Development and validation of analytical procedure for analysis of Amoxiciline, Metronidazole and Omeprazole, used as anti-Helicobacter pylori agents alone and in mixture

被引:0
|
作者
Maslarska, Vania [1 ]
Peikova, Lily [2 ]
Georgieva, Maya [2 ]
Ivanova, Stefka [3 ]
Smerikarova, Miglena [1 ]
Balkanski, Stefan [4 ]
Bozhanov, Stanislav [1 ]
机构
[1] Med Univ Sofia, Dept Chem, Fac Pharm, Sofia, Bulgaria
[2] Med Univ Sofia, Dept Pharmaceut Chem, Fac Pharm, Sofia, Bulgaria
[3] Med Univ Pleven, Dept Pharmaceut Chem & Pharmacognosy, Fac Pharm, Pleven, Bulgaria
[4] Bulgarian Pharmaceut Union, Sofia, Bulgaria
关键词
Helicobacter pylori; simultaneous determination; HPLC-UV; Amoxicillin Trihydrate; Metronidazole; Omeprazole; analysis; PROTON-PUMP INHIBITOR; SPECTROPHOTOMETRIC DETERMINATION; CHROMATOGRAPHY; SPIRAMYCIN;
D O I
10.3897/pharmacia.70.e109211
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Background: The contemporary treatment of ulcerogenic diseases and gastroesophageal reflux disease is related usually to application of a combination of imidazole-based antibacterial, antibiotic and proton pump inhibitor. In the current study, the three most common representatives Amoxicilline (AMO), Metronidazole (MET) and Omeprazole (OME), respectively, are subjected to analysis through classical analytical procedure, providing high level accuracy, sensitivity and good separation abilities. As such a UV/VIS method was applied as a well known identification and quantitation technique for analyses in various samples. Furthermore, this technique is known to be a good detection method in combination with chromatographic systems. Purpose: A simple, specific, accurate and precise reverse phase-high performance liquid chromatographic method has been developed for the simultaneous determination of Amoxicillin Trihydrate (AMO), Metronidazole (MET) and Omeprazole (OME) in synthetic mixture. Materials and methods: Some important parameters like pH of the mobile phase, concentration of the acid or buffer solution, percentage and type of the organic modifier, etc. were tested for a good chromatographic separation. The sample was analyzed using a mobile phase of Acetonitrile: Phosphate buffer (pH=7.6 +/- 0.1) (40:60 v/v). The flow rate was 1.0 mL/ min with detection at 280 nm. Results: The retention time for AMO, MET and OME was found to be 1.67, 2.86 and 5.99 min respectively, and the recoveries in the synthetic mixture were between 98 and 102%. The validated method was linear over the concentration range of 25 to 200 mu g/mL for AMO, 12.5 to 100 mu g/mL for MET and 5-40 mu g/mL for OME, with a correlation coefficient > 0.999. Conclusion: The developed method has been validated in accordance with theInternational Conference onHarmonization (ICH) guidelines and showed excellent linearity, accuracy, precision, specificity, robustness, as well as system suitability results within the acceptance criteria.
引用
收藏
页码:681 / 688
页数:8
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