Mass screening for inborn error of amino acid metabolism using HPLC
Author(s)
Jasco

This report concerns the simultaneous analysis of the anomalous metabolic amino acids of three illnesses targeted by the Ministry for Health and Welfare (homocystinuria, maple syrup urine disease, phenylketonuria): methionine (Met), leucine (Leu), phenylalanine (Phe), valine (Val), tyrosine (Tyr), isoleucine (Ile).

The time for analysis of a single specimen is 15 minutes. Detection employs OPA post column derivatization. The use of a micro-plate enables easy simultaneous pre-processing of multiple samples.