One-step extraction of polar drugs from plasma by Parallel Artificial Liquid Membrane Extraction

Research output: Contribution to journalJournal articleResearchpeer-review

Standard

One-step extraction of polar drugs from plasma by Parallel Artificial Liquid Membrane Extraction. / Pilařová, Veronika; Sultani, Mumtaz; Ask, Kristine Skoglund; Nováková, Lucie; Pedersen-Bjergaard, Stig; Gjelstad, Astrid.

In: Journal of Chromatography B: Analytical Technologies in the Biomedical and Life Sciences, Vol. 1043, 17.02.2017, p. 25-32.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Pilařová, V, Sultani, M, Ask, KS, Nováková, L, Pedersen-Bjergaard, S & Gjelstad, A 2017, 'One-step extraction of polar drugs from plasma by Parallel Artificial Liquid Membrane Extraction', Journal of Chromatography B: Analytical Technologies in the Biomedical and Life Sciences, vol. 1043, pp. 25-32. https://doi.org/10.1016/j.jchromb.2016.09.019

APA

Pilařová, V., Sultani, M., Ask, K. S., Nováková, L., Pedersen-Bjergaard, S., & Gjelstad, A. (2017). One-step extraction of polar drugs from plasma by Parallel Artificial Liquid Membrane Extraction. Journal of Chromatography B: Analytical Technologies in the Biomedical and Life Sciences, 1043, 25-32. https://doi.org/10.1016/j.jchromb.2016.09.019

Vancouver

Pilařová V, Sultani M, Ask KS, Nováková L, Pedersen-Bjergaard S, Gjelstad A. One-step extraction of polar drugs from plasma by Parallel Artificial Liquid Membrane Extraction. Journal of Chromatography B: Analytical Technologies in the Biomedical and Life Sciences. 2017 Feb 17;1043:25-32. https://doi.org/10.1016/j.jchromb.2016.09.019

Author

Pilařová, Veronika ; Sultani, Mumtaz ; Ask, Kristine Skoglund ; Nováková, Lucie ; Pedersen-Bjergaard, Stig ; Gjelstad, Astrid. / One-step extraction of polar drugs from plasma by Parallel Artificial Liquid Membrane Extraction. In: Journal of Chromatography B: Analytical Technologies in the Biomedical and Life Sciences. 2017 ; Vol. 1043. pp. 25-32.

Bibtex

@article{39e173ecd8a24b60af75156a596d8af4,
title = "One-step extraction of polar drugs from plasma by Parallel Artificial Liquid Membrane Extraction",
abstract = "The new microextraction technique named parallel artificial liquid membrane extraction (PALME) was introduced as an alternative approach to liquid-liquid extraction of charged analytes from aqueous samples. The concept is based on extraction of analytes across a supported liquid membrane sustained in the pores of a thin polymeric membrane, a well-known extraction principle also used in hollow fiber liquid-phase microextraction (HF-LPME). However, the new PALME technique offers a more user-friendly setup in which the supported liquid membrane is incorporated in a 96 well plate system. Thus, high-throughput is achievable, in addition to the green chemistry offered by using PALME. The consumption of organic solvent is minimized to 3-5μL per sample. With a sample volume of 250μL and acceptor solution volume of 50μL, a maximal enrichment factor of five is achievable. Based on these parameters, a new method for extraction of polar basic drugs was developed in the present work. The basic drugs hydralazine, ephedrine, metaraminol, salbutamol, and cimetidine were used as model analytes, and were extracted from alkalized human plasma into an aqueous solution via the supported liquid membrane. The extraction was promoted by a carrier dissolved in the membrane, creating a temporary ion-pair complex between the hydrophilic drug and the carrier. As the model analytes were extracted directly into an aqueous solution, there was no need for evaporation of the extract before injection into LC-MS. Hence, the sample preparation is performed in one step. With optimized conditions, the extraction recoveries were in the range 50-89% from human plasma after 45min extraction. The data from the method evaluation were satisfactory and in line with current guidelines, and revealed an extraction method with substantial potential for high throughput bioanalysis of polar basic drugs.",
author = "Veronika Pila{\v r}ov{\'a} and Mumtaz Sultani and Ask, {Kristine Skoglund} and Lucie Nov{\'a}kov{\'a} and Stig Pedersen-Bjergaard and Astrid Gjelstad",
note = "Copyright {\textcopyright} 2016 Elsevier B.V. All rights reserved.",
year = "2017",
month = feb,
day = "17",
doi = "10.1016/j.jchromb.2016.09.019",
language = "English",
volume = "1043",
pages = "25--32",
journal = "Journal of Chromatography B: Analytical Technologies in the Biomedical and Life Sciences",
issn = "1570-0232",
publisher = "Elsevier",

