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Determination of neopterin, kynurenine, tryptophan and creatinine in human serum by high throuput HPLC
L. Krcmova, D. Solichova, B. Melichar, M. Kasparova, J. Plisek, L. Sobotka, P. Solich
Jazyk angličtina Země Anglie, Velká Británie
Typ dokumentu časopisecké články, práce podpořená grantem
- MeSH
- fosfáty chemie MeSH
- koncentrace vodíkových iontů MeSH
- kreatinin krev MeSH
- kynurenin krev MeSH
- lidé MeSH
- neopterin krev MeSH
- pufry MeSH
- reprodukovatelnost výsledků MeSH
- tryptofan krev MeSH
- vysokoúčinná kapalinová chromatografie přístrojové vybavení metody MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
A new HPLC method for simultaneous determination of neopterin, creatinine, kynurenine and tryptophan in human serum was developed and validated. Monolithic stationary phase's technology (two monolithic columns RP-18e were connected with guard monolithic cartridge 4.6 mm × 50 mm+3.0 mm × 100 mm and 4.6 × 10 mm) and special auto sampler for micro titration plates (samples are storage in dark cooled place protected against evaporation) were combined with easy sample preparation step. As mobile phase 15 mmol/L phosphate buffer at pH 4.50 was used. Neopterin and tryptophan were detected using fluorescent detection and kynurenine and creatinine were detected by diode-array detection. This method may be suitable for large sequences of samples in clinical research and routine practice.
Citace poskytuje Crossref.org
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- $a Determination of neopterin, kynurenine, tryptophan and creatinine in human serum by high throuput HPLC / $c L. Krcmova, D. Solichova, B. Melichar, M. Kasparova, J. Plisek, L. Sobotka, P. Solich
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- $a A new HPLC method for simultaneous determination of neopterin, creatinine, kynurenine and tryptophan in human serum was developed and validated. Monolithic stationary phase's technology (two monolithic columns RP-18e were connected with guard monolithic cartridge 4.6 mm × 50 mm+3.0 mm × 100 mm and 4.6 × 10 mm) and special auto sampler for micro titration plates (samples are storage in dark cooled place protected against evaporation) were combined with easy sample preparation step. As mobile phase 15 mmol/L phosphate buffer at pH 4.50 was used. Neopterin and tryptophan were detected using fluorescent detection and kynurenine and creatinine were detected by diode-array detection. This method may be suitable for large sequences of samples in clinical research and routine practice.
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