Novel Worm-like Micelles for Hydrochloride Doxorubicin Delivery: Preparation, Characterization, and In Vitro Evaluation

Yaning Yang, Chen Ge, Jun He, Wei-gen Lu
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Abstract

Doxorubicin hydrochloride (DOX) is one of the widely used antineoplastic agents in treating various cancers, yet it is always associated with the occurrence of adverse reactions that limit its clinical use. Currently, encapsulating DOX in micelles may represent a promising strategy to reduce toxicity and side effects of the drug. This study aimed to explore a novel acitretin-based surfactant (ACMeNa) with good solid stability to encapsulate DOX to form micelles (ACM-DOX). In this work, ACM-DOX micelles were prepared by a microfluidic method free of organic solvents. The characteristics of ACM-DOX micelles were assessed, including morphology, particle size, stability, entrapment efficiency, and drug loading. An in vitro cytotoxicity experiment of the micelles on MDA-MB-231 (a human breast cancer cell line) was also performed. The micelle formation mechanism suggested that the insoluble ACMeNa/DOX complex was formed by electrostatic interaction, and subsequently encapsulated by self-assembly into micelles. The designed ACM-DOX micelles had an average particle size of 19.4 ± 0.2 nm and a zeta potential of −43.7 ± 2.4 mV, with entrapment efficiency and drug loading efficiency of 92.4 ± 0.5% and 33.4 ± 0.3%, respectively. The ACM-DOX micelles had worm-like structures under a Cryo-transmission electron microscope and exhibited good stability within 8 hours after reconstitution and 4- to 32-fold dilution of its reconstituted solution. ACM-DOX micelles released 80% of DOX within 24 hours in a medium of pH = 5.0, and its drug profile can be described by a first-order model. Moreover, ACM-DOX micelles showed cytotoxicity against MDA-MB-231 in a dose-dependent manner, and displayed a higher antitumor activity as compared with free DOX, with IC50 values of DOX and ACM-DOX micelles being 6.80 ± 0.50 and 4.64 ± 0.32 μg/mL, respectively. Given above, ACMeNa has great application potential as a DOX carrier for the treatment of cancers.
用于盐酸阿霉素递送的新型蠕虫状胶束:制备、表征和体外评价
盐酸多柔比星(DOX)是目前广泛应用于各种癌症的抗肿瘤药物之一,但其不良反应的发生限制了其临床应用。目前,将DOX包封在胶束中可能是一种很有前途的策略,可以减少药物的毒性和副作用。本研究旨在探索一种具有良好固体稳定性的新型actretina基表面活性剂(ACMeNa),用于包封DOX形成胶束(ACM-DOX)。在这项工作中,ACM-DOX胶束是通过微流控方法制备的,不含有机溶剂。评估了ACM-DOX胶束的特性,包括形态、粒径、稳定性、包封效率和载药量。并进行了胶束对人乳腺癌细胞系MDA-MB-231的体外细胞毒性实验。胶束形成机制表明,不溶性ACMeNa/DOX配合物是通过静电相互作用形成的,然后通过自组装封装成胶束。设计的ACM-DOX胶束平均粒径为19.4±0.2 nm, zeta电位为- 43.7±2.4 mV,包封效率为92.4±0.5%,载药效率为33.4±0.3%。在低温透射电子显微镜下,ACM-DOX胶束具有蠕虫状结构,并且在重组后8小时内表现出良好的稳定性,并将重组后的溶液稀释4至32倍。在pH = 5.0的介质中,ACM-DOX胶束在24小时内释放80%的DOX,其药物谱可以用一阶模型描述。此外,ACM-DOX胶束对MDA-MB-231表现出剂量依赖性的细胞毒性,与游离DOX相比,其抗肿瘤活性更高,DOX和ACM-DOX胶束的IC50值分别为6.80±0.50和4.64±0.32 μg/mL。综上所述,ACMeNa作为DOX载体在癌症治疗中具有很大的应用潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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