A review on analytical method development and validation of Erlotinib
نویسندگان
چکیده
In this review article determines the different analytical methods for quantitative establishment of Erlotinib by using HPLC, HPLCMS, HPLC-UV, LC-MS/MS. Pharmaceutical method development requires valid procedures and qualitative analysis in Pharmaceuticals dosage formulations human serum. This assessment explains that superiority HPLC/LC-MS reviewed is based on drugs formulations, (API), biological fluids such as serum plasma.
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ژورنال
عنوان ژورنال: International Journal of Health Care and Biological Sciences
سال: 2023
ISSN: ['2582-7499']
DOI: https://doi.org/10.46795/ijhcbs.v4i1.433