Ceramic-based multisite microelectrode arrays for simultaneous measures of choline and acetylcholine in CNS.

A ceramic-based microelectrode array (MEA) with enzyme coatings for the accurate measurement of acetylcholine (ACh) in brain tissues is presented. Novel design features allow for self-referencing recordings for improved limits of detection and highly selective measurements of ACh and choline (Ch), simultaneously. Design and fabrication features also result in minimal tissue damage during implantation and improved enzyme coatings due to isolated recording sites. In these studies we have used a recombinant human acetylcholinesterase enzyme coating, which has better reproducibility than other commercially available enzymes. The precisely patterned recording site dimensions, low limit of detection (0.2 micro M) and fast response time ( approximately 1s) allow for second-by-second measurements of ACh and Ch in brain tissues. An electropolymerized meta-phenylenediamine (mPD) layer was used to exclude interfering substances from being recorded at the platinum recording sites. Our studies support that the mPD layer was stable for over 24h under in vitro and in vivo recording conditions. In addition, our work supports that the current configuration of the MEAs produces a robust design, which is suited for measures of ACh and Ch in rat brain.

[1]  C. Choi,et al.  Glucose sensor using a microfabricated electrode and electropolymerized bilayer films. , 2002, Biosensors & bioelectronics.

[2]  K. Moxon,et al.  Ceramic-based multisite microelectrodes for electrochemical recordings. , 2000, Analytical chemistry.

[3]  K. Mitchell,et al.  Acetylcholine and choline amperometric enzyme sensors characterized in vitro and in vivo. , 2004, Analytical chemistry.

[4]  Doretti,et al.  Acetylcholine biosensor involving entrapment of acetylcholinesterase and poly(ethylene glycol)-modified choline oxidase in a poly(vinyl alcohol) cryogel membrane. , 2000, Enzyme and microbial technology.

[5]  L. Descarries The hypothesis of an ambient level of acetylcholine in the central nervous system , 1998, Journal of Physiology-Paris.

[6]  G. Gerhardt,et al.  Second‐by‐second measurement of acetylcholine release in prefrontal cortex , 2006, The European journal of neuroscience.

[7]  S. Ito,et al.  Simultaneous Determination of Choline and Acetylcholine Based on a Trienzyme Chemiluminometric Biosensor in a Single Line Flow Injection System , 2003, Analytical sciences : the international journal of the Japan Society for Analytical Chemistry.

[8]  Tianyan You,et al.  Characterization of platinum nanoparticle-embedded carbon film electrode and its detection of hydrogen peroxide. , 2003, Analytical chemistry.

[9]  J. Lowry,et al.  Characterization in vitro and in vivo of the oxygen dependence of an enzyme/polymer biosensor for monitoring brain glucose , 2002, Journal of Neuroscience Methods.

[10]  Craig A. Grimes,et al.  Encyclopedia of Sensors , 2006 .

[11]  G. Gerhardt,et al.  L-lactate measures in brain tissue with ceramic-based multisite microelectrodes. , 2005, Biosensors & bioelectronics.

[12]  I. Karube,et al.  Ultramicrobiosensors for Monitoring of Neurotransmitters , 1992, Annals of the New York Academy of Sciences.

[13]  G. S. Wilson,et al.  Direct measurement of glutamate release in the brain using a dual enzyme-based electrochemical sensor , 1994, Brain Research.

[14]  J. Lowry,et al.  Biosensor for neurotransmitter L-glutamic acid designed for efficient use of L-glutamate oxidase and effective rejection of interference. , 1997, The Analyst.

[15]  Jin Dai,et al.  Atypical, but Not Typical, Antipsychotic Drugs Increase Cortical Acetylcholine Release without an Effect in the Nucleus Accumbens or Striatum , 2002, Neuropsychopharmacology.

[16]  L. Descarries,et al.  Ultrastructural evidence for diffuse transmission by monoamine and acetylcholine neurons of the central nervous system. , 2000, Progress in brain research.

[17]  Francois Pomerleau,et al.  Chronic second‐by‐second measures of l‐glutamate in the central nervous system of freely moving rats , 2007, Journal of neurochemistry.

