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载阿霉素的双离子固体脂质纳米粒抑制 U87MG 细胞的生长。

Catanionic solid lipid nanoparticles carrying doxorubicin for inhibiting the growth of U87MG cells.

机构信息

Department of Chemical Engineering, National Chung Cheng University, Chia-Yi 62102, Taiwan, ROC.

出版信息

Colloids Surf B Biointerfaces. 2011 Jul 1;85(2):131-7. doi: 10.1016/j.colsurfb.2011.02.011. Epub 2011 Feb 17.

Abstract

Catanionic solid lipid nanoparticles (CASLNs), loaded with doxorubicin (Dox) and grafted with anti-epithelial growth factor receptor (EGFR) (anti-EGFR/Dox-CASLNs), were applied to suppressing propagation of malignant U87MG cells. U87MG cells were cultured with anti-EGFR/Dox-CASLNs for assessing the cell viability and EGFR expression. When the concentration of catanionic surfactants, containing hexadecyltrimethylammonium bromide and sodium anionic sodium dodecylsulfate, was 1mM, CASLNs entrapped the largest quantity of Dox. The order of cacao butter (CB) in the entrapment efficiency of Dox was 50% CB>0% CB>100% CB. In addition, the release rate of Dox and the antiproliferative effect on U87MG cells were in the following order: 100% CB>0% CB>50% CB. A high level of CB in anti-EGFR/Dox-CASLNs reduced the cytotoxicity to human brain-microvascular endothelial cells. The immunochemical staining revealed that the crosslinked anti-EGFR on the surface of Dox-CASLNs preserved a high specificity in recognizing EGFR on U87MG cells and inducing growth-inhibition effect. The innovated anti-EGFR/Dox-CASLNs can be an effective delivery system with high targeting efficacy against the growth of brain glioblastomas carcinoma.

摘要

季铵盐固体脂质纳米粒(CATANIONIC SOLID LIPID NANOPARTICLES,简称 CASLNs),负载阿霉素(DOXORUBICIN,简称 Dox)并接枝抗表皮生长因子受体(ANTI-EPIDERMAL GROWTH FACTOR RECEPTOR,简称 EGFR)(ANTI-EGFR/Dox-CASLNs),被应用于抑制恶性 U87MG 细胞的增殖。将 U87MG 细胞与抗 EGFR/Dox-CASLNs 一起培养,以评估细胞活力和 EGFR 表达。当包含十六烷基三甲基溴化铵和十二烷基硫酸钠的季铵盐表面活性剂浓度为 1mM 时,CASLNs 包封了最大量的 Dox。可可脂(COCOA BUTTER,简称 CB)在 Dox 包封效率中的顺序为 50% CB>0% CB>100% CB。此外,Dox 的释放速率和对 U87MG 细胞的增殖抑制作用的顺序为:100% CB>0% CB>50% CB。抗 EGFR/Dox-CASLNs 中 CB 含量高会降低对人脑微血管内皮细胞的细胞毒性。免疫化学染色显示,Dox-CASLNs 表面交联的抗 EGFR 保持了对 U87MG 细胞上 EGFR 的高特异性,并诱导生长抑制作用。这种创新的抗 EGFR/Dox-CASLNs 可以成为一种有效的靶向递药系统,对脑胶质瘤癌的生长具有很高的靶向疗效。

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