Volume 11 Issue 5
Oct.  2021
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Shuning Li, Zhenyao Lu, Li Jiao, Ran Zhang, Yu Hong, Jiye Aa, Guangji Wang. Quantitative determination of D4-cystine in mice using LC-MS/MS and its application to the assessment of pharmacokinetics and bioavailability[J]. Journal of Pharmaceutical Analysis, 2021, 11(5): 580-587. doi: 10.1016/j.jpha.2020.08.010
Citation: Shuning Li, Zhenyao Lu, Li Jiao, Ran Zhang, Yu Hong, Jiye Aa, Guangji Wang. Quantitative determination of D4-cystine in mice using LC-MS/MS and its application to the assessment of pharmacokinetics and bioavailability[J]. Journal of Pharmaceutical Analysis, 2021, 11(5): 580-587. doi: 10.1016/j.jpha.2020.08.010

Quantitative determination of D4-cystine in mice using LC-MS/MS and its application to the assessment of pharmacokinetics and bioavailability

doi: 10.1016/j.jpha.2020.08.010
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This study was financially supported by the National Natural Science Foundation of the People's Republic of China (Grant Nos.: 81773814 and 81530098), the National Key Special Project of Science and Technology for Innovation Drugs of China (Project No.: 2017ZX09301013), and the National Key Research and Development Program (Grant No.: 2018YFC0807404).

  • Received Date: Mar. 25, 2020
  • Rev Recd Date: Jul. 20, 2020
  • Available Online: Jan. 11, 2022
  • Publish Date: Oct. 15, 2021
  • Cystine is the primary source material for the synthesis of glutathione. However, the pharmacokinetics and tissue distribution of cystine are largely unknown. A surrogate analyte D4-cystine was employed to generate calibration curves for the determination of levels of D4-cystine and endogenous cystine in mice by liquid chromatography-tandem mass spectrometry (LC-MS/MS). Validation assessments proved the sensitivity, specificity and reproducibility of the method with a lower limit of quantification (LLOQ) of 5 ng/mL over 5–5000 ng/mL in plasma. The pharmacokinetics of D4-cystine were evaluated after administering injections and oral solutions, both of which minimally impacted endogenous cystine levels. The absolute bioavailability of cystine was 18.6%, 15.1% and 25.6% at doses of 25, 50 and 100 mg/kg, respectively. Intravenously injected D4-cystine resulted in dramatically high plasma levels with reduced levels in the brain and liver. Intragastrically administered D4-cystine resulted in high levels in the plasma and stomach with relatively low levels in the lung, kidney, heart and brain.
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