2019
DOI: 10.3390/molecules24112037
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Liquid Chromatography-Tandem Mass Spectrometry of Desoxo-Narchinol a and Its Pharmacokinetics and Oral Bioavailability in Rats and Mice

Abstract: Desoxo-narchinol A is one of the major active constituents from Nardostachys jatamansi, which has been reported to possess various pharmacological activities, including anti-inflammatory, antioxidant, and anticonvulsant activity. A simple and sensitive liquid chromatography-tandem mass spectrometry (LC-MS/MS) method was developed and validated for the quantification of desoxo-narchinol A in two different biological matrices, i.e., rat plasma and mouse plasma, using sildenafil as an internal standard (IS). The … Show more

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Cited by 3 publications
(2 citation statements)
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“…This phenomenon was almost the same as that reported in a previous study, 28,35,36 and it may have been caused by a variety of factors, such as fractionated gastric emptying, enterohepatic circulation and separated "absorption windows". [37][38][39] However, the mechanism of this phenomenon in the pharmacokinetic study needs further detailed investigation. All in all, these results should drive further studies of eriocitrin and promote research into developing efficacy in clinical therapeutic studies.…”
Section: Pharmacokinetic Studymentioning
confidence: 99%
“…This phenomenon was almost the same as that reported in a previous study, 28,35,36 and it may have been caused by a variety of factors, such as fractionated gastric emptying, enterohepatic circulation and separated "absorption windows". [37][38][39] However, the mechanism of this phenomenon in the pharmacokinetic study needs further detailed investigation. All in all, these results should drive further studies of eriocitrin and promote research into developing efficacy in clinical therapeutic studies.…”
Section: Pharmacokinetic Studymentioning
confidence: 99%
“…The absorbed drug superimposed in the blood, and the double peak phenomenon of the drug-time curve appeared. 38,39 In Fig. 3 The concentration-time curve of plasma eupatorin in rats after single oral medication (50 mg kg À1 ).…”
Section: Pharmacokinetic Studymentioning
confidence: 99%