Department of Pharmaceutics, School of Pharmacy, Fudan University & Key Laboratory of Smart Drug Delivery (Fudan University), Ministry of Education, Shanghai 201203, PR China.
College of Pharmaceutical Sciences, Southwest University & Chongqing Engineering Research Center for Pharmaceutical Process and Quality Control, Chongqing 400716, PR China.
Adv Drug Deliv Rev. 2015 Aug 1;90:101-18. doi: 10.1016/j.addr.2015.04.025. Epub 2015 May 8.
Protein and peptide toxins offer an invaluable source for the development of actively targeted drug delivery systems. They avidly bind to a variety of cognate receptors, some of which are expressed or even up-regulated in diseased tissues and biological barriers. Protein and peptide toxins or their derivatives can act as ligands to facilitate tissue- or organ-specific accumulation of therapeutics. Some toxins have evolved from a relatively small number of structural frameworks that are particularly suitable for addressing the crucial issues of potency and stability, making them an instrumental source of leads and templates for targeted therapy. The focus of this review is on protein and peptide toxins for the development of targeted drug delivery systems and molecular therapies. We summarize disease- and biological barrier-related toxin receptors, as well as targeted drug delivery strategies inspired by those receptors. The design of new therapeutics based on protein and peptide toxins is also discussed.
蛋白质和肽毒素为主动靶向药物传递系统的发展提供了宝贵的资源。它们与多种同源受体强烈结合,其中一些受体在疾病组织和生物屏障中表达甚至上调。蛋白质和肽毒素或其衍生物可以作为配体促进治疗剂在组织或器官特异性积累。一些毒素是从相对较少的结构框架进化而来的,这些结构框架特别适合解决效力和稳定性的关键问题,使它们成为靶向治疗的先导和模板的重要来源。本综述的重点是用于开发靶向药物传递系统和分子治疗的蛋白质和肽毒素。我们总结了与疾病和生物屏障相关的毒素受体,以及受这些受体启发的靶向药物传递策略。还讨论了基于蛋白质和肽毒素的新型治疗剂的设计。