Optimation and validation of analytical method of cotrimoxazole in tablet and plasma in vitro by high performance liquid chromatography

Journal of Bioanalysis and Biomedicine

Volumn 4, Issue 2, 2012, Pages 26-29

  Harmita, ^a   Mansur, Umar ^a   Sartika, Jenni ^a  

^a UNIVERSITY OF INDONESIA   (Indonesia)

Author keywords

Hplc; Sulfamethoxazole; Trimethoprim; Validation

Indexed keywords

ACETIC ACID; ACETONITRILE; COTRIMOXAZOLE; SODIUM HYDROXIDE; SULFADIMIDINE; TRIETHYLAMINE; WATER;

ACCURACY; ARTICLE; COLUMN CHROMATOGRAPHY; CONCENTRATION (PARAMETERS); DRUG BLOOD LEVEL; DRUG DETERMINATION; DRUG STABILITY; FLOW RATE; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; HUMAN; IN VITRO STUDY; LIMIT OF QUANTITATION; PH MEASUREMENT; PROCESS DEVELOPMENT; PROCESS OPTIMIZATION; REPRODUCIBILITY; ROOM TEMPERATURE; VALIDATION PROCESS;

EID: 84864799163     PISSN: None     EISSN: 1948593X     Source Type: Journal    
DOI: 10.4172/1948-593X.1000059     Document Type: Article

References (25)

1. Blood (2009) January 8, 2010
2. Departemen Kesehatan Republik Indonesia (1995) Farmakope Indonesia (Ed. ke-4) Jakarta.
3. Evans, Gary (Ed.) (2004) A handbook of bioanalysis and drug metabolism. USA: CRC Press.
4. Food and Drug Administration (1994) Validation of chromatographic methods. Reviewer guidance
5. Food and Drug Administration (2000) Analytical procedures and method validation. Guidance for industry, Februari 2, 2010.
6. Food and Drug Administratio (2001) Bioanalytical method validation. Guidance for industry. November 15, 2009.
7. Food and Drug Administration (2003) Q1A(R2) Stability testing of new drug substances and products. Guidance for industry, November 15, 2009
8. Galichet, Laurent Y (Ed.) (2005) Clarke's analysis of drugs and poisons. London: Pharmaceutical Press.
9. Gandjar, Ibnu G, Rohman A (2007) Kimia farmasi analisis. Yogyakarta: Pustaka Pelajar.
10. Gilman AG (2006) The Pharmacological basis of therapeutics (11th ed.) USA: Macmillan Publishing.
11. Gunawan, Gan S (Ed.) (2008) Farmakologi dan terapi (Ed. ke-5). Jakarta: Balai Penerbit FK UI.
12. Hadjar, Mohammad MI (1985) Teknik analisis obat dalam cairan biologis dengan GLC dan HPLC. In: Cermin Dunia Kedokteran (No. 37, hlm. 26-31) Jakarta: Pusat Penelitian dan Pengembangan PT. Kalbe Farma.
13. Harmita (2006) Buku ajar analisis fisikokimia. Depok: Departemen Farmasi FMIPA Universitas Indonesia.
14. Katzung BG, Masters SB, Trevor AJ (2009) Basic and clinical pharmacology. McGraw-Hill San Fransisco.
15. Laizure SC, Holden CL, Stevens RC (1990) Ion-paired high-performance liquid chromatographic separation of trimethoprim, sulfamethoxazole and N4-acetylsulfamethoxazole with solid-phase extraction. In: Lunn, George. & Schmuff, Norman. (1997) HPLC Methods for Pharmaceutical Analysis. USA: Wiley Interscience.
16. Mistri HN, Jangid AG, Pudage A, Shah A, Shrivastav PS (2009) Simultaneous determination of sulfamethoxazole and trimethoprim in microgram quantities from low plasma volume by liquid chromatography-tandem mass spectrometry. Microchemical Journal 94: 130-138.
17. Moffat AC (Ed.) (1986) Clarke's isolation and identification of drugs in pharmaceuticals, body fluid, and post mortem material (2nd ed.) London: The Pharmaceutical Press.
18. Moore KHP, Brouwer KLR (1995) High-performance liquid chromatographic evaluation of the effect of heat treatment on trimethoprim and sulfamethoxazole stability in serum. In: Lunn, George & Schmuff, Norman. (1997) HPLC Methods for Pharmaceutical Analysis. USA: Wiley Interscience.
19. Ronn Anita M, Mutabingwa TK, Angelo KS (1999) A reversed-phase high-performance liquid chromatography method for the determination of cotrimoxazole (trimethoprim/sulphamethoxazole) in children treated for malaria. Desember 8, 2009.
20. Henner ST (Ed.) (2005) Preparative chromatography of fine chemicals and pharmaceutical agents. Germany: Wiley-VCH.
21. Wu-Pong SL, Yu S, Andrew BC (2004) Applied biopharmaceutics and pharmacokinetics (5th ed.) USA: Appeton & Lange.
22. James S, Boylan James C (Ed.) (1988) Encyclopedia of pharmaceutical technology. Vol.1. New York, USA.
23. Synder Lloyd R, Kirkland, Joseph J, Glajch (1997) Practical HPLC method development (2nd ed.). USA: John Wiley & Sons.
24. The United State Pharmacopeial Convention (2006) United states of pharmacopeia 30 - national formulary 25, USA
25. Vogel, Arthur Israel (1989) Textbook of quantitative chemical analysis. Inggris: Longman Scientific & Technical.