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Physiologically based pharmacokinetic modeling of the inhibitory effect of dapagliflozin on intestinal and renal SGLT
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Yu ZHANG1, 2, Pan-pan XIE1, Ya-mei LI1, 2, Xue-mei HE1, Yue LIU1, Ai-xin SHI1, *
Acta Pharmaceutica Sinica | 2022, 57(6) : 1874 - 1879
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Acta Pharmaceutica Sinica | 2022, 57(6): 1874-1879
Original Articles
Physiologically based pharmacokinetic modeling of the inhibitory effect of dapagliflozin on intestinal and renal SGLT
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Yu ZHANG1, 2, Pan-pan XIE1, Ya-mei LI1, 2, Xue-mei HE1, Yue LIU1, Ai-xin SHI1, *
Affiliations
  • 1. Clinical Trial Center, Beijing Hospital, National Center of Gerontology; Institute of Geriatric Medicine, Chinese Academy of Medical Sciences, Beijing 100730, China
  • 2. Life Science and Biological Pharmacy Academy, Shenyang Pharmaceutical University, Shenyang 110016, China
Published: 2022-06-12 doi: 10.16438/j.0513-4870.2022-0094
Outline
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This study establishes and optimizes the physiologically based pharmacokinetics (PBPK) model for dapagliflozin, predicts the drug distribution into relevant tissues, and calculates the inhibitory effect on the sodium-glucose cotransporters (SGLTs) in the intestine and renal proximal tubule. Based on literature data, a PBPK model for oral administration in healthy adults was established and the predicted blood concentration-time curve characteristics, the main pharmacokinetic parameters (PK), and drug excretion in urine were compared with the published data. To verify and optimize the model and verify the accuracy of the tissue distribution and concentration predictions, a pharmacodynamics model (PD) was established. Urine glucose excretion (UGE) was simulated at the corresponding times. The characteristics of the drug-time curve predicted by the model are similar to those of the measured curve, and the ratio of the main PK parameters to the measured values is within a two-fold range; the accuracy of the established PBPK model is good. The maximal inhibition obtained with 10 mg of dapagliflozin on the duodenum and jejunum segment sodium-glucose co-transporter 1 (SGLT1s) was 1.6%-4.7%, and the inhibition rate of the sodium-glucose co-transporter 2 (SGLT2s) in the proximal tubule of the kidney was as high as 99.9%. At a dose of 10 mg, dapagliflozin delayed intestinal glucose absorption while occupying most of the sites (99.9%) of the renal sodium-glucose cotransporter 2 and inhibiting its glucose reabsorption. This physiological-pharmacokinetic model for dapagliflozin in healthy adults can provide meaningful guidance for exploring pharmacological mechanisms and potential toxicity of gliflozin by simulating drug distribution in different tissues.

dapagliflozin  /  physiologically based pharmacokinetics  /  drug tissue concentration distribution  /  sodium-glucose cotransporter  /  inhibitory effect
Yu ZHANG, Pan-pan XIE, Ya-mei LI, Xue-mei HE, Yue LIU, Ai-xin SHI. Physiologically based pharmacokinetic modeling of the inhibitory effect of dapagliflozin on intestinal and renal SGLT[J]. Acta Pharmaceutica Sinica, 2022 , 57 (6) : 1874 -1879 . DOI: 10.16438/j.0513-4870.2022-0094
Year 2022 volume 57 Issue 6
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Article Info
doi: 10.16438/j.0513-4870.2022-0094
  • Receive Date:2022-01-19
  • Online Date:2025-12-23
  • Published:2022-06-12
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History
  • Received:2022-01-19
  • Revised:2022-04-08
Funding
Affiliations
    1. Clinical Trial Center, Beijing Hospital, National Center of Gerontology; Institute of Geriatric Medicine, Chinese Academy of Medical Sciences, Beijing 100730, China
    2. Life Science and Biological Pharmacy Academy, Shenyang Pharmaceutical University, Shenyang 110016, China
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表12种不同金属材料的力学参数

Family
属数
Number of
genus
种数
Number of
species
占总种数比例
Percentage of
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种数
Number of
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占总种数比例
Percentage of total
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鹅膏菌科Amanitaceae 2 11 5.26 鹅膏菌属 Amanita 10 4.78
小菇科 Mycenaceae 2 12 5.74 丝盖伞属 Inocybe 5 2.39
多孔菌科 Polyporaceae 8 14 6.70 蜡蘑属 Laccaria 5 2.39
红菇科 Russulaceae 3 23 11.00 小皮伞属 Marasmius 6 2.87
小菇属 Mycena 11 5.26
光柄菇属 Pluteus 5 2.39
红菇属 Russula 17 8.13
栓菌属 Trametes 5 2.39
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