{"paper_id":"ad2acc34-2865-4013-9379-5c721c60796e","body_text":"Aloe  L. is the largest genus in the Xanthorrhoeaceae family, and geographically restricted to Old World [ 1 ]. Its name derives from the Arabic word “Alloeh”, meaning “shining bitter substance” [ 2 ].  Aloe  plants have been widely known and used for centuries as topical and oral therapeutic agent due to their health, beauty, medicinal, and skin care properties [ 2 , 3 ].  Aloe arborescens ,  Aloe barbadensis ,  Aloe ferox , and  Aloe vera  are among the well-investigated  Aloe  species. Presently, they account among the most economically important medicinal plants and are commonly used in primary health treatment, where they play a pivotal role in the treatment of various types of diseases, through biochemical and molecular pathway modulation [ 4 ]. Indeed,  Aloe  plants have been reported for multiple biological properties, including antibacterial and antimicrobial, antitumor, anti-inflammatory, anti-arthritic, anti-rheumatoid, anticancer, and antidiabetic activities, detoxification, treating constipation, flushing out toxins and wastes from the body, promoting digestion (on gastrointestinal disorders treatment), and reducing illnesses likelihood, as well as for immune system deficiencies [ 3 , 4 , 5 , 6 , 7 , 8 , 9 ]. Besides, several clinical trials validated the use of  Aloe  gel against several diseases, such as diabetes or antihyperglycemic, wound, and burn-healing topical agents [ 5 , 10 , 11 ]. The main commercial forms used in the food, cosmetics, and pharmaceutical industries [ 12 , 13 ] consisting of the plant’s fleshy leaves, gel, and latex are pills, jellies, creams, drinks, liquid, sprays, ointments, and lotions [ 3 , 13 ]. The nutrients and phytochemicals that have been identified in  Aloe  plants include vitamins, minerals, enzymes, simple and complex polysaccharides, fatty acids, indoles, alkanes, pyrimidines, aldehydes, dicarboxylic acids, ketones, phenolic compounds, phytosterols, and alkaloids with potential biological and toxicological activities [ 3 , 6 , 9 ]. On a side note,  A. vera  gel coating has demonstrated postharvest preservative and stabilizing effects in some foods and beverages, and for instance, table grapes [ 14 , 15 ]. However,  A. vera  administration is often related to kidney dysfunction, diarrhea, electrolyte imbalance, and conventional drug interactions. In addition,  Aloe  topical application has been associated with erythema, contact dermatitis episodes, and phototoxicity [ 3 ].  Aloe  fleshy leaves, gel, and latex are the base of the main commercial forms of aloe products (e.g., pills, jellies, creams, drinks, liquids, sprays, ointments, and lotions) [ 3 , 13 ].\nIn view of the ethnopharmacological uses and pharmacological properties of  Aloe  plants, this review narratively summarized the botany, phytochemical composition, ethnobotanical uses, food preservative effects, and preclinical and clinical efficacy of  Aloe  plants to provide further direction for its utilization in human welfare.\n\nAloe  genus is a monoecious, perennial species with shallow roots.  Aloe  species are mostly inhabitants of arid climates, and are widely distributed in Africa, India, and other arid areas. The largest number of  Aloe  species is approximately 140, and most are found in South Africa [ 1 ]. However, they could also be grown in subtropical summer rainfall and winter rainfall regions [ 16 ]. The major factors restraining genus distribution are fire tolerance, soil moisture, rainfall, and temperature.  Aloe  species occupy a wide diversity of habitats, varying from sea level to altitudes of 2700 m, and from closed-canopy forests to desert shrub lands. However, some individual species showed particular geography restriction [ 17 ], although seed pollinator morphology and specificity also effect  Aloe  species distribution [ 18 ].\nAloe  species can be cultivated in a wide range of soils. The most desirable soil texture is a loamy mixture with pH ranging from 7.0 to 8.5. Nonetheless, some species, such as  Aloe commixta ,  Aloe haemanthifolia ,  Aloe plicatilis , and most grass aloe species prefer to grow in acidic soils [ 19 ]. Temperature requirements for  Aloe  growth range from 4 °C to 21 °C; however, this cold tolerant genus could maintain its growth even below 4 °C. Under optimal environmental conditions,  Aloe  species can reach heights of up to 61–99 cm. Regarding flowering duration, it may vary from May to June [ 19 ]. Some  Aloe  species appeared to react to soil mineral composition and produce differently colored flower varieties [ 20 ]. Although few  Aloe  genus species require specific pH and mineral composition, the majority of them can thrive in almost any soil type, and require little or no soil preparation before soil planting [ 21 , 22 ]. The ideal soil for establishment after  Aloe  species nursing is well-drained sandy soil or rocky sites. The adult plants of some  Aloe  species (e.g.,  A. greatheadii  and  A. secundiflora ) can act as nurse plants themselves, colonizing, and ameliorating harsh conditions in sparsely vegetated or completely denuded landscapes [ 23 , 24 ].  Aloe  species could also be effective agents for degraded rangeland treatment because of their mate (similar to root systems), which increases soil binding and stabilization [ 23 ].\n\nVarious species of  Aloe  genus plants have been proven to exert a diverse range of pharmacological activities. In addition, aloes are now considered to be a very interesting source of bioactive compounds [ 25 ]. Concurrently, some of the pharmacological activities reported, which support the traditional usages of each aloe species, have also been attributed to the presence of a wide range of phytoconstituents.\nAloe  plant leaves, which are the most commonly used medicinal parts, are heterogeneous and can be divided into three major parts, namely: (i) the outer green epidermis, primarily consisting of structural components; (ii) the outer pulp region below the epidermis, consisting of vascular bundles where the bitter latex or sap is derived; and (iii) the inner leaf pulp, consisting of aloe gel and containing parenchyma cells. Regarding the different composition of these leaf portions, they are also likely to have distinct classes of bioactive compounds, which is believed to contribute to the different biological properties of leaves [ 26 ]. Briefly, the outer green epidermis has been reported to contain anthraquinones, pre-anthraquinones, and their corresponding glycosides [ 27 ], while the outer pulp region below the epidermis contains latex that predominantly consists of phenolic compounds, including anthraquinones and pre-anthraquinones, anthrones, chromones, coumarins, flavonoids, and pyrones [ 28 ]. On the other hand, the inner leaf pulp contains a high acemannan polysaccharide content, as well as a wide variety of phytochemicals, among them alkaloids, anthraquinones, anthrones, chromones, coumarins, flavonoids, and pyrones [ 27 , 29 ]. Pulp also contains vitamins, minerals, enzymes, and proteins [ 3 ]. Indeed, many authors believe that the various biological activities related to different  Aloe  species should be ascribed to a synergistic action between several compounds rather than a single chemical substance [ 29 , 30 ].\nBased on our literature search, various review articles that discuss  Aloe  phytochemical content are mostly focused on  Aloe vera  [ 2 , 31 ], with only Cock [ 26 ] providing a review article on the  Aloe  genus, which mainly focused on the close relationship between plants phytoconstituents and antioxidant capacity. However, most of the phytochemicals identified in the genus  Aloe  were not properly associated with the respective  Aloe  species from which they were isolated. Moreover, not all of the phytochemicals were completely cited by Cock [ 26 ], although he did cite all of the reports made by original authors. Prior to presenting our own report on  Aloe  species phytoconstituents, we take this opportunity to acknowledge the work of Cock [ 26 ], highlighting both bioactive compounds generally isolated and identified from the  Aloe  genus. Indeed, in his article, Cock [ 26 ] divided the discussion on  Aloe  genus phytoconstituents into several significant classes, namely anthraquinones, anthrones, chromones, coumarins, pyrans, pyrones, alkaloids, benzene, naphthalene, and furan derivatives.\nVarious types of anthraquinones were also reported to be presented in  Aloe  species leaves, such as aloesaponarin, chrysophanol, and its progenitor prechrysophanol, desoxyerythrolaccin, 1,5-dihydroxy-3-hydroxy methylanthraquinone, helminthosporin, 7-hydroxyaloe emodin, isoxanthorin, laccaic acid- d -methyl ester, nataloe emodin, and its ester nataloe emodin-8-methyl ester, aloechrysone, and aloesaponol. In addition,  Aloe  anthraquinones are often present as  O -glycosides, such as aloe emodin-11- O -rhamnoside, nataloe emodin-2- O -glucoside, aloesaponol-6- O -glucoside, aloesaponol-8- O -glucoside, and aloesaponol- O -methyl-4- O -glucoside. Other than that, leaf exudates from several  Aloe  species, such as  Aloe saponaria  Haw. and  Aloe elgonica  Bullock were also reported to contain anthraquinone dimers, such as asphodelin and bianthracene, and its glycosylated dimer derivative elgonicardine [ 26 ]. The hydroxylated derivatives of aloin, such as 5-hydroxyaloin A, 7-hydroxyaloin, and 10-hydroxyaloin B, as well as their acetate derivatives, 5-hydroxyaloin A 6′- O -acetate, 7-hydroxyaloin-6′- O -monoacetate, and 10-hydroxyaloin-6- O -acetate have also been identified. Except for  A. saponaria  and  A. elgonica , no other  Aloe  species were reported in the discussion, despite the numerous mentioned anthraquinones isolated from this plant.