Milligan Joshua J, Saha Soumen, Jenkins Irene C, Chilkoti Ashutosh
Department of Biomedical Engineering, Duke University, Durham, NC 277018, USA.
Department of Biomedical Engineering, Duke University, Durham, NC 277018, USA.
Curr Opin Biotechnol. 2022 Apr;74:146-153. doi: 10.1016/j.copbio.2021.11.006. Epub 2021 Dec 15.
Small molecule drugs suffer from poor in vivo half-life, rapid degradation, and systemic off-target toxicity. To address these issues, researchers have developed nanoparticles that significantly enhance the delivery of many drugs while reducing their toxicity and improving targeting to specific organs. Recombinantly synthesized biomaterials such as elastin-like polypeptides (ELPs) have unique attributes that greatly facilitate the rational design of nanoparticles for drug delivery. These attributes include biocompatibility, precise control over amino acid sequence design, and stimuli-responsive self-assembly into nanostructures that can be loaded with a range of drugs to enhance their pharmacokinetics and pharmacodynamics, significantly improving their therapeutic efficacy over the free drugs. This review summarizes recent developments in genetically encoded, self-assembling ELP nanoparticles and their applications for drug delivery.
小分子药物存在体内半衰期短、快速降解以及全身脱靶毒性等问题。为了解决这些问题,研究人员开发了纳米颗粒,可显著提高多种药物的递送效率,同时降低其毒性并改善对特定器官的靶向性。重组合成的生物材料,如弹性蛋白样多肽(ELP),具有独特的特性,极大地促进了用于药物递送的纳米颗粒的合理设计。这些特性包括生物相容性、对氨基酸序列设计的精确控制,以及对刺激响应的自组装成纳米结构,该结构可装载一系列药物以增强其药代动力学和药效学,显著提高其相对于游离药物的治疗效果。本综述总结了基因编码的、自组装的ELP纳米颗粒的最新进展及其在药物递送中的应用。