Nanomaterial Platforms for Endometriosis: A Systematic Review

Hong-yu Chen , Na Li , Xiao-dan Zhu , Xiang-cheng Pan , En-yuan Tian , Fang-fang Lang , Wei Tian

Current Medical Science ›› : 1 -13.

PDF
Current Medical Science ›› :1 -13. DOI: 10.1007/s11596-026-00239-z
Review
review-article
Nanomaterial Platforms for Endometriosis: A Systematic Review
Author information +
History +
PDF

Abstract

Endometriosis (EM) is a chronic, estrogen-dependent inflammatory disease affecting approximately 10% of women of reproductive age worldwide, causing debilitating pelvic pain, infertility, and substantially impaired quality of life. Conventional hormonal therapies and surgery are limited by systemic side effects, high recurrence rates, and failure to maintain adequate drug concentrations at ectopic lesion sites. Nanotechnology-based drug delivery has emerged as a promising strategy for directing therapeutic agents to ectopic lesion sites, potentially reducing the systemic toxicity that limits current pharmacological options. We systematically review three nanomaterial platforms—hydrogels, extracellular vesicles (EVs), and inorganic nanoparticles—with attention to their physicochemical properties, therapeutic rationale, and preclinical findings, as well as the specific strengths and unresolved limitations of each platform. We further compare how each platform addresses the core pathological processes of EM, namely, persistent inflammation, progressive fibrosis, and pathological angiogenesis. We hope that this review will assist researchers in comparing nanocarrier strategies and identifying more realistic pathways for clinical application in EM.

Keywords

Nanomaterials / Endometriosis / Hydrogel / Extracellular vesicle / Inorganic nanoparticle / Drug delivery

Cite this article

Download citation ▾
Hong-yu Chen, Na Li, Xiao-dan Zhu, Xiang-cheng Pan, En-yuan Tian, Fang-fang Lang, Wei Tian. Nanomaterial Platforms for Endometriosis: A Systematic Review. Current Medical Science 1-13 DOI:10.1007/s11596-026-00239-z

登录浏览全文

4963

注册一个新账户 忘记密码

References

[1]

Mehedintu C, Plotogea MN, Ionescu S, et al.. Endometriosis still a challenge. J Med Life, 2014, 7(3): 349-357

[2]

Chapron C, Marcellin L, Borghese B, et al.. Rethinking mechanisms, diagnosis and management of endometriosis. Nat Rev Endocrinol, 2019, 15(11): 666-682

[3]

Taylor HS, Kotlyar AM, Flores VA. Endometriosis is a chronic systemic disease: clinical challenges and novel innovations. Lancet., 2021, 397(10276): 839-852

[4]

Rolla E. Endometriosis: advances and controversies in classification, pathogenesis, diagnosis, and treatment. F1000Res. 2019;8:529

[5]

Saunders PTK, Horne AW. Endometriosis: Etiology, pathobiology, and therapeutic prospects. Cell., 2021, 184(11): 2807-2824

[6]

Kho RM, Andres MP, Borrelli GM, et al.. Surgical treatment of different types of endometriosis: Comparison of major society guidelines and preferred clinical algorithms. Best Pract Res Clin Obstet Gynaecol, 2018, 51: 102-110

[7]

Kalaitzopoulos DR, Samartzis N, Kolovos GN, et al.. Treatment of endometriosis: a review with comparison of 8 guidelines. BMC Womens Health, 2021, 21(1): 397

[8]

Bayda S, Adeel M, Tuccinardi T, et al.. The history of nanoscience and nanotechnology: from chemical-physical applications to nanomedicine. Molecules., 2019, 25(1): 112

[9]

McNeil SE. Nanotechnology for the biologist. J Leukoc Biol, 2005, 78(3): 585-594

[10]

Padmanabhan J, Kyriakides TR. Nanomaterials, inflammation, and tissue engineering. Wiley Interdiscip Rev Nanomed Nanobiotechnol, 2015, 7(3): 355-370

