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通过反相微乳液制备的荧光聚氨酯纳米胶囊:用作生物载体的表面功能化

Fluorescent polyurethane nanocapsules prepared via inverse miniemulsion: surface functionalization for use as biocarriers.

作者信息

Paiphansiri Umaporn, Dausend Julia, Musyanovych Anna, Mailänder Volker, Landfester Katharina

机构信息

Institute of Organic Chemistry III-Macromolecular Chemistry and Organic Materials, University of Ulm, Albert-Einstein-Allee 11, 89081 Ulm, Germany.

出版信息

Macromol Biosci. 2009 Jun 11;9(6):575-84. doi: 10.1002/mabi.200800293.

Abstract

The functionalization of well-defined PU nanocapsules with an aqueous core prepared by performing a polyaddition at the interface of inverse (water-in-oil) miniemulsion droplets is demonstrated. The miniemulsion technique involving the nanoreactor concept allows one to obtain an encapsulation efficiency as high as 90% within the nanocapsules. A pH independent fluorescent dye is used as a model system for the aqueous core. By varying the molar ratio of the diol to the diisocyanate at a fixed surfactant concentration, the shell thickness of the nanocapsules can be finely tuned. The carboxy- and amino-functionalized surface of the nanocapsules can be tailored by an in-situ carboxymethylation reaction and by physical adsorption of a cationic polyelectrolyte, i.e. PAEMA or PEI. The increased uptake of amino-functionalized fluorescent nanocapsules by HeLa cells clearly demonstrates the potential of the functionalized nanocapsules to be successfully exploited as biocarriers.

摘要

通过在反相(水包油)微乳液滴的界面进行加成聚合制备具有水相核的明确的聚氨酯纳米胶囊的功能化得以展示。涉及纳米反应器概念的微乳液技术能够使纳米胶囊内的包封效率高达90%。一种与pH无关的荧光染料被用作水相核的模型体系。在固定的表面活性剂浓度下,通过改变二醇与二异氰酸酯的摩尔比,可以精细调节纳米胶囊的壳厚度。纳米胶囊的羧基和氨基功能化表面可通过原位羧甲基化反应以及阳离子聚电解质(即聚甲基丙烯酸二甲氨基乙酯或聚乙烯亚胺)的物理吸附来定制。HeLa细胞对氨基功能化荧光纳米胶囊摄取的增加清楚地证明了功能化纳米胶囊作为生物载体成功应用的潜力。

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