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使用脂质体模板制备单分散且尺寸可控的聚乙二醇水凝胶纳米颗粒。

Preparation of monodisperse and size-controlled poly(ethylene glycol) hydrogel nanoparticles using liposome templates.

作者信息

An Se Yong, Bui Minh-Phuong Ngoc, Nam Yun Jung, Han Kwi Nam, Li Cheng Ai, Choo Jaebum, Lee Eun Kyu, Katoh Shigeo, Kumada Yoichi, Seong Gi Hun

机构信息

Department of Applied Chemistry, Hanyang University, Ansan 426-791, South Korea.

出版信息

J Colloid Interface Sci. 2009 Mar 1;331(1):98-103. doi: 10.1016/j.jcis.2008.11.022. Epub 2008 Nov 17.

Abstract

Liposomes were used as templates to prepare size-controlled and monodisperse poly(ethylene glycol) (PEG) hydrogel nanoparticles. The procedure for the preparation of PEG nanoparticles using liposomes consists of encapsulation of photopolymerizable PEG hydrogel solution into the cavity of the liposomes, extrusion through a membrane with a specific pore size, and photopolymerization of the contents inside the liposomes by UV irradiation. The size distributions of the prepared particles were 1.32+/-0.16 microm (12%), 450+/-62 nm (14%), and 94+/-12 nm (13%) after extrusion through membrane filters with pore sizes of 1 microm, 400 nm, and 100 nm, respectively. With this approach, it is also possible to modify the surface of the hydrogel nanoparticles with various functional groups in a one-step procedure. To functionalize the surface of a PEG nanoparticle, methoxy poly(ethylene glycol)-aldehyde was added as copolymer to the hydrogel-forming components and aldehyde-functionalized PEG nanoparticles could be obtained easily by UV-induced photopolymerization, following conjugation with poly-L-lysine-FITC through amine-aldehyde coupling. The prepared PEG particles showed strong fluorescence from FITC on the edge of the particles using confocal microscopy. The immobilization of biomaterials such as enzymes in hydrogel particles could be performed with loading beta-galactosidases during the hydration step for liposome preparation without additional procedures. The resorufin produced by applying resorufin beta-D-galactopyranoside as the substrate showed the fluorescence under the confocal microscopy.

摘要

脂质体被用作模板来制备尺寸可控且单分散的聚乙二醇(PEG)水凝胶纳米颗粒。使用脂质体制备PEG纳米颗粒的过程包括将可光聚合的PEG水凝胶溶液封装到脂质体腔内,通过具有特定孔径的膜进行挤压,以及通过紫外线照射使脂质体内的内容物发生光聚合。分别通过孔径为1微米、400纳米和100纳米的膜过滤器挤压后,所制备颗粒的尺寸分布分别为1.32±0.16微米(12%)、450±62纳米(14%)和94±12纳米(13%)。通过这种方法,还可以在一步操作中用各种官能团修饰水凝胶纳米颗粒的表面。为了使PEG纳米颗粒表面功能化,将甲氧基聚乙二醇醛作为共聚物添加到形成水凝胶的组分中,通过紫外线诱导的光聚合反应,随后通过胺醛偶联与聚-L-赖氨酸-异硫氰酸荧光素(poly-L-lysine-FITC)结合,可轻松获得醛基功能化的PEG纳米颗粒。使用共聚焦显微镜观察,所制备的PEG颗粒在颗粒边缘显示出强烈的异硫氰酸荧光素(FITC)荧光。在脂质体制备的水合步骤中,在不进行额外操作的情况下加载β-半乳糖苷酶,就可以将酶等生物材料固定在水凝胶颗粒中。以试卤灵β-D-吡喃半乳糖苷作为底物产生的试卤灵在共聚焦显微镜下显示出荧光。

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