[11]

Kunzmann A, Andersson B, Thurnherr T, et al.. Toxicology of engineered nanomaterials: focus on biocompatibility, biodistribution and biodegradation. Biochim Biophys Acta, 2011, 1810(3): 361-373

[12]

Siivola KM, Burgum MJ, Suárez-Merino B, et al.. A systematic quality evaluation and review of nanomaterial genotoxicity studies: a regulatory perspective. Part Fibre Toxicol, 2022, 19(1): 59

[13]

Sharifi M, Sohrabi MJ, Hosseinali SH, et al.. Enzyme immobilization onto the nanomaterials: Application in enzyme stability and prodrug-activated cancer therapy. Int J Biol Macromol, 2020, 143: 665-676

[14]

Farokhzad OC, Langer R. Impact of nanotechnology on drug delivery. ACS Nano, 2009, 3(1): 16-20

[15]

Volpini C, Bloise N, Dominoni M, et al.. The nano-revolution in the diagnosis and treatment of endometriosis. Nanoscale, 2023, 15(43): 17313-17325

[16]

Mitchell MJ, Billingsley MM, Haley RM, et al.. Engineering precision nanoparticles for drug delivery. Nat Rev Drug Discov, 2021, 20(2): 101-124

[17]

Patra JK, Das G, Fraceto LF, et al.. Nano based drug delivery systems: recent developments and future prospects. J Nanobiotechnol, 2018, 16(1): 71

[18]

Kaith BS, Singh A, Sharma AK, et al.. Hydrogels: synthesis, classification, properties and potential applications—a brief review. J Polym Environ, 2021, 29(12): 3827-3841

[19]

Seliktar D. Designing cell-compatible hydrogels for biomedical applications. Science, 2012, 336(6085): 1124-1128

[20]

Ahmad Z, Salman S, Khan SA, et al.. Versatility of hydrogels: from synthetic strategies, classification, and properties to biomedical applications. Gels, 2022, 8(3): 167

[21]

Gutierrez AM, Frazar EM, X Klaus MV, et al. Hydrogels and hydrogel nanocomposites: enhancing healthcare through human and environmental treatment. Adv Healthc Mater. 2022;11(7):2101820.

[22]

Saboktakin MR, Tabatabaei RM. Supramolecular hydrogels as drug delivery systems. Int J Biol Macromol, 2015, 75: 426-436

[23]

Gu D, O’Connor AJ, G H Qiao G, et al. Hydrogels with smart systems for delivery of hydrophobic drugs. Expert Opin Drug Deliv. 2017;14(7):879–895.

[24]

Oliva N, Conde J, Wang K, et al.. Designing hydrogels for on-demand therapy. Acc Chem Res, 2017, 50(4): 669-679

[25]

Li Z, Li G, Xu J, et al.. Hydrogel transformed from nanoparticles for prevention of tissue injury and treatment of inflammatory diseases. Adv Mater, 2022, 34(16 ArticleID: 2270119

[26]

Hewlings SJ, Kalman DS. Curcumin: a review of its effects on human health. Foods., 2017, 6(10): 92

[27]

Urošević M, Nikolić L, Gajić I, et al.. Curcumin: biological activities and modern pharmaceutical forms. Antibiotics (Basel), 2022, 11(2): 135

[28]

Liu X, Yan S, Wu H, et al.. Interventional hydrogel microsphere controlled-releasing curcumin for photothermal therapy against endometriosis. Adv Funct Mater, 2024, 34(26): 2315907

[29]

Yue K, Trujillo-de Santiago G, Alvarez MM, et al.. Synthesis, properties, and biomedical applications of gelatin methacryloyl (GelMA) hydrogels. Biomaterials, 2015, 73: 254-271

[30]

