治疗性脂质体与活性分子协同作用,增强靶向治疗。

IF 3.9 4区 医学 Q1 PHARMACOLOGY & PHARMACY
Alireza Partoazar, Ramin Goudarzi, Ahmad Reza Dehpour
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引用次数: 0

摘要

由磷脂(PLs)单独或与活性分子组成的脂质体在改善严重疾病如阿尔茨海默病、骨质疏松症和炎症等方面具有重要的潜力。例如,在病理条件下,PLs表现出抗炎、抗氧化、神经保护和成骨特性,从而加速了药物的治疗效果。这些药理学性质可由PLs或脂质体的类型和剂量调节。它们通过信号通路、下调或上调基因表达、氧化应激平衡等生物学机制影响疾病。有趣的是,在实验模型中,含有磷脂酰丝氨酸等必需PLs的脂质体与姜黄素或阿仑膦酸钠等活性分子可以协同改善骨质疏松症等某些疾病。因此,我们旨在强调各种PLs或脂质体的独特优势,重点是它们不同的治疗方式和增强脂质体在实验研究中的协同作用。这些特性表明,通过减少慢性疾病的药物使用来提高药物疗效和减轻副作用是一种有希望的方法,然而,它们的临床转化需要进一步验证安全性和有效性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Therapeutic liposomes synergize with active molecules to enhance targeted therapy.

Liposomes composed of phospholipids (PLs) either alone or with an active molecule, can reveal a significant potential in the improvement of severe disorders such as Alzheimer's disease, osteoporosis, and inflammatory conditions. For instance, PLs exhibit anti-inflammatory, antioxidant, neuroprotective, and osteogenic properties in pathological conditions which accelerate the therapeutic effect of the drugs. These pharmacological properties can be modulated by the type and dose of PLs or liposome administration. They affect disorders through the signalling pathways, down or upregulation of gene expression, balance of oxidative stress, and other biological mechanisms. Interestingly, liposomes containing essential PLs like phosphatidylserine with active molecules such as curcumin or alendronate could synergistically improve certain diseases like osteoporosis in experimental models. Accordingly, we aimed to highlight the unique advantages of various PLs or liposomes with an emphasis on their diverse therapeutic modalities and potentiation of liposomes in synergy with the cargos in experimental studies. These properties suggest a promising approach to enhance drug efficacy and mitigate the side effects through reduced drug usage in chronic diseases, however, their clinical translation requires further validation of safety and effectiveness in human.

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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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