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利用抗原-抗体相互作用进行粒子靶向的可行性和限制。

Feasibility and constraints of particle targeting using the antigen-antibody interaction.

机构信息

Institute of Chemical Technology Prague, Department of Chemical Engineering, Technická 3, Prague 6, 166 28, Czech Republic.

出版信息

Nanoscale. 2013 Dec 7;5(23):11490-8. doi: 10.1039/c3nr04340a. Epub 2013 Oct 29.

Abstract

This work is concerned with the surface modification of fluorescent silica nanoparticles by a monoclonal antibody (M75) and the specific bioadhesion of such particles to surfaces containing the PG domain of carbonic anhydrase IX (CA IX), which is a trans-membrane protein specifically expressed on the surfaces of several tumor cell lines. The adhesion strength of antibody-bearing silica nanoparticles to antigen-bearing surfaces was investigated under laminar flow conditions in a microfluidic cell and compared to the adhesion of unmodified silica nanoparticles and nanoparticles coupled with an unspecific antibody. Adhesion to cancer cells using flow cytometry was also investigated and in all cases the adhesion strength of M75-modified nanoparticles was significantly stronger than for the unmodified or unspecific nanoparticles, up to several orders of magnitude in some cases. The specific modification of nano- and microparticles by an antibody-like protein therefore appears to be a feasible approach for the targeting of tumor cells.

摘要

这项工作涉及通过单克隆抗体 (M75) 对荧光二氧化硅纳米粒子进行表面修饰,以及此类粒子特异性地粘附到含有碳酸酐酶 IX (CA IX) PG 结构域的表面,CA IX 是一种跨膜蛋白,特异性表达在几种肿瘤细胞系的表面。在微流控细胞中,在层流条件下研究了带有抗体的二氧化硅纳米粒子在带有抗原的表面上的粘附强度,并将其与未修饰的二氧化硅纳米粒子和与非特异性抗体偶联的纳米粒子的粘附进行了比较。还使用流式细胞术研究了对癌细胞的粘附,在所有情况下,M75 修饰的纳米粒子的粘附强度都明显强于未修饰或非特异性纳米粒子,在某些情况下要强几个数量级。因此,通过类似抗体的蛋白质对纳米粒子和微粒子进行特异性修饰似乎是一种针对肿瘤细胞的靶向方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7254/4047836/8e9fd0a9101a/c3nr04340a-f1.jpg

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