[18]  Laurent Descarries,et al.  Diffuse transmission by acetylcholine in the CNS , 1997, Progress in Neurobiology.

[19]  N. Hampp,et al.  Potentiometric thick-film sensor for the determination of the neurotransmitter acetylcholine. , 1994, The Analyst.

[20]  G. Gerhardt,et al.  o-Phenylenediamine-modified carbon fiber electrodes for the detection of nitric oxide. , 1996, Analytical chemistry.

[21]  Martyn G Boutelle,et al.  An amperometric glucose-oxidase/poly(o-phenylenediamine) biosensor for monitoring brain extracellular glucose: in vivo characterisation in the striatum of freely-moving rats , 1998, Journal of Neuroscience Methods.

[22]  G. Gerhardt,et al.  Clearance of Exogenous Dopamine in Rat Dorsal Striatum and Nucleus Accumbens: Role of Metabolism and Effects of Locally Applied Uptake Inhibitors , 1993, Journal of neurochemistry.

[23]  S. Higson,et al.  A novel electro-optical sensor format with generic applicability for exploitation with NAD(P) dependent enzymes. , 2003, Biosensors & bioelectronics.

[24]  B. Waterhouse Methods in Drug Abuse Research : Cellular and Circuit Level Analyses , 2002 .

[25]  G. Gerhardt,et al.  Self-referencing ceramic-based multisite microelectrodes for the detection and elimination of interferences from the measurement of L-glutamate and other analytes. , 2001, Analytical chemistry.

[26]  G. Gerhardt,et al.  Rapid assessment of in vivo cholinergic transmission by amperometric detection of changes in extracellular choline levels , 2004, The European journal of neuroscience.

[27]  N. Kulagina,et al.  Pharmacological evidence for the selectivity of in vivo signals obtained with enzyme-based electrochemical sensors , 2001, Journal of Neuroscience Methods.

[28]  G. Gerhardt,et al.  Ceramic-based multisite microelectrode array for rapid choline measures in brain tissue , 2003 .

[29]  G. Gerhardt,et al.  Microelectrode array studies of basal and potassium‐evoked release of l‐glutamate in the anesthetized rat brain , 2006, Journal of neurochemistry.

[30]  F. Pomerleau,et al.  Real Time in Vivo Measures of l‐Glutamate in the Rat Central Nervous System Using Ceramic‐Based Multisite Microelectrode Arrays , 2003, Annals of the New York Academy of Sciences.

[31]  Microdialysis without acetylcholinesterase inhibition reveals an age-related attenuation in stimulated cortical acetylcholine release , 2003, Neurobiology of Aging.

[32]  G. Gerhardt,et al.  Regional effects of aging on dopaminergic function in the Fischer-344 rat , 1992, Neurobiology of Aging.

[33]  K. Torimitsu,et al.  On-line electrochemical sensor for selective continuous measurement of acetylcholine in cultured brain tissue. , 1998, Analytical chemistry.

[34]  G. S. Wilson,et al.  Electrochemically mediated electrodeposition/electropolymerization to yield a glucose microbiosensor with improved characteristics. , 2002, Analytical chemistry.

[35]  G. S. Wilson,et al.  Fundamental studies of glucose oxidase deposition on a Pt electrode. , 2002, Analytical chemistry.

[36]  Jochen Klein,et al.  Effects of nicotinamide on central cholinergic transmission and on spatial learning in rats , 1996, Pharmacology Biochemistry and Behavior.

[37]  P. Zambonin,et al.  Electrosynthesized poly(pyrrole)/poly(2-naphthol) bilayer membrane as an effective anti-interference layer for simultaneous determination of acethylcholine and choline by a dual electrode amperometric biosensor. , 2006, Biosensors & bioelectronics.

[38]  A. Michael,et al.  Amperometric microsensors for monitoring choline in the extracellular fluid of brain , 1996, Journal of Neuroscience Methods.

[39]  Francois Pomerleau,et al.  Improved ceramic-based multisite microelectrode for rapid measurements of l-glutamate in the CNS , 2002, Journal of Neuroscience Methods.