Delivery of Oleanolic Acid with Improved Antifibrosis Efficacy by a Cell Penetrating Peptide P10

被引:5
|
作者
Wang, Lidan [1 ,2 ]
Geng, Jingping [1 ,3 ]
Wang, Hu [1 ,4 ]
机构
[1] China Three Gorges Univ, Med Sch, Dept Microbiol & Immunol, Yichang 443002, Peoples R China
[2] Chinese Med Hosp Puyang, Lab Med Dept, Puyang 457000, Peoples R China
[3] Univ Warsaw, Ctr New Technol, Interdisciplinary Lab Mol Biol & Biophys, PL-02097 Warsaw, Poland
[4] Johns Hopkins Univ, Inst Cell Engn, Sch Med, Baltimore, MD 21215 USA
关键词
Cell penetrating peptide; Drug delivery; Oleanolicacid; Fibrosis; NUCLEIC-ACID; IDENTIFICATION; EFFICIENCY;
D O I
10.1021/acsptsci.3c00087
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Oleanolicacid (OA), a common pentacyclic triterpenoid found inplants, has several therapeutic uses, including the treatment of hepatopathydisorders. However, due to OA's weak permeability and limitedbioavailability, its therapeutic advantages are limited. Here, weshowed that a short peptide known as p10 not only binds to OA butalso rapidly enhances OA delivery into cultured hepatic stellate cells(HSCs), lowers their synthesis of fibrogenic proteins, and furtherreduces the HSC migration capacity. Our findings show that noncovalentlyconjugating short peptides to OA improves its pharmacological efficacyand permeability.
引用
收藏
页码:1006 / 1014
页数:9
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