Article
Determination of asperosaponin VI in rat plasma by HPLC-ESI-MS and its application to preliminary pharmacokinetic studies.
China Pharmaceutical University, Ministry of Education, Nanjing, China.
Biomedical Chromatography (impact factor:
1.97).
09/2009;
24(5):550-5.
DOI:10.1002/bmc.1325
pp.550-5
Source: PubMed
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Citations (0)
- Cited In (1)
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Article: Response surface methodology to optimize enzymatic preparation of deapio-platycodin d and platycodin d from radix platycodi.
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ABSTRACT: In the present work, we reported the enzymatic preparation of deapio-platycodin D (dPD) and platycodin D (PD) optimized by response surface methodology (RSM) from Radix Platycodi. During investigation of the hydrolysis of crude platycosides by various glycoside hydrolases, snailase showed a strong ability to transform deapio-platycoside E (dPE) and platycoside E (PE) into dPD and PD with 100% conversion. RSM was used to optimize the effects of the reaction temperature (35-45 °C), enzyme load (5-20%), and reaction time (4-24 h) on the conversion process. Validation of the RSM model was verified by the good agreement between the experimental and the predicted values of dPD and PD conversion yield. The optimum preparation conditions were as follows: temperature, 43 °C; enzyme load, 15%; reaction time, 22 h. The biotransformation pathways were dPE→dPD3→dPD and PE→PD3→PD, respectively. The determined method may be highly applicable for the enzymatic preparation of dPD and PD for medicinal purposes and also for commercial use.International Journal of Molecular Sciences 01/2012; 13(4):4089-100. · 2.60 Impact Factor
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Keywords
0.05% formic acid-methanol
akebia saponin D
asperosaponin VI
calibration curve
Chromatographic separation
Dipsacaceae
Dipsacus asper Wall
inter-assay variability values
internal standard
lower limit
mobile phase
oral administration
pharmacokinetic study
protein precipitation
quantification
selected ion monitoring mode
sensitive high-performance liquid chromatography-electrospray ionization-mass spectrometry
target ions
typical bioactive triterpenoid saponin
validated method