Liu Zhibo, Chen Xiaoyuan
Laboratory of Molecular Imaging and Nanomedicine, National Institute of Biomedical Imaging and Bioengineering, National Institutes of Health, Bethesda, MD 20892, USA.
Chem Soc Rev. 2016 Mar 7;45(5):1432-56. doi: 10.1039/c5cs00158g.
Albumin is the most abundant circulating protein in plasma and has recently emerged as a versatile protein carrier for drug targeting and for improving the pharmacokinetic profile of peptide or protein based drugs. Three drug delivery technologies related to albumin have been developed, which include the coupling of low-molecular weight drugs to exogenous or endogenous albumin, conjugating bioactive proteins by albumin fusion technology (AFT), and encapsulation of drugs into albumin nanoparticles. This review article starts with a brief introduction of human serum albumin (HSA), and then summarizes the mainstream chemical strategies of developing HSA binding molecules for coupling with drug molecules. Moreover, we also concisely condense the recent progress of the most important clinical applications of HSA-binding platforms, and specify the current challenges that need to be met for a bright future of HSA-binding.
白蛋白是血浆中含量最丰富的循环蛋白,最近已成为一种多功能蛋白载体,用于药物靶向以及改善基于肽或蛋白质的药物的药代动力学特征。已开发出三种与白蛋白相关的药物递送技术,包括将低分子量药物与外源性或内源性白蛋白偶联、通过白蛋白融合技术(AFT)共轭生物活性蛋白,以及将药物封装到白蛋白纳米颗粒中。本文首先简要介绍人血清白蛋白(HSA),然后总结开发用于与药物分子偶联的HSA结合分子的主流化学策略。此外,我们还简要概括了HSA结合平台最重要的临床应用的最新进展,并明确了为实现HSA结合的光明未来需要应对的当前挑战。