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载有促凋亡剂的 TSPO 配体-葡聚糖纳米胶粒递送至神经胶质瘤细胞系。

Delivery of Proapoptotic Agents in Glioma Cell Lines by TSPO Ligand-Dextran Nanogels.

机构信息

Department of Pharmacy-Drug Sciences, University of Bari "Aldo Moro", Via Orabona, St. 4, 70125 Bari, Italy.

Institute for Physical and Chemical Processes (IPCF)-CNR, SS Bari, Via Orabona, St. 4, 70125 Bari, Italy.

出版信息

Int J Mol Sci. 2018 Apr 11;19(4):1155. doi: 10.3390/ijms19041155.

Abstract

Translocator protein 18-kDa (TSPO) is a versatile mitochondrial target for molecular imaging and therapy. Moreover, selective TSPO ligands have been widely investigated for diagnostic purposes and explored to target drug delivery systems directed to cancer cells overexpressing TSPO. Indeed, poly(d,l-lactic-co-glycolic acid (PLGA) polymers and nanocarriers decorated with TSPO ligands are capable of transporting TSPO ligands inside cancer cells, inducing survival inhibition in cancer cells and producing mitochondrial morphology modification. The aim of this work was to prepare nanogels (NGs) made with TSPO ligand dextran conjugates (TSPO-Dex) that are useful as potential delivery systems of two TSPO ligands as apoptotic agents. Synthesis and complete characterization of TSPO-dextran conjugates, an average molecular weights analysis, TSPO ligand release profiles, thermal behaviour and swelling studies were achieved. NG preparation, characterization and in vitro biological studies were also performed. The release of TSPO ligands released from dextran conjugates at 37 °C occurred in human serum at a faster rate than that detected in phosphate buffer. Cytotoxicity studies demonstrated that NGs produced from TSPO ligand-dextran conjugates induce survival inhibition in rat C6 glioma cell lines. Cellular uptake was also proven by fluorescence microscopy.

摘要

转位蛋白 18kDa(TSPO)是一种多功能的线粒体靶点,可用于分子成像和治疗。此外,选择性 TSPO 配体已被广泛研究用于诊断目的,并探索将其用于靶向表达 TSPO 的癌细胞的药物递送系统。事实上,聚(丙交酯-共-乙交酯)(PLGA)聚合物和用 TSPO 配体修饰的纳米载体能够将 TSPO 配体运送到癌细胞内,诱导癌细胞的生存抑制,并产生线粒体形态修饰。本工作的目的是制备用 TSPO 配体葡聚糖缀合物(TSPO-Dex)制成的纳米凝胶(NGs),作为两种 TSPO 配体作为凋亡剂的潜在递送系统。完成了 TSPO-葡聚糖缀合物的合成和全面表征,包括平均分子量分析、TSPO 配体释放曲线、热行为和溶胀研究。还进行了 NG 的制备、表征和体外生物学研究。在 37°C 下,TSPO 配体从葡聚糖缀合物中释放的释放速度比在磷酸盐缓冲液中检测到的释放速度更快。细胞毒性研究表明,由 TSPO 配体-葡聚糖缀合物产生的 NGs 诱导大鼠 C6 神经胶质瘤细胞系的生存抑制。荧光显微镜也证明了细胞摄取。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7add/5979576/db126e4a0748/ijms-19-01155-g001.jpg

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