FENG Guo, WU Zeng-guang, HE Xin, et al. Tissue Distribution of 3,29-Dibenzoyl Rarounitriol from Trichosanthis Semen in Rats by UPLC-MS/MS[J]. Chinese journal of experimental traditional medical formulae, 2017, 23(21): 86-92.
FENG Guo, WU Zeng-guang, HE Xin, et al. Tissue Distribution of 3,29-Dibenzoyl Rarounitriol from Trichosanthis Semen in Rats by UPLC-MS/MS[J]. Chinese journal of experimental traditional medical formulae, 2017, 23(21): 86-92. DOI: 10.13422/j.cnki.syfjx.2017210086.
Objective: To investigate the tissue distribution of 3
29-dibenzoyl rarounitriol from Trichosanthis Semen in rats after oral administration. Method: The stomach
heart
liver
spleen
lung and kidney in healthy male SD rats were taken at 0.5
1
3
6 h after intragastric administration
tissue homogenates and pretreatment were performed.ZORBAX C18 column(2.1 mm×50 mm
3.5 μm) was adopted with mobile phase of 10 mmol·L-1 ammonium acetate (containing 0.1% formic acid)-methanol for gradient elution
flow rate was 0.5 mL·min-1
the injection volume of 10 μL.A triple quadrupole tandem mass spectrometry equipped with electrospray ionization source was used as detector and operated by multiple reaction monitoring (MRM) positive ion mode of the transitions m/z 684.7-527.6
m/z 472.4-436.4 for 3
29-dibenzoyl rarounitriol and terfenadine
respectively. Result: After intragastric administration of 3
29-dibenzoyl rarounitriol in rats
peak concentration in the lung reached at 0.5 h
that in the heart
liver
spleen and kidney reached at 1.0 h
but that in the stomach at 3.0 h.The distribution of drug in the stomach and lung is large
its concentration in the stomach at 3.0 h was (405.8±114.8) ng·g-1;but the drug distributed fastest in the lung
it can reached a high concentration of (338.8±85.5) ng·g-1 at 0.5 h
distribution of 3
29-dibenzoyl rarounitriol in the heart
liver
spleen and kidney was low
the drug concentration in each organ were significantly reduced at 6.0 h. Conclusion: After intragastric administration of 3
29-dibenzoyl rarounitriol
it can be distributed to each organ tissue
which has high concentration in the stomach and lung
and this drug can still maintain a high level after 3 h
but its concentrations in the heart
liver
spleen and kidney are relatively low
which may be related to the nature characteristics and the acting features of itself.