Dipartimento di Chimica Organica, "A. Mangini", University, Viale Risorgimento 4, 40136 Bologna, Italy.
Adv Healthc Mater. 2012 May;1(3):342-7. doi: 10.1002/adhm.201100047. Epub 2012 Apr 5.
A simple method for the synthesis of lipophilic Ag NPs have been developed. The coated Ag NPs have been entrapped into a FDA-approved and targetable PEG-based polymeric nanoparticles, and this nanocarrier has been conjugated with the peptide chlorotoxin. Uptake experiments have shown a cell-specific recognition of the Ag-1-PNPs-Cltx on U87MG cell lines in comparison to Balb/3T3. The uptake of Ag into the cells was quantified and an interesting cytotoxic effect (IC50 = 45 μM) has been found on glioblastoma cell lines.
已经开发出一种简单的方法来合成亲脂性 Ag NPs。将包覆的 Ag NPs 包封在一种 FDA 批准的、靶向性的基于 PEG 的聚合物纳米颗粒中,这种纳米载体与肽氯毒素结合。与 Balb/3T3 相比,摄取实验表明,Ag-1-PNPs-Cltx 在 U87MG 细胞系上具有细胞特异性识别。已经定量了 Ag 进入细胞的情况,并在神经胶质瘤细胞系上发现了有趣的细胞毒性作用(IC50 = 45 μM)。