\nWithin the anthrones class, barbaloin, which referred to  C -glycosyl anthrone isomers aloin A and aloin B, was the first  Aloe  anthrone to be isolated and can be detected in nearly 100  Aloe  species, including  A. vera  and  A. ferox  leaves [ 26 ]. In addition, homonataloin and nataloin were consequently isolated from  A. marlothii  Berger. Other anthrones, some of them containing additional rhamnose, cinnamic, or coumaroyl moieties, have also been isolated from various  Aloe  species leaves, which include aloinoside, aloe barbendol, aloe-emodin anthrone, chrysophanolanthrone, aloe emodin-10-C-rhamnoside, 8- O -methyl-7-hydroxyaloin, 6′- O -cinnamoyl-8- O -methyl-7-hydroxyaloin, 6′- O - p -coumaroyl-7-hydroxyaloin, 7-hydroxyaloin-4′,6′- O -diacetate, 6′- O -cinnamoyl-5-hydroxyaloin A, microstigmin A, deacetyllittoraloin, littoraloin, littoraloside, microdontin, and homonataloside [ 26 ].\nAnother phytochemical group, known as chromones, are the most abundant phenolic compound class in  Aloe  leaves [ 26 ]. Aloeresin A and aloesin (previously known as aloeresin B), as well as 2′- p - O -methlcoumaroylaloesin, have been classified as some of the most commonly found  Aloe  leaf constituents. In addition, several isomeric and substituted isomeric forms, including aloeresin C, aloeresin D, aloeresin E, aloeresin F, iso-aloeresin A, and iso-aloeresin D have also been reported. These were later followed by the successful identification of a wide variety of chromones from distinct  Aloe  species, including methylated derivatives, such as 7- O -methylaloesin, 7- O -methylaloesinol, 7- O -methylaloeresin A, 8-[ C - B - D -[2- O -( E )-cinnamoyl]glucopyranosyl]-2-[( R )-2-hydroxypropyl]-7-methoxy-5-methylchromone, 8- C -glycosyl-7- O -methylaloediol, 8- C -glycosyl-7- O -methyl- S -aloesol, 2-acetonyl-7-hydroxy-8-(2-furanonyl)-7-hydroxy-5-methylchromone, and 7-hydroxy-2,5-dimethylchromone. In addition to these, chromones containing cinnamic and coumaroyl moieties, such as 8- C -glycosyl-(2′- O -cinnamoyl)-7- O -methyl-aloediol, 8,2-acetonyl-8-(2′,6′-di- O , O -coumaroyl)-glucopyranosyl-7-hydroxy-5-methylchromone, 2-acetonyl-8-(2′,cinnamoyl)-glucopyranosyl-7-hydroxy-5-methylchromone, 6′- O -coumaroylaloesin, and 2′- p - O -methlcoumaroylaloesin have also been identified [ 26 ]. Unfortunately, for any of the chromones cited, not one specific  Aloe  species was excerpted.\nFeralolide and dihydroisocoumarin glycoside are coumarins that have been identified in  A. ferox  and  A. hildebrandtii  [ 26 ], respectively. Pyrans (e.g., bisbenzopyran) and pyrones (e.g., aloenin, aloenin aglycone, aloenin acetal, aloenin B, and aloe-2″- p - O -coumaroyl ester) have also been identified in several  Aloe  species leaf exudates [ 26 ]. Except for  A. ferox  and  A. hildebrandtii , the other  Aloe  species, from which coumarins, pyrans, and pyrones were isolated, were not revealed.\nSeveral alkaloids have been isolated from several  Aloe  species [ 26 ].  N -methyltyramine and  O , N -dimethyltyramine have been reported as being the most common  Aloe  alkaloids, whereas γ-coniceine was only found in a few species. In contrast, coniine has only been reported to occur in one species,  Aloe viguieri  Perrier [ 26 ]. Except for  A. viguieri , the other  Aloe  species, from which the alkaloids were identified, were not quoted.\nSeveral benzene, naphthalene, and furan-based bioactive compounds have also been identified as common constituents of  Aloe  plants [ 26 ]. Among the identified benzene derivatives are protocatechuic acid, methyl- p -coumarate, and pluridone, which have been identified in several  Aloes . Fluridone, which is the only sulfur derivative containing the benzene derivative identified from  Aloe  plants, was identified from  A. pluridens  Haw. Various naphthalene derivatives, namely aglycone isoeleutherol, isoeleutherol-5- O -glucoside, feroxidin, feroxidin A, feroxidin B, and plicataloside, have been isolated from  Aloe  plants, with aglycone isoeleutherol and isoeleutherol-5- O -glucoside specifically detected from  Aloes  roots portions. In addition to these, several of the naphthalene compounds, such as 5-OH-3-methylnaphto[2,3-c]furan-4(1 H )-one, 3-methylnaphto[2,3-c]furan-4(9 H )-one, and 3-methylnaphto[2,3-c]furan-4,9-dione have been found to contain a furan moiety [ 26 ]. Except for  A. pluridens , the other  Aloe  species, from which the benzene, naphthalene, and furan derivatives were identified, were not named.\nSeveral flavonoids were also detected in  Aloe  plants, with only naringenin, apigenin, isovitexin, and dihydro-isorhamnetin cited as being the major ones [ 26 ]. Nevertheless, the actual  Aloe  plants, from which flavonoids have been isolated, were not cited.\nPhytosterols, such as cholesterol, campesterol, β-sitosterol, and lupeol together with their glucosides have also been cited to be present in  Aloe  leaves [ 26 ]. However, the actual  Aloe  plants, from which the sterols were isolated, were not mentioned.\nAlthough a number of other secondary metabolites were claimed to be present in  Aloe  leaves, Cock [ 26 ] only specifically cited the presence of tannins. Moreover, the actual  Aloe  plants, from which the secondary metabolites were isolated, were not indicated.\nPolysaccharides are the non-phenolic components that are present in high abundance in  Aloe  leaf gels [ 26 ]. However, their presence within  Aloe  leaves are variable, and there is huge diversity among the different individual  Aloes . According to Femenia et al. [ 32 ], polysaccharides composition and concentration also change with seasonal variations and growing environment conditions. Although several polysaccharides were detected in  Aloe  species, Cock [ 26 ] only mentioned acemannan (a long chain polymer of β (1→4) linked galactomannan saccharides). Unfortunately, the exact species from which polysaccharides were isolated were not mentioned.\nCock [ 26 ] also cited the presence of various vitamins, namely vitamin C (ascorbic acid), vitamin B1 (thiamine), vitamin B2 (riboflavin), vitamin B6 (pyridoxal phosphate), vitamin B12 (cyanocobalamin), and vitamin E (α-tocopherol) in unspecified  Aloe  leaf gels.\nMoreover, Cock [ 26 ] also mentioned that leaf gels from several  Aloe  species contain inorganic minerals, including magnesium, zinc, calcium, potassium, sodium, iron, phosphorous, manganese, copper, and molybdenum. However, species were not mentioned.\nCock [ 26 ] claimed that his review article on  Aloe  genus is not a comprehensive report. This claim was further supported by the lack of information with regard to  Aloe ’ s  phytoconstituents, such as no information on: (i) types of  Aloe  parts or extracts used to isolate bioactive compound(s); (ii)  Aloe  plants species used in the isolation of bioactive compound(s); and (iii) the location from which  Aloe  plants were collected, to name a few. Moreover, several phytoconstituents that were reported in some articles were not mentioned at all by Cock [ 26 ]. Taking these issues into consideration, the present review was performed with an attempt to provide more detail with regard to  Aloe  genus-isolated phytoconstituents.\nMany reports have been published concerning  Aloe  phytochemicals. Due to their economic and medical importance,  Aloe  phytoconstituents, especially those from the  A. arborescens ,  A. barbadensis ,  A. ferox , and  A. vera  species, have been intensively investigated. The summary of phytochemical studies on  Aloe  species, including plant parts, principal constituents, and corresponding literatures is represented in  Table 1 ,  Table 2 ,  Table 3 ,  Table 4  and  Table 5 , according to investigated extraction methods. In most cases, leaf  Aloe  plants exudates were collected and used for phytoconstituent investigation purposes. Some researchers used fresh plant materials.  Aloe  plant extract chemical compositions were analyzed by solvent fractionation, column chromatography, preparative thin-layer chromatography (TLC), high-performance liquid chromatography (HPLC), HPLC–mass spectrometry (MS), and gas chromatography–mass spectrometry (GC–MS). In general, around 20 chemical constituents, including aloin A, aloin B, aloinoside A, and aloinoside B, aloesin, plicataloside, isovitexin, and aloe emodin were reported as principal  Aloe  species components.\nThe chemical structure of main  Aloe  species phytochemicals is represented in  Figure 1 .\n\nThis section summarizes the traditional use of  Aloe  plants for treating various ailments from different parts of the world. Among 446  Aloe  species, belonging to the Xanthorrhoeaceae family,  Aloe vera  (L.) Burm. f., also known as  A. barbadensis  Mill., is the most commonly used species in traditional medicine in Indian subcontinent. Other species reported to be used are  A. arborescens ,  A. littoralis , and  A. pirottae . Akaberi et al. [ 95 ] provided the most recent review of the  Aloe  species’ therapeutic effects in traditional and modern medicine. Gastrointestinal activities, hepatoprotective properties, and beneficial effects against skin problems, such as wounds, injuries, and infective diseases, are among the most frequently reported  Aloe  species properties [ 95 ].\nMost of the  Aloe  plants usage reports are documented from Asia (India and Nepal), and a few exist from other parts of the world, mostly from Africa through ethnomedicine studies.  A. vera  is commonly called Ghiu kumari in India and Nepal.\nAs previously introduced, the most widely used part of  Aloe  is the leaf. The most commonly used part is leaf gel, which is effective for treating cuts and burns, gastrointestinal disorders, and maintaining blood pressure. Jelly obtained from the leaf is used to treat cuts, burns, and other skin complaints in the Indian subcontinent [ 96 , 97 , 98 , 99 , 100 ]. It is also eaten by people suffering from high blood pressure, gastritis, and stomach-related diseases [ 96 ]. In Sikkim-India,  A. vera  is used for its antihyperglycemic effect [ 101 ]. The  A. vera  purgative property is also documented in the Sikkim government database [ 99 ].