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Bioactivation and reactivity research advances - 2023 year in review.
Wang, Shuai; Argikar, Upendra A; Chatzopoulou, Maria; Cho, Sungjoon; Crouch, Rachel D; Dhaware, Deepika; Gu, Ting-Jia; Heck, Carley J S; Johnson, Kevin M; Kalgutkar, Amit S; Liu, Joyce; Ma, Bin; Miller, Grover P; Rowley, Jessica A; Seneviratne, Herana Kamal; Zhang, Donglu; Khojasteh, S Cyrus.
Afiliação
  • Wang S; Department of Drug Metabolism and Pharmacokinetics, Genentech, Inc., South San Francisco, CA, USA.
  • Argikar UA; Non-clinical Development, Bill and Melinda Gates Medical Research Institute, Cambridge, MA, USA.
  • Chatzopoulou M; Translational Science, UCB Biopharma UK, Slough, UK.
  • Cho S; Department of Drug Metabolism and Pharmacokinetics, Genentech, Inc., South San Francisco, CA, USA.
  • Crouch RD; Department of Pharmacy and Pharmaceutical Sciences, Lipscomb University College of Pharmacy, Nashville, TN, USA.
  • Dhaware D; DMPK and Safety Sciences, Orion Pharma, Espoo, Finland.
  • Gu TJ; Department of Drug Metabolism and Pharmacokinetics, Genentech, Inc., South San Francisco, CA, USA.
  • Heck CJS; Medicine Design, Pfizer Worldwide Research, Development and Medical, Groton, CT, USA.
  • Johnson KM; Drug Metabolism and Pharmacokinetics, Inotiv, Maryland Heights, MO, USA.
  • Kalgutkar AS; Medicine Design, Pfizer Worldwide Research, Development and Medical, Cambridge, MA, USA.
  • Liu J; Department of Drug Metabolism and Pharmacokinetics, Genentech, Inc., South San Francisco, CA, USA.
  • Ma B; Department of Drug Metabolism and Pharmacokinetics, Genentech, Inc., South San Francisco, CA, USA.
  • Miller GP; Department of Biochemistry and Molecular Biology, University of Arkansas for Medical Sciences, Little Rock, AR, USA.
  • Rowley JA; Translational Science, UCB Biopharma UK, Slough, UK.
  • Seneviratne HK; Department of Chemistry and Biochemistry, University of Maryland, Baltimore County, Baltimore, MD, USA.
  • Zhang D; Department of Drug Metabolism and Pharmacokinetics, Genentech, Inc., South San Francisco, CA, USA.
  • Khojasteh SC; Department of Drug Metabolism and Pharmacokinetics, Genentech, Inc., South San Francisco, CA, USA.
Drug Metab Rev ; : 1-38, 2024 Jul 17.
Article em En | MEDLINE | ID: mdl-38963129
ABSTRACT
Advances in the field of bioactivation have significantly contributed to our understanding and prediction of drug-induced liver injury (DILI). It has been established that many adverse drug reactions, including DILI, are associated with the formation and reactivity of metabolites. Modern methods allow us to detect and characterize these reactive metabolites in earlier stages of drug development, which helps anticipate and circumvent the potential for DILI. Improved in silico models and experimental techniques that better reflect in vivo environments are enhancing predictive capabilities for DILI risk. Further, studies on the mechanisms of bioactivation, including enzyme interactions and the role of individual genetic differences, have provided valuable insights for drug optimizations. Cumulatively, this progress is continually refining our approaches to drug safety evaluation and personalized medicine.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: Drug Metab Rev Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: Drug Metab Rev Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos