LNCaP公司
体内
外体
癌症研究
内化
肽
前列腺癌
靶向给药
微泡
体外
纳米载体
癌症
化学
医学
药理学
细胞
生物
药品
生物化学
内科学
小RNA
基因
生物技术
作者
Maja Severic,Guanglong Ma,Sara Pereira,Amalia Ruiz,Calvin C.L. Cheung,Wafa’ T. Al-Jamal
标识
DOI:10.1016/j.jconrel.2020.12.017
摘要
The present work describes the engineering of anti-PSMA peptide-decorated exosome mimetics (EMs) targeting advanced prostate cancer (PC). The targeted EMs were produced from anti-PSMA peptide, WQPDTAHHWATL, expressing U937 monoblastic cells, followed by successive extrusion cycles. The engineered EMs were nanosized, produced at a high yield, and displayed the anti-PSMA peptide, exosomal markers and monocytes proteins on their surface. As anticipated, PSMA-EMs showed increased cellular internalization in PSMA positive PC cell lines (LNCaP and C4-2B), compared to unmodified EMs. Most importantly, higher tumour targeting was observed in solid C4-2B tumours, following intravenous administration, confirming their targeting ability in vivo. Overall, our study indicates that the engineered anti-PSMA peptide-targeted EMs can be a promising drug delivery system for advanced PC.
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