\nSushen et al. [ 102 ] have documented the extensive uses of  A. vera  in the traditional health care system in India. They report that juice preparation is used for sunstroke; leaf gel is useful to treat gastric intestinal problems, such as indigestion, candidiasis, constipation, diarrhea, colitis, and digestive issue relief, such as heartburn and irritable bowel syndrome. Chewing  A. vera  leaf or massaging on gums with an index finger gently using its gel will cure bleeding gums and toothache; it can also be used to treat menstrual cramps; gel mixed with a pinch of patika (alum, potassium aluminum sulfate) and put on a cloth can be put on eyes to cure eye problems. Leaf gel has several use reports. Leaf gel powder is mixed with raw turmeric juice, and a few drops is put into the ear and nose three to four times a day to reduce infections. Leaf gels are also mixed with a pinch of dried turmeric powder, a pinch of powdered dried seeds of bitter gourd, and a little sugar to make it sweet, and taken two times a day. It is also mixed with a few drops of raw garlic juice and a pinch of dried turmeric powder to make a homogeneous paste, and two to three spoons are taken three times a day for diarrhea; gel is used for uterine cancer and cervical cancer; it is also used for constipation, rectal infection, and ulcers. Several other leaf gel uses have been documented, and some other  A. vera  uses include: lowering cholesterol in blood; for miscarriage and anti-abortive treatment; treating arthritis, joint pains, body pains, and muscle pain; increasing potentiality and sperm count; treating heart disease, depression, stress release, anger management, stability management, and so on. Also reported is for cuts and wounds, white hair reduction, hair fall, ticks, mites, dandruff, baldness, grey hair, dry split hair, etc. In India, it is also used for piles, lower abdomen pain, migraine, breast pain, tuberculosis, stomach ulcers, heartburn, indigestion, dysentery, sexually transmitted infections, endometriosis, fibroids presence in uterus, gonorrhea, etc. Pimples and achiness are also treated with  A. vera . Protection from ultraviolet (UV) irradiation, post-operative care, stretch marks, learning and memory improvement, cancer, diabetes, hepatitis, AIDS, and weight loss are other uses of  Aloe  leaf gel.\nLeaves are also chewed to cure skin and uterine disorders and treat jaundice in Nepal [ 103 , 104 , 105 ]. In India, leaves are used for stomachic, tonic, purgative and anthelmintic purposes; juice is put on the head in high fever to reduce body temperature [ 106 ]. Leaf juice is also applied on fresh burns. Juice is also given to diabetic patients and for urinal troubles [ 105 ]. The Limboo tribe of Sikkim use leaf juice on burnt wounds, which also helps cool pain [ 107 ]. Whole plant juice, pulp, or paste is used as a remedy in intestinal worms in children, as well as a hepatic stimulant, stomachic, and liver and spleen enlargement [ 108 ].\nLeaf juice is given for a stomachache and as a tonic [ 109 ]. Juice is also commonly used in case of constipation [ 109 , 110 ]. Leaf juice given in case of indigestion, hemorrhoids, and peptic ulcers [ 111 ]. Juice is also used in rheumatic pains, fever, jaundice, menstrual disorder, suppression, and gonorrhea, and juice is applied locally for burns and skin irritation [ 101 ].\nLeaf pulp is also taken to treat dysentery [ 112 ] and other stomach disorders in Nepal [ 113 ]. It is used to cure burn wounds and regulate menstruation, constipation, and ascariasis [ 99 ]. The use of  A. vera  as an emmenagogue is also reported from Panchthar Nepal [ 97 ]. Leaf is used in catarrh, cough, and overheating problems [ 114 ], and  Aloe  species leaf gel, including  A. vera , is also used for diabetes [ 115 , 116 , 117 ].\nA. vera  is also used to treat fresh and bleeding or infected wounds, burns, eczema, and dandruff in Mexico [ 118 ]. It is also used to treat HIV in South Africa [ 119 , 120 ]. Pulp and juice obtained from  A. arborescens  is used on dermatosis and against articular pains in Italy [ 121 ].\nA. littoralis  is used to treat  Bilharzia  in the traditional health care system of Namibia [ 122 ]. Another species reported to be used in traditional medicine from Africa is  A. pirottae , but its detailed use is not mentioned [ 123 ].\n\nNowadays, the food industry looks for new sources of natural compounds with different properties [ 124 , 125 , 126 , 127 , 128 , 129 , 130 , 131 , 132 ]. It is considered that, through the plant kingdom,  Aloe  species, especially  A. vera , is one of the most applied medical plants worldwide [ 133 ]. These plants have been used in folk medicine from different therapeutic purposes, due to its purgative effect, for skin disorder healing and beauty treatments. Numerous reports show that the  Aloe  leaf possesses a wild spectrum of activities, including, anticancer, antioxidant, anti-inflammatory, immunomodulatory, hepatoprotective, antiulcer, and antidiabetic as well as found application in dermatology, to treat radiation-caused skin conditions and in gastroenterology or gynecology as a bactericidal, viricidal, or fungicidal. The widespread use of this plant is the result,  inter alia , of the content of approximately 200 biologically active compounds, as previously introduced, characterized by a synergistic effect. In cosmetology,  Aloe  species are used in creams, soaps, and shampoos production. Not least, industrial applications of these plants include beverages, ice cream, food supplements, and others [ 16 , 30 ]. Despite the industrial use of plants belonging to the  Aloe  genus, previous studies of antimicrobial properties are mainly directed toward isolates obtained from human skin. Undoubtedly, these plants are characterized by their natural antimicrobial potential, and their use in food production.\n\nIn vitro studies have shown that  A. vera  is characterized by activity against Gram-negative and Gram-positive bacteria. Petroleum ether, dichloromethane, and water extracts of upper stem, young bark, mature bark, leaves and roots of  A. barberae  from South Africa were evaluated for their antimicrobial activity against Gram-positive ( Bacillus subtilis ,  Staphylococcus aureus ) and Gram-negative ( Escherichia coli ,  Klebsiella pneumoniae ) bacteria [ 71 ]. Petroleum ether and dichloromethane extracts of mature bark, leaves, and roots exhibited significant activity against all bacteria, with minimum inhibitory concentrations (MIC) ranging from 0.195 mg/mL to 1.56 mg/mL. In another study, the authors evaluated the antimicrobial properties and phenolic contents of medicinal plants used by the Venda people. It was found that  A. chabaudii  roots exhibited low levels of phenolic compounds as also weak antimicrobial activities against  B. subtilis ,  S. aureus E. coli , and  K. pneumoniae  [ 134 ]. Generally, it is believed that  A. vera  acetone extracts exhibit stronger activity against  S. aureus ,  Streptococcus pyogenes ,  Pseudomonas aeruginosa , and  E. coli  compared to aqueous or ethanol extracts. Lawrence et al. [ 67 ] documented the antibacterial property of  A. vera  gel extracted using different solvents. They found differences between the extract activities against  S. aureus ,  S. pyogenes ,  B. subtilis ,  E. coli ,  Ps. aeruginosa ,  K. pneumoniae ,  Salmonella typhi , and  Bacillus cereus . In general, the results of the agar well diffusion method showed that the inhibition zones ranged from 12.66 mm ( E. coli ) to 23.33 mm ( B. cereus ). On the other hand, methanol extract exhibited the strongest activity against  B. cereus  (22.33 mm) followed by  S. pyogenes  (15 mm), and the least for  S. typhi  (9.66 mm). Finally, according the results obtained in their research, acetone extract gave the lowest values of inhibition zones, ranging from 6.00 mm ( E. coli ) to 7.33 mm ( S. pyogenes ). What is more, no differences between acetone and controls were noted for  P. aeruginosa  and  S. typhi . In general, it is well noted that plant extracts show greater antibacterial activity against Gram-positive than Gram-negative bacteria [ 135 ]. Also, in the study of Ferro et al. [ 136 ], Gram-positive bacterium  S. pyogenes  was more susceptible to  A. vera  gel than Gram-negative  Shigella flexneri . The effective growth inhibition was achieved with aloe concentrations of more than 100 mg/mL for  S. flexneri  and 25 mg/mL for  Streptococcus pyogenes . The authors found that sap extract was more effective than leaf extract against  E. coli ,  B. subtilis ,  S. aureus , and  P. aeruginosa . Sap water extract (100 µg/mL) showed the strongest inhibitory properties against  B. subtilis  and  P. aeruginosa . Jonson et al. [ 137 ] studied antibacterial activity of leaf extract from  Aloe vera ,  Datura stromonium ,  Pongamia pinnata ,  Lantona camara , and  Calotropis procera . They found that from all of the tested alcoholic and aqueous extracts,  A. vera  showed the strongest activity against  E. coli  and  S. aureus . What is more, aloe polysaccharides were used in tea tree or palmarosa essential oil combinations as a natural strategy against  Xanthomonas fragariae  (bacterial angular leaf spot disease, which is an important strawberry disease responsible for significant yield losses) [ 138 ]. It was found that these preparations reduce disease severity and activate plant defenses, and that  Aloe  polysaccharides alone reduced  X. fragariae  growth by up to 44%. The authors concluded that tested essential oils and polysaccharides from aloe can be considered as potential agents for plant disease control and could play a significant role in product formulation for strawberry leaf spot control. The essential oils into aloe polysaccharide preparation contributed more effectively to reduce the disease severity, either by its antimicrobial activity or by the plants’ defense mechanism activation. The antimicrobial activities of  A. vera  juice were tested in the work of Alemda and Agaoglu [ 139 ].