拟肽
药物输送
药理学
抗菌剂
广谱
癌症治疗
药品
抗药性
医学
计算生物学
化学
生物
癌症
组合化学
肽
生物化学
微生物学
有机化学
内科学
作者
Liming Lin,Jiaying Chi,Yilang Yan,Rui Luo,Xiaoqian Feng,Yingjun Zheng,Dongyi Xian,Xin Li,Guilan Quan,Daojun Liu,Chuanbin Wu,Chao Lu,Xin Pan
标识
DOI:10.1016/j.apsb.2021.07.014
摘要
Membrane-disruptive peptides/peptidomimetics (MDPs) are antimicrobials or anticarcinogens that present a general killing mechanism through the physical disruption of cell membranes, in contrast to conventional chemotherapeutic drugs, which act on precise targets such as DNA or specific enzymes. Owing to their rapid action, broad-spectrum activity, and mechanisms of action that potentially hinder the development of resistance, MDPs have been increasingly considered as future therapeutics in the drug-resistant era. Recently, growing experimental evidence has demonstrated that MDPs can also be utilized as adjuvants to enhance the therapeutic effects of other agents. In this review, we evaluate the literature around the broad-spectrum antimicrobial properties and anticancer activity of MDPs, and summarize the current development and mechanisms of MDPs alone or in combination with other agents. Notably, this review highlights recent advances in the design of various MDP-based drug delivery systems that can improve the therapeutic effect of MDPs, minimize side effects, and promote the co-delivery of multiple chemotherapeutics, for more efficient antimicrobial and anticancer therapy. This review summarizes recent advances of membrane-disruptive peptides/peptidomimetics-based therapeutics, combination therapy, and delivery systems for antibacterial and anti-tumor applications.
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