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无表面活性剂制备具有低细胞毒性的高度稳定两性离子聚(酰胺-胺)纳米凝胶。

Surfactant-free preparation of highly stable zwitterionic poly(amido amine) nanogels with minimal cytotoxicity.

机构信息

Department of Biomaterials Science and Technology, MIRA Institute for Biomedical Technology and Technical Medicine, Faculty of Science and Technology, University of Twente, P.O. Box 217, 7500 AE Enschede, The Netherlands.

Department of Biomaterials Science and Technology, MIRA Institute for Biomedical Technology and Technical Medicine, Faculty of Science and Technology, University of Twente, P.O. Box 217, 7500 AE Enschede, The Netherlands.

出版信息

Acta Biomater. 2016 Jan;30:126-134. doi: 10.1016/j.actbio.2015.10.037. Epub 2015 Oct 28.

Abstract

UNLABELLED

Narrowly dispersed zwitterionic poly(amido amine) (PAA) nanogels with a diameter of approximately 100nm were prepared by a high-yielding and surfactant-free, inverse nanoprecipitation of PAA polymers. The resulting, negatively charged, nanogels (PAA-NG1) were functionalized with N,N-dimethylethylenediamine via EDC/NHS coupling chemistry. This resulted in nanogels with a positive surface charge (PAA-NG2). Both types of nanogels were fluorescently labelled via isothiocyanate coupling. PAA-NG1 displays high colloidal stability both in PBS and Fetal Bovine Serum solution. Moreover, both nanogels exhibit a distinct zwitterionic swelling profile in response to pH changes. Cellular uptake of FITC-labelled nanogels with RAW 264.7, PC-3 and COS-7 cells was evaluated by fluorescence microscopy. These studies showed that nanogel surface charge greatly influences nanogel-cell interactions. The PAA polymer and PAA-NG1 showed minimal cell toxicity as was evaluated by MTT assays. The findings reported here demonstrate that PAA nanogels possess interesting properties for future studies in both drug delivery and imaging.

STATEMENT OF SIGNIFICANCE

The use of polymeric nanoparticles in biomedical applications such as drug delivery and imaging, shows great potential for medical applications. However, these nanoparticles are often not stable in biological environments. Zwitterionic polymers have shown excellent biocompatibility, but these materials are not easily degradable in biological environments. With the aim of developing a nanoparticle for drug delivery and imaging we synthesized a biomimetic and readily biodegradable zwitterionic polymer, which was incorporated into nanogels. These nanogels showed excellent stability in the presence of serum and minimal cytotoxicity, which was tested in three cell lines. Because of their negative surface charge and excellent serum stability, these nanogels are therefore promising carriers for drug delivery and molecular imaging.

摘要

未标记

通过高收率且无表面活性剂的聚(酰胺-胺)(PAA)聚合物的反相胶束沉淀制备了直径约为 100nm 的分散性窄的两性离子 PAA 纳米凝胶。所得带负电荷的纳米凝胶(PAA-NG1)通过 EDC/NHS 偶联化学用 N,N-二甲基乙二胺进行功能化。这导致纳米凝胶带有正表面电荷(PAA-NG2)。这两种类型的纳米凝胶均通过异硫氰酸酯偶联进行荧光标记。PAA-NG1 在 PBS 和胎牛血清溶液中均显示出高胶体稳定性。此外,两种纳米凝胶在响应 pH 值变化时均显示出独特的两性离子溶胀特性。通过荧光显微镜评估了 RAW 264.7、PC-3 和 COS-7 细胞对 FITC 标记的纳米凝胶的细胞摄取。这些研究表明,纳米凝胶表面电荷极大地影响了纳米凝胶-细胞相互作用。通过 MTT 测定评估了 PAA 聚合物和 PAA-NG1 的细胞毒性最小。这里报道的研究结果表明,PAA 纳米凝胶具有用于药物输送和成像的未来研究的有趣特性。

意义声明

在药物输送和成像等生物医学应用中使用聚合物纳米粒子在医学应用中显示出巨大的潜力。然而,这些纳米粒子在生物环境中通常不稳定。两性离子聚合物显示出优异的生物相容性,但这些材料在生物环境中不易降解。为了开发用于药物输送和成像的纳米粒子,我们合成了一种仿生且易于生物降解的两性离子聚合物,将其掺入纳米凝胶中。这些纳米凝胶在存在血清时显示出极好的稳定性,并且在三种细胞系中测试时细胞毒性最小。由于其负表面电荷和出色的血清稳定性,因此这些纳米凝胶是药物输送和分子成像的有前途的载体。

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