\nIn the work of Dharajiya et al. [ 140 ],  A. barbadensis  leaf extract antibacterial activity was evaluated against  E. coli ,  P. aeruginosa ,  B. cereus , and  Serratia marcescens . They found maximum inhibitory activities against  S. marcescens  (hexane extract) and  B. cereus  (methanol extract). In general, the authors noted that methanol extract showed an inhibitory effect against all of the tested bacterial strains, while ethyl acetate extract showed no inhibitory activities. Similar results of antibacterial activity against  E. coli ,  B. subtilis ,  S. epidermidis , and  S sonnei  were obtained by Coopoosamy and Magwa [ 79 ]. They found that the MIC of emodin and aloin A ranged from 62.5 mg/mL against  B. subtilis  and  E. coli  to 250 mg/mL against  S. epidermidis  and  S. sonnei  [ 79 , 141 ].  A. vera  sap and leaf extracts were investigated for antimicrobial properties by Abakar et al. [ 142 ]. The disc diffusion method revealed that juice inhibits  Mycobacterium smegmatis ,  K. pneumoniae ,  Enterococcus faecalis ,  Micrococcus luteus , and  Bacillus sphericus  growth. They concluded that the juice obtained from aloe can be used for antimicrobial activity in cosmetics, pharmacy, and the food industry.  S. mutans  growth inhibition was subject of investigation by Jain et al. [ 143 ]. The authors used crude, organic solvent-based and aqueous extracts from  A. vera  leaves, neem ( Azadirachta indica ), tulsi ( Ocimum tenuiflorum ), amla fruits ( Emblica officinalis ), garlic cloves ( Allium sativum ), and ginger rhizomes ( Zingiber officinale ). The MIC results determined by the agar well diffusion method showed that 25 mg/mL of organic solvents extract inhibited tested bacterium growth. On the other hand, the MIC values for aqueous extract equaled 50 mg/mL. It is worth noting that the organic solvent extract activity from aloe was comparable to garlic and alma. The antibacterial activity of polysaccharides from  Aloe  spp. has been attributed to phagocytic leucocytes stimulation to destroy bacteria.  A. vera  compounds with particular antimicrobial activity are saponins, acemannan, and anthraquinones derivatives [ 144 ].  Aloe -emodin effect on  Helicobacter pylori  N-acetyltransferase activity showed dose-dependent inhibition [ 145 ]. Cellini et al. [ 146 ] attributed  H. pylori  inhibition to the polysaccharides that are present in gel, exhibiting an anti-adhesive effect.  A. vera  aqueous extract effect on  E. coli  morphological and physiological properties were described by Kargaran et al. [ 147 ]. They found that the aloe extract MIC value equaled 2.23 mg/mL. What is more, another aloe plant— A. ferox —is known to show activity against wild bacteria.  A. ferox -isolated compounds (aloe emodin, chrysophanol, and aloin) activity were investigated by Kambizi et al. [ 56 ]. They found that aloe emodin and alonin A exhibit inhibitory activities against  B. cereus ,  B. subtilis ,  S. aureus ,  E. coli ,  Staphylococcus epidermidis , and  Shigella sonnei . Chrysophanol was characterized by weaker antibacterial action, inhibiting  B. subtilis ,  S. epidermidis , and  E. coli  strains. On the other hand, pyrocatechol, 2-vinyl crotonaldehyde, ascorbic acid,  p -coumaric acid, and cinnamic acid isolated from plant have shown a wide spectrum of antibacterial activity [ 148 ].\nRadi et al. [ 149 ] evaluated the effect of gelatin coating incorporated with  A. vera  gel and green and black tea extracts on the physicochemical, microbial, and sensorial properties of fresh-cut oranges stored at 4 °C for 17 days. They noted that coating materials with gelatin incorporated with  A. vera  and green tea extracts successfully retarded microbial growth and extended shelf life during storage. Chen et al. [ 150 ] showed that the antimicrobial activities of composite films increased as the amount of aloe gel powder used in composite films increased. The average area of inhibitory zones of  Citrobacter freundii ,  Escherichia coli ,  Enterobacter aerogenes ,  Serratia marcescens ,  S. aureus , and  B. cereus  for films with aloe⁄gelatin (1:4) and aloe⁄gelatin (4:1) compositions were 1.63 ÷ 2.38 mm and 3.82 ÷ 4.80 mm, respectively.  A. vera  potential application as an edible coating was provided by Benítez et al. [ 151 ]. They found significant microbial population reduction in fresh-cut kiwifruit treated with 15%  A. vera  during 11 days of storage. The results at the last day of analysis were 4.97 log CFU (colony-forming units)/g for 15% aloe and 5.75 log CFU/g for control. What is more, they found that  A. vera  can be used as a coating to both extend postharvest shelf life and maintain product sensory properties through the storage period [ 152 ]. Similar results were obtained by Sogvar et al. [ 153 ] on aloe coatings that have been used to maintain the quality of postharvest strawberry fruits. The application of aloe and 5% of ascorbic acid reduced the mesophilic bacteria population from 3.63 log CFU/g for control to 3.13 log CFU/g.\nAloe  species’ availability, safety, and bioactivity make them an interesting alternative as control agent used in preharvest and postharvest fungal diseases of fruits and vegetables. Studies showed that  A. vera  reduces  Penicillium ,  Botrytis , and  Alternaria  spore survival by up to 20% [ 154 ], as well as inhibits  Fusarium ,  Rhizoctonia , and  Colleotrichum  mycelium growth by up to 38% [ 155 ]. What is more, in the work of Castillo et al. [ 156 ], it was reported that  A. vera  gel inhibits  Penicillium digitatum  and  Botrytis cinerea .  A. vera  gel was analyzed as an antifungal agent against six fungi causing plant diseases:  Fusarium oxysporum ,  Alternaria alternate ,  Colletotrichum gloeosporioides ,  Bipolaris spicifera ,  Curvularia hawaiiensis , and  Botryotinia fuckeliana . It was found that gel was most effective against  F. oxysporum  [ 157 ]. The authors found that films with the highest  A. vera  ratio were effective in controlling fungal contamination. Nectarine treated with  A. vera  gel alone, or with the addition of thymol, inhibited the fungal growth of inoculated  Rhizopus stolonifer ,  Botrytis cinerea , and  Penicillium digitatum . Therefore,  Aloe  application led to a significantly lower fungal infection (two to threefold) than in non-treated nectarines. It was found that the addition of thymol did not generally improve the aloe gel efficacy to reduce infection [ 158 ]. In the work of Vieira et al. [ 159 ], chitosan and  A. vera  liquid fraction coatings presented the best uniformly coat blueberry surface characteristics. The authors showed that the microbiological growth of  Botrytis cinerea  was reduced by 42% in coated blueberries after 25 days. Overall, coatings extended the shelf life of blueberries for five days (compared with the control sample), demonstrating that a chitosan and  A. vera  combination shows high potential in expanding shelf life. The antifungal activity from eight  Aloe  species gels ( A. arborescens  Mill.,  A. aristata  Haw.,  A. claviflora  Strydenburg,  A. ferox  Mill.,  A. mitriformis  Mill.,  A. saponaria  Ait.,  A. striata  Haw., and  A. vera  L.) were evaluated against  B. cinerea ,  P. digitatum ,  Penicillium expansum , and  P. italicum  [ 160 ]. The authors concluded that antifungal activity was higher for  A. ferox ,  A. mitriformis , and  A. saponaria  than  A. vera , which can be correlated with aloin content. Nidiry et al. [ 161 ] have also reported that aloin and aloe-emodin from  A. vera  could be important antifungal moieties. Guillén et al. [ 160 ] reported that  A. arborescens  could be even more effective than  A. vera  gel for preservative purposes in edible coatings, affecting climacteric fruit quality.  A. vera  and green tea extracts used in gelatin-based edible coating for fresh-cut oranges reduced the total fungal count [ 149 ].  A. vera  coatings effectively controlled or inhibited fungal populations during strawberry storage, and therefore was considered an effective natural agent against bacteria and yeasts-associated postharvest diseases [ 153 ]. The total number of yeasts and molds obtained for fresh-cut kiwi samples coated with aloe were about 10 times lower than for the control sample. Additionally, an  A. vera  coating maintained fruit firmness, and prevented ascorbic acid losses and yellowing due to ripening. In contrast, fruit treated with an alginate-based coating had higher microorganism counts than the control samples [ 152 ]. Benítez et al. [ 151 ] studied the efficacy of an edible coating based on  A. vera  gel at different concentrations: 1% ( v / v ), 5% ( v / v ), and 15% ( v / v ). They found that an aloe coating reduced respiration rates and microbial spoilage in sliced kiwi fruit. After seven days of storage, yeast and molds load dropped by approximately one logarithmic unit for slices coated with 15% and 5%. Similar findings were stated by Martínez-Romero et al. [ 162 ]. In their work, an  A. vera  gel coating maintained ready-to-eat pomegranate arils. The authors used different aloe concentrations, as well as aloe plus ascorbic acid, and found that  A. vera  treatments led to significantly lower counts of both mesophilic aerobics, and yeasts and molds. What is more, aloe coatings led to firmness retention and increased the total anthocyanins and total phenolics levels. The antifungal effects of 2% ( w / v )  A. vera  were also evaluated against  Colletotrichum gloeosporioides  on avocado fruit by Bill et al. [ 163 ]. According to the results, aloe showed weaker properties than thyme oil with chitosan combination.  