A Systematic Review on Metabolite Profiling in Anticancer Drug Development

Authors

  • Nadda Muhamad Chulabhorn International College of Medicine, Thammasat University, Pathum Thani 12120, Thailand.
  • Kesara Na-Bangchang Chulabhorn International College of Medicine, Thammasat University, Pathum Thani 12120, Thailand. Center of Excellence in Pharmacology and Molecular Biology of Malaria and Cholangiocarcinoma, Chulabhorn International College of Medicine, Thammasat University, Pathum Thani 12120, Thailand and Drug Discovery and Development Center, Office of Advanced Sciences and Technology, Thammasat University, Pathum Thani 12120, Thailand.

DOI:

https://doi.org/10.9734/bpi/capr/v5/16964D

Keywords:

Metabolism, metabolite profile, anticancer, herbal medicine, cancer

Abstract

One of the most important pharmacokinetic processes is drug metabolism, which is crucial to medication development. The examination of the metabolite profile is essential because the metabolites produced may be helpful for therapy or cause major harm. The objective of this systematic review is to summarize the research articles relating to the metabolite profile investigation of conventional drugs and herb-derived compounds for cancer chemotherapy, to examine factors influencing metabolite profiling of these drugs/compounds and determine the relationship between therapeutic efficacy and toxicity of their metabolites. The literature search was performed through PubMed, and ScienceDirect searches up to January 2019. It was discovered that the creation of metabolites was influenced by four primary variables, including species, gender, drug administration route, and dose. There are certain metabolites that have been classified as hazardous or active.  This information is important for cancer chemotherapy and the development of anticancer drugs.  

Published

2022-07-22

How to Cite

Nadda Muhamad, & Kesara Na-Bangchang. (2022). A Systematic Review on Metabolite Profiling in Anticancer Drug Development. Challenges and Advances in Pharmaceutical Research Vol. 5, 36–106. https://doi.org/10.9734/bpi/capr/v5/16964D