Design of a self-cleaning thermoresponsive nanocomposite hydrogel membrane for implantable biosensors.

Following implantation of a biosensor, adhesion of proteins and cells and eventual fibrous encapsulation will limit analyte diffusion and impair sensor performance. A thermoresponsive nanocomposite hydrogel was developed as a self-cleaning biosensor membrane to minimize the effect of the host response and its utility for an optical glucose sensor, demonstrated here. It was previously reported that thermoresponsive nanocomposite hydrogels prepared from photopolymerization of an aqueous solution of N-isopropylacrylamide (NIPAAm) and polysiloxane colloidal nanoparticles released adhered cells with thermal cycling. However, poly(N-isopropylacrylamide) hydrogels exhibit a volume phase transition temperature (VPTT) of approximately 33-34 degrees C, which is below body temperature. Thus, the hydrogel would be in a collapsed state in vivo, which would ultimately limit diffusion of the target analyte (e.g., glucose) to the encapsulated sensor. In this study, the VPTT of the nanocomposite hydrogel was increased by introducing N-vinylpyrrolidone (NVP) as a comonomer, so that the hydrogel was in the swollen state in vivo. This thermoresponsive nanocomposite hydrogel was prepared by the photopolymerization of an aqueous solution of NIPAAm, NVP, and polysiloxane colloidal nanoparticles. In addition to a VPTT a few degrees above body temperature, the hydrogel also exhibited good mechanical strength, glucose diffusion, and in vitro cell release upon thermal cycling. Thus, this nanocomposite hydrogel may be useful as a biosensor membrane to minimize biofouling and extend the lifetime and efficiency of implantable glucose sensors and other biosensors.

[1]  A. Entezami,et al.  Effect of synthesis method and buffer composition on the LCST of a smart copolymer of N-isopropylacrylamide and acrylic acid , 2007 .

[2]  The effect of preparation temperature on the swelling behavior of poly (N-isopropylacrylamide) gels , 2000 .

[3]  T. Okano,et al.  Thermo-responsive culture dishes allow the intact harvest of multilayered keratinocyte sheets without dispase by reducing temperature. , 2001, Tissue engineering.

[4]  Buddy D. Ratner,et al.  A paradigm shift: biomaterials that heal , 2007 .

[5]  W. N. Chen,et al.  Engineering cell de-adhesion dynamics on thermoresponsive poly(N-isopropylacrylamide). , 2008, Acta biomaterialia.

[6]  V. Choudhary,et al.  Synthesis and characterization of poly(N‐isopropylacrylamide) films by photopolymerization , 2006 .

[7]  Hang Song,et al.  Effects of internal microstructures of poly(N-isopropylacrylamide) hydrogels on thermo-responsive volume phase-transition and controlled-release characteristics , 2006 .

[8]  Thermoreversible hydrogels. XII. Effect of the polymerization conditions on the swelling behavior of the N-isopropylacrylamide gel , 2000 .

[9]  Yong Pei,et al.  The effect of pH on the LCST of poly(N-isopropylacrylamide) and poly(N-isopropylacrylamide-co-acrylic acid) , 2004, Journal of biomaterials science. Polymer edition.

[10]  A. Han,et al.  Thermoresponsive nanocomposite hydrogels with cell-releasing behavior. , 2008, Biomaterials.

[11]  A. Moes,et al.  Effect of some physiological and non-physiological compounds on the phase transition temperature of thermoresponsive polymers intended for oral controlled-drug delivery. , 2001, International journal of pharmaceutics.

[12]  Yuichi Mori,et al.  Cell Culture on a Thermo-Responsive Polymer Surface , 1990, Bio/Technology.

[13]  Norihiro Kato,et al.  Microporous, fast response cellulose ether hydrogel prepared by freeze-drying. , 2004, Colloids and surfaces. B, Biointerfaces.

[14]  C. Chu,et al.  Thermosensitive PNIPAAm cryogel with superfast and stable oscillatory properties. , 2003, Chemical communications.

[15]  Clark M. Blatteis,et al.  Physiology and Pathophysiology of Temperature Regulation , 1998 .

[16]  P. Lianos,et al.  Photophysical behavior of terpyridine-lanthanide ion complexes incorporated in a poly(N,N-dimethylacrylamide) hydrogel. , 2006, Langmuir : the ACS journal of surfaces and colloids.

