2-Deoxyglucose Dendrimer-Enabled Niclosamide Delivery to FRβ-Expressing Macrophages Alleviates Endometriosis Progression and Associated Hyperalgesia

Anubhav Dhull, Dhull A, Mingxin Shi, Harvey ME, Madeleine E. Harvey, Taylor M Page, Sharma R, Rishi Sharma, Kenneth John Goody, Goody KJ, Aqib Iqbal Dar, Dar AI, Nash S. Moawad, Vijay Kumar Sirohi, Sirohi VK, Cooke PS, Paul S. Cooke, Kanako Hayashi, Anjali Anjali Sharma, Anjali Sharma
Advanced healthcare materials · 2026 · vol. 15(37) , pp. e71661 · doi:10.1002/adhm.71661 · PMID:42670248 · PMC13650810 · W7128485652
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A niclosamide-loaded dendrimer targeted to folate receptor-β-positive macrophages reduced lesion burden and hyperalgesia in a mouse endometriosis model, demonstrating the therapeutic potential of this nonhormonal nanomedicine.

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Abstract

Endometriosis (EuE) is a chronic, incurable disease. Due to limited efficacy, high recurrence rates, and serious side effects of current treatments, development of new, targeted, nonhormonal therapies is urgently needed. We previously reported that niclosamide, an FDA-approved anthelmintic drug, attenuates endometriotic lesion growth. We further identified folate receptor-β (FRβ)-positive macrophages as contributors to disease progression. Significantly, niclosamide inhibits FRβ+ macrophages and reduces inflammation, innervation, and angiogenesis. To develop niclosamide as a nonhormonal and selective immune cell-targeted therapy for EuE, we engineered a folic acid (FA)-conjugated 2-deoxyglucose dendrimer (FA-2DG-D) using click chemistry to enable selective FRβ-mediated uptake. Conjugation of niclosamide to FA-2DG-D yielded a targeted nanotherapeutic (FA-2DG-D-Niclo) with enhanced aqueous solubility, controlled intracellular release, and excellent batch-to-batch reproducibility. In a mouse model of EuE, FA-2DG-D demonstrated lesion-specific accumulation and selective internalization by FRβ+ macrophages with minimal off-target organ retention. A single intraperitoneal dose of FA-2DG-D-Niclo (25 or 50 mg/kg/bw of niclosamide) significantly reduced FRβ+ macrophage burden, suppressed lesion number and volume, and markedly improved EuE-associated hyperalgesia at 2 weeks post-treatment. Together, these findings establish FRβ+ macrophages as a potential target in EuE and present FA-2DG-D-Niclo as a nonhormonal, macrophage-focused nanomedicine for precise and effective endometriosis treatment.

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MeSH descriptors

Dendrimers Dendrimers Dendrimers Deoxyglucose Deoxyglucose Deoxyglucose Endometriosis Endometriosis Endometriosis Endometriosis Endometriosis Folate Receptor 2 Folate Receptor 2 Folate Receptor 2 Hyperalgesia Hyperalgesia Hyperalgesia Hyperalgesia Hyperalgesia Macrophages

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Papers in the corpus that this work cites (lower rings, blue) and that cite this one (upper rings, green). Dot size scales with the paper's in-corpus citation count — bigger dot = more influential within the endo/adeno field. Click a dot to open that paper. Outer rings show 2-hop neighbours — papers reached through the immediate citers/citees. [ collapse to 1-hop ]

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SciLite annotations

chemicals 7
niclosamide niclosamide niclosamide niclosamide folic acid 2-hydroxymethylglutarate polycarbazole polymer
organisms 1
transgenic mice

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