A. vera  gel was evaluated for their antifungal activity in the study of Sitara et al. [ 164 ]. The authors noted that 0.35% of tested gel completely inhibited plant pathogenic fungal growth for  Alternaria alternata  and  Drechslera hawaiensis . In comparison with the control medium, significant growth inhibition was also found in  Aspergillus niger ,  A. flavus , and  P. digitatum . Hassanpour [ 165 ] found that coating materials containing  A. vera  gel reduce fungal decay of raspberry fruits ( Rubus  spp.) during eight days’ incubation at 4 °C, without differences between different gel levels. Functional films with  A. vera  gel were noted to increase different papaya fruits ( Carica papaya ) shelf life during 15 days of storage [ 166 ]. The authors found that  A. vera  gel significantly inhibited papaya fruits ripping. Generally,  A. vera  use as a functional film component was also noted for grapes ( Vitis vinifera ) [ 167 ], pineapple ( Ananas comosus ) [ 168 ], or tomatoes [ 169 ] as well as cherry tomatoes [ 158 ].\nIn other studies,  A. ferox  methanol extract showed activity against  Candida albicans  with an MIC value of 20 mg/mL, while the MIC of aloin used against these yeasts equaled 5 mg/mL. On the other hand,  Aloe ferox  acetone extract was shown to exhibit fungicidal activity at 10 mg/mL against five fungal strains:  Alternaria alternata ,  A. niger ,  Mucor hiemalis ,  Penicillium notatum , and  Schizophyllum commune  [ 170 ]. Abakar et al. [ 142 ] noted that sap water extract and  A. vera  leaves exhibited intermediate susceptibility against  A. niger  and  C. albicans . Subramanian et al. [ 171 ] found that  A. vera  leaf gel ethanol extract showed strong activity against  Aspergillus fumigatus ,  A. niger ,  A. flavus ,  Fusarium oxysporum , and  Microsporum canis . On the other hand,  A. vera  fresh leaf hydroalcoholic extract showed antifungal activity against  Botrytis gladiolorum ,  Fusarium oxysporum , and  Penicillium gladioli  mycelial growth [ 172 ].  A. vera  gel and leaf extract activity against  Trichophyton mentagrophytes ,  T. schoeleinii ,  M. canis , and  Candida albicans  were evaluated by Olaleye et al. [ 173 ]. In this research, only gel inhibited  T. mentagrophytes  growth, while leaf extract possessed inhibitory effects on  C. albicans . The antifungal activity against  Aspergillus niger ,  A. flavus ,  Aspergillus oryzae ,  Penicillium chrysogenum , and  Trichoderma viride  were evaluated by Dharajiya et al. [ 140 ]. Maximum inhibitory activity was found for aqueous extract against  A. niger . On the other hand, methanol extract showed weak inhibitory activity against  A. oryzae . Two extracts (hexane and ethyl acetate) failed to express antifungal activity against any of the fungal strains used in the study. What is more, the authors found that  P. chrysogenum  and  T. viride  were found to be resistant to the tested extracts. Das et al. [ 148 ] have reported that a protein isolated from  A. vera  shows antifungal activity against  Candida  species, specifically  C. paraprilosis ,  C. krusei , and  C. albicans . Sequencing analysis showed the isolate to be a lectin-like protein that inhibits trypsin, revealing a protease inhibitory function.\n\nIn the following subsections, different in vitro and in vivo  Aloe  plant species biological effects are carefully described and briefly resumed in  Table 6 .\nA. vera  has been used for the treatment of skin damage in several cultures [ 174 ]. In vitro extracts of  A. vera  stimulated several cell type proliferations. In many researches, treatment with whole  A. vera  gel extracts resulted in faster wounds healing [ 175 , 176 ]. The mannose 6-phosphate present in  A. vera  gel is considered to be the active ingredient for wound healing [ 177 ]. Mannose 6-phosphate heals wounds by increasing cell phagocytic activity [ 178 ]. It is thought that mannose 6-phosphate increases the wound area contraction rate [ 179 ] and collagen synthesis [ 180 ]. During wound healing, the polysaccharides that are present in  A. vera  induce fibroblasts proliferation and hyaluronic acid and hydroxyproline production, which play an important role in extracellular matrix remodeling [ 5 ]. A class of plant growth regulators, gibberellins, which are available in  A. vera , also enhance collagen and elastin formation for breaking strength improvement, by interfering with a collagen cross-link for wound contraction, reducing wrinkle formation [ 2 , 181 , 182 , 183 ]. Polysaccharides and glycoproteins isolated from plants were reported to have wound-healing activity [ 184 , 185 ]. The wound-healing activity of saponin that is present in  A. vera  was also reported [ 186 ]. Acemannan is considered to be a main functional component of  A. vera ; it is composed of a long chain of acetylated mannose [ 33 , 135 , 184 ]. Indeed, acemannan stimulates wound healing and hard tissue regeneration by inducing cell proliferation [ 187 ]. Eight  Aloe  species ( A. arborescens ,  A. brevifolia ,  A. eru ,  A. ferox ,  A. grandidentata ,  A. perfoliata ,  A. saponaria , and  A. vera ) also provided significant accelerating effects on diabetic wound healing in rats following the topical application of leaf methanol extracts [ 36 ].\nAloe  products have been used for drug absorption enhancement with low bioavailability due to extensive efflux [ 188 ]. Carien et al. [ 188 ] demonstrated an increase in drug permeability in the presence of  Aloe vera  gel and whole leaf materials. This is thought to be attributed to the opening of tight junctions by  A. vera  gel and precipitated polysaccharides. Laxatives are substances that loosen stools.  Aloe  is also used as a laxative due to its ability to reduce intestinal water absorption. Anthraquinones that are present in plants act as potent laxatives through mucous secretion stimulation, thereby increasing intestinal water content [ 189 ]. Active anthraquinones, such as aloin, aloe-emodin, and emodin are linked to aloe purgative action [ 5 , 190 ]. Aloin, which is present in gel, can be metabolized by colonic flora to reactive aloe-emodin, which is responsible for purgative activity [ 5 , 133 ]. Five phytosterols that are present in  A. vera  gel are able to reduce visceral fat accumulation, and influence glucose and lipid metabolism in animal model experiments. They also reduced large-sized intestinal polyps [ 5 ]. Aloe-emodin, emodin, and rhein synergistically exerted a potentiating purgative effect on mice [ 191 ].  A. vera  laxative effect was shown after 6–24 h or more from oral anthraquinone administration [ 192 ].\nA. ferox  is widely used for its potent laxative and cathartic effects, which are attributed to anthraquinones and in particular to aloe-emodin [ 193 ].  A. ferox  leaf water extract displayed in vivo laxative effects via improved intestinal motility in loperamide-induced constipated rats [ 194 ].\nIn addition to its laxative properties,  Aloe  could strengthen the stomach, and was traditionally used as a carminative and appetizer agent. It has also been suggested for relieving stomach pain [ 95 ].  Aloe  was known as a good remedy for hemorrhoids and anal disorder treatment. Clinical and experimental studies have shown that  Aloe  preparation administration is useful for a wide range of gastrointestinal problems.  Aloe  extract and a number of its compounds have been shown to ameliorate inflammation and improve clinical and histopathological colitis symptoms in animal models. Significant antiulcer and gastroprotective activities were also observed after administration of  Aloe- containing preparation [ 95 ].  Aloe  is thought to be a potential agent in treatment of gastrointestinal cancers [ 195 , 196 ].\nCyclooxygenase (COX) enzymes (also known as prostaglandin-H 2 -synthases) act as catalysts in the production of prostaglandins (highly active pro-inflammatory mediators) from arachidonic acid (hydrolytically released from membrane phospholipids) during inflammatory processes [ 197 ]. Prostaglandin production inhibition by inhibiting COX enzymes, particularly the COX-2 enzyme (an isoform induced under pathological conditions) is one of the mechanisms of action of some non-steroidal anti-inflammatory drugs (NSAIDs) used for the symptomatic treatment of inflammation. Although different levels of activity (against COX-1 only) were reported in 51 different  Aloe  species [ 198 ], COX-1 isoform inhibition is not desirable, because this enzyme is largely known to be constitutively expressed in most tissues for maintaining some physiological functions [ 199 ].  Aloe  administration has been demonstrated to result in phagocytic and proliferative activity raise by inhibiting COX pathways and reducing prostaglandin E2 production [ 200 , 201 ]. Lindsey et al. [ 202 ] reported that  A. ferox  methanol extract exhibited COX-1 inhibitory effects. Albumin transcription levels and tumor necrosis factor (TNF)-α genes are involved in the early phase of acute inflammatory response. In rats treated with aloe-emodin, an abolishment of albumin gene transcription was observed. TNF-α was weakly detectable in livers after aloe-emodin administration. Histological analysis showed a reduced inflammatory infiltration of the lymphocytes and Kupffer cells observed in rats treated with aloe-emodin [ 203 ].  A. vera  can inhibit the inflammatory process following burn injury by reducing leukocyte adhesion and pro-inflammatory cytokine production [ 204 ].  