多功能靶向多西他赛加巴库奇醇胶束治疗卵巢癌的侵袭和转移。

Qi-Yan Li, Ri-Ran Zhu, Hai-Ying Yu, Chun-Lin Liu, Fei-Yan Diao, Ya-Qi Jiang, Yong-Qiang Lin, Xue-Tao Li, Wei-Jian Wang
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引用次数: 0

摘要

肿瘤的侵袭和转移给卵巢癌(OC)的治疗带来了巨大挑战,使其难以治愈。基质金属蛋白酶(MMP)反应性控释胶束制剂是一种潜在的治疗方法,已引起人们的关注。在这项研究中,我们开发了一种新型 PEG5000-PVGLIG-hyaluronic acid 多西他赛/巴库昔醇(PP-HA-DTX/BAK)胶束制剂,该制剂具有理想的粒度、窄 PDI 和约 -5mV 的 ZETA 电位等特性。HA的表面修饰有助于向肿瘤内部渗透,而DSPE-PEG2000-PVGLIG-PEG5000的加入则有助于掩盖DSPE-PEG2000-HA,减少脱靶效应,延长药物在体内的循环时间。体外和体内实验均表明,这些胶束能有效抑制 OC 细胞的增殖、侵袭和转移,同时促进细胞凋亡。因此,我们的研究结果表明,PP-HA-DTX/BAK胶束是治疗OC的一种安全有效的治疗策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Multifunctional targeting of docetaxel plus bakuchiol micelles in the treatment of invasion and metastasis of ovarian cancer.

The invasion and metastasis of tumors pose significant challenges in the treatment of ovarian cancer (OC), making it difficult to cure. One potential treatment approach that has gained attention is the use of matrix metalloproteinase reactive controlled release micelle preparations. In this study, we developed a novel PEG5000-PVGLIG-hyaluronic acid docetaxel/bakuchiol (PP-HA-DTX/BAK) micelles formulation with desirable characteristics such as particle size, narrow polydispersity index, and a ZETA potential of approximately -5 mV. The surface modification with HA facilitates tumor penetration into the tumor interior, while the incorporation of DSPE-PEG2000-PVGLIG-PEG5000helps conceal DSPE-PEG2000-HA, reducing off-target effects and prolonging drug circulation timein vivo. Bothin vitroandin vivoexperiments demonstrated that these micelles effectively inhibit proliferation, invasion, and metastasis of OC cells while promoting apoptosis. Therefore, our findings suggest that PP-HA-DTX/BAK micelles represent a safe and effective therapeutic strategy for treating OC.

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