Next-generation cancer nanotherapeutics: Pluronic® F127 based mixed micelles for enhanced drug delivery.

IF 3.1 4区 医学 Q2 PHARMACOLOGY & PHARMACY
Krishna Bhalodi, Charmy Kothari, Shital Butani
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引用次数: 0

Abstract

Cancer, projected to become the second leading cause of mortality globally, underscores the critical need for precise drug delivery systems. Nanotechnology, particularly micelles, has emerged as a promising avenue. These nano-sized colloidal dispersions (< 100 nm) utilize amphiphilic molecules featuring a hydrophilic tail and hydrophobic core, facilitating efficient drug encapsulation and delivery. Pluronic® F127, a triblock copolymer (PEO101-PPO56-PEO101), has emerged as a promising drug carrier due to its non-ionic, less-toxic nature, which prolongs drug circulation time and improves drug delivery across blood-brain and intestinal barriers. Mixed micelles, formed using Pluronic® F127 combined with other polymers, surfactants, and drugs, enhance drug solubility, stability, and targeted delivery. This review highlights the key features of mixed micelles, including enhanced pharmacokinetics and targeting abilities, folic acid (FA) conjugation strategies, superior cytotoxicity with reduced side effects, overcoming multidrug resistance, and versatility across various cancer types and compounds. Additionally, the potential for clinical translation of Pluronic® F127-based mixed micelle in cancer treatment is discussed, addressing current challenges and paving the way for optimized applications.

新一代癌症纳米疗法:基于 Pluronic® F127 的混合胶束用于增强药物输送。
癌症预计将成为全球第二大死亡原因,这凸显了对精确给药系统的迫切需求。纳米技术,尤其是胶束,已成为一种前景广阔的途径。这些纳米尺寸的胶体分散体(® F127,一种三嵌段共聚物(PEO101-PPO56-PEO101),因其非离子、低毒性而成为一种很有前途的药物载体,可延长药物的循环时间,改善药物通过血脑屏障和肠道屏障的输送。使用 Pluronic® F127 与其他聚合物、表面活性剂和药物结合形成的混合胶束可提高药物的溶解度、稳定性和靶向给药效果。本综述重点介绍了混合胶束的主要特点,包括增强药代动力学和靶向能力、叶酸(FA)共轭策略、卓越的细胞毒性并减少副作用、克服多药耐药性以及在各种癌症类型和化合物中的通用性。此外,还讨论了基于 Pluronic® F127 的混合胶束在癌症治疗中的临床应用潜力,以应对当前的挑战并为优化应用铺平道路。
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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来源期刊
CiteScore
6.20
自引率
5.60%
发文量
142
审稿时长
4-8 weeks
期刊介绍: Naunyn-Schmiedeberg''s Archives of Pharmacology was founded in 1873 by B. Naunyn, O. Schmiedeberg and E. Klebs as Archiv für experimentelle Pathologie und Pharmakologie, is the offical journal of the German Society of Experimental and Clinical Pharmacology and Toxicology (Deutsche Gesellschaft für experimentelle und klinische Pharmakologie und Toxikologie, DGPT) and the Sphingolipid Club. The journal publishes invited reviews, original articles, short communications and meeting reports and appears monthly. Naunyn-Schmiedeberg''s Archives of Pharmacology welcomes manuscripts for consideration of publication that report new and significant information on drug action and toxicity of chemical compounds. Thus, its scope covers all fields of experimental and clinical pharmacology as well as toxicology and includes studies in the fields of neuropharmacology and cardiovascular pharmacology as well as those describing drug actions at the cellular, biochemical and molecular levels. Moreover, submission of clinical trials with healthy volunteers or patients is encouraged. Short communications provide a means for rapid publication of significant findings of current interest that represent a conceptual advance in the field.
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