Dong-mei Wang,Jing-fan Zhou,Xiao-bin Zhong,Jie Feng.Determination and Pharmacokinetic Study of Nitidine Chloride in Rat Plasma after Intragastrical Administration by LC-ESI-MS/MS Method[J].Chinese Herbal Medicines (CHM),2017,9(4):376-380
Determination and Pharmacokinetic Study of Nitidine Chloride in Rat Plasma after Intragastrical Administration by LC-ESI-MS/MS Method
  
DOI:10.1016/S1674-6384(17)60118-7
中文关键词:  
英文关键词:nitidine chloride  pharmacokinetics  Zanthoxylum nitidum (Roxb.) DC.
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Author NameAffiliation
Dong-mei Wang 1. School of Pharmaceutical Sciences, Guangxi Medical University, Nanning 530021, China 2. The Third Affiliated Hospital of Guangxi Medical University, Nanning 530031, China 
Jing-fan Zhou School of Pharmaceutical Sciences, Guangxi Medical University, Nanning 530021, China 
Xiao-bin Zhong School of Pharmaceutical Sciences, Guangxi Medical University, Nanning 530022, China 
Jie Feng School of Pharmaceutical Sciences, Guangxi Medical University, Nanning 530023, China 
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英文摘要:
      Objective To study the pharmacokinetics of nitidine chloride (NC) in rat plasma after intragastrical (i.g.) administration. Methods A liquid chromatography-electrospray ionization-mass/mass sprectrometry (LC-ESI-MS/MS) was used and carbamazepine was used as an intermal standard (I.S.). The rat plasma samples were deproteinized with acetonitrile and the resultant supernatant was assayed on an analytical DiamonsilTM ODS C18 column (2.1 mm × 150 mm) equipped with a C18 guard column (4 mm × 20 mm) with a mobile phase of acetonitrile–10 mM ammonium acetate buffer–formic acid (35: 65: 0.2, v/v/v) at the flow rate of 0.25 mL/min. The LC–MS was carried out on a triple-quadrupole mass spectrometry equipped with an ESI and positive selected-ion monitoring. Target ions were monitored at [M - Cl]+ m/z 348.2 for NC and [M + H]+ m/z 237.2 for I.S., respectively. Results The simple one step deproteinize and rapid analysis method were successfully used in pharmacokinetic study on NC after i.g. administration. The linear relationship was good over the range of 2.5 – 1000.0 ng/ml (r2 = 0.999 2) in rat plasma. The lower limit of quantification and detection were 2.5 and 1.6 ng/ml, respectively. The extraction recovery was in the range of 86.54 – 98.60%. The intra- and inter-day precisions (relative standard deviation) were less than 6.00%, with accuracies deviation between 89.40 to 95.57%. A two-compartment pharmacokinetic open model was proposed and validated to explain the apparent biphasic disposition of NC in rat plasma after i.g. administration. Conclusion This study was successfully applied to a pharmacokinetic study of NC in rats plasma following i.g. administration and could be used for preclinical and clinical pharmacokinetic evaluation of NC.
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