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氨等离子体处理的聚丙烯腈纳米纤维膜:通过戊二醛偶联化学固定蛋白质的坚固基底,用于生物传感器应用。

Ammonia plasma-treated electrospun polyacrylonitryle nanofibrous membrane: the robust substrate for protein immobilization through glutaraldhyde coupling chemistry for biosensor application.

机构信息

Institute for Nanoscience and Nanotechnology, Sharif University of Technology, Tehran, Iran.

Stem Cell Technology Research Center, 19977-75555, Tehran, Iran.

出版信息

Sci Rep. 2017 Aug 25;7(1):9441. doi: 10.1038/s41598-017-10040-7.

Abstract

The surface of polyacrylonitrile electrospun nanofibrous membrane (PAN NFM) was aminated by the ammonia plasma treatment. The content of amine groups has been estimated for different time of plasma treatment. The newly generated amine groups were successfully activated by glutaraldehyde (Ga) for the covalent attachment of the protein molecules on the NFM surface. Bio-functionalization of ammonia plasma treated PAN NFM was carried out by the primary antibodies (Ab) immobilization as a protein model through Ga coupling chemistry. For comparison, the immobilization of Ab was also performed through physical interactions. Attenuated total reflection-fourier transform infrared spectroscopy (ATR-FTIR) was used for the characterization of surface functional groups of PAN NFM after different modifications. The surface morphology of the NFM after immobilization was characterized using scanning electron microscope (SEM). The efficacy of Ab immobilization was estimated by enzyme-linked immuno sorbent assay (ELISA) method. X- Ray photoelectron spectroscopy (XPS) was performed to confirm the covalent immobilization of Ab on the modified PAN NFM. Results show that ammonia plasma treatment effectively increased the amount of Ab immobilization through Ga coupling chemistry. Our findings suggest that this is a versatile model for the preparation of stable bio-functionalized NFM which is applicable in different field of biomedical science.

摘要

聚丙烯腈电纺纳米纤维膜(PAN NFM)的表面通过氨等离子体处理进行了氨基化。已经估计了不同等离子体处理时间的胺基含量。新生成的胺基通过戊二醛(Ga)成功激活,用于在 NFM 表面上共价连接蛋白质分子。通过 Ga 偶联化学,通过固定化一级抗体(Ab)作为蛋白质模型,对氨等离子体处理的 PAN NFM 进行了生物功能化。为了进行比较,还通过物理相互作用进行了 Ab 的固定化。衰减全反射-傅里叶变换红外光谱(ATR-FTIR)用于表征不同修饰后的 PAN NFM 的表面功能基团。使用扫描电子显微镜(SEM)对固定化后的 NFM 的表面形貌进行了表征。通过酶联免疫吸附测定(ELISA)法评估了 Ab 固定化的效果。X 射线光电子能谱(XPS)用于证实 Ab 在修饰的 PAN NFM 上的共价固定化。结果表明,氨等离子体处理通过 Ga 偶联化学有效地增加了 Ab 的固定化量。我们的研究结果表明,这是一种用于制备稳定生物功能化 NFM 的通用模型,适用于生物医学科学的不同领域。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd26/5573414/b7dd80e849b9/41598_2017_10040_Fig1_HTML.jpg

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