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通过模拟酶催化原子转移自由基聚合将pH响应性聚合物刷表面固定在介孔二氧化硅纳米颗粒上以实现可控的药物释放

Surface Immobilization of pH-Responsive Polymer Brushes on Mesoporous Silica Nanoparticles by Enzyme Mimetic Catalytic ATRP for Controlled Cargo Release.

作者信息

Zhou Hang, Wang Xin, Tang Jun, Yang Ying-Wei

机构信息

College of Chemistry, International Joint Research Laboratory of Nano-Micro Architecture Chemistry (NMAC), Jilin University, Changchun 130012, China.

出版信息

Polymers (Basel). 2016 Aug 2;8(8):277. doi: 10.3390/polym8080277.

Abstract

Peroxidase mimetic catalytic atom transfer radical polymerization (ATRP) was first used to install tertiary amine-functionalized polymer brushes on the surface of mesoporous silica nanoparticles (MSNs) in a facile and highly efficient manner. Poly(,-dimethylaminoethyl methacrylate) (PDMAEMA) brushes-grafted MSNs were fabricated by biocompatible deuterohemin-β-Ala-His-Thr-Val-Glu-Lys (DhHP-6)-catalyzed surface-initiated ATRP (SI-ATRP). The resulting organic⁻inorganic hybrid nanocarriers were fully characterized by Fourier transform-infrared spectroscopy (FT-IR), thermogravimetric analysis (TGA), X-ray photoelectron spectroscopy (XPS), powder X-ray diffraction (XRD), SEM, TEM, Elemental analysis, Zeta-potential, and N₂ adsorption⁻desorption isotherms, which demonstrated the successful coating of pH-responsive polymers on the MSN surface. Rhodamine 6G (Rh6G) dyes were further loaded within the mesopores of this nanocarrier, and the release of Rh6G out of MSNs in a controlled fashion was achieved upon lowing the solution pH. The electrostatic repulsion of positively-charged tertiary ammonium of PDMAEMAs in acidic environments induced the stretching out of polymer brushes on MSN surfaces, thus opening the gates to allow cargo diffusion out of the mesopores of MSNs.

摘要

过氧化物酶模拟催化原子转移自由基聚合(ATRP)首次被用于以简便且高效的方式在介孔二氧化硅纳米颗粒(MSNs)表面接上叔胺功能化聚合物刷。通过生物相容性的氘代血红素-β-丙氨酸-组氨酸-苏氨酸-缬氨酸-谷氨酸-赖氨酸(DhHP-6)催化的表面引发原子转移自由基聚合(SI-ATRP)制备了接枝聚(甲基丙烯酸-2-二甲氨基乙酯)(PDMAEMA)刷的MSNs。通过傅里叶变换红外光谱(FT-IR)、热重分析(TGA)、X射线光电子能谱(XPS)、粉末X射线衍射(XRD)、扫描电子显微镜(SEM)、透射电子显微镜(TEM)、元素分析、zeta电位和N₂吸附-脱附等温线对所得的有机-无机杂化纳米载体进行了全面表征,这些表征证明了pH响应性聚合物成功包覆在MSN表面。罗丹明6G(Rh6G)染料进一步负载在该纳米载体的介孔内,通过降低溶液pH值实现了Rh6G从MSNs中以可控方式释放。在酸性环境中,PDMAEMAs带正电荷的叔铵的静电排斥作用导致聚合物刷在MSN表面伸展,从而打开通道,使货物从MSNs的介孔中扩散出来。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/47ae/6432388/ab502d4e27c5/polymers-08-00277-sch001.jpg

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