Utility of in vitro drug metabolism data in predicting in vivo metabolic clearance
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A value of 45 mg/g liver or 52.5 mg/g is commonly used as MPPGL.
“Generally, a value of 45 mg/g liver [60] originally obtained from rat data, or 52.5 mg/g based on hepatocyte data reported in the literature via back calculation, is commonly used as MPPGL.”
From Interpretation of Non-Clinical Data for Prediction of Human Pharmacokinetic Parameters: In Vitro-In Vivo Extrapolation and Allometric Scaling (2019) · cites this paper as [60]
Houston found that a direct physiological scaling factor incorporated to predict CLH using in vitro hepatocytes and rat microsomes data yielded adequate evidence supporting IVIVE.
“A direct physiological scaling factor was incorporated to predict CLH using in vitro hepatocytes and rat microsomes data by Houston [60].”
From Interpretation of Non-Clinical Data for Prediction of Human Pharmacokinetic Parameters: In Vitro-In Vivo Extrapolation and Allometric Scaling (2019) · cites this paper as [60]
Although CLint,in vitro obtained from dexamethasone-treated microsomes provided an accurate estimate of 77% of the observed CLint,in vivo, the limitation similar to that of Houston persisted.
“Although a CLint, in vitro obtained from dexamethasone-treated microsomes provided an accurate estimate of 77% of the observed CLint, in vivo, the limitation similar to that of Houston [60] persisted.”
From Interpretation of Non-Clinical Data for Prediction of Human Pharmacokinetic Parameters: In Vitro-In Vivo Extrapolation and Allometric Scaling (2019) · cites this paper as [60]
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“Although a CLint, in vitro obtained from dexamethasone-treated microsomes provided an accurate estimate of 77% of the observed CLint, in vivo, the limitation similar to that of Houston [60] persisted.”
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Liver organoids: Current advances and future applications for hepatology
Kim, Y., Kang, M., Mamo, M. G., Adisasmita, M., Huch, M., & Choi, D. (2025) · Clinical and Molecular Hepatology · doi:10.3350/cmh.2024.1040 · Cited by 26 · see citing works
- Authors
- Brian Houston, J.
- Venue
- Biochemical Pharmacology
- Publisher
- Elsevier BV
- Published
- 1994-04
- Volume
- 47
- Issue
- 9
- Pages
- 1469-1479
- ISSN
- 0006-2952 (ISSN-L)
- OpenAlex
- W2064799851
- Cited by
- 925
- References
- 0
- Citations by year
- 2026: 27 · 2025: 36 · 2024: 33 · 2023: 29 · 2022: 30 · 2021: 32 · 2020: 34 · 2019: 24 · 2018: 27 · 2017: 23 · 2016: 33 · 2015: 27 · 2014: 29 · 2013: 35 · 2012: 42
- FWCI
- 6.72
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Biochemical Pharmacology (publishedVersion)
- PubMed (publishedVersion)
- Research Explorer (The University of Manchester) (publishedVersion)
- Topics
- Life Sciences › Pharmacology, Toxicology and Pharmaceutics › Pharmacology › Pharmacogenetics and Drug Metabolism
- Health Sciences › Medicine › Oncology › Drug Transport and Resistance Mechanisms
- Life Sciences › Pharmacology, Toxicology and Pharmaceutics › Pharmacology › Drug-Induced Hepatotoxicity and Protection
- Keywords
- tubulin polymerization inhibitors, in vitro metabolism, G2/M cell cycle arrest, mitotic arrest, lymphoma, liver microsomal stability, anticancer agents
- MeSH terms
- Animals, Biotransformation, Pharmaceutical Preparations, Metabolic Clearance Rate, Microsomes, Liver, Pharmacokinetics, In Vitro Techniques
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Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
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