Analysis of simvastatin in pharmaceutical preparations by high performance thin layer chromatography

Authors

  • SN MEYYANATHAN Dept. de Química Farmacéutica, J.S.S. College of Pharmacy, Ootacamund – 643 001, Tamilnadu, India
  • GVS RAMASARMA Dept. de Química Farmacéutica, J.S.S. College of Pharmacy, Ootacamund – 643 001, Tamilnadu, India
  • B SURESH Dept. de Química Farmacéutica, J.S.S. College of Pharmacy, Ootacamund – 643 001, Tamilnadu, India

Keywords:

HPTLC, Simvastatin, Fexofenadine, Tablets

Abstract

A new simple, precise, rapid, and selective high-performance thin layer chromatography (HPTLC) method has beendeveloped for the analysis of simvastatin in pharmaceutical preparations. The method uses fexofenadine as an internalstandard. The stationary phase was silica gel 60 F254 prewashed with methanol; ethyl acetate - methanol - ammoniasolution 25% (7:1.5:0.5, v/v) was used as mobile phase. Detection and quantification were performed densitometricallyat λ = 220nm. The linear range of the analysis was 0.08 - 0.8 μg and the percentage recovery was 100.7 %.

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References

The United States Pharmacopeia The national formulary. Asian ed. Rockville MD 1999. P.1521.

Takano T, Abe S, Hata S. Selected ion monitoring method for quantifying simvastatin and its acid form in human plasma

using the ferrocenylboronate derivative. Biomed Environ Mass Spectrom 1990 Sep; (19) 9: 577-581.

Morris MJ, Gilbert JD, Hsich JYK, Matuszewski BK, Ramjit HG, Bayne WF. Determination of the HMG-CoA reductase inhibitors simvastatin, lovastatin and pravastatin in plasma by gas chromatography - chemical-ionization mass spectrometry. Biol Mass Spectrom 1993 Jan; (22) 1: 1-8.

Cai KH, Zheng WH, Zhou Y, Lin GY, Zhao XL. Analysis method and pharmacokinetic studies of simvastatin in plasma. Fenxi Huaxue 1999 Nov 20; (27) 11:1254 -1257.

Carlucci G, Mazzeo P, Biordi L, Bologna M. Simultaneous determination of simvastatin and its hydroxy acid form in

human plasma by high-performance liquid chromatography with UV detection. J Pharm Biomed Anal 1992 Sep; (10) 9: 693-697.

Ochiai H, Uchiyama N, Imagaki K, Hata S, Kamei T. Determination of simvastatin and its active metabolite in human

plasma by column-switching high-performance liquid chromatography with fluorescence detection after derivatization

with 1-bromoacetylpyrene. J Chromatogr Biomed Appl 1997 June 20; 694(1): 211- 217.

Tan L, Yang LL, Zhang X, Yuan YS, Ling SS. Determination of simvastatin in human plasma by high-performance liquid chromatography. Sepu 2000 May; (18) 3: 232 -234.

Jemal M, Ouyang Z, Powell ML.Direct-injection LC-MS-MS method for high-throughput simultaneous quantitation of simvastatin and simvastatin acid in human plasma. J Pharm Biomed Anal 2000 Aug 15; (23) 2-3: 323 - 340.

Zhao JJ, Xie IH, Yang AY, Road cap BA, Rogers JD. Quantitation of simvastatin and its - hydroxy-acid in human plasma by liquid-liquid cartridge extraction and liquid chromatography-tandem mass spectrometry. J Mass Spectrometry 2000 Sep; (35) 9:1133 - 1143.

Published

2004-03-20

How to Cite

1.
MEYYANATHAN S, RAMASARMA G, SURESH B. Analysis of simvastatin in pharmaceutical preparations by high performance thin layer chromatography. Ars Pharm [Internet]. 2004 Mar. 20 [cited 2024 Jul. 22];45(2):121-9. Available from: https://revistaseug.ugr.es/index.php/ars/article/view/5108

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Original Articles