scholarly journals Enzymatic assay of d-glucuronate using uronate dehydrogenase

2009 ◽  
Vol 392 (2) ◽  
pp. 183-185 ◽  
Author(s):  
Tae Seok Moon ◽  
Sang-Hwal Yoon ◽  
Mary-Jane Tsang Mui Ching ◽  
Amanda M. Lanza ◽  
Kristala L. Jones Prather
Author(s):  
B Lefrère ◽  
D Wohrer ◽  
C Godefroy ◽  
M Soichot ◽  
A Mihoubi ◽  
...  

Abstract We report the case of an 11-month-old male infant with a complex congenital heart disease who was admitted in the intensive care unit following cardiorespiratory arrest at home. Toxicological urine screening reported an ethanol concentration of 0.65 g/L using an enzymatic assay, without suspicion of alcohol intake; a significant amount of ethanol concentration was found in two plasma samples using the same enzymatic assay. Plasma and urine ethanol concentrations were below the limit of quantification (LOQ) when tested using a gas chromatography method. Urine ethanol level was also below the LOQ when tested by enzymatic assay after an initial urine ultrafiltration. These results confirmed our suspicion of matrix interference due to elevated lactate and lactate dehydrogenase levels interfering in the enzymatic assay. This analytical interference, well-known in postmortem samples, extensively studied in vitro, has been rarely reported in vivo, especially in children. To the best of our knowledge, this case is only the sixth one reported in an infant’s plasma and the first initially discovered from urine. Indeed, as for ethanol, this last matrix has not been studied in the context of this artifact that may induce false-positive ethanol results while seeking a diagnosis in life-threatening or fatal situations that are potentially subject to forensic scrutiny. In parallel to a synthetic literature review, we propose a simple, informative decision tree, in order to help health professionals suspecting a false-positive result when performing an ethanol assay.


1980 ◽  
Vol 21 (2) ◽  
pp. 259-261
Author(s):  
H Fromm ◽  
P Amin ◽  
H Klein ◽  
I Kupke
Keyword(s):  

2021 ◽  
Vol 39 ◽  
pp. 116160
Author(s):  
Rossella Capochiani de Iudicibus ◽  
Petr Tomek ◽  
Brian D. Palmer ◽  
Sofian M. Tijono ◽  
Jack U. Flanagan ◽  
...  

1997 ◽  
Vol 43 (3) ◽  
pp. 533-538 ◽  
Author(s):  
James R Etchison ◽  
Hudson H Freeze

Abstract We describe a new and improved enzymatic assay for determining the concentration of d-mannose in sera. Serum d-glucose is selectively converted to glucose-6 phosphate with the highly specific thermostable glucokinase (EC 2.7.1.2) from Bacillus stearothermophilus. The anionic reaction products and excess substrates are removed by a rapid and simple anion-exchange chromatography step in microcentrifuge spin columns. d-Mannose in the glucose-depleted sample is then assayed spectrophotometrically by using coupled enzymatic reactions. The quantitative elimination of glucose from the serum samples allowed the accurate and reproducible assay of serum mannose in the 0–200 μmol/L range. Recovery of mannose added to serum (5–200 μmol/L) was 94% ± 4.4%. The intraassay CV was 6.7% at 40 μmol/L mannose (n = 5; 39.6 ± 1.6 μmol/L) and 4.4% at 80 μmol/L (n = 11; 75.0 ± 1.8 μmol/L); the interassay CV at these concentrations was 12.2% (n = 7; 36.9 ± 2.1 μmol/L) and 9.8% (n = 7; 74.2 ± 2.7 μmol/L), respectively. Sera from 11 healthy human volunteers contained an average of 54.1 ± 11.9 μmol/L mannose (range 36–81 μmol/L).


2001 ◽  
Vol 25 (2) ◽  
pp. 77-80 ◽  
Author(s):  
B. Blomme ◽  
P. Lheureux ◽  
E. Gerlo ◽  
V. Maes
Keyword(s):  

Sign in / Sign up

Export Citation Format

Share Document