An automated fluorometric procedure for histidine in blood

We have adapted the sample procurement procedure of blood spotted on filter paper for use with an automated fluorometric method for histidine which is based on the reaction of the amino acid with O-phthaldialdehyde in alkaline solution. Histidine was eluted from blood spotted on filter paper by an a...

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Published inClinica chimica acta Vol. 36; no. 1; pp. 105 - 111
Main Authors Hill, Hoyle D., Summer, George K., Newton, Dale A.
Format Journal Article
LanguageEnglish
Published Netherlands Elsevier B.V 1972
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Abstract We have adapted the sample procurement procedure of blood spotted on filter paper for use with an automated fluorometric method for histidine which is based on the reaction of the amino acid with O-phthaldialdehyde in alkaline solution. Histidine was eluted from blood spotted on filter paper by an alcoholic diluent, and samples and standards were analyzed at a rate of 40/h with a 1:2 sample-to-wash ratio. The reaction product was stabilized by addition of a phosphoric acid solution and measured in a standard fluorometer. The fluorescence is linear for increasing concentrations of histidine, carry-over is negligible, and reproducibility is excellent. The mean percentage recovery was 92% over a concentration range of 2–40 mg/100 ml histidine added to whole blood. Blood obtained from 130 newborn infants 1–3 days after birth revealed a mean and standard deviation of 3.7 ± 0.9 mg/100 ml. The method is rapid and sensitive, and should be applicable to detection of histidinemia and to studies on other clinical and biological problems in human populations.
AbstractList We have adapted the sample procurement procedure of blood spotted on filter paper for use with an automated fluorometric method for histidine which is based on the reaction of the amino acid with O-phthaldialdehyde in alkaline solution. Histidine was eluted from blood spotted on filter paper by an alcoholic diluent, and samples and standards were analyzed at a rate of 40/h with a 1:2 sample-to-wash ratio. The reaction product was stabilized by addition of a phosphoric acid solution and measured in a standard fluorometer. The fluorescence is linear for increasing concentrations of histidine, carry-over is negligible, and reproducibility is excellent. The mean percentage recovery was 92% over a concentration range of 2–40 mg/100 ml histidine added to whole blood. Blood obtained from 130 newborn infants 1–3 days after birth revealed a mean and standard deviation of 3.7 ± 0.9 mg/100 ml. The method is rapid and sensitive, and should be applicable to detection of histidinemia and to studies on other clinical and biological problems in human populations.
Author Newton, Dale A.
Summer, George K.
Hill, Hoyle D.
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Cites_doi 10.1136/adc.38.197.80
10.1016/S0022-3476(62)80109-7
10.1093/clinchem/11.5.541
10.1093/clinchem/15.5.361
10.1542/peds.34.2.182
10.1093/clinchem/15.5.381
10.1016/S0021-9258(19)52394-8
10.1016/0009-8981(70)90225-1
10.1016/0003-2697(70)90135-1
10.1056/NEJM196108032650504
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SubjectTerms Administration, Oral
Aldehydes
Amino Acid Metabolism, Inborn Errors - blood
Amino Acid Metabolism, Inborn Errors - diagnosis
Autoanalysis
Chemistry, Clinical - instrumentation
Fluorometry
Histidine - administration & dosage
Histidine - blood
Humans
Infant, Newborn
Kinetics
Methods
Phthalic Acids
Title An automated fluorometric procedure for histidine in blood
URI https://dx.doi.org/10.1016/0009-8981(72)90164-7
https://www.ncbi.nlm.nih.gov/pubmed/5007692
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