4.3 Article

Quantitative determination of Cpd118, A novel FBPase inhibitor, in dog plasma by HPLC-MS/MS

Journal

BIOANALYSIS
Volume 13, Issue 11, Pages 865-873

Publisher

Newlands Press Ltd
DOI: 10.4155/bio-2021-0035

Keywords

bioavailability; Cpd118; FBPase inhibitor; LC-MS/MS; pharmacokinetic profile

Funding

  1. National Science and Technology Major Project of China [2018ZX09711001-002, 2018ZX09711002-003-012]

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This study developed and validated an HPLC-MS/MS method for quantifying Cpd118, a fructose-1,6-bisphosphatase inhibitor for controlling gluconeogenesis in Type 2 diabetes mellitus. The method was shown to be sensitive, accurate, and successfully applied in pharmacokinetic studies of Cpd118 in dogs.
Aim: A HPLC-MS/MS method was first developed and validated for the quantification of Cpd118, a novel fructose-1, 6-bisphosphatase inhibitor for controlling gluconeogenesis in Type 2 diabetes mellitus. Materials & methods: Cpd118 was extracted from dog plasma following acetonitrile protein precipitation, separated by HPLC on a CAPCELL PAK ADME column (3.5 mu m, 2.1 mm x 100 mm) and quantified using negative heated electrospray ion source-MS/MS. Results: Cpd118 was quantified from plasma using the method described above over a linear range of 10-20,000 ng/ml, with interday and intraday assay accuracy from -11.78 to 4.01% and the precision was <= 11.15%. Conclusion: The method was sensitive and selective for the quantification of Cpd118 and was successfully used to the pharmacokinetic and bioavailability study of Cpd118 in dogs.

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