Development of fast, precise and selective RP-HPLC methods for identification of possible degradation products of ivermectin in isolated rat hepatocytes and in different pH media
Publication details: Karnataka Association of Pharmaceutical Teachers of India (APTI) 2022Edition: Vol.56(2), Apr-JuneDescription: 546-552pSubject(s): Online resources: In: Indian journal of pharmaceutical education and researchSummary: Aim: A new stability indicating RP-HPLC based methods were developed to identify the possible degradation products of Ivermectin in isolated rat hepatocytes and in different pH media using a C18 RP column. Complete validation, including linearity, accuracy, recovery, precision, robustness, stability, and peak purity, was performed. Materials and Methods: HPLC system of UltiMateDionex 3000 DAD with LiChrosorb C18 Column were used in this study. During the investigation, for the removal of interfering fraction of isolated rat hepatocytes a purification procedure, consisting of protein precipitation followed by double filtration was developed. Results: Method I was applied effectively and the results indicated two major hepatic metabolites of Ivermectin. Method II was developed to monitor the chemical stability in close to physiological conditions. The appearance of a new peak and the proportional decrease in the sample concentration indicate a liability in buffer with pH12. Conclusion: The obtained results demonstrated that the degradation products of Ivermectin in hepatic cells and in alkali media are different.| Item type | Current library | Status | Barcode | |
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School of Pharmacy Archieval Section | Not for loan | 2022-1447 |
Aim: A new stability indicating RP-HPLC based methods were developed to identify the
possible degradation products of Ivermectin in isolated rat hepatocytes and in different
pH media using a C18 RP column. Complete validation, including linearity, accuracy,
recovery, precision, robustness, stability, and peak purity, was performed. Materials
and Methods: HPLC system of UltiMateDionex 3000 DAD with LiChrosorb C18 Column
were used in this study. During the investigation, for the removal of interfering fraction
of isolated rat hepatocytes a purification procedure, consisting of protein precipitation
followed by double filtration was developed. Results: Method I was applied effectively
and the results indicated two major hepatic metabolites of Ivermectin. Method II was
developed to monitor the chemical stability in close to physiological conditions. The
appearance of a new peak and the proportional decrease in the sample concentration
indicate a liability in buffer with pH12. Conclusion: The obtained results demonstrated
that the degradation products of Ivermectin in hepatic cells and in alkali media are
different.
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