| Literature DB >> 32779988 |
Maki Miyamoto1, Yohei Kosugi1, Shinji Iwasaki1, Ikumi Chisaki1, Sayaka Nakagawa1, Nobuyuki Amano1, Hideki Hirabayashi1.
Abstract
The unbound fractions in plasma (f up) in two mouse models of humanized liver mice, PXB and humanized TK-NOG mice, were compared with human f up values using equilibrium dialysis method. A good relationship between f up values obtained from PXB mice and humans was observed; the f up of 34/39 compounds (87.2%) in PXB mice were within 3-fold of human f up. In contrast, a weak correlation was observed between human and humanized TK-NOG mouse f up values; the f up of 15/24 compounds (62.5%) in humanized TK-NOG mice were within 3-fold of human f up. As different profiles of plasma protein binding (PPB) profiles were observed between PXB and humanized TK-NOG mice, f up evaluation is necessary in each mouse model to utilize these humanized liver mice for pharmacological, drug-drug interaction (DDI), and toxicity studies. The unbound fraction in the mixed plasma of human and SCID mouse plasma (85:15) was well correlated with f up in PXB mice (38/39 compounds within a 3-fold). Thus, this artificial PXB mouse plasma could be used to evaluate PPB.Entities:
Keywords: Albumin; PXB mouse; TK-NOG mouse; alpha-1 acid glycoprotein; chimeric humanized mouse; plasma protein binding; unbound fraction
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Year: 2020 PMID: 32779988 DOI: 10.1080/00498254.2020.1808735
Source DB: PubMed Journal: Xenobiotica ISSN: 0049-8254 Impact factor: 1.908