线粒体靶向脂质体给药-治疗潜力和挑战。

IF 4.3 4区 医学 Q1 PHARMACOLOGY & PHARMACY
Lissette Sanchez-Aranguren, Mohamad Anas Al Tahan, Muhammad Uppal, Parag Juvale, Mandeep Kaur Marwah
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引用次数: 0

摘要

脂质体作为治疗药物的纳米载体,是转化医学研究的热点。考虑到它们的生物相容性,脂质体是一种适合的药物输送系统,具有高效的治疗效果和最小的场外毒性。在人类疾病的不同情况下,不仅要维持治疗药物水平,而且要将它们靶向到适当的细胞内隔室。线粒体调节细胞信号、钙平衡和能量产生,在各种人类疾病中起着至关重要的作用。关注线粒体靶向药物传递的概念在几十年前就提出了,但这一想法的实际应用及其在临床应用中的转化仍在发展中。线粒体靶向脂质体提供了标准药物递送系统的替代方案,潜在地减少了脱靶相互作用、副作用和药物剂量或频率。为了推动这一领域的发展,必须整合各种学科,如高效化学设计、药理学、药剂学和细胞生物学。本文综述了针对线粒体的新型脂质体药物传递系统的设计、开发和表征方面的科学进展,同时回顾了它们的翻译潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Mitochondrial-targeted liposome-based drug delivery - therapeutic potential and challenges.

Liposomes, as nanocarriers for therapeutics, are a prominent focus in translational medicine. Given their biocompatibility, liposomes are suitable drug delivery systems rendering highly efficient therapeutic outcomes with minimal off-site toxicity. In different scenarios of human disease, it is essential not only to maintain therapeutic drug levels but also to target them to the appropriate intracellular compartment. Mitochondria regulate cellular signalling, calcium balance, and energy production, playing a crucial role in various human diseases. The notion of focusing on mitochondria for targeted drug delivery was proposed several decades ago, yet the practical application of this idea and its translation to clinical use is still in development. Mitochondrial-targeted liposomes offer an alternative to standard drug delivery systems, potentially reducing off-target interactions, side effects, and drug dosage or frequency. To advance this field, it is imperative to integrate various disciplines such as efficient chemical design, pharmacology, pharmaceutics, and cell biology. This review summarises scientific advances in the design, development and characterisation of novel liposome-based drug delivery systems targeting the mitochondria while revisiting their translational potential.

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来源期刊
CiteScore
9.10
自引率
0.00%
发文量
165
审稿时长
2 months
期刊介绍: Journal of Drug Targeting publishes papers and reviews on all aspects of drug delivery and targeting for molecular and macromolecular drugs including the design and characterization of carrier systems (whether colloidal, protein or polymeric) for both vitro and/or in vivo applications of these drugs. Papers are not restricted to drugs delivered by way of a carrier, but also include studies on molecular and macromolecular drugs that are designed to target specific cellular or extra-cellular molecules. As such the journal publishes results on the activity, delivery and targeting of therapeutic peptides/proteins and nucleic acids including genes/plasmid DNA, gene silencing nucleic acids (e.g. small interfering (si)RNA, antisense oligonucleotides, ribozymes, DNAzymes), as well as aptamers, mononucleotides and monoclonal antibodies and their conjugates. The diagnostic application of targeting technologies as well as targeted delivery of diagnostic and imaging agents also fall within the scope of the journal. In addition, papers are sought on self-regulating systems, systems responsive to their environment and to external stimuli and those that can produce programmed, pulsed and otherwise complex delivery patterns.
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