Preparation of letrozole dispersed pHEMA/AAm-g-LDPE drug release system: In-vitro release kinetics for the treatment of endometriosis

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This study prepared and characterized a letrozole-loaded pHEMA/AAm-g-LDPE system, finding that cross-linker concentration controls drug release, with the optimized sample releasing 72% drug over 72 hours in simulated uterine fluid.

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Abstract

This paper focuses on the development of a drug delivery system for systemically controlled release of a poorly soluble drug, letrozole. The work meticulously describes the preparation and characterizations of 2-hydroxyethyl methacrylate (HEMA) polymerization onto hydrophilic acrylamide grafted low-density polyethylene (AAm-g-LDPE) surface for targeted drug release system. The surface morphology and thickness measurement of coated pHEMA layer were measured using scanning electron microscopy (SEM). The swelling study was done in deionized (DI) water and simulated uterine fluid (SUF, pH = 7.6). In vitro release of letrozole from the system was performed in SUF. Further, the release kinetics of letrozole from the system was studied using different mathematical models. The results, suggest that the rate of drug release can be altered by varying the concentrations of cross-linker in pHEMA. The optimized sample released 72% drug at the end of 72 h of measurement.

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Condition tags

endometriosis

MeSH descriptors

Acrylamide Drug Liberation Endometriosis Letrozole Polyethylene Polyhydroxyethyl Methacrylate Acrylamide Animals Cell Death Cell Death Cell Survival Cell Survival Endometriosis Female Kinetics Letrozole Letrozole Mice NIH 3T3 Cells Polyethylene

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Source provenance

europepmc
last seen: 2026-09-06T06:16:21.322493+00:00
pubmed
last seen: 2026-05-13T22:22:48.502547+00:00
unpaywall
last seen: 2026-05-14T19:30:52.867331+00:00
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