色谱

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三相中空纤维式液相微萃取用于快速富集血浆中的尼古丁

杨新磊,罗明标,唐毓萍   

  1. Key Laboratory of Nuclear Resources and Environment of Ministry of Education, East China Institute of Technology, Nanchang  330013, China
  • 收稿日期:2006-07-10 修回日期:2006-08-28 出版日期:2006-11-30 发布日期:1986-06-25
  • 通讯作者: 罗明标

Enrichment of Nicotine in Plasma with Three-Phase Hollow Fiber Based Liquid Phase Microextraction

YANG Xinlei, LUO Mingbiao, TANG Yuping   

  1. Key Laboratory of Nuclear Resources and Environment of Ministry of Education, East China Institute of Technology, Nanchang  330013, China
  • Received:2006-07-10 Revised:2006-08-28 Online:2006-11-30 Published:1986-06-25
  • Contact: LUO Mingbiao

摘要: 建立了一种以三相中空纤维式液相微萃取(TP-HF-LPME)进行样品前处理,采用高效液相色谱快速、准确测定血浆中尼古丁含量的方法。研究表明该方法集萃取、富集、净化为一步,极大地简化了传统血浆成分测定的前处理过程,是一种快速、有效、绿色的前处理方法。方法的线性范围为0.1~50 mg/L,相关系数(r2)为0.9996,检测限为0.05 mg/L (信噪比为3),相对标准偏差小于5%。

关键词: 高效液相色谱, 尼古丁, 血浆 , 样品前处理, 液相微萃取

Abstract: A novel method for fast determination of nicotine in plasma was established by using high performance liquid chromatography (HPLC) coupled with a three-phase hollow fiber based liquid phase microextraction (TP-HF-LPME) technique for sample preparation. The microextraction was mediated by the pH difference between the environment inside and outside of an organic phase immobilized in the pores formed in the wall of a polypropylene hollow fiber. The pH value of the medium outside the organic phase was adjusted by adding a dilute KOH solution to form a basic donor phase while the pH value of the inner media was set to pH 3 to form an acceptor phase using a 10 mmol/L KH2PO4 solution. On working conditions, neutral nicotine molecules were firstly extracted from the original sample solution to the organic phase, and then the analyte was extracted from the organic phase to the acceptor phase. After described extraction time, 4 μL of acceptor phase was withdrawn and directly injected into HPLC system for analysis. Parameters related to TP-HF-LPME (organic solvent, pH of acceptor and donor phase, stirring rate, salt effect, methanol content in acceptor phase and extraction time) were also optimized experimentally. The proposed method integrates extraction, enrichment and clean-up into a single step, dramatically simplifying the traditional procedure to prepare a liquid sample with complex matrices such as plasma. It has been demonstrated to be a very fast, effective and virtually "green" sample preparation technique, which provided a good linear range (0.1-50 mg/L) with r2 of 0.9996, a low detection limit (0.05 mg/L, S/N= 3) and a satisfactory relative standard deviation (<5%).

Key words: high performance liquid chromatography (HPLC), nicotine, plasma , sample preparation, liquid phase microextraction