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A Simple and Sensitive LC-MS/MS Method for Determination of Four Major Active Diterpenoids from Andrographis paniculata in Human Plasma and Its Application to a Pilot Study.
Pholphana, Nanthanit; Panomvana, Duangchit; Rangkadilok, Nuchanart; Suriyo, Tawit; Ungtrakul, Teerapat; Pongpun, Wanwisa; Thaeopattha, Saichit; Satayavivad, Jutamaad.
Afiliação
  • Pholphana N; Laboratory of Pharmacology, Chulabhorn Research Institute, Bangkok, Thailand.
  • Panomvana D; Translational Research Unit (TRU), Chulabhorn Research Institute, Bangkok, Thailand.
  • Rangkadilok N; Laboratory of Pharmacology, Chulabhorn Research Institute, Bangkok, Thailand.
  • Suriyo T; Laboratory of Pharmacology, Chulabhorn Research Institute, Bangkok, Thailand.
  • Ungtrakul T; Chulabhorn Hospital, Bangkok, Thailand.
  • Pongpun W; Chulabhorn Hospital, Bangkok, Thailand.
  • Thaeopattha S; Translational Research Unit (TRU), Chulabhorn Research Institute, Bangkok, Thailand.
  • Satayavivad J; Laboratory of Pharmacology, Chulabhorn Research Institute, Bangkok, Thailand.
Planta Med ; 82(1-2): 113-20, 2016 Jan.
Article em En | MEDLINE | ID: mdl-26576030
Andrographis paniculata contains four major active diterpenoids, including andrographolide (1), 14-deoxy-11, 12-didehydroandrographolide (2), neoandrographolide (3), and 14-deoxyandrographolide (4), which exhibit differences in types and/or degrees of their pharmacological activity. Previous pharmacokinetic studies in humans reported only the parameters of compound 1 and its analytical method in human plasma. The purpose of this study was to develop a simple, sensitive, and selective liquid chromatography tandem-mass spectrometry technique for the simultaneous determination of all four major active diterpenoids in the A. paniculata product in human plasma. These four diterpenoids in plasma samples were extracted by a simple protein precipitation method with methanol and separated on a Kinetex C18 column using a gradient system with a mobile phase of acetonitrile and water. The liquid chromatography tandem-mass spectrometry was performed in the negative mode, and the multiple reaction monitoring mode was used for the quantitation. The method showed a good linearity over a wide concentration range of 2.50-500 ng/mL for 1 and over the range of 1.00-500 ng/mL for the other diterpenoids with a correlation coefficient R(2) > 0.995. The lower limit of quantification of 1 was found to be 2.50 ng/mL, while those of the other diterpenoids were 1.00 ng/mL. The intraday and interday accuracy (relative error) ranged from 0.03 % to 10.03 %, and the intraday and interday precisions (relative standard deviation) were in the range of 2.05-9.67 %. The extraction recovery (86.54-111.56 %) with a relative standard deviation of 2.78-8.61 % and the matrix effect (85.15-112.36 %) were within the acceptance criteria. Moreover, these four major active diterpenoids were stable in plasma samples at the studied storage conditions with a relative error ≤-9.79 % and a relative standard deviation ≤ 9.26 %. Hence, this present method was successfully validated and used in the pilot study to determine the pharmacokinetic parameters of all four major active diterpenoids in human plasma after multiple oral doses of the A. paniculata product were administered to a healthy, Thai female volunteer.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Espectrometria de Massas / Cromatografia Líquida / Andrographis / Diterpenos Tipo de estudo: Diagnostic_studies Limite: Humans Idioma: En Revista: Planta Med Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Tailândia

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Espectrometria de Massas / Cromatografia Líquida / Andrographis / Diterpenos Tipo de estudo: Diagnostic_studies Limite: Humans Idioma: En Revista: Planta Med Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Tailândia