Chemiluminescence determination of terbutaline sulfate in bovine urine and pharmaceutical preparations based on enhancement of the 2-phenyl-4, 5-di (2-furyl) imidazole-potassium ferricyanide system

Journal of Pharmaceutical and Biomedical Analysis

Volumn 58, Issue 1, 2012, Pages 141-145

  Han, Lu ^a   Zhang, Yumin ^a   Kang, Jing ^a   Tang, Jieli ^a   Zhang, Yihua ^a  

^a JILIN UNIVERSITY   (China)

Author keywords

2 Phenyl 4, 5 di (2 furyl) imidazole; Chemiluminescence; Potassium ferricyanide; Terbutaline sulfate

Indexed keywords

2 PHENYL 4,5 DI (2 FURYL)IMIDAZOLE; IMIDAZOLE DERIVATIVE; POTASSIUM FERRICYANIDE; TERBUTALINE SULFATE; UNCLASSIFIED DRUG;

ARTICLE; CHEMOLUMINESCENCE; CONCENTRATION (PARAMETERS); COW; DRUG DETERMINATION; DRUG SYNTHESIS; NONHUMAN; PRIORITY JOURNAL; SENSITIVITY ANALYSIS; URINE;

ANIMALS; CATTLE; FERRICYANIDES; IMIDAZOLES; LUMINESCENCE; LUMINESCENT MEASUREMENTS; PHARMACEUTICAL PREPARATIONS; TERBUTALINE;

EID: 80255138117     PISSN: 07317085     EISSN: 1873264X     Source Type: Journal    
DOI: 10.1016/j.jpba.2011.09.011     Document Type: Article

References (18)

1. Radziszewski B.R. Untersuchungen über hydrobenzamid, amarin und lophin. Chem. Ber. 1877, 10:70-75.
2. MacDonald A., Chan K.W., Nieman T.A. Lophine chemiluminescence for metal ion determinations. Anal. Chem. 1979, 51:2077-2082.
3. Fridman N., Kaftory M., Speiser S. Structures and photophysics of lophine and double lophine derivatives. Sens. Actuators 2007, B 126:107-115.
4. Nakashima K., Fukuzaki Y., Nomura R., Shimoda R., Nakamurafl Y., Kurodafl N., Akiyama S., Irgum K. Fluorescence and chemiluminescence properties of newly developed lophine analogues. Dyes Pigments 1998, 38:127-136.
5. 2-agonists in urine by gas chromatography-mass spectrometry for application in doping control. Anal. Chim. Acta 2000, 418:79-92.
6. Martineau L., Horan M.A., Rothwell N.J., Little R.A. Salbutamol, a beta 2-adrenoceptor agonist increases skeletal muscle strength in young men. Clin. Sci. 1992, 8:615-621.
7. Kim K.H., Kim H.J., Kim J.H., Shin S.D. Determination of terbutaline enantiomers in human urine by coupled achiral-chiral high-performance liquid chromatography with fluorescence detection. J. Chromatogr. B 2001, 751:69-77.
8. Herring V.L., Johnson J.A. Simple method for determination of terbutaline concentration by high-performance liquid chromatography. J. Chromatogr. B 2000, 741:307-312.
9. Doerge D.R., Bajic S., Blankenship L.R., Preece S.W., Churchwell M.I. Determination of β-agonist residues in human plasma using liquid chromatography/atmospheric pressure chemical ionization mass spectrometry and tandem mass spectrometry. J. Mass Spectrom. 1995, 30:911-916.
10. Li S., Wang J.S., Zhao S.L. Determination of terbutaline sulfate by capillary electrophoresis with chemiluminescence detection. J. Chromatogr. B 2009, 877:155-158.
11. Lu W.Z., Cole R.B. Determination of chiral pharmaceutical compounds, terbutaline, ketamine and propranolol, by on-line capillary electrophoresis-electrospray ionization mass spectrometry. J. Chromatogr. B 1998, 714:69-75.
12. Yilmaz N., Ö zkan S.A., Uslu B., Şentürk Z., Biryol I. Determination of terbutaline based on oxidation voltammetry. J. Pharm. Biomed. Anal. 1998, 17:349-355.
13. Wang Z.P., Zhang Z.J., Fu Z.F., Zhang X. Sensitive flow-injection chemiluminescence determination of terbutaline sulfate based on enhancement of the luminol-permanganate reaction. Anal. Bioanal. Chem. 2004, 378:834-840.
14. Lv Y., Zhang Z.J., Hu Y.F., He D.Y., He S.H. A novel chemiluminescence method for determination of terbutaline sulfate based on potassium ferricyanide oxidation sensitized by rhodamine 6G. J. Pharm. Biomed. Anal. 2003, 32:555-561.
15. He D.Y., Zhang Z.J., Zhou H.J., Huang Y. Micro flow sensor on a chip for the determination of terbutaline in human serum based on chemiluminescence and a molecularly imprinted polymer. Talanta 2006, 69:1215-1220.
16. Debus H. Ueber die einwirkung des ammoniaks auf glyoxal. Liebigs Ann. Chem. 1858, 107:199-208.
17. Tsunenaga M., Iga H., Kimura M. Location effect of an OH group on the chemiluminescence efficiency of 4-hydroperoxy-2-(o-, m-, or p-hydroxyphenyl)-4, 5-diphenyl-4H-isoimidazoles. Tetrahedron Lett. 2005, 46:1877-1880.
18. Evmiridis N.P. Prospects of using chemiluminescence emission generated during oxidation of pyrogallol with periodate for the determination of pyrogallol with flow injection. Analyst 1988, 113:1051-1056.