Aloe  polysaccharide pretreatment can attenuate cerebral ischemia and reperfusion injury in severe traumatic–hemorrhagic rats, through inhibiting systemic inflammatory response, leukocyte aggregation, and lipid peroxidation in the brain [ 205 ]. An acidic polysaccharide and a protein with the molecular weight (MW) of 14 kDa from  A. vera  have also been shown to have anti-inflammatory activity [ 2 ]. A cinnamic acid ester of aloesin found in  A. vera  has the ability to reduce croton oil-induced inflammation [ 148 ]. The C-glucosyl chromone isolated from  A. vera  gel extracts was also found to have anti-inflammatory properties [ 206 ]. The anthraquinones and chromones that are present in aloe inner gel possess strong anti-inflammatory effects in murine macrophages [ 200 ]. Fresh  A. vera  gel was reported for the significant reduction of acute inflammation in rats [ 207 ]. It is also reported that  A. vera  extract helped in decreasing inflammation by 48% in a rat arthritic inflammatory model [ 208 ].\nMorphofunctional and molecular changes induced by carbon tetrachloride (CCl 4 ) were reduced through aloe-emodin administration in rats [ 203 ]. Anthraquinone is likely to protect against hepatocyte death, lipid peroxidation, and the subsequent inflammatory response [ 133 ]. Phytosterols found in aloe, specifically lophenol and cycloartanol, have the ability to induce fatty acid synthesis downregulation and fatty acid oxidation upregulation in the liver, resulting in intra-abdominal fat reduction and hyperlipidemia improvement. An improvement in metabolic syndrome-related disorders and liver steatosis was obtained in aloe sterol-treated diabetic fatty rats. The results also showed that aloe suppressed obesity-induced inflammatory response by reducing cytokine levels [ 74 ].  A. vera  gel extract can also prevent ethanol-induced fatty liver by suppressing mRNA lipogenic gene expression in the liver.  Aloe  gel also has the therapeutic potential to decrease cholesterol levels and cardiovascular disease risk [ 209 ]. In another study investigating  A. vera  extract effect on lindane (LD)-induced hepatoxicity and genotoxicity, leaf extract (1.0 mL/kg body weight, b.w.) decreased serum glutamate pyruvate transaminase (GPT), glutamate oxaloacetate transaminase (GOT), gamma-glutamyl transferase (GGT), and alkaline phosphatase (ALP) levels induced by 100 mg/kg b.w. LD [ 210 ]. In addition to  A. vera , hepatoprotective activity was also reported for other  Aloe  genus species, including  A. arborescens .  A. arborescens  was reported to be most active in liver diseases treatment, particularly cancers [ 211 ].\nFree radical overproduction, including reactive oxygen species (ROS) resulting in oxidative stress, is known to be associated with the development of many diseases [ 226 , 243 , 277 ]. An antioxidant is a substance that significantly delays or inhibits oxidizable substrate oxidation at low concentrations [ 278 ]. In the literature,  A. vera  compounds were highlighted for their antioxidant activities [ 37 , 279 , 280 ]. It has been reported that  A. vera  leaf epidermis and flower methanol extracts exerted in vitro antioxidant effects [ 281 ].  Aloe  gel showed free radical scavenging activity on 2,2-diphenyl-1-picrylhydrazyl (DPPH), 2,20-azinobis-(3-ethylbenzothiazoline-6-sulfonic acid) (ABTS)+•, and nitric oxide radicals [ 212 ].  A. ferox  antioxidant capacity was determined using oxygen radical absorbance capacity (ORAC) and ferric reducing antioxidant power (FRAP) analyses.  A. ferox  antioxidant activity was attributed to its phytochemical composition. Thus, it can be used in alleviating symptoms or preventing oxidative stress-related diseases [ 44 ]. Aloeresins in  A. ferox  displayed strong antioxidant activity [ 213 ]. These 7-hydroxychromones, such as aloesin from an aloe extract, suppress free radical generation and reactive oxygen species (ROS) production, thereby preventing and treating ROS-mediated and other oxidative process-associated conditions [ 214 ]. Also,  A. ferox  leaves methanol extract showed good DPPH scavenging activity [ 215 ]. 5-Methylchromones aloesin, aloeresin A, and aloesone, which are compounds present in  A. barbadensis  and  A. arborescens , exhibited the most radical scavenging activity by DPPH and ORAC assays [ 50 ]. The in vitro antioxidant activity of  A. arborescens  [ 94 ],  A. ferox  [ 44 , 58 , 59 ],  Aloe greatheadii  var.  davyana  [ 282 ],  A. harlana  [ 283 ],  A. saponaria  [ 284 ],  A. marlothii , and  A. melanacantha  [ 285 ] leaf extracts were reported in the literature. Sazhina et al. [ 216 ] reported that leaf extracts from 15  Aloe  species exhibited high antioxidant activity. However, the potent antioxidant activity measured in these in vitro studies needs to be followed up with appropriate in vivo assays. The absorption and bioavailability issues of such antioxidants following consumption also require investigation [ 198 ]. A protective potential of  Aloe  polysaccharides against 2,20-azobis(2-amidinopropane) dihydrochloride induced oxidative stress and cell death in kidney epithelial cells (Vero cells), as well as in an in vivo zebrafish model were shown [ 217 ]. Antioxidant compounds present in  A. saponaria  gel exerted antinociceptive and anti-inflammatory effects by the topical treatment of an ultraviolet B-induced sunburn model [ 286 ]. In another study,  A. barbadensis  extract displayed significant antioxidant activity in diabetic rats by increasing superoxide dismutase (SOD) enzyme activity and reducing lipid peroxidation [ 218 ].\nA. vera  has in vitro antibacterial activity against Gram-negative and Gram-positive bacteria. Thus, it has been described as an antibacterial agent, as previously introduced. Antibacterial activity has been attributed to their polysaccharides, which trigger phagocytic leucocytes to destroy bacteria [ 75 ]. Indeed,  A. vera  gel extract antibacterial activity against Gram-positive and Gram-negative bacteria was showed in other studies [ 136 , 219 ]. An experiment proved that  A. vera  acetone extract was more active against  S. aureus ,  Streptococcus pyogenes ,  P. aeruginosa , and  E. coli  compared to aqueous or ethanol extracts [ 6 ].  A. ferox  is used to treat distinct infections, particularly those that are sexually transmitted, internal parasites, gonorrhoea, and syphilis in South Africa [ 220 ]. Aloe-emodin and aloin A isolated from  A. ferox  exhibited antibacterial activity against  Bacillus cereus ,  B. subtilis ,  S. aureus ,  S. epidermidis ,  E. coli , and  Shigella sonnei , while chrysophanol only led to  B. subtilis ,  S. epidermidis , and  E. coli  growth inhibition [ 56 ]. Aloe-emodin and aloin A showed antibacterial activity against  B. subtilis ,  E. coli ,  S. epidermidis , and  S. sonnei  [ 79 ]. An  Aloe  methanol extract and aloin had inhibitory effects against  Neisseria gonorrhoeae  [ 221 ]. The antimicrobial activities of 10 different South African  Aloe  species extracts were listed in another study [ 198 ]. Antimicrobial activities were reported for  A. arborescens  leaf ethyl acetate (against  E. coli ) [ 222 ],  A. barberae  root and leaf dichloromethane (against  E. coli  and  C. albicans ) [ 71 ], and  A. marlothii  leaf dichloromethane (against  S. aureus ) [ 223 ] extracts. Of particular interest are the inhibitory effects demonstrated by ethyl acetate and the methanol extracts of  A. arborescens  and  A. striatula  leaves, respectively, against ampicillin-resistant  E. coli  [ 222 ]. Pyrocatechol, a hydroxylated phenol that is present in  A. vera , is known to have toxic effects on microorganisms [ 57 , 224 ]. The water and carbohydrates present in  A. vera  gel have very strong antibacterial potential against  P. aeruginosa  and mycobacterium strains, such as  Mycobacterium smegmatis ,  Mycobacterium fortuitum ,  Mycobacterium kansasii , and  Mycobacterium tuberculosis  [ 192 , 225 , 226 ].\nAloe-emodin exerted  H. pylori  inhibition, which is the microorganism that is responsible for gastritis, peptic ulcer, gastric adenocarcinoma, and MALT (mucosa-associated lymphoid tissue) lymphoma [ 145 ]. In another study,  A. vera  gel exhibited inhibitory effects on multi-resistant  H. pylori  strains, with its activity being attributed to the anti-adhesive effect of gel polysaccharides [ 146 ]. Also, it was reported that  A. vera  inner gel has antibacterial activity against both susceptible and resistant  H. pylori  strains and it can be used as a natural agent for  H. pylori  gastric infection treatment [ 227 ].\nThe topical antibacterial as well as anti-inflammatory properties of aloe are embodied in a patent application of a laxative suppository preparation that is used for the treatment of hemorrhoids and bacterial infections of the anus [ 141 ].\nA protein (MW 14 kDa) isolated from  A. vera  displayed antifungal activity against different  Candida  species, specifically  Candida parapsilosis ,  Candida krusei , and  Candida albicans  [ 148 ].  A. vera  removed  Candida  infections through promoting alkalization and alleviating constipation [ 228 ]. The saponins that are available strongly act against bacteria, viruses, fungi, and yeasts [ 67 ]. A report showed that  A.vera  pulp inhibitory activity on  Fusarium oxysporum  and its liquid fraction reduced  Rhizoctonia solani ,  F. oxysporum , and  Colletotrichum coccodes  colony growth rates [ 229 ]. Some studies reported unspecified  A. ferox  ‘juice’ antifungal activity against  Trichophyton  spp. causing athlete’s foot and thrush [ 230 ]. Low activity was recorded for methanol extract against  C. albicans  [ 221 ]. Again,  A. ferox  acetone extract was found to be fungicidal against five fungi [ 170 ].\nIn many research studies, it has been reported that  A. vera  showed antiviral activity preventing virus adsorption, attachment, or entry into host cells. Zandi and Rastian [ 287 ] showed that  A. vera  gel had antiviral activity against herpes simplex virus (HSV) type 2 strains. Anthraquinone derivatives, such as aloe-emodin, emodin, and chrysophanol, which are present in aloe, have been reported to exhibit antiviral activity, also displaying inhibitory mechanisms against influenza A virus replication and virus-induced cytopathic effect [ 231 ].  