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R P McKnight

Publications and source records attributed to R P McKnight.

5 recordsLinked to original sources

Evaluation of the PaT Stat Kinetic UV Test set for the determination of phenylalanine and tyrosine in serum or plasma.

We have evaluated the PaT Stat Kinetic UV Test Kit for the simultaneous determination of phenylalanine (Phe) and tyrosine (Tyr) in plasma or serum. The Phe and Tyr concentrations measured with the kit show a coefficient of variation of about 15% for both within- and between-day determinations. The assays for both Phe and Tyr are linear to concentrations of at least 18 mg/dL without predilution of the specimen. Concentration differences of as little as 0.5 mg/dL are distinguishable. No significant interference was found from either phenylpyruvate or phenyllactate at levels up to 0.5 mM, nor from bilirubin, haemoglobin, or triglycerides at levels well above those generally found in clinical specimens. A comparative study of 70 clinical specimens, using the kit method and an amino acid analyzer (AAA) showed a linear relationship. Least-squares analysis of the data yielded the following parameters (AAA as reference): slope = 0.93 to 1.00, intercept = 0.04 to 0.21, correlation coefficient = 0.97 to 0.98. We conclude that the kit is suitable for the determination of Phe and Tyr in plasma or serum and can enable any laboratory equipped with a recording UV-spectrophotometer to assay these two amino acids for the dietary management of PKU.

Adult↗

Evaluation of a method for enzymic radiochemical assay of tobramycin and amikacin in serum.

This enzymic radiochemical procedure for measuring tobramycin and amikacin in serum is based on the transfer of the 14C-acetyl group from [14C]acetyl-coenzyme A to the 6' nitrogen atom of the drug by the enzyme kanamycin 6'-acetyltransferase (EC 2.3.1.55). The transfer, stoichiometric and quantitative, is complete after 10-min incubation at 37 degrees C. The labeled acetylaminoglycoside is adsorbed onto phosphocellulose paper discs, which are washed to removed any unreacted [14C]acetyl-coenzyme A. The radioactivity is then eluted into liquid scintillation counting vials and counted for 1 min each. The assay detects as little as 2 ng of either drug and the standard curve is linear into the toxic range of concentrations. Most of the commonly administered aminoglycosides act as substrates in the assay, except for the C1 component of gentamicin C complex. Neither hemolysis, lipemia, nor icterus interfere with the assay. Results compare favorably with those determined by radioimmunoassay and a microbiological method.

Amikacin↗

Thermodynamic parameters for the intramolecular disordered-to-beta transition of poly(L-tyrosine) in aqueous solution.

We have examined the disordered-to-beat transition of two samples of high molecular wieght poly(L-tyrosine), a polypeptide with an ionizing side chain, by potentiometric titration of solutions of this polymer in aqueous buffer. The degree of ionization was determined spectrophotometrically from the absorption of the tyrosinate anion at 293.5 nm. By using polymer solutions of high dilution the region of the conformational transition was separated from that of aggregation. As a consequence it was possible to obtain titration data for the intramolecular transition which we believe are free of interference from aggregation. For this transition we found that deltaHO=-1330 cal/mol of residue. The two samples gave values of -3.42+/-0.14 and -3.85+/-0.10 u for the change in entropy. Possible artifactual origins for this distinction have been examined and may be dicounted. Rather, it probably reflects a difference in the beta structures formed which depends on molecular weight.

Hydrogen-Ion Concentration↗