Feng T, Wei Y, Lee RJ, et al.. Liposomal curcumin and its application in cancer. Int J Nanomedicine, 2017, 12: 6027-6044

[31]

Maiorana A, Maranto M, Restivo V, et al.. Evaluation of long-term efficacy and safety of dienogest in patients with chronic cyclic pelvic pain associated with endometriosis. Arch Gynecol Obstet, 2024, 309(2): 589-597

[32]

Wu M, Zhang Q, Shang L, et al.. Microfluidics-derived hierarchical microparticles for the delivery of dienogest for localized endometriosis therapy. Acta Biomater, 2024, 178: 257-264

[33]

Vercellini P, Buggio L, Berlanda N, et al.. Estrogen-progestins and progestins for the management of endometriosis. Fertil Steril, 2016, 106(7): 1552-1571.e2

[34]

Chien AJ, Goss PE. Aromatase inhibitors and bone health in women with breast cancer. JCO, 2006, 24(33): 5305-5312

[35]

Mukherjee AG, Wanjari UR, Nagarajan D, et al.. Letrozole: Pharmacology, toxicity and potential therapeutic effects. Life Sci, 2022, 310 ArticleID: 121074

[36]

Tian W, Wang C, Chu R, et al.. Injectable hydrogel nanoarchitectonics with near-infrared controlled drug delivery for in situ photothermal/endocrine synergistic endometriosis therapy. Biomater Res, 2023, 27(1): 100

[37]

Malaguarnera M, Giugno I, Seminara G, et al.. Liver damage induced by danazol. Drug Investig, 1994, 8(2): 122-125

[38]

Nomura K, Murakami K, Shozu M, et al.. Local application of danazol-loaded hyaluronic acid hydrogel to endometriosis in a rat model. Fertil Steril, 2006, 85(Suppl 1): 1157-1167

[39]

Kooijmans SAA, Stremersch S, Braeckmans K, et al.. Electroporation-induced siRNA precipitation obscures the efficiency of siRNA loading into extracellular vesicles. J Control Release, 2013, 172(1): 229-238

[40]

Sheta M, Taha EA, Lu Y, et al.. Extracellular vesicles: new classification and tumor immunosuppression. Biology, 2023, 12(1): 110

[41]

Buzas EI. The roles of extracellular vesicles in the immune system. Nat Rev Immunol, 2023, 23(4): 236-250

[42]

Yang B, Chen Y, Shi J. Exosome biochemistry and advanced nanotechnology for next-generation theranostic platforms. Adv Mater, 2019, 31(2 ArticleID: e1802896

[43]

Ma Y, Dong S, Li X, et al.. Extracellular vesicles: an emerging nanoplatform for cancer therapy. Front Oncol, 2020, 10 ArticleID: 606906

[44]

Haney MJ, Klyachko NL, Zhao Y, et al.. Exosomes as drug delivery vehicles for Parkinson’s disease therapy. J Control Release, 2015, 207: 18-30

[45]

Wang L, Yu X, Zhou J, et al.. Extracellular vesicles for drug delivery in cancer treatment. Biol Proced Online, 2023, 25(1): 28

[46]

Zhang D, Lee H, Jin Y. Delivery of functional small RNAs via extracellular vesicles in vitro and in vivo. RNA Interference and CRISPR Technologies: Technical Advances and New Therapeutic Opportunities. New York, NY: Springer, 2020:107–117.

