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透明质酸修饰的混合纳米胶束的制备及其用于靶向递送亲脂性药物至 CD44 过表达的癌细胞。

Preparation of hyaluronic acid-decorated mixed nanomicelles for targeted delivery of hydrophobic drugs to CD44-overexpressing cancer cells.

机构信息

Department of Chemical Engineering, Faculty of Engineering, Arak University, 38156-8-8349 Arak, Iran.

Department of Material Science and Engineering, Faculty of Engineering, Arak University, Arak 38156-8-8349, Iran.

出版信息

Int J Pharm. 2021 Jan 5;592:120052. doi: 10.1016/j.ijpharm.2020.120052. Epub 2020 Nov 5.

Abstract

Most of the employed methods for preparation of targeted nanoparticles containing hydrophobic herbal drugs have multiple surface modifications with time-consuming steps. The present research was aimed to develop a facile method for preparation of hyaluronic acid (HA)-decorated mixed nanomicelles loaded with curcumin (as a hydrophobic drug model) to provide an efficient drug delivery system for targeted therapy of breast cancer cells with high expression of CD44 receptor. To this end, curcumin was first encapsulated in the hydrophobic core of Pluronic F127/didecyldimethylammonium bromide (PD) mixed nanomicelles using thin-film hydration method. Then, negatively charged HA was coated on the positively charged surface of PD mixed nanomicelles via electrostatic interactions. The drug loading and entrapment efficiency of the targeted nanomicelles were 2.8% and 95.1%, respectively. The average hydrodynamic size of the prepared nanomicelles before and after coating with HA were 19.8 and 35.8 nm, respectively. Moreover, in vitro cytotoxicity analyses showed that, HA-coated PD (HA-PD) mixed nanomicelles can enhance the cytotoxicity of curcumin against MDA-MB-231 cancer cells compared to non-targeted ones (PD mixed nanomicelles), and free curcumin. The IC concentrations of free curcumin, curcumin-loaded PD mixed nanomicelles, and curcumin-loaded HA-PD mixed nanomicelles were 4.11, 3.20, and 2.83 μg/mL, respectively, after 48 h incubation with MDA-MB-231 cancer cells. Our results suggest that, curcumin-loaded HA-PD mixed nanomicelles may be considered as a promising targeted anticancer drug delivery system for breast cancer therapy and/or delivering other hydrophobic drugs to different kinds of cancer cells with CD44-receptor overexpression.

摘要

大多数用于制备含疏水草药的靶向纳米粒子的方法都需要经过多次表面修饰,步骤繁琐耗时。本研究旨在开发一种简便的方法,用于制备透明质酸(HA)修饰的载姜黄素(作为疏水药物模型)混合纳米胶束,为高表达 CD44 受体的乳腺癌细胞的靶向治疗提供高效的药物传递系统。为此,首先采用薄膜水化法将姜黄素包封在 Pluronic F127/双十二烷基溴化铵(PD)混合纳米胶束的疏水性内核中。然后,通过静电相互作用将带负电荷的 HA 涂覆在 PD 混合纳米胶束的带正电荷表面上。靶向纳米胶束的载药量和包封效率分别为 2.8%和 95.1%。HA 修饰前后制备的纳米胶束的平均水动力粒径分别为 19.8nm 和 35.8nm。此外,体外细胞毒性分析表明,与非靶向的 PD 混合纳米胶束和游离姜黄素相比,HA 修饰的 PD(HA-PD)混合纳米胶束可以增强姜黄素对 MDA-MB-231 癌细胞的细胞毒性。游离姜黄素、载姜黄素 PD 混合纳米胶束和载姜黄素 HA-PD 混合纳米胶束在与 MDA-MB-231 癌细胞孵育 48 小时后的 IC浓度分别为 4.11μg/mL、3.20μg/mL 和 2.83μg/mL。我们的结果表明,载姜黄素 HA-PD 混合纳米胶束可能被认为是一种有前途的用于乳腺癌治疗的靶向抗癌药物传递系统,也可用于将其他疏水药物递送至不同类型的高表达 CD44 受体的癌细胞。

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