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A biodegradable CO2-based polymeric antitumor nanodrug via a one-pot surfactant- and solvent-free miniemulsion preparation

机译:通过一锅表面活性剂和无溶剂微乳剂制剂的一种可生物降解的CO2基聚合物抗肿瘤纳米抗体

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摘要

In the present study, low molecular weight poly(propylene carbonate) (PPC, M-n = 3500), a biodegradable liquid polymer easily prepared from carbon dioxide (CO2), was modified into poly(propylene carbonate)diacrylate (PPC-DA) by acylation, and methoxy poly(ethylene glycol) (mPEG) was modified into methoxy poly(ethylene glycol) acrylate (mPEG-A). Using PPC-DA as the dispersant to dissolve hydrophobic doxorubicin (DOX) and the initiator, and with mPEG-A as the co-monomer and polymerisable surfactant, a biodegradable nanodrug with excellent biocompatibility was prepared by shear emulsification polymerization without surfactants or organic solvent residues. The nanodrug can be efficiently endocytosed by tumor cells and can rapidly release doxorubicin triggered by the acidic endosomal pH. As evidenced by experiments in tumor-bearing mice, such a nanodrug is stealthy during blood circulation, and targets tumor sites with high efficiency. Moreover, this nanodrug is more effective and less toxic than free doxorubicin. This study provides a green and versatile approach for preparing biodegradable nanodrugs via a simple and efficient process. Moreover, this study extends the applications of CO2 based polymers in the biomedical field, promoting the development of CO2 polymerization fixation.
机译:在本研究中,低分子量聚(碳酸亚丙酯)(PPC,Mn = 3500),通过酰化将易于用二氧化碳(CO2)制备的可生物降解的液体聚合物(CO 2),通过酰化改性聚(碳酸亚丙酯)二丙烯酸酯(PPC-DA)然后将甲氧基聚(乙二醇)(MPEG)改性为甲氧基聚(乙二醇)丙烯酸酯(MPEG-A)。使用PPC-DA作为分散剂以溶解疏水性多柔比蛋白(DOX)和引发剂,并用MPEG-A作为共聚单体和可聚合表面活性剂,通过剪切乳化聚合而没有表面活性剂或有机溶剂残留物制备具有优异生物相容性的可生物降解的纳米树脂。纳米树脂可以通过肿瘤细胞有效内吞,可以快速释放由酸性内体pH引发的多柔比星。如在携带肿瘤小鼠的实验所证明的情况下,这种纳米树脂在血液循环过程中是隐身的,并且效率高靶向肿瘤部位。此外,该纳米抑郁型比游离多柔比蛋白更有效且毒性较小。该研究提供了一种通过简单有效的方法制备可生物降解的纳米树脂的绿色和多功能的方法。此外,该研究扩展了基于CO 2的聚合物在生物医学领域的应用,促进了CO2聚合固定的发育。

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