Aloe  was shown to increase CD 4  count, which results from an immune system improvement. This may be beneficial to HIV-infected patients. It is thought that CD 4  count raise can be attributed to in vitro HIV inhibition by acemannan or the immune-modulatory effects of aloe components [ 232 ]. Similarly, aloe-emodin displayed promising effects in reducing herpes simplex virus Type I and Type II infection. It can also inhibit viruses, such as  Varicella zoster  virus (VSV), influenza virus, and pseudorabies virus [ 181 , 233 ]. In various studies, it was reported that polysaccharide acemannan prevented human lung epithelial cell-bacteria adhesion, and also reduced herpes simplex virus infection [ 288 , 289 , 290 ]. In vitro and in vivo antiviral effects have also been observed for  A. ferox  and  A. secundiflora  leaf extracts, respectively [ 291 , 292 ].\nMalaria is a deadly disease that infects over 150 million humans annually in Africa alone [ 293 ]. The protozoan  Plasmodium falciparum  is the deadliest causative  Plasmodium  species. Traditionally, aloes are not known to possess antimalarial properties, but several scientific studies indicated that some  Aloe  species can be used to treat malaria-related symptoms. Van Zyl and Viljoen [ 294 ] evaluated 34  Aloe  species and their main constituents for antiplasmodial activity using titrated [3 H ]-hypoxanthine incorporation assay. It was found that several methanol extracts inhibited  Plasmodium falciparum  growth by 50% in concentrations of 32–77 mg/mL. Clarkson et al. [ 295 ] in vitro tested 134 plant species against  P. falciparum  strain D10 using parasite lactate dehydrogenase (pLDH) assay.  A. ferox  organic extract (DCM, dichloromethane/MeOH 1:1) displayed promising antiplasmodial effects (IC 50  8 mg/mL), while aqueous extracts did not show any activity [ 295 ].  Aloe marlothii  (whole plant) dichloromethane extract demonstrated good activity (IC 50  of 3.5 mg/mL) against  P. falciparum  [ 295 ].  A. maculata  [ 295 ] whole plant and  A. viridiflora  [ 294 ] leaf extracts showed mild activity.  A. marlothii  [ 295 ] root and  A. speciosa ,  A. suprafoliata , and  A. wickensii  [ 294 ] leaf extracts showed weak activity. These findings indicate that the  Aloe  genus may be used as a potential antimalarial drug.\nThe in vitro anthelmintic activity of the crude aqueous extract obtained from  A. ferox  was examined on eggs and larvae of the nematode parasite  Haemonchus contortus .  A. ferox  extracts showed 100% egg hatch inhibition at 20 mg/mL and larval development inhibition at 2.5 mg/mL [ 296 ].\nAloin, an anthraquinone that is a natural compound and the main  Aloe  ingredient, has been proposed as a potential therapeutic option in cancer, wherein it showed chemoprotective effects against 1,2-dimethylhydrazine-induced colon preneoplastic lesions in Wistar rats [ 234 ]. Indeed, aloin treatment inhibited vascular endothelial growth factor (VEGF) secretion in cancer cells. VEGF is one of the most important proangiogenic cytokines, which is known and well characterized as a tumor neovascularization inducer. Aloin treatment has shown to significantly inhibit VEGF-induced angiogenic response in human endothelial cells, in vitro, triggering proliferation inhibition and endothelial cell migration. Aloin was found to inhibit tumor angiogenesis and growth by signal transducer and activator of transcription 3 (STAT3) activation [ 235 ].\nAloe-emodin (1,8-dihydroxy-3-hydroxymethyl-9,10-anthracenedione) is an anthracenedione derivative from  A. vera  leaves. Recent reports have shown that aloe-emodin possesses antiproliferation effects in some cancer cells types, such as lung, squamous, glioma, and neuroectodermal cancer cells [ 236 , 237 ]. Aloe-emodin is also an anthraquinone subtype; it is a natural compound that has traditionally been found to have diverse biological activities, with anticancer functions among them [ 238 , 239 ]. Aloe-emodin has been found to possess an antiproliferation effect on some cancer cells types, inhibiting both N-acetyl transferase activity and gene expression. This effect plays a crucial role in aryl amine carcinogens metabolism, which is found in human malignant melanoma cells [ 240 , 241 ]. Recently, Lin et al. [ 241 ] demonstrated that aloe-emodin induced apoptosis in T24 human bladder cancer cells. Aloin, which is derived from  A. vera  leaves, has been shown to possess anticancer effects too [ 241 ], as it inhibits tumor angiogenesis and growth via blocking STAT3 activation, therefore displaying a potential as drug candidate for cancer therapy [ 242 ]. Anthraquinone derivatives, such as emodin-like natural (emodin, rhein, and aloin) and synthetic (anthraquinone-2-sulfonic acid) anthraquinones have recently been shown to protect amyloid β and aggregation-induced cell death through antiaggregating effects, and/or enhancing phosphatidylinositol-3-kinase/protein kinase B mediated survival mechanisms, which suggests that anthraquinone-2-sulfonic acid could be a new neuroprotective compound and a novel caspase inhibitor [ 148 , 243 ].\nAn investigation showed that polysaccharide acemannan inhibits benzopyrene binding with primary rat hepatocytes and thereby prevents cancer initiating benzopyrene DNA adduct formation [ 184 , 244 ]. In chemoprevention,  A. vera  gel stimulate glutathione S-transferase induction, which inhibits phorbol myristate acetate tumor-promoting effects [ 245 , 246 ]. Similarly, aloin inhibited cancer cells by altering a cell cycle through the mitochondrial-dependent pathway, which leads to cell membrane integrity loss and apoptosis [ 247 ]. A study demonstrated aloin protective effects on inducible nitric oxide synthase (iNOS) and NFκB synthesis induced in HaCat cells by ultraviolet (UV) B irradiation. Aloin inhibited NFκB and P65 activity by downregulating iNOS mRNA expression caused by UVB irradiation [ 248 ]. Aloe-emodin produced antitumor effects in P-glycoprotein overexpressing cell lines [ 249 ]. In addition, barbaloin, physcion, chrysophanol, aloesin, diethylhexyl phthalate, and an N-terminal octapeptide were reported to have cytotoxic activity on cancer cells [ 225 , 250 , 251 , 252 , 253 ]. Acemannan acts as a very active anticancer agent. Acemannan stimulated TNF-α, IL-1, and interferon production by macrophages and deactivated cancer cells [ 254 ]. In an experiment, aloin was tested on human uterine carcinoma HeLaS3 cells [ 297 ]. Aloin showed antiproliferative effects through arresting the cell cycle in the S phase and significantly increasing HeLaS3 cells apoptosis. This emphasized that aloin can be used for treating human cervical carcinoma in the future. It was also applied to radiosensitize HeLaS3 cells, which suggests an aloin cytotoxic adjuvant effect [ 298 ].\nA. ferox  is also used as an anticancer agent [ 299 , 300 , 301 ]. Aloe-emodin has been reported to have selective activity against neuroectodermal tumors, with practically no effect on normal cells [ 300 ]. Aloe-emodin promoted cell death through specific drug uptake by neuroectodermal tumors [ 302 ].\nThe treatment of diabetes using various natural active compounds is still high-priority research. There are instances to consider  A. vera  as an antidiabetic agent. In vivo and in vitro studies strongly demonstrated that the water soluble fraction of  Aloe  species possesses glucose-lowering activities, and some of its components modulate glucose transporter-4 mRNA expression [ 255 ]. Studies have proved that the polysaccharides that are present in the plant protects β-cells from oxidative damage by alloxan [ 37 , 148 , 256 ]. It was reported that they helped reduce fasting blood glucose levels in alloxan-induced diabetic mice [ 257 ]. Polysaccharides play a major role in antidiabetic activities by increasing insulin levels, and hence, show hypoglycemic effects [ 183 , 258 ]. Phytosterols, such as lophenol, 24-methyl-lophenol, 24-ethyl-lophenol, cycloartanol, and 24-methylene cycloartanol were reported for their beneficial effects in diabetes and obesity [ 74 ]. A report gave confirmation of the clinical and experimental hypoglycemic conditions, due to  A. vera  sap oral intake continuously for four to 14 weeks [ 257 ]. One study discussed aloe-emodin-8- O -glycoside efficacy, isolated from  A. vera  gel, in enhancing glucose transport through proximal and distal marker modulation involved in glucose uptake and its transformation into glycogen [ 259 ]. Tanaka et al. [ 73 ] reported reductions in both the fasting and random blood glucose levels of db/db diabetic mice that were chronically treated with the same  A. vera  gel phytosterols [ 73 ]. Jain et al. [ 260 ] found that  A. vera  gel has significant antidiabetic and cardioprotective effects, as it significantly reduced oxidative stress in streptozotocin-induced diabetic rats and improved antioxidant status [ 260 ].\nA recent study confirmed that phytosterols administration isolated from  A. vera  gel reduced visceral fat mass and improved hyperglycemia in Zucker diabetic fatty rats [ 261 ].  Aloe succotrina  leaf dried pulp exerted remarkable antihyperlipidemic effects in high-fat diet and fructose-induced hyperlipidemic rats. It also significantly decreased the total serum cholesterol, total triglycerides, low-density lipoprotein (LDL), very low-density lipoprotein (VLDL), and high-density lipoprotein (HDL) cholesterol levels [ 262 ]. In polycystic ovarian syndrome (PCOS), rats treated with  A. vera  gel, plasma triglyceride, and LDL cholesterol levels decreased, while HDL cholesterol levels increased and PCOS were significantly reduced.  Aloe  gel also improved the reversion of abnormal estrous cyclicity, glucose intolerance, and lipid metabolizing enzyme activities [ 263 , 264 , 265 ].\nEmodin and aloe-emodin isolated from  A. vera  gel suppressed breast cancer cell proliferation by targeting estrogen receptor-α protein stability through distinct mechanisms. This aspect suggests a possible anthraquinone application in preventing breast cancer cell proliferation through estrogen receptor-α inhibition [ 52 ].  