Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 1999
Determination of the histamine metabolite tele-methylimidazoleacetic acid and of creatinine in urine by the same HPLC system.
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Granerus G, Lönnqvist B, Wass U
Аннотация
OBJECTIVE AND DESIGN: To develop an HPLC method with UV detection for determination of tele-methylimidazoleacetic acid (t-MelmAA) in urine of man or animals, which is reliable, simple and less expensive than existing GC/MS techniques.
METHOD: The elaborated procedure enables separation of t-MelmAA from its pros-isomer (p-MelmAA) as well as from imidazoleacetic acid. As an internal standard tele-ethylimidazoleacetic acid (t-EtlmAA) is used. The acids, after being converted to their stable isopropylesters, are extracted at pH 6.0-6.5. The further separation prior to HPLC utilises a small cellulose phosphate column. The HPLC system is isocratic with a C18 column and mobile phase consisting of an aqueous solution of SDS at pH 3.5 mixed with acetonitrile (65:35). An advantage of this system is that it can be used to determine the urine creatinine concentration to express excreted t-MelmAA in mmol/mol creatinine.
RESULTS AND CONCLUSIONS: The method applicability is demonstrated in repeated studies in mastocytosis patients. The broad range of excretion values, from normal up to a high level (0.9 to 30 mmol/mol creatinine), indicates that it can be satisfactorily used for evaluation of histamine turnover under various clinical conditions. The method appears to be a good alternative to GC/MS based ones.
METHOD: The elaborated procedure enables separation of t-MelmAA from its pros-isomer (p-MelmAA) as well as from imidazoleacetic acid. As an internal standard tele-ethylimidazoleacetic acid (t-EtlmAA) is used. The acids, after being converted to their stable isopropylesters, are extracted at pH 6.0-6.5. The further separation prior to HPLC utilises a small cellulose phosphate column. The HPLC system is isocratic with a C18 column and mobile phase consisting of an aqueous solution of SDS at pH 3.5 mixed with acetonitrile (65:35). An advantage of this system is that it can be used to determine the urine creatinine concentration to express excreted t-MelmAA in mmol/mol creatinine.
RESULTS AND CONCLUSIONS: The method applicability is demonstrated in repeated studies in mastocytosis patients. The broad range of excretion values, from normal up to a high level (0.9 to 30 mmol/mol creatinine), indicates that it can be satisfactorily used for evaluation of histamine turnover under various clinical conditions. The method appears to be a good alternative to GC/MS based ones.