Simultaneous Estimation of Cal DL-2-Hydroxy,4-methyl thio-butyrate and Ca-2-oxo3-phenyl Propionate in Alpha-Ketoanalogues Tablets by Validated RP-HPLC Method

被引:0
|
作者
Panda, Shambo [1 ,2 ]
Bose, Anindya [1 ]
Debnath, Biplab [2 ]
Nath, Rajarshi
Das, Arijit [3 ]
Ghosh, Somsubhra [4 ]
机构
[1] Siksha O Anusandhan Deemed Univ, Sch Pharmaceut Sci, Dept Pharmaceut Anal, Bhubaneswar, Odisha, India
[2] Bharat Technol, Dept Pharmaceut Chem, Howrah, West Bengal, India
[3] Bharat Technol, Dept Pharmacol, Howrah, West Bengal, India
[4] Neotia Univ, Sch Pharm, Dept Pharmaceut Anal, Diamond Harbour, West Bengal, India
关键词
Alpha-Ketoanalogues; Chronic kidney disease; Chromatography; Method Validation; Simultaneous estimation; Formulation; ACID;
D O I
10.5530/ijper.58.3.101
中图分类号
G40 [教育学];
学科分类号
040101 ; 120403 ;
摘要
Introduction: Alpha-Ketoanalogues is a dietary supplement drug containing Calcium-DLthe management of chronic renal disease. Objectives: In this study, a simple RP-HPLC method has been developed to simultaneously determine Calcium-DL-2-hydroxy-4-(methylthio) butyrate Materials and Methods: The compounds were separated in a single run using a Waters XBridge 250 mm x 4.6 mm C18 column with 5 mu m particle size and 130 & Aring; pore size. Elution was carried out via gradient mode with the UV detector wavelength set at 210 nm. The mobile phase selected was a binary mixture of ammonium hydrogen sulphate buffer (pH 7.0) and acetonitrile at a 1.0 mL/min flow rate. Results: The retention time of CHMB and COPP was found to be about 7 min and 20 min, respectively. The chromatographic method shows detector linearity in 50-150% of the operating range with the square of correlation coefficient at 0.9998 and 0.9999 for these two compounds, respectively. The parentage recovery of both CHMB and COPP was within 98-102% range. The method validation was carried out per the USP (chapter 1225) and ICH guidelines (Q2-R2). The developed method was found to be specific, precise, linear, robust, and accurate. Conclusion: This method could be utilized to assay tablet formulation of CHMB and COPP during the in-process and finished product quality control.
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页码:925 / 930
页数:6
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