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纤维素接枝聚(丙交酯)纳米胶束的自组装和紫杉醇载药量。

Self-assembly and paclitaxel loading capacity of cellulose-graft-poly(lactide) nanomicelles.

机构信息

State Key Laboratory of Pulp and Paper Engineering, South China University of Technology, Guangzhou, China.

出版信息

J Agric Food Chem. 2012 Apr 18;60(15):3900-8. doi: 10.1021/jf3001873. Epub 2012 Apr 4.

Abstract

A series of amiphiphilic cellulose-based graft copolymers (MCC-g-PLA) with various molecular factors were synthesized in ionic liquid BmimCl and characterized by FT-IR, (1)H NMR, (13)C NMR, XRD, and TGA. Their solubility in a variety of solvents was compared. The prepared MCC-g-PLA copolymers can self-assemble into spherical nanomicelles (10-50 nm) in aqueous solution. The self-assembly behaviors of the MCC-g-PLA copolymers were systematically investigated by fluorescence probe. Furthermore, the hydrophobic antitumor drug paclitaxel (PTX) was successfully encapsulated into the MCC-g-PLA micelles. The drug encapsulation efficiency and loading content were found to be as high as 89.30% (w/w) and 4.97%, respectively. Results in this study not only suggest a promising cellulose-based antitumor drug carrier but also provide information for property-directed synthesis of the cellulose graft PLA copolymers.

摘要

一系列具有不同分子因素的两亲性纤维素接枝共聚物(MCC-g-PLA)在离子液体 BmimCl 中合成,并通过 FT-IR、(1)H NMR、(13)C NMR、XRD 和 TGA 进行了表征。比较了它们在各种溶剂中的溶解度。制备的 MCC-g-PLA 共聚物可以在水溶液中自组装成球形纳米胶束(10-50nm)。通过荧光探针系统地研究了 MCC-g-PLA 共聚物的自组装行为。此外,疏水性抗肿瘤药物紫杉醇(PTX)成功地封装到 MCC-g-PLA 胶束中。药物包封效率和载药量分别高达 89.30%(w/w)和 4.97%。本研究的结果不仅为基于纤维素的抗肿瘤药物载体提供了有希望的方案,也为基于纤维素的接枝 PLA 共聚物的性能导向合成提供了信息。

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