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pH-sensitive PEG-based micelles for tumor targeting.

机译:pH敏感的基于PEG的胶束用于靶向肿瘤。

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A new acid sensitive nanocarrier based on lipid core micelles has been investigated for tumor targeted drug delivery. Sulfadimethoxine-PEG-phospholipid unimer (SD-PEG-DSPE) was designed to endow micelles with pH responsiveness in the physiopathologic range. The unimer was synthesized according to a two-step procedure. Potentiometric analysis showed that SD-PEG-DSPE has pK(a) of 6.7. In water, the unimers assembled spontaneously in 20 nm size micelles with 60 muM critical micelle concentration. The particle size was not affected by the pH in the 6.2-7.4 range. The micelles loaded paclitaxel very efficiently and released the drug slowly regardless the incubation pH. Fluorescence spectroscopy and cytofluorimetry carried out by MCF7 tumor cell incubation with labeled SD-PEG-DSPE micelles at pH 7.4 and 6.2 showed that micelles associate with cells mostly at acidic pH with a time-dependent behavior. A cell subpopulation took up the nanocarrier more efficiently at pH 6.2. Confocal microscopy confirmed that under these conditions the systems are taken up by cells or fuse with cellular membrane. Cytotoxicity studies demonstrated that the SD-PEG-DSPE micelles deliver more efficiently paclitaxel at pH 6.2 than at neutral pH confirming that the cell internalization can be triggered by the external environmental conditions.
机译:已经研究了一种基于脂质核心胶束的新型酸敏感性纳米载体,用于肿瘤靶向药物的递送。磺胺二甲氧嘧啶-PEG-磷脂单体(SD-PEG-DSPE)旨在赋予胶束以生理病理范围内的pH响应性。根据两步程序合成了单体。电位分析表明SD-PEG-DSPE的pK(a)为6.7。在水中,单聚体自发组装在20 nm大小的胶束中,临界胶束浓度为60μM。粒径不受6.2-7.4范围内的pH值的影响。不管孵育的pH值如何,胶束都能非常有效地加载紫杉醇,并缓慢释放药物。通过MCF7肿瘤细胞与标记的SD-PEG-DSPE胶束在pH 7.4和6.2的孵育进行的荧光光谱和细胞荧光分析表明,胶束主要在酸性pH下与细胞缔合,具有时间依赖性。在pH 6.2下,细胞亚群更有效地吸收了纳米载体。共聚焦显微镜证实,在这些条件下,系统被细胞吸收或与细胞膜融合。细胞毒性研究表明,SD-PEG-DSPE胶束在pH 6.2时比在中性pH时更有效地递送紫杉醇,这证实了细胞内在化可以由外部环境条件触发。

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