化学
体内分布
寡核苷酸
肾
结合
肽
靶向治疗
药物输送
靶向给药
药理学
癌症研究
计算生物学
生物化学
内科学
DNA
癌症
体外
有机化学
数学分析
生物
医学
数学
作者
Morgane Mannes,Dora Mugoli Chigoho,Charlotte Martin,Thomas Barlow,Tine L.M. Hectors,Tom C Govaerts,Peter Kayaert,Kirsten De Ridder,Carole Delachaume,Béatrice Vayssière,Martin J. I. Andrews,Sophie Hernot,Steven Ballet
标识
DOI:10.1021/acs.jmedchem.5c01893
摘要
Targeted drug delivery has emerged as a crucial strategy to enhance efficacy and minimize side effects from off-target interactions, a particularly relevant approach for kidney diseases, where many treatments suffer from poor targeting efficiency. In this study, we benchmarked a series of peptides previously identified for their kidney-targeting potential, utilizing them as targeting moieties for an oligonucleotide aimed at repressing HIF-1α expression in renal tubular cells. The peptides were synthesized, radiolabeled, and evaluated for their biodistribution profiles in mice. The best-performing peptide was conjugated to the oligonucleotide of interest, leveraging its kidney-targeting properties to optimize the delivery. We demonstrated that conjugation of the oligonucleotide to a kidney-targeting peptide preserved its repressing HIF-1α activity, while increasing accumulation 10-fold in the kidneys. The results from this study offer valuable insights into the potential of kidney-targeting peptides as a novel strategy to improve the efficacy and safety of therapies for kidney diseases.
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