The Experts below are selected from a list of 1449 Experts worldwide ranked by ideXlab platform

Zhihong Jiang - One of the best experts on this subject based on the ideXlab platform.

Deokchun Yang - One of the best experts on this subject based on the ideXlab platform.

Dong Hwan Sohn - One of the best experts on this subject based on the ideXlab platform.

  • simultaneous determination of Ginsenoside Rb1 and rg1 in human plasma by liquid chromatography mass spectrometry
    Journal of Pharmaceutical and Biomedical Analysis, 2004
    Co-Authors: Hye Young Ji, Seung Goo Chang, Dong Hwan Sohn
    Abstract:

    Abstract A liquid chromatographic–mass spectrometric (LC/MS) method for the simultaneous determination of Ginsenoside Rb 1 and Rg 1 in human plasma was developed. The method involved the protein precipitation followed by analysis of Ginsenoside Rb 1 and Rg 1 in an Atlantis C 18 column with the gradient elution of acetonitrile and ammonium formate (10 mM, pH 3.0) at a flow rate of 0.2 ml/min. The analytes were determined using electrospray negative ionization mass spectrometry in the selected ion monitoring mode. The standard curves for Ginsenoside Rb 1 and Rg 1 were linear over the concentration range of 10.0–1000 ng/ml. The lower limit of quantification was 10.0 ng/ml using 100 μl plasma sample. The coefficient of variation of intra- and inter-day assays for Ginsenoside Rb 1 and Rg 1 at three quality control levels ranged from 1.0 to 6.8% and 5.4 to 9.8%, respectively. Ginsenoside Rb 1 and Rg 1 were stable in blank human plasma at room temperature for 24 h and following three freeze–thaw cycles.

  • Simultaneous determination of Ginsenoside Rb1 and Rg1 in human plasma by liquid chromatography–mass spectrometry
    Journal of pharmaceutical and biomedical analysis, 2004
    Co-Authors: Hye Won Lee, Seung Goo Chang, Dong Hwan Sohn, Hae Kyoung Kim, Hui Hyun Kim, Jaebaek Kim, Hye Suk Lee
    Abstract:

    Abstract A liquid chromatographic–mass spectrometric (LC/MS) method for the simultaneous determination of Ginsenoside Rb 1 and Rg 1 in human plasma was developed. The method involved the protein precipitation followed by analysis of Ginsenoside Rb 1 and Rg 1 in an Atlantis C 18 column with the gradient elution of acetonitrile and ammonium formate (10 mM, pH 3.0) at a flow rate of 0.2 ml/min. The analytes were determined using electrospray negative ionization mass spectrometry in the selected ion monitoring mode. The standard curves for Ginsenoside Rb 1 and Rg 1 were linear over the concentration range of 10.0–1000 ng/ml. The lower limit of quantification was 10.0 ng/ml using 100 μl plasma sample. The coefficient of variation of intra- and inter-day assays for Ginsenoside Rb 1 and Rg 1 at three quality control levels ranged from 1.0 to 6.8% and 5.4 to 9.8%, respectively. Ginsenoside Rb 1 and Rg 1 were stable in blank human plasma at room temperature for 24 h and following three freeze–thaw cycles.

Xiao Ling Fang - One of the best experts on this subject based on the ideXlab platform.

  • oral absorption of Ginsenoside Rb1 using in vitro and in vivo models
    Planta Medica, 2006
    Co-Authors: Yunjuan Wu, Xiao Ling Fang
    Abstract:

    This research attempts to clarify the cause for poor oral absorption of Ginsenoside Rb 1 (Rb 1 ), one main ingredient of the well known Panax notoginseng saponins (PNS) for curing hemorrhage. Caco-2 cell monolayers were used as an in vitro model to reveal the transport mechanism of Rb 1 across the intestinal mucosa. Moreover, the serum concentration-time profiles of Rb 1 after tail venous (IV), portal venous (PV), intraduodenal (ID) and peroral (PO) administration to rats were compared to evaluate the first-pass effects of stomach, intestine and liver. In vitro experiments showed that uptake by Caco-2 cell monolayers was temperature dependent, but was not influenced by cyclosporine A and ketoconazole. The change in the apical pH showed no obvious effects on the uptake of Rb 1 . The uptake and transport were non-saturable, and flux from the apical compartment to the basolateral compartment (A-B) increased linearly with increasing concentration, which indicated a passive transport. Meanwhile, an apparent permeability coefficient of (5.90 ± 1.02)×10 -8 cm/s (C 0 = 1 mg/mL) predicted an incomplete absorption. The investigation on the pharmacokinetic behavior of Rb 1 after different routes of administration to rats showed a significant difference between PO (F PO was 0.64%), ID (F ID was 2.46%) and PV (F PV was 59.49%) administration, and the first-pass effect of the intestine is more significant than that of the stomach and liver in the absorption process. In summary, elimination in the stomach, large intestine and liver contributed to the poor absorption of Rb 1 , but the low membrane permeability might be a more important factor dominating the extent of absorption.

  • Pharmacokinetics and bioavailability of Ginsenoside Rb1 and Rg1 from Panax notoginseng in rats.
    Journal of ethnopharmacology, 2003
    Co-Authors: Xiao Ling Fang, Dao Feng Chen
    Abstract:

    Panax notoginseng is used as a therapeutic agent to stop haemorrhages and a tonic to promote health in Chinese medicine. Currently saponins of P. notoginseng (PNS) are especially given attentions for their hemorheological properties. The pharmacokinetic profiles of the main PNS are still not accurately investigated. Therefore, our preliminary aim is to elucidate the pharmacokinetic features of Ginsenoside Rb(1) (Rb(1)) and Ginsenoside Rg(1) (Rg(1)), two of the main PNS in rats. Firstly, quantitive analysis of Rb(1) and Rg(1) in saponins of P. notoginseng was studied and the most suitable assay method by HPLC for blood sample were established. Then Rb(1) and Rg(1) in the same serum were determined after administering PNS to rats. The decline of Rb(1) in serum could be described by a two-compartment model. The half-life of alpha phase was 23.40 min and that of beta phase was 17.96 h. Rb(1) was absoRbed from the digestive tract and the bioavailability via P.O. was 4.35%. The pharmacokinetics of Rg(1) in rats also could be described by a two-compartment model. The half-lives of Rg(1) were 24.23 min for alpha phase and 14.13 h for beta phase. Rg(1) could be absoRbed in the digestive tract and the oral bioavailability was 18.40%. Both of the low oral bioavailability of Rb(1) and rapid reduction of Rg(1) in blood indicated that formula modification is necessary.

Tianxiu Qian - One of the best experts on this subject based on the ideXlab platform.