Magnetically separable bimodal mesoporous carbons with a large capacity for the immobilization of biomolecules

被引:36
作者
Sevilla, Marta [1 ]
Valle-Vigon, Patricia [1 ]
Tartaj, Pedro [2 ]
Fuertes, Antonio B. [1 ]
机构
[1] CSIC, Inst Nacl Carbon, E-33080 Oviedo, Spain
[2] CSIC, Inst Ciencia Mat Madrid, E-28049 Madrid, Spain
关键词
DIRECT ELECTRON-TRANSFER; MOLECULAR-SIEVES; INORGANIC NANOPARTICLES; ENZYME IMMOBILIZATION; SYNTHETIC ROUTE; DRUG-DELIVERY; SILICA MATRIX; ADSORPTION; HEMOGLOBIN; FABRICATION;
D O I
10.1016/j.carbon.2009.05.004
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
A method for the fabrication of carbon-based mesoporous magnetic composites with a large capacity for the adsorption/immobilization of biomolecules is presented. The composites consist of iron oxide spinel nanoparticles inserted into the pores of templated unimodal or bimodal mesoporous carbons. The deposition of the magnetic iron oxide nanoparticles was carried out following two synthetic routes: (1) the direct incorporation of nanoparticles into the pores of the templated carbons and (2) the insertion of nanoparticles into the mesopores of the carbon-silica composite followed by the selective removal of silica framework. The carbon-iron oxide magnetic composites prepared according to route 2 were found to have better textural properties (larger BET surface areas and pore volumes) and significantly higher capacity for the adsorption of hemoglobin and immobilization of lysozyme. The amounts of hemoglobin or lysozyme adsorbed/immobilized by these materials were 176 mg hemoglobin g(-1) support and 131 mg lysozyme g(-1) support using route,1 and 430 mg hemoglobin g(-1) support and 322 mg lysozyme g(-1) support by route 2. Furthermore, we have demonstrated that, when no inorganic nanoparticles are deposited, the bimodal mesoporous carbon shows exceptionally a large immobilization capacity for hemoglobin (830 mg g(-1) support) and lysozyme (510 mg g(-1)). (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2519 / 2527
页数:9
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