A. vera  gel also helped in maintaining ovarian steroid status in polycystic ovary-like condition, where steroidogenesis is altered and the estrogen and testosterone ratio is disturbed [ 263 ].\nA. vera  gel has the ability to minimize gastric ulcers in both humans and animals [ 30 , 267 ].  A. vera  leaf extracts have also been widely recommended for digestion promotion and in peptic ulcer treatment due to its prominent cytoprotective action, whereby  A. vera  gel exhibited antibacterial activity against both susceptible and resistant  H. pylori  strains and acted as a promising effective natural agent in combination with antibiotics on  H. pylori  gastric infection treatment [ 5 , 266 ]. However, studies have confirmed that  A. vera  gel could not prevent ethanol-induced gastric lesions in rats [ 267 ]. In rats, gastric acid secretion and hydrochloric acid induced-gastric mucosa damage was investigated after  A. vera  aqueous ethanol extract application.  A. vera  extract exhibited dose-dependent inhibitory effects on gastric acid secretions by direct interaction with acid-producing cells or with H2-receptors on parietal cells. A report confirmed that  A. vera  extract showed cytoprotective activity at low doses [ 268 ]. Another report demonstrated that a mixed treatment with  A. vera  and sucralfate reduced gastric inflammation, enhanced epithelial cell proliferation, elongated gastric glands, and reduced ulcer sizes [ 269 ].\nA. vera  can be used on cardiovascular disorders treatment. It stimulated fibroblast cells for making new tissues. Proteoglycans and collagens are formed, thus reducing cardiovascular disorders risk, after fibroblasts stimulation [ 190 ].\nCollagen, elastin, and hyaluronic acid are the major components of the skin dermis layer. Collagen forms the three-dimensional structure of skin, and elastin maintains its elasticity, whereas hyaluronic acid restores skin moisture levels. Fibroblasts are mainly responsible for collagen activation, hyaluronic acid, and elastin in the skin dermis layer, and thereby maintain extracellular matrix homeostasis [ 270 , 271 , 272 ].  Aloe  sterols promoted collagen production and thereby increased type I and type III collagen synthesis gene expression in human dermal fibroblasts. Sterols also increased the hyaluronic acid content of the dermal extracellular matrix. Therefore, they can improve skin moisture [ 273 ]. The melanocytic effects of  A. vera  leaf extract and aloin have been reported by Ali et al. [ 274 ], suggesting that they can be useful for hyperpigmentation treatment. Aloesin was reported to have tyrosinase inhibitory activity, which may be helpful in hyperpigmentation treatment, corresponding to melanin formation, such as melasma and ephelides [ 275 ]. Also, the skin cell proliferating activity of an  Aloe  glycopeptide (G1G1M1DI2) (MW 5.500 Da) was reported [ 303 ].\nA. vera  was reported to trigger collagen and elastin fiber production, making skin more elastic and less wrinkled, but the exact mechanism is not well understood [ 4 , 177 ].\nAn  Aloe  glycoprotein (10 kDa) was found to reduce histamine release and promote leukotriene synthesis and secretion in the activated lung mast cells of guinea pigs. Furthermore, glycoprotein dose-dependently decreased protein kinase C and phospholipase C activities, inhibiting diacylglycerol and phospholipase A activity and blocking Ca 2+  influx during mast cell activation [ 276 ].\nFollowing  Aloe  extracts administration, marked improvements in learning, memory, and cognitive function and Alzheimer disease have also been reported [ 304 , 305 , 306 , 307 ].  Aloe  gel potential on Parkinson disease has also been reported in mice [ 308 ]. Moreover,  Aloe  leaf powder aqueous extract showed anticonvulsant activity in mice [ 309 ].\n\nAloe  is known as healing plant. It has been used for traditional medical purposes in several cultures [ 220 ], and its distinct therapeutic properties have been reported ( Table 7 ). Some of them are attributed to the specific compounds that are present in  Aloe .\nIn traditional medicine,  A. ferox  leaves and roots are applied topically, sometimes mixed with animal fat, or taken internally to treat eczema, dermatitis, and acne. They are also used in the treatment of various other skin diseases or conditions, such as skin cancer, burns, and psoriasis [ 44 ]. Epidermal melanin overproduction, synthesized by tyrosinase action, causes skin hyperpigmentation. The aloesin and arbutin present in  Aloe  can inhibit tyrosinase activity in a synergistic manner [ 310 ]. In fact, it has been reported that aloesin can inhibit hyperpigmentation in human skin after UV radiation in a dose-dependent manner, while co-treatment with aloesin and arbutin exerted an additive effect [ 311 ].  A. barbadensis  [ 312 ] and  A. arborescens  [ 313 ] wound-healing properties were also reported. In a clinical study, burn wound healing was found to be remarkably earlier in  A. vera -treated patients than in those who were treated with 1% silver sulfadiazine cream and a burn dressing for superficial and partial thickness burn treatment [ 314 ]. In another clinical study, it was shown that re-epithelialization and partial thickness burn wound healing was significantly faster in  Aloe- treated sites compared to the silver sulfadiazine-treated ones. The results confirmed that  Aloe  cream can be used to treat second-degree burn wounds, too [ 315 ]. A significant improvement in burning wound healing after  A. vera  treatment was observed in rat models [ 316 , 317 ].\nA report of a clinical study has shown that the oral administration of 2%  A. vera  gel is not only effective in decreasing pain score and wound size in recurrent aphthous stomatitis patients, but also in decreasing the aphthous wound-healing period [ 266 ]. It has been reported that  A. vera  extracts may be used to treat the external parts of eye inflammations, such as the cornea [ 318 ].  A. vera  gel had strong immunomodulatory activity, downregulating lipopolysaccharide-induced inflammatory cytokine production and NLRP3 (NACHT, LRR, and PYD domains-containing protein 3) inflammasome expression in human macrophages [ 319 ]. Acemannan stimulated immunity through potentiating the lymphocyte response to alloantigen with nitric oxide production activation by macrophages and cytokines, such as interleukin (IL)-1, IL-6, interferon (IFN), and TNF-α. It enhanced phagocytosis and also increased circulating monocyte and macrophage levels [ 254 , 320 , 321 ]. Polysaccharide aloeride activated nuclear factor (NF)-ĸB in human macrophages similar to bacterial endotoxin [ 75 ].\nIn general, the α-amylase that is present in human pancreatic cell helps control starch hydrolysis inside the body, and hence protects from postprandial hyperglycemia. Postprandial hyperglycemia is characterized by a rapid increase in blood glucose levels in diabetic patients. An investigation confirmed that  A. vera  decreased diabetes severity by lowering blood glucose levels in type 2 diabetic patients [ 322 ]. Other clinical studies have suggested that  A. vera  gel may act as a safe antihyperglycemic and antihypercholesterolemic agent in type 2 diabetic patients, without any significant effects on other normal blood lipid levels or liver/kidney function [ 323 ].\nIn a randomized controlled trial,  A. vera  gel complex reduced body weight, body fat mass, and insulin resistance in obese pre-diabetic and early non-treated diabetic patients [ 322 ]. Further, in a pilot study, two  Aloe  products in pre-diabetic patients over an eight-week period, tended to revert impaired fasting glucose levels and impaired glucose tolerance observed in pre-diabetes/metabolic syndrome conditions [ 322 ].\nA. vera  antihyperlipidemic activity has also been reported. It had beneficial effects on fatty streak development prevention, and may help in reducing atherosclerosis development through risk factor modification [ 323 ].  A. vera  leaf gel efficacy was checked in hyperlipidemic type 2 diabetic patients in a randomized double-blind placebo-controlled clinical trial, wherein it reduced total cholesterol and low-density lipoprotein (LDL) levels [ 323 ].\nIt has been shown that acquired immune deficiency syndrome (AIDS) can be treated by using  A. vera  extracts in many reports. A daily intake of a minimum dose of 1200 mg of  A. vera  active ingredients improved AIDS symptoms. It soothed the wound and burn of internal organs, and hence acted as a promising AIDS drug. The mannose-6-phosphate present in  A. vera  can also inhibit the HIV-1 virus that causes AIDS [ 324 ].\nIt has been shown that acemannan hydrogels heal aphthous ulcers and reduce pain [ 325 ].  A. vera  is very effective for gum diseases, such as gingivitis and periodontitis [ 327 ]. Besides, it has been reported that  A. vera  mouthwash reduced plaque and gingivitis, though less than chlorhexidine [ 326 ].\n\nThe therapeutic effects of  Aloe  species in traditional and modern medicines are well documented. The present report highlights the research progress on  Aloe  spp. botany, phytochemical composition, ethnobotanical uses, food preservation, and preclinical and clinical efficacy. Of special attention are aloin A, aloin B, aloinoside A, aloinoside B, aloesin, plicataloside, isovitexin, and aloe-emodin, because of their prominent biological activity and abundance in  Aloe  plants. Therefore, considering the data presented here, and namely taking into consideration both its valuable phytoconstituents and wide beneficial effects, the  Aloe  species may be considered as economically important matrices for food, medical, and pharmaceutical industries.","source_license":"CC-BY-4.0","license_restricted":false}