癌症治疗的创新:内源性刺激反应脂质体作为先进的纳米载体。

IF 5.5 3区 医学 Q1 PHARMACOLOGY & PHARMACY Pharmaceutics Pub Date : 2025-02-13 DOI:10.3390/pharmaceutics17020245
Jazmín Torres, Johanna Karina Valenzuela Oses, Antonio María Rabasco-Álvarez, María Luisa González-Rodríguez, Mónica Cristina García
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引用次数: 0

摘要

最近纳米技术的进步通过脂质体(L)的发展彻底改变了癌症治疗——这是全球最紧迫的健康挑战之一,也是导致死亡的主要原因之一。脂质体是基于脂质的纳米囊泡,以其生物相容性和封装亲水性和亲脂性药物的能力而闻名。最近的创新导致了刺激反应型L的产生,它们释放有效载荷以响应特定的内源性或外源性触发。双反应和多反应L,对多种刺激作出反应,提供更高的精度,提高治疗效果,同时减少全身毒性。此外,这些智能L可以调整其物理化学性质和形态,以实现位点特异性靶向和药物控制释放,提高治疗效果,同时最大限度地减少不良反应。本文综述了内源性刺激反应型脂质体纳米载体的最新研究进展,以及整合内外触发的双反应型和多反应型纳米载体,重点介绍了它们的设计策略、机制及其在癌症治疗中的应用。
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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Innovations in Cancer Therapy: Endogenous Stimuli-Responsive Liposomes as Advanced Nanocarriers.

Recent advancements in nanotechnology have revolutionized cancer therapy-one of the most pressing global health challenges and a leading cause of death-through the development of liposomes (L), lipid-based nanovesicles known for their biocompatibility and ability to encapsulate both hydrophilic and lipophilic drugs. More recent innovations have led to the creation of stimuli-responsive L that release their payloads in response to specific endogenous or exogenous triggers. Dual- and multi-responsive L, which react to multiple stimuli, offer even greater precision, improving therapeutic outcomes while reducing systemic toxicity. Additionally, these smart L can adjust their physicochemical properties and morphology to enable site-specific targeting and controlled drug release, enhancing treatment efficacy while minimizing adverse effects. This review explores the latest advancements in endogenous stimuli-responsive liposomal nanocarriers, as well as dual- and multi-responsive L that integrate internal and external triggers, with a focus on their design strategies, mechanisms, and applications in cancer therapy.

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来源期刊
Pharmaceutics
Pharmaceutics Pharmacology, Toxicology and Pharmaceutics-Pharmaceutical Science
CiteScore
7.90
自引率
11.10%
发文量
2379
审稿时长
16.41 days
期刊介绍: Pharmaceutics (ISSN 1999-4923) is an open access journal which provides an advanced forum for the science and technology of pharmaceutics and biopharmaceutics. It publishes reviews, regular research papers, communications,  and short notes. Covered topics include pharmacokinetics, toxicokinetics, pharmacodynamics, pharmacogenetics and pharmacogenomics, and pharmaceutical formulation. Our aim is to encourage scientists to publish their experimental and theoretical details in as much detail as possible. There is no restriction on the length of the papers. The full experimental details must be provided so that the results can be reproduced.
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