[47]

Liang Y, Iqbal Z, Wang J, et al.. Cell-derived extracellular vesicles for CRISPR/Cas9 delivery: engineering strategies for cargo packaging and loading. Biomater Sci, 2022, 10(15): 4095-4106

[48]

Skardal A, Murphy SV, Crowell K, et al.. A tunable hydrogel system for long-term release of cell-secreted cytokines and bioprinted in situ wound cell delivery. J Biomed Mater Res B Appl Biomater, 2017, 105(7): 1986-2000

[49]

Wang Y, Li J. Current progress in growth factors and extracellular vesicles in tendon healing. Int Wound J, 2023, 20(9): 3871-3883

[50]

Bernardo ME, Fibbe WE. Mesenchymal stromal cells: sensors and switchers of inflammation. Cell Stem Cell, 2013, 13(4): 392-402

[51]

Zheng X, Zhao D, Liu Y, et al.. Regeneration and anti-inflammatory effects of stem cells and their extracellular vesicles in gynecological diseases. Biomed Pharmacother, 2023, 168 ArticleID: 115739

[52]

Habata S, Mamillapalli R, Ucar A, et al.. Donor mesenchymal stem cells program bone marrow, altering macrophages, and suppressing endometriosis in mice. Stem Cells Int, 2023, 2023: 1598127

[53]

Meligy FY, Elgamal DA, Abdelzaher LA, et al.. Adipose tissue-derived mesenchymal stem cells reduce endometriosis cellular proliferation through their anti-inflammatory effects. Clin Exp Reprod Med, 2021, 48(4): 322-336

[54]

Hirakawa T, Yotsumoto F, Shirasu N, et al.. Trophic and immunomodulatory effects of adipose tissue derived stem cells in a preclinical murine model of endometriosis. Sci Rep, 2022, 12(1): 8031

[55]

Huang SJ, Huang CY, Huang YH, et al.. A novel therapeutic approach for endometriosis using adipose-derived stem cell-derived conditioned medium- A new hope for endometriotic patients in improving fertility. Front Endocrinol, 2023, 14: 1158527

[56]

Bjorkman S, Taylor HS. microRNAs in endometriosis: biological function and emerging biomarker candidates. Biol Reprod, 2019, 100(5): 1135-1146

[57]

Zhang Y, Chang X, Wu D, et al.. Down-regulation of exosomal miR-214-3p targeting CCN2 contributes to endometriosis fibrosis and the role of exosomes in the horizontal transfer of miR-214-3p. Reprod Sci, 2021, 28(3): 715-727

[58]

Wu D, Lu P, Mi X, et al. Exosomal miR-214 from endometrial stromal cells inhibits endometriosis fibrosis. MHR Basic Sci Reprod Med. 2018:357–365.

[59]

Li Q, Yuan M, Jiao X, et al.. M1 macrophage-derived nanovesicles repolarize M2 macrophages for inhibiting the development of endometriosis. Front Immunol, 2021, 12 ArticleID: 707784

[60]

Dad HA, Gu TW, Zhu AQ, et al.. Plant exosome-like nanovesicles: emerging therapeutics and drug delivery nanoplatforms. Mol Ther, 2021, 29(1): 13-31

[61]

Choo YW, Kang M, Kim HY, et al.. M1 macrophage-derived nanovesicles potentiate the anticancer efficacy of immune checkpoint inhibitors. ACS Nano, 2018, 12(9): 8977-8993

[62]

Amin MMJ, Trevelyan CJ, Turner NA. microRNA-214 in health and disease. Cells, 2021, 10(12): 3274

[63]

Alshammari BH, Lashin MMA, Mahmood MA, et al.. Organic and inorganic nanomaterials: fabrication, properties and applications. RSC Adv, 2023, 13(20): 13735-13785

[64]

Mattoussi H, Rotello VM. Inorganic nanoparticles in drug delivery. Adv Drug Deliv Rev, 2013, 65(5): 605-606

[65]

Ni D, Bu W, Ehlerding EB, et al.. Engineering of inorganic nanoparticles as magnetic resonance imaging contrast agents. Chem Soc Rev, 2017, 46(23): 7438-7468

[66]

Qian X, Han X, Chen Y. Insights into the unique functionality of inorganic micro/nanoparticles for versatile ultrasound theranostics. Biomaterials, 2017, 142: 13-30

[67]

