Development of a self-cleaning sensor membrane for implantable biosensors

被引:34
|
作者
Gant, Rebecca M. [1 ]
Hou, Yaping [1 ]
Grunlan, Melissa A. [1 ]
Cote, Gerard L. [1 ]
机构
[1] Texas A&M Univ, Dept Biomed Engn, College Stn, TX 77843 USA
关键词
foreign body response; biocompatible; thermoresponsive; smart polymers; PNIPAAm; CALCIUM ALGINATE MEMBRANES; DIFFUSION-COEFFICIENTS; DRUG-RELEASE; IN-VIVO; GLUCOSE; HYDROGELS; DETACHMENT; SURFACES; DELIVERY; BEHAVIOR;
D O I
10.1002/jbm.a.32135
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Fibrous tissue encapsulation may slow the diffusion of the target analyte to an implanted sensor and compromise the optical signal. Poly(N-isopropylacrylamide) (PNIPAAm) hydrogels are thermoresponsive, exhibiting temperature-modulated swelling behavior that could be used to prevent biofouling. Unfortunately, PNIPAAm hydrogels are limited by poor mechanical strength. In this Study, a unique thermoresponsive nanocomposite hydrogel was developed to create a mechanically robust Self-cleaning sensor membrane for implantable biosensors. This hydrogel was prepared by the photochemical cure of all aqueous solution of NIPAAm and copoly(dimethylsiloxane/ methylvinylsiloxane) colloidal nanoparticles (similar to 219 nm). At temperatures above the volume phase transition temperature (VPTT) of approximately 33-34 degrees C, the hydrogel des-wells and becomes hydrophobic, whereas lowering the temperature below the VPTT causes the hydrogel to swell and become hydrophilic. The potential of this material to minimize biofouling via temperature-modulation while maintaining sensor viability was investigated using glucose as a target analyte. PNIPAAm composite hydrogels with and without poration were compared to a pure PNIPAAm hydrogel and a nonthermoresponsive poly (ethylene glycol) (PEG) hydrogel. Poration led to a substantial increase in diffusion. Cycling the temperature of the nanocomposite hydrogels around the VPTT caused significant detachment of GFP-H2B 3T3 fibroblast cells. (C) 2008 Wiley Periodicals, Inc. J Biomed Mater Res 90A: 695-701,2009
引用
收藏
页码:695 / 701
页数:7
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