Absolute bioavailability and intravenous pharmacokinetics of N‐acetyl‐D‐mannosamine in humans

The low oral bioavailability of ManNAc is likely due to poor absorption (rather than first-pass hepatic extraction) due to its high polarity. In addition, zero-order absorption explains why the systemic exposure to ManNAc does not increase proportionally with dose.

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Publication Details

Journal
British Journal of Clinical Pharmacology
Published
2025-09-18
DOI
https://doi.org/10.1002/bcp.70292
Citations
1
Primary Topic
Chronic Lymphocytic Leukemia Research
Type
article
Field-Weighted Citation Impact
1.63

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Absolute bioavailability and intravenous pharmacokinetics of N‐acetyl‐D‐mannosamine in humans

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Absolute bioavailability and intravenous pharmacokinetics of N‐acetyl‐D‐mannosamine in humans

O. S. Pavlova, Gianfranco Fornasini, Guy Ludbrook, Allan M. Evans, Tahlia R. Meola, Stephanie E. Reuter, Sumit Kumar Jain
article en
1 citations

Abstract

The low oral bioavailability of ManNAc is likely due to poor absorption (rather than first-pass hepatic extraction) due to its high polarity. In addition, zero-order absorption explains why the systemic exposure to ManNAc does not increase proportionally with dose.

British Journal of Clinical PharmacologyVol. 92(2)
South Australia Pathology (AU), University of South Australia (AU)
University of South Australia
Openalex Percentile: Top 13%
Chronic Lymphocytic Leukemia Research
1.63
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