HPLC method for amino acids profile in biological fluids and inborn metabolic disorders of aminoacidopathies

Indian Journal of Clinical Biochemistry

Volumn 17, Issue 2, 2002, Pages 7-26

  Babu, S V Suresh ^a   Shareef, M M ^a   Shetty, A Pavan Kumar ^a   Shetty, K Taranath ^a  

^a NATIONAL INSTITUTE OF MENTAL HEALTH AND NEUROSCIENCES   (India)

Author keywords

Amino acidopathies; Amino acids profile; Inborn metabolic disorders; O pthalaldehyde; Reverse phase HPLC

Indexed keywords

EID: 77949807992     PISSN: 09701915     EISSN: None     Source Type: Journal    
DOI: 10.1007/BF02867967     Document Type: Article

References (23)

1. Walker.V and Mills,G.A, (1995) Quantitative methods for amino acid analysis in biological fluids. Ann. Clin. Biochem. 32, 28-57
2. Andersson.A. Isaksson, A., Bratstrom, L and Bjorn, H. (1993) Homocysteine and other thiols in plasma and thiol specific postcolumn derivatization. Clin. Chem. 39, 1590-1597.
3. Deyl, Z., Hyanek. J and Horakova, M. (1986) Profiling of amino acids in body fluids and tissues by means of liquid chromatography. J. Chromatogr. 379, 177-250.
4. Jacobsen, D.W. (1998) Homocysteine and vitamins in cardiovascular disease. Clin. Chem. 44, 1833-1843
5. Hankey, G.J and Eikelboom, J.W. (1999) Homocysteine and vascular disease. The Lancet 354,407-413
6. Welch, G.N and Loscalzo, J (1998) Homocysteine and atherothrombosis. New Engl. J. Med. 338, 1042-1050
7. Boushey, C. J., Beresford, S. A. A., Omen, G. S., and Motulsky, A.G.(1995). A quantitative assessment of plasma homocysteine as a risk factor in vascular disease. JAMA. 274, 1049 -1057
8. Graham. I. M., Daly, L. E, Refsum, H. M., Robinson, K., Brattstrom, L.E., Ueland, Per M., Palma-Reis, R.J., Boers, G. H., Sheahan, R. G., Israelsson, Bo., Uiterwaal., C. S., Meleady, R., McMaster, D., Verhoef, P., Witterman, J., Rubba, P., Bellet, H., Wutreccht, J.C., deWalk, H. W., Luis, C. S., Parrot-Rouland, F. M., Tan, K.S., Higgins, I., Garcon, D., Medrano, M.J., Candito, M., Evans, A. E. and Andria, G. (1997) Plasma homocysteine as a risk factor for vascular disease: European concerted action project. JAMA, 277, 1775-1781
9. Frantzen, F., Faaren, A. L., Alfheim, I and Nordhei, A. K. (1998) Enzyme conversion immuno assay for determining total homocysteine in plasma or serum. Clin. Chem.44, 311-316
10. Refsum, H., Ueland, P.M., and Svardal, A. M. (1989) Fully automated fluorescence assay for determining total homocysteine in plasma. Clin. Chem. 35, 1921-1927
11. Robenstein, D. L., and Yamaahita, G. T (1989) Determination of homocysteine, penicillamine and their symmetrical and mixed disulfides by liquid chromatography with electrochemical detection. Anal. Biochem. 80, 259-263
12. Thomson, S. B and Tucker, D. J (1985) Determination of homocysteine in urine. J. Chromatogr. 338,201-208
13. Pastore, A., Massoud, R., Motti, C., Russo, A. Lo., Fucci, G., Cortese, C and Federici, G. (1998) Fully automated assay for total homocysteine, cysteine, cysteinylglycine, glutathione, cysteamine and 2-mercaptopropionylglycine in plasma and urine. Cin. Chem.44, 825-832
14. Mansoor, M. A., Svardal, A M and Ueland, P.M (1992) Determination of the in vivo redox status of cysteine, cysteinylglycine, homocysteine and glutathione in human plasma. Anal. Biochem. 200, 218-229
15. Hyland, K. and Bottiglieri; T. (1992) Measurement of total plasma and cerebrospinal fluid homocysteine by fluorescence following high performance liquid chromatography and pre column derivatization with opthalaldehyde. J. Chromatogr. 579, 55-62.
16. Bradford, M. (1976) A rapid and sensitive method for the quantification of micrograms quantities of protein utilizing the principle of protein dye binding. Anal. Biochem. 76, 248-254.
17. Varley, H., Gowenlock, A. H. and Bell, M.(1980). Practical Clinical Biochemistry. Vol I, Fifth edn (1980). William Heinemann Medical Books Lts, London, p 491-494.
18. Turnell. D. C and Cooper, J.D.H. (1982) Rapid assay for amino acids in serum or urine by precolumn derivatization and reversed phase liquid chromatography. Clin. Chem. 28, 527-531.
19. Tom Teerlink, Paul, A.M., Van Leeuwen and Alexander, H. (1994) Plasma amino acids determined by liquid chromatography within 17 minutes. Clin. Chem. 40, 245-249.
20. Hamesh, A and Jhonson, M.W (2001 ) Nonketotic hyperglycinemia In: The Metabolic & Molecular Bases of inherited Diseases. Eight edition Vol II. Eds. Scriver, CR., Beaudet, A.I., Sly, W.S and Valle, D. McGraw Hill Med Publication Division, New York. p. 2065-2078
21. Valle, D and Simell, O. (2001 ). The hyperornithinemias. In: The Metabolic & Molecular Bases of inherited Diseases. Eighth edition Vol II Eds. Scriver, CR., Beaudet, A.I., Sly, W.S and Valle, D. McGraw Hill Med Publication Division, New York. p. 1857-1895
22. Chung, D.T. and Shih, V.E., (2001). Maple syrup urine disease (Branched chain ketoaciduria). In: The Metabolic & Molecular Bases of inherited Diseases eight edition Vol II Edis. Scriver, CR., Beaudet, A.I., Sly, W.S and Valle, D. McGraw Hill Med Publication Division, New York. p. 1971-2005
23. Mudd, S.H., Levy, H.L. and Kraus, J.P (2001). Disorders of transulfuration. In: The Metabolic & Molecular Bases of inherited Diseases eight edition Vol II Eds. Scriver, CR., Beaudet, A.I., Sly, W.S and Valle, D. Mcgraw Hill Med Publication Division, New York, p.2007-2056