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Study on In Vitro Metabolism and In Vivo Pharmacokinetics of Beauvericin.
- Source :
-
Toxins . Jul2022, Vol. 14 Issue 7, pN.PAG-N.PAG. 18p. - Publication Year :
- 2022
-
Abstract
- Beauvericin (BEA) is a well-known mycotoxin produced by many fungi, including Beaveria bassiana. The purpose of this study was to evaluate the in vitro distribution and metabolism characteristics as well as the in vivo pharmacokinetic (PK) profile of BEA. The in vitro metabolism studies of BEA were performed using rat, dog, mouse, monkey and human liver microsomes, cryopreserved hepatocytes and plasma under conditions of linear kinetics to estimate the respective elimination rates. Additionally, LC-UV-MSn (n = 1~2) was used to identify metabolites in human, rat, mouse, dog and monkey liver microsomes. Furthermore, cytochrome P450 (CYP) reaction phenotyping was carried out. Finally, the absolute bioavailability of BEA was evaluated by intravenous and oral administration in rats. BEA was metabolically stable in the liver microsomes and hepatocytes of humans and rats; however, it was a strong inhibitor of midazolam 1′-hydroxylase (CYP3A4) and mephenytoin 4′-hydroxylase (CYP2C19) activities in human liver microsomes. The protein binding fraction values of BEA were >90% and the half-life (T1/2) values of BEA were approximately 5 h in the plasma of the five species. The absolute bioavailability was calculated to be 29.5%. Altogether, these data indicate that BEA has great potential for further development as a drug candidate. Metabolic studies of different species can provide important reference values for further safety evaluation. [ABSTRACT FROM AUTHOR]
- Subjects :
- *BEAUVERICIN
*LIVER microsomes
*PHARMACOKINETICS
*CYTOCHROME P-450
*METABOLISM
Subjects
Details
- Language :
- English
- ISSN :
- 20726651
- Volume :
- 14
- Issue :
- 7
- Database :
- Academic Search Index
- Journal :
- Toxins
- Publication Type :
- Academic Journal
- Accession number :
- 158318689
- Full Text :
- https://doi.org/10.3390/toxins14070477