Drug and metabolite concentrations in tissues in relationship to tissue adverse findings: a review
- PMID: 21241198
- DOI: 10.1517/17425255.2011.545053
Drug and metabolite concentrations in tissues in relationship to tissue adverse findings: a review
Abstract
Introduction: Drug blood (or plasma) levels measured during safety preclinical investigations do not always correlate with toxicological findings. Concentrations in target tissues or, even better, at target receptors would probably be more relevant. In addition, toxicity may be caused by drug metabolites which, in turn, can be tissue specific. Tissue concentrations and tissue metabolism may be crucial for interpreting tissue toxicity.
Areas covered: This paper, starting from the authors' direct experience, focuses on distribution of the parent compound and metabolites in target toxicity tissues and presents a review of several examples where organ or tissue concentrations have been either useful or not relevant for interpreting safety findings. Regulatory aspects and technological progresses are also mentioned.
Expert opinion: The authors advocate directing more attention and efforts toward investigating tissue distribution: this approach might reduce late stage attrition. When unexpected tissue toxicity is found, measuring drug concentrations in the target tissue and characterising and measuring tissue metabolites could bring relevant information for interpreting the adverse finding. Evidence of slow accumulation of a long lasting metabolite in a tissue should be considered as an alert: this evidence can be obtained during short-term toxicity studies.
Similar articles
-
Complicating factors in safety testing of drug metabolites: kinetic differences between generated and preformed metabolites.Toxicol Appl Pharmacol. 2006 Dec 1;217(2):143-52. doi: 10.1016/j.taap.2006.08.009. Epub 2006 Sep 1. Toxicol Appl Pharmacol. 2006. PMID: 17055014
-
Metabolites in safety testing.Bioanalysis. 2009 Oct;1(7):1193-200. doi: 10.4155/bio.09.98. Bioanalysis. 2009. PMID: 21083045
-
Interpretation and considerations on the safety evaluation of human drug metabolites.Chem Res Toxicol. 2009 Jul;22(7):1217-20. doi: 10.1021/tx900124j. Chem Res Toxicol. 2009. PMID: 19563206 Review.
-
Applicability of bioanalysis of multiple analytes in drug discovery and development: review of select case studies including assay development considerations.Biomed Chromatogr. 2006 May;20(5):383-414. doi: 10.1002/bmc.594. Biomed Chromatogr. 2006. PMID: 16307470 Review.
-
Structural alert/reactive metabolite concept as applied in medicinal chemistry to mitigate the risk of idiosyncratic drug toxicity: a perspective based on the critical examination of trends in the top 200 drugs marketed in the United States.Chem Res Toxicol. 2011 Sep 19;24(9):1345-410. doi: 10.1021/tx200168d. Epub 2011 Jul 11. Chem Res Toxicol. 2011. PMID: 21702456 Review.
Cited by
-
Exploring the antimalarial and antioxidant efficacy of transition metal(II) chelates of thiosemicarbazone ligands: spectral investigations, molecular docking, DFT, MESP and ADMET.Biometals. 2024 Feb;37(1):247-265. doi: 10.1007/s10534-023-00546-1. Epub 2023 Nov 8. Biometals. 2024. PMID: 37938497
-
Differences in Multicomponent Pharmacokinetics, Tissue Distribution, and Excretion of Tripterygium Glycosides Tablets in Normal and Adriamycin-Induced Nephrotic Syndrome Rat Models and Correlations With Efficacy and Hepatotoxicity.Front Pharmacol. 2022 Jun 9;13:910923. doi: 10.3389/fphar.2022.910923. eCollection 2022. Front Pharmacol. 2022. PMID: 35754482 Free PMC article.
-
Spatial analysis of drug absorption, distribution, metabolism, and toxicology using mass spectrometry imaging.Biochem Pharmacol. 2022 Jul;201:115080. doi: 10.1016/j.bcp.2022.115080. Epub 2022 May 10. Biochem Pharmacol. 2022. PMID: 35561842 Free PMC article. Review.
-
A Nanostructured Matrices Assessment to Study Drug Distribution in Solid Tumor Tissues by Mass Spectrometry Imaging.Nanomaterials (Basel). 2017 Mar 21;7(3):71. doi: 10.3390/nano7030071. Nanomaterials (Basel). 2017. PMID: 28336905 Free PMC article.
-
Heterogeneity of paclitaxel distribution in different tumor models assessed by MALDI mass spectrometry imaging.Sci Rep. 2016 Dec 21;6:39284. doi: 10.1038/srep39284. Sci Rep. 2016. PMID: 28000726 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical
