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Parallel artificial liquid membrane extraction: micro-scale liquid-liquid-liquid extraction in the 96-well format.
Astrid Gjelstad1, Knut Einar Rasmussen, Marthe Petrine Parmer
1School of Pharmacy, University of Oslo, PO Box 1068 Blindern, 0316 Oslo, Norway. astrid.gjelstad@farmasi.uio.no
Bioanalysis
|June 8, 2013
Summary
A new parallel artificial liquid membrane extraction method was developed for analyzing drugs in human plasma. This technique offers efficient extraction with good sensitivity and linearity for key analytes.
Area of Science:
- Analytical Chemistry
- Biochemistry
Background:
- A novel approach, parallel artificial liquid membrane extraction (PALME), is introduced for analytical liquid-liquid-liquid membrane extraction.
- PALME utilizes a sandwich design with donor and acceptor plates separated by artificial liquid membranes, adapting hollow-fiber liquid-phase microextraction to a 96-well plate format.
Purpose of the Study:
- To develop and validate a new parallel artificial liquid membrane extraction technique for the analysis of basic drugs in human plasma.
- To assess the efficiency, sensitivity, and linearity of the PALME method using LC-MS/MS.
Main Methods:
- Development of a parallel artificial liquid membrane extraction setup in a 96-well plate format.
- Extraction of four basic drugs (pethidine, nortriptyline, methadone, haloperidol) from human plasma samples.
- Analysis of extracted drugs using liquid chromatography-tandem mass spectrometry (LC-MS/MS).
Main Results:
- Successful extraction of four basic drugs from human plasma within 30 minutes.
- Extraction recoveries ranged from 34% to 74% for the model analytes.
- Achieved low limits of quantification (LOQs) between 0.01-0.35 ng/ml, with linearity (R² > 0.9955) and relative standard deviation (RSD) values below 12%.
Conclusions:
- Liquid-liquid-liquid membrane extraction was successfully implemented using a modified 96-well plate format.
- The parallel artificial liquid membrane extraction method provides a viable and efficient approach for drug analysis in biological matrices.
- The developed method demonstrates good performance characteristics for the quantitative analysis of basic drugs in human plasma.