Yanar F, Carugo D, Zhang X. Hybrid nanoplatforms comprising organic nanocompartments encapsulating inorganic nanoparticles for enhanced drug delivery and bioimaging applications. Molecules, 2023, 28(15): 5694

[68]

Ahmad F, Salem-Bekhit MM, Khan F, et al.. Unique properties of surface-functionalized nanoparticles for bio-application: functionalization mechanisms and importance in application. Nanomaterials (Basel), 2022, 12(8): 1333

[69]

Kiio TM, Park S. Physical properties of nanoparticles do matter. J Pharm Investig, 2021, 51(1): 35-51

[70]

Périgo EA, Hemery G, Sandre O, et al.. Fundamentals and advances in magnetic hyperthermia. Appl Phys Rev, 2015, 2(4 ArticleID: 041302

[71]

Celardo I, Pedersen JZ, Traversa E, et al.. Pharmacological potential of cerium oxide nanoparticles. Nanoscale, 2011, 3(4): 1411

[72]

Park Y, Demessie AA, Luo A, et al.. Targeted nanoparticles with high heating efficiency for the treatment of endometriosis with systemically delivered magnetic hyperthermia. Small, 2022, 18(24 ArticleID: e2107808

[73]

Palzer J, Eckstein L, Slabu I, et al.. Iron oxide nanoparticle-based hyperthermia as a treatment option in various gastrointestinal malignancies. Nanomaterials (Basel), 2021, 11(11): 3013

[74]

Avasthi A, Caro C, Pozo-Torres E, et al.. Magnetic nanoparticles as MRI contrast agents. Top Curr Chem, 2020, 378(3): 40

[75]

Lingasamy P, Tobi A, Haugas M, et al.. Bi-specific tenascin-C and fibronectin targeted peptide for solid tumor delivery. Biomaterials, 2019, 219 ArticleID: 119373

[76]

Simón-Gracia L, Kiisholts K, Petrikaitė V, et al.. Homing peptide-based targeting of tenascin-C and fibronectin in endometriosis. Nanomaterials (Basel), 2021, 11(12): 3257

[77]

Cho H, Shim MK, Moon Y, et al.. Tumor-specific monomethyl auristatin E (MMAE) prodrug nanoparticles for safe and effective chemotherapy. Pharmaceutics, 2022, 14(10): 2131

[78]

Moses AS, Taratula OR, Lee H, et al.. Nanoparticle-based platform for activatable fluorescence imaging and photothermal ablation of endometriosis. Small, 2020, 16(18 ArticleID: e1906936

[79]

Park JM, Choi HE, Kudaibergen D, et al.. Recent advances in hollow gold nanostructures for biomedical applications. Front Chem, 2021, 9 ArticleID: 699284

[80]

Guo X, Li W, Zhou J, et al.. Specific photothermal ablation therapy of endometriosis by targeting delivery of gold nanospheres. Small, 2017, 13(15): 1603270

[81]

Singh KR, Nayak V, Sarkar T, et al.. Cerium oxide nanoparticles: properties, biosynthesis and biomedical application. RSC Adv, 2020, 10(45): 27194-27214

[82]

Chaudhury K, Babu KN, Singh AK, et al.. Mitigation of endometriosis using regenerative cerium oxide nanoparticles. Nanomed Nanotechnol Biol Med, 2013, 9(3): 439-448

[83]

Dudley AC, Griffioen AW. Pathological angiogenesis: mechanisms and therapeutic strategies. Angiogenesis, 2023, 26(3): 313-347

Funding

Shandong Province Maternal and Child Health Youth Science and Technology Innovation Project(SFYZXJJ-2024032)

Shandong Provincial Postdoctoral Science Foundation(SDCX-ZG-202503168)

China Postdoctoral Science Foundation(2025M782217)

RIGHTS & PERMISSIONS

The Author(s), under exclusive licence to the Huazhong University of Science and Technology

PDF

6

Accesses

0

Citation

Detail

Sections
Recommended

/