药物输送
药品
药理学
生物相容性
药代动力学
体内
弹性蛋白
靶向给药
合理设计
药效学
纳米技术
化学
计算生物学
医学
材料科学
生物
生物技术
有机化学
病理
作者
Joshua J. Milligan,Soumen Saha,Irene Jenkins,Ashutosh Chilkoti
标识
DOI:10.1016/j.copbio.2021.11.006
摘要
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.
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