Rapid high performance liquid chromatography method for erlotinib quantification in vitro: Application to study the effect of resveratrol on metabolism and cellular uptake of erlotinib

• Published in: Fundamental & clinical pharmacology 2023-10, Vol.37 (5), p.983-993
• Main Authors: Zayed, Aref, Al Hroot, Jomana, Mayyas, Abdulraouf, Al-Husein, Belal
• Format: Article
• Language: English
• Subjects: Cancer; Chromatography; Colorectal carcinoma; Cytochrome; Cytochrome P450; Cytochromes P450; Drug interaction; Drug interactions; Growth factors; Hepatocytes; High performance liquid chromatography; In vitro methods and tests; Liquid chromatography; LITAF protein; Liver; Liver cancer; Lung cancer; Metabolism; Metabolites; Microsomes; Non-small cell lung carcinoma; Pancreatic cancer; Pharmacology; Photodiodes; Resveratrol; Stability analysis
• ISSN: 0767-3981; 1472-8206
• DOI: 10.1111/fcp.12914

Erlotinib is a selective epidermal growth factor receptor inhibitor that is used for the treatment of non-small cell lung cancer and pancreatic cancer. Its metabolism is mainly mediated by cytochrome P450 3A (CYP 3A). Resveratrol, a natural compound found in many plants and supplements, is known to inhibit CYP3A enzyme, therefore, it may act as an inhibitor for the metabolism of erlotinib. Development of a rapid high performance liquid chromatography with photodiode array detection (HPLC-PDA) method for the quantification of erlotinib in liver microsomes and cancer cells and its application to study resveratrol effect on metabolism and cellular uptake of erlotinib. HPLC-PDA was used to develop an efficient bioanalytical method with a 2.5-min runtime preceded by a simple protein precipitation step. The method was validated according to the European Medicines Agency guidelines. Erlotinib metabolic stability and resveratrol effect on erlotinib metabolite formation were evaluated in rat liver microsomes. Furthermore, the method was used to measure the intracellular concentrations of erlotinib in cancer colorectal cells and investigating resveratrol effect on the cellular uptake of erlotinib. A rapid HPLC-PDA method was developed and validated for the first time to address potential drug interaction of erlotinib with resveratrol. Resveratrol was a strong inhibitor of erlotinib metabolism in vitro with IC  = 4.03 μM. Resveratrol, however, had no effect on erlotinib cellular uptake after 1 h incubation in human colorectal cancer cells. The study suggests that resveratrol may produce a potential herb-drug interaction with erlotinib at the metabolism level and should be investigated in patients in the clinic.