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L K Noyes

Publications and source records attributed to L K Noyes.

5 recordsLinked to original sources

Long-term implantation of voltammetric oxidase/peroxide glucose sensors in the rat peritoneum.

Methods for designing, fabricating, testing in vitro and in vivo, and improving chronically implantable oxidase/peroxide-type polarographic glucose sensors are described. Voltammetric means to evaluate oxygen supply to the sensor and to measure the nearby microcirculation with hydrogen washout techniques using the implanted glucose sensor are outlined. Because some peritoneally implanted sensors have, perhaps surprisingly, remained functional for months, such devices may prove with further development to be useful as the sensing components in artificial pancreatic beta cells for the control of diabetes.

Animals↗

Rapid electroenzymatic measurement of lactate in microsamples of spinal fluid.

A lactate sensor, which makes possible rapid direct measurement of L-lactate in small samples of spinal fluid, has been developed. This enzyme electrode gives a linear current output as a function of hydrogen peroxide generated by a lactate oxygen oxidoreductase sandwiched between two membranes. The membranes serve to support the oxidase, prevent the diffusion of soluble electroactive species such as urate, ascorbate, and phenolic drugs such as acetaminophen, and to form a diffusion-limited path for the lactate. A 10 or 25 microL sample of spinal fluid is injected into a 350 microL thermostated chamber containing a suitable buffer and the electrode's sensing surface. The method has been tested by analysis of spinal fluid, with amounts of lactate up to 15 mmol/L, by comparison with a photoenzymatic method. A correlation coefficient of 0.999 was found. With a new cellulose ester membrane, acetaminophen levels up to 10 mmol/L did not interfere. A YSI glucose analyzer can be converted to a lactate analyzer by changing the O-ring mounted enzyme transducer membrane.

Electrodes↗

Rapid micromeasurement of lactate in whole blood.

A new lactate sensor makes it possible to measure the lactate content of whole blood directly in less than 1 min, using only a 10-microL blood sample. The procedure works equally well with plasma, serum, spinal fluid, other body fluids, or tissue homogenates. The instrument is calibrated with lactate standards between 0 and 15 mMol/L. The sensor, a polarographic enzyme electrode, gives a current which is a linear function of the lactate concentration. There is no interference from glucose, pyruvate, alcohol, ascorbate, anticoagulants, lidocaine, acetaminophen, or other drugs and metabolites commonly encountered in critically ill patients. The lactate sensor is composed of a peroxide sensor and an enzyme transducer membrane. The lactate is stoichiometrically converted to pyruvate and hydrogen peroxide by lactate oxygen oxidoreductase derived from Pediococcus species. The oxygen required for the enzymatic oxidation is supplied via an air-permeable silicone elastomeric membrane used for stirring. Comparison of our new electroenzymatic method with the Boehringer-Mannheim photoenzymatic method gives correlations of 0.997 for both whole blood and plasma.

Alcohol Oxidoreductases↗