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建立了一种 HPLC/MS/MS 法同时测定大鼠血浆中替硝唑、达克罗宁和氯己定的浓度,并将其应用于成膜溶液的药代动力学研究。

Development of a HPLC/MS/MS method for simultaneous determination of tinidazole, dyclonine and chlorhexidine in rat plasma and its application in the pharmacokinetic research of a film-forming solution.

机构信息

Hebei Medical University, 361 East Zhongshan Road, Shijiazhuang 050017, China.

出版信息

J Pharm Biomed Anal. 2012 Mar 25;62:224-7. doi: 10.1016/j.jpba.2012.01.009. Epub 2012 Jan 16.

DOI:10.1016/j.jpba.2012.01.009
PMID:22305084
Abstract

A rapid and sensitive HPLC/MS/MS method was developed and validated for simultaneous determination of tinidazole, dyclonine and chlorhexidine, the three main components of a film-forming solution, in rat plasma. The plasma samples were pretreated by solid phase extraction (SPE) method. Separation was achieved on a Phenomenex Gemini C(18) column (50 mm × 2.0 mm, 5 μm) using an isocratic mobile phase system composed of methanol-ammonium formate (10 mM)-formic acid (56:44:0.2, v/v/v) (pH 3.5) at a flow rate of 0.2 mL/min. Analytes were determined by tandem mass spectrometry with electrospray positive ionization and multiple-reaction monitoring (MRM) mode. The monitoring ions were (m/z) 247.4 → (m/z) 81.9 for tinidazole, (m/z) 290.1 → (m/z) 97.8 for dyclonine, (m/z) 505.0 → (m/z) 335.3 for chlorhexidine and (m/z) 282.1 → (m/z) 212.0 for phentolamine (internal standard). The calibration curves were linear in the range of 2-1000 ng/mL for the three components. The precision and accuracy of the method were well within the generally accepted criteria for biomedical analysis. It has been successfully applied to the pharmacokinetic research of a film-forming solution in rat.

摘要

建立并验证了一种用于同时测定大鼠血浆中薄膜形成溶液三种主要成分替硝唑、达克罗宁和洗必泰的快速灵敏的 HPLC/MS/MS 方法。采用固相萃取(SPE)法预处理血浆样品。分离在 Phenomenex Gemini C(18)柱(50mm×2.0mm,5μm)上进行,采用甲醇-甲酸铵(10mM)-甲酸(56:44:0.2,v/v/v)(pH3.5)为流动相,流速为 0.2mL/min,采用等度洗脱。采用电喷雾正离子化和多反应监测(MRM)模式进行串联质谱分析。监测离子分别为替硝唑(m/z)247.4→(m/z)81.9、达克罗宁(m/z)290.1→(m/z)97.8、洗必泰(m/z)505.0→(m/z)335.3 和苯芐胺(内标,m/z)282.1→(m/z)212.0。三种成分的校准曲线在 2-1000ng/mL 范围内呈线性。该方法的精密度和准确度均符合生物医学分析的一般公认标准。该方法已成功应用于大鼠薄膜形成溶液的药代动力学研究。

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