Journal of Liquid Chromatography & Related Technologies, 2012
A rapid, simple, sensitive, and selective chromatographic method has been developed for the simul... more A rapid, simple, sensitive, and selective chromatographic method has been developed for the simultaneous estimation of atorvastatin calcium, losartan potassium, atenolol, and aspirin in marketed formulation. The separation was carried out on a KYA TECH HiQ Sil C18HS (250 × 4.6 mm i.d., 5 µm particle size) column using a mobile phase of acetonitrile: 0.02 M potassium dihydrogen phosphate buffer (pH 3.4) (70:30% v/v). The chromatographic analysis has been carried out using flow rate of 1 mL/min and detection at 236 nm. The proposed method was applied for analysis of ATN, ASP, LOS and ATO from plasma. ATO showed a linear response in the concentration range of 4–24 µg/mL, LOS and ATN showed a linear response in the concentration range of 20–120 µg/mL and ASP showed a linear response in the concentration range of 30–180 µg/mL in tablet formulation analysis. ATO, LOS, ASP, and ATN showed a linear response in the concentration range of 25–150, 50–300, 100–600, and 50–300 ng/mL in plasma analysis, respectively. The proposed methods for analysis of the four drugs from marketed formulation and plasma have been validated as per ICH and USFDA guidelines, respectively. Thus, proposed methods have their applications in field of bioequivalence and pharmacokinetic studies.
Journal of Liquid Chromatography & Related Technologies, 2012
A rapid, simple, sensitive, and selective chromatographic method has been developed for the simul... more A rapid, simple, sensitive, and selective chromatographic method has been developed for the simultaneous estimation of atorvastatin calcium, losartan potassium, atenolol, and aspirin in marketed formulation. The separation was carried out on a KYA TECH HiQ Sil C18HS (250 × 4.6 mm i.d., 5 µm particle size) column using a mobile phase of acetonitrile: 0.02 M potassium dihydrogen phosphate buffer (pH 3.4) (70:30% v/v). The chromatographic analysis has been carried out using flow rate of 1 mL/min and detection at 236 nm. The proposed method was applied for analysis of ATN, ASP, LOS and ATO from plasma. ATO showed a linear response in the concentration range of 4–24 µg/mL, LOS and ATN showed a linear response in the concentration range of 20–120 µg/mL and ASP showed a linear response in the concentration range of 30–180 µg/mL in tablet formulation analysis. ATO, LOS, ASP, and ATN showed a linear response in the concentration range of 25–150, 50–300, 100–600, and 50–300 ng/mL in plasma analysis, respectively. The proposed methods for analysis of the four drugs from marketed formulation and plasma have been validated as per ICH and USFDA guidelines, respectively. Thus, proposed methods have their applications in field of bioequivalence and pharmacokinetic studies.
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