Qing ZHANG, Qing WANG, Jin-tang CHENG, et al. Analysis of Excretion Behavior of GK-A from Ginkgo Semen in Urine and Bile of Rats[J]. Chinese journal of experimental traditional medical formulae, 2020, 26(3): 96-101.
DOI:
Qing ZHANG, Qing WANG, Jin-tang CHENG, et al. Analysis of Excretion Behavior of GK-A from Ginkgo Semen in Urine and Bile of Rats[J]. Chinese journal of experimental traditional medical formulae, 2020, 26(3): 96-101. DOI: 10.13422/j.cnki.syfjx.20191354.
Analysis of Excretion Behavior of GK-A from Ginkgo Semen in Urine and Bile of Rats
a antitussive compound separated from Ginkgo Semen
in the urine and bile of rats.
Method:
2
UPLC-MS/MS was used to determine the concentration of GK-A in rat urine and bile samples. The separation was performed on a C
18
column
the mobile phase consisted of 0.1%formic acid aqueous solution (A) and acetonitrile (B) for gradient elution (0-1 min
95%A; 1-3 min
95%-85%A; 3-7.5 min
85%-40%A; 7.5-8 min
40%A). The detection was carried out by a triple quadrupole mass spectrometer in the positive ion mode with an electrospray ionization (ESI). Multiple reaction monitoring (MRM) mode was employed. After intragastric administration of GK-A
the urine and bile samples were collected at different time points
and the contents of GK-A in the samples were determined
and the cumulative excretion and cumulative excretion rate were calculated.
Result:
2
After 72 h of administration
the cumulative excretion of GK-A in urine was (12.35±2.69) μg
and the cumulative excretion rate was (0.58±0.13)%. Meanwhile
after 24 h of administration
the cumulative excretion of GK-A in bile was (55.16±29.22) μg
and the cumulative excretion rate was (1.57±0.83)%. Only a small amount of GK-A was excreted from urine and bile of rats with a slow speed.
Conclusion:
2
After intragastric administration
the excretion of GK-A in rat urine and bile is not the main elimination pathway.
K Wada , S Ishigaki , K Ueda , et al . Studies on the constitution of edible and medicinal plants. I. Isolation and identification of 4- O -methylpyridoxine,toxic principle from the seed of Ginkgo biloba L. [J]. Chem Pharm Bull(Tokyo) , 1988 , 36 ( 5 ): 1779 - 1782 .
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Related Institution
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