主动靶向型载奥拉帕尼PEI-PLGA纳米粒的制备表征及抗三阴乳腺癌研究

胡慧平, 汪汉香, 付之文, 刘金梅, 李石军, 张玉, 史琛

中国药学杂志 ›› 2022, Vol. 57 ›› Issue (17) : 1447-1452.

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中国药学杂志 ›› 2022, Vol. 57 ›› Issue (17) : 1447-1452. DOI: 10.11669/cpj.2022.17.008
论著

主动靶向型载奥拉帕尼PEI-PLGA纳米粒的制备表征及抗三阴乳腺癌研究

  • 胡慧平, 汪汉香, 付之文, 刘金梅, 李石军, 张玉, 史琛*
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Preparation, Characterization and Anticancer Effect of Active-targeted Olaparib-loaded PEI-PLGA Nanoparticles

  • HU Hui-ping, WANG Han-xiang, FU Zhi-wen, LIU Jin-mei, LI Shi-jun, ZHANG Yu, SHI Chen*
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摘要

目的 构建具有肿瘤细胞特异靶向性的纳米给药系统,研究该纳米粒的体外抗三阴乳腺癌作用。方法 采用乳化扩散溶剂挥发法制备包载奥拉帕尼的聚乙烯亚胺-聚乳酸-羟基乙酸共聚物(PEI-PLGA)纳米粒,进一步用透明质酸修饰,制备靶向载药纳米粒。采用激光粒度仪和透射电镜对纳米粒的形态、粒径大小、电位及分布情况进行表征。CCK-8法检测纳米粒对MDA-MB-231细胞的毒性作用,通过共聚焦显微镜观察细胞对目标纳米粒的靶向摄取,生物透射电镜观察细胞内部形态变化分析凋亡情况。结果 成功制备奥拉帕尼靶向载药纳米粒(HA-Ola-PPNPs),粒径为(166.2±0.842) nm,大小分布均匀,呈圆形或椭圆形,稳定性良好;奥拉帕尼包载于PEI-PLGA纳米粒中能够起到药物缓释作用;CCK-8实验结果显示纳米粒组均呈现出时间依赖和剂量依赖性细胞毒性,且HA-Ola-PPNPs对癌细胞具有更强的杀伤作用;激光共聚焦结果说明了HA与CD44受体的主动靶向结合可以显著提高MDA-MB-231细胞对目标纳米粒的摄取;生物透射电镜观察显示HA-Ola-PPNPs能够有效诱导MDA-MB-231细胞发生凋亡。结论 本研究成功制备了具有CD44受体特异性靶向的载药纳米粒,为三阴乳腺癌的临床治疗提供一种新策略。

Abstract

OBJECTIVE To synthesize the active-targeted olaparib-loaded polyethyleneimine-polyllactic-co-glycolic acid(PEI-PLGA) nanoparticles(HA-Ola-PPNPs) and investigate the therapy of triple negative breast cancer in vitro.METHODS The olaparib-loaded PEI-PLGA nanoparticles were prepared by the emulsion solvent diffusion evaporation method. And further modified with hyaluronic acid(HA) to prepare HA-Ola-PPNPs. The synthesis of HA-Ola-PPNPs was verified by dynamic light scattering(DLS) and transmission electron microscopy(TEM), the cytotoxicity was measured by CCK-8.Confocal microscopy was used to observe the uptake of NPs. Biological TEM was used to observe the morphological changes of cells and analyze the apoptosis.RESULTS The mean size of HA-Ola-PPNPs was (166.2±0.842)nm and showed negatively charged surface (-12.3±1.63)mV. The encapsulation efficiency of HA-Ola-PPNPs was (80.44±6.218)%. CCK-8 results showed that all the nanoparticles presented time-dependent and dose-dependent cytotoxicity, and HA-Ola-PPNPs exhibited efficient in vitro antitumor activities. The binding of HA to CD44 receptor could significantly improve the uptake of HA-Ola-PPNPs by MDA-MB-231 cells.And HA-Ola-PPNPs could effectively induce apoptosis of MDA-MB-231 cells.CONCLUSION In this study, active-targeted HA-Ola-PPNPs are successfully prepared, which could provide a new strategy for the clinical treatment of triple negative breast cancer(TNBC).

关键词

奥拉帕尼 / 纳米粒 / 透明质酸 / 三阴乳腺癌 / 主动靶向

Key words

olaparib / nanoparticle / hyaluronic acid / triple-negative breast cancer / active-target

引用本文

导出引用
胡慧平, 汪汉香, 付之文, 刘金梅, 李石军, 张玉, 史琛. 主动靶向型载奥拉帕尼PEI-PLGA纳米粒的制备表征及抗三阴乳腺癌研究[J]. 中国药学杂志, 2022, 57(17): 1447-1452 https://doi.org/10.11669/cpj.2022.17.008
HU Hui-ping, WANG Han-xiang, FU Zhi-wen, LIU Jin-mei, LI Shi-jun, ZHANG Yu, SHI Chen. Preparation, Characterization and Anticancer Effect of Active-targeted Olaparib-loaded PEI-PLGA Nanoparticles[J]. Chinese Pharmaceutical Journal, 2022, 57(17): 1447-1452 https://doi.org/10.11669/cpj.2022.17.008
中图分类号: R944    R965   

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基金

国家自然科学基金项目资助(82073402)
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