[17]  Chaobin He,et al.  The effect of salt and pH on the phase-transition behaviors of temperature-sensitive copolymers based on N-isopropylacrylamide. , 2004, Biomaterials.

[18]  M. S. Jones Effect of pH on the lower critical solution temperatures of random copolymers of N-isopropylacrylamide and acrylic acid , 1999 .

[19]  N. Uyanik,et al.  Investigation of the effect of type and concentration of ionizable comonomer on the collapse behavior of N-isopropylacrylamide copolymer gels in water , 1999 .

[20]  Luke M. Geever,et al.  The effect of salts and pH buffered solutions on the phase transition temperature and swelling of thermoresponsive pseudogels based on N-isopropylacrylamide , 2007 .

[21]  E. Chiellini,et al.  Polymers in Medicine , 1983 .

[22]  Junru Wu,et al.  Subcutaneous Tissue Mechanical Behavior is Linear and Viscoelastic Under Uniaxial Tension , 2003, Connective tissue research.

[23]  Leslie D. Montgomery,et al.  Effect of ambient temperature on the thermal profile of the human forearm, hand, and fingers , 2006, Annals of Biomedical Engineering.

[24]  James D. Hardy,et al.  Basal Metabolism, Radiation, Convection and Vaporization at Temperatures of 22 to 35°C. Six Figures , 1938 .

[25]  T. Okano,et al.  Thermo-sensitive polymers as on-off switches for drug release , 1987 .

[26]  Jan Feijen,et al.  Effect of comonomer hydrophilicity and ionization on the lower critical solution temperature of N-isopropylacrylamide copolymers , 1993 .

[27]  G. Stephanopoulos,et al.  Diffusion coefficients of glucose and ethanol in cell‐free and cell‐occupied calcium alginate membranes , 1986, Biotechnology and bioengineering.

[28]  J Werner,et al.  Temperature profiles with respect to inhomogeneity and geometry of the human body. , 1988, Journal of applied physiology.

[29]  Chih-Chang Chu,et al.  Thermoresponsive hydrogel with rapid response dynamics , 2003, Journal of materials science. Materials in medicine.

[30]  J. Knochel,et al.  Medical progress: Heat stroke , 2002 .

[31]  K. Amighi,et al.  Evaluation of a new controlled-drug delivery concept based on the use of thermoresponsive polymers. , 2002, International journal of pharmaceutics.

[32]  Mark E Meyerhoff,et al.  In vivo chemical sensors: tackling biocompatibility. , 2006, Analytical chemistry.

[33]  Klaus D. Jandt,et al.  Temperature-sensitive PVA/PNIPAAm semi-IPN hydrogels with enhanced responsive properties. , 2009, Acta biomaterialia.

[34]  G. Brengelmann,et al.  Control of skin blood flow in the neutral zone of human body temperature regulation. , 1996, Journal of applied physiology.

[35]  G. Coté,et al.  Development of a self-cleaning sensor membrane for implantable biosensors. , 2009, Journal of biomedical materials research. Part A.

[36]  T. Okano,et al.  Thermo‐responsive polymeric surfaces; control of attachment and detachment of cultured cells , 1990 .

[37]  R. Freitag Synthetic Polymers for Biotechnology and Medicine , 2002 .

[38]  Kevin E. Healy,et al.  Synthesis and characterization of injectable poly(N-isopropylacrylamide)-based hydrogels that support tissue formation in vitro , 1999 .

[39]  Valery V. Tuchin,et al.  Handbook of Optical Sensing of Glucose in Biological Fluids and Tissues , 2008 .

[40]  D. Kazan,et al.  Structure and protein separation efficiency of poly(N‐isopropylacrylamide) gels: Effect of synthesis conditions , 1998 .

[41]  Armando Venâncio,et al.  Characterization of sugar diffusion coefficients in alginate membranes , 1997 .

[42]  J. Teixeira,et al.  Model identification and diffusion coefficients determination of glucose and malic acid in calcium alginate membranes , 1994 .

[43]  Frank N. Jones,et al.  Organic Coatings: Science and Technology , 1992 .

[44]  Peter Tikuisis,et al.  Forearm temperature profile during the transient phase of thermal stress , 2004, European Journal of Applied Physiology and Occupational Physiology.

[45]  C. Bowman,et al.  Mechanical properties of hydrogels and their experimental determination. , 1996, Biomaterials.