Curcumin loaded hyaluronan modified niosomes: Preparation, characterization and anti-cancer activity on triple-negative breast cancer cells

IF 4.9 3区 医学 Q1 PHARMACOLOGY & PHARMACY Journal of Drug Delivery Science and Technology Pub Date : 2025-03-28 DOI:10.1016/j.jddst.2025.106869
Mozhgan Abasi , Zaynab Sadeghi Ghadi , Younes Pilehvar , Pedram Ebrahimnejad
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Abstract

Curcumin is a herbal polyphenolic compound with anti-cancer properties, but its low solubility, stability and bioavailability limit its therapeutic potential. In this study, we developed niosomes, nanosized vesicles composed of tween 80, Sorbitan monostearate, cholesterol and hyaluronan, as a novel delivery system for curcumin. The curcumin-loaded hyaluronan modified niosomes (cur-nio) were prepared by thin-film hydration method and characterized for their morphology, zeta potential, particle size and in vitro drug release. The anti-cancer activity and apoptotic effect of cur-nio were evaluated on MDA-MB-231 cell line by MTT assay, Real time PCR and Annexin V-FITC/PI staining. Moreover, migration and invasion phenotypes of cells were determined by transwell assays and wound healing assays. We were also interested in determining cur-nio effects on tumorigenicity of MDA-MB-231 cells by mammosphere formation assay. The results showed that the cur-nio had a spherical shape, a negative charge, a mean diameter of about 251 ± 7.14 nm and a high encapsulation efficiency of about 97.96 ± 0.55. The cur-nio exhibited a sustained release profile of curcumin. The cur-nio showed significant inhibition of cell viability and induction the expression of essential apoptotic genes compared to free curcumin and blank niosomes. The IC50 value of cur-nio was about 30 μM, which was approximately 2 times lower than that of free curcumin. Also, our results showed that cur-nio significantly inhibits cell migration, invasion, mammosphere formation and proliferation rate in vitro.These findings suggest that niosomes are a promising carrier for enhancing the delivery and efficacy of curcumin in cancer therapy.

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姜黄素负载透明质酸修饰乳质体:制备、表征及对三阴性乳腺癌细胞的抗癌活性
姜黄素是一种具有抗癌作用的草药多酚类化合物,但其低溶解度、稳定性和生物利用度限制了其治疗潜力。在这项研究中,我们开发了纳米小体,由80、山梨糖单硬脂酸酯、胆固醇和透明质酸组成的纳米小泡,作为姜黄素的一种新的递送系统。采用薄膜水合法制备了载姜黄素透明质酸修饰乳小体(curc -nio),并对其形貌、zeta电位、粒径和体外释药性能进行了表征。采用MTT法、Real - time PCR法和Annexin V-FITC/PI染色对MDA-MB-231细胞株的抗癌活性和凋亡作用进行了评价。此外,通过transwell实验和伤口愈合实验确定细胞的迁移和侵袭表型。我们还对通过乳腺球形成试验确定curnio对MDA-MB-231细胞致瘤性的影响感兴趣。结果表明,所制得的cu -nio呈球形,带负电荷,平均直径约为251±7.14 nm,包封效率约为97.96±0.55。姜黄素具有缓释特性。与游离姜黄素和空白niosomes相比,curc -nio对细胞活力有明显的抑制作用,并能诱导凋亡必需基因的表达。姜黄素的IC50值约为30 μM,比游离姜黄素低约2倍。此外,我们的研究结果表明,curc -nio显著抑制细胞迁移、侵袭、乳腺球形成和体外增殖率。这些结果表明,niosomes是一种很有希望的载体,可以增强姜黄素在癌症治疗中的传递和疗效。
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来源期刊
CiteScore
8.00
自引率
8.00%
发文量
879
审稿时长
94 days
期刊介绍: The Journal of Drug Delivery Science and Technology is an international journal devoted to drug delivery and pharmaceutical technology. The journal covers all innovative aspects of all pharmaceutical dosage forms and the most advanced research on controlled release, bioavailability and drug absorption, nanomedicines, gene delivery, tissue engineering, etc. Hot topics, related to manufacturing processes and quality control, are also welcomed.
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