化学
体内分布
体内
选择性
生物物理学
渗透(战争)
肽
药理学
磁导率
药物输送
药品
吲哚青绿
血脑屏障
配体(生物化学)
体外
毒品携带者
P-糖蛋白
临床前影像学
药代动力学
靶向给药
不利影响
环肽
作者
Kensuke Asukabe,Nagi Yamashita,Runa Fujimoto,Kotaro Sakamoto,Eijiro Miyako
标识
DOI:10.1021/acs.bioconjchem.5c00352
摘要
KS-487 is a cyclic peptide previously reported to bind low-density lipoprotein receptor-related protein 1 (LRP1) and exhibit blood-brain barrier (BBB) permeability. In this study, we evaluated the in vivo BBB permeability and selectivity of KS-487 in comparison with those of Angiopep-2 (ANG2), a widely used linear LRP1-binding peptide. Indocyanine green (ICG)-labeled KS-487 and ANG2 were subcutaneously administered to mice, and their biodistribution was assessed at 24, 48, and 72 h by using in vivo imaging. ICG-KS-487 and ICG-ANG2 displayed comparable brain permeability and nearly identical time-course profiles. Notably, ICG-KS-487 demonstrated greater brain selectivity, defined as the ratio of brain to liver accumulation at 72 h. No adverse effects, including weight loss or histopathological abnormalities in major organs, were observed in mice treated with ICG-KS-487. These findings highlight the remarkable brain-targeting properties and safety profile of KS-487, supporting its potential utility as a targeting ligand for drug delivery to treat brain-related disorders.
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