}

RIS

TY - JOUR

T1 - One-step extraction of polar drugs from plasma by Parallel Artificial Liquid Membrane Extraction

AU - Pilařová, Veronika

AU - Sultani, Mumtaz

AU - Ask, Kristine Skoglund

AU - Nováková, Lucie

AU - Pedersen-Bjergaard, Stig

AU - Gjelstad, Astrid

N1 - Copyright © 2016 Elsevier B.V. All rights reserved.

PY - 2017/2/17

Y1 - 2017/2/17

N2 - The new microextraction technique named parallel artificial liquid membrane extraction (PALME) was introduced as an alternative approach to liquid-liquid extraction of charged analytes from aqueous samples. The concept is based on extraction of analytes across a supported liquid membrane sustained in the pores of a thin polymeric membrane, a well-known extraction principle also used in hollow fiber liquid-phase microextraction (HF-LPME). However, the new PALME technique offers a more user-friendly setup in which the supported liquid membrane is incorporated in a 96 well plate system. Thus, high-throughput is achievable, in addition to the green chemistry offered by using PALME. The consumption of organic solvent is minimized to 3-5μL per sample. With a sample volume of 250μL and acceptor solution volume of 50μL, a maximal enrichment factor of five is achievable. Based on these parameters, a new method for extraction of polar basic drugs was developed in the present work. The basic drugs hydralazine, ephedrine, metaraminol, salbutamol, and cimetidine were used as model analytes, and were extracted from alkalized human plasma into an aqueous solution via the supported liquid membrane. The extraction was promoted by a carrier dissolved in the membrane, creating a temporary ion-pair complex between the hydrophilic drug and the carrier. As the model analytes were extracted directly into an aqueous solution, there was no need for evaporation of the extract before injection into LC-MS. Hence, the sample preparation is performed in one step. With optimized conditions, the extraction recoveries were in the range 50-89% from human plasma after 45min extraction. The data from the method evaluation were satisfactory and in line with current guidelines, and revealed an extraction method with substantial potential for high throughput bioanalysis of polar basic drugs.

AB - The new microextraction technique named parallel artificial liquid membrane extraction (PALME) was introduced as an alternative approach to liquid-liquid extraction of charged analytes from aqueous samples. The concept is based on extraction of analytes across a supported liquid membrane sustained in the pores of a thin polymeric membrane, a well-known extraction principle also used in hollow fiber liquid-phase microextraction (HF-LPME). However, the new PALME technique offers a more user-friendly setup in which the supported liquid membrane is incorporated in a 96 well plate system. Thus, high-throughput is achievable, in addition to the green chemistry offered by using PALME. The consumption of organic solvent is minimized to 3-5μL per sample. With a sample volume of 250μL and acceptor solution volume of 50μL, a maximal enrichment factor of five is achievable. Based on these parameters, a new method for extraction of polar basic drugs was developed in the present work. The basic drugs hydralazine, ephedrine, metaraminol, salbutamol, and cimetidine were used as model analytes, and were extracted from alkalized human plasma into an aqueous solution via the supported liquid membrane. The extraction was promoted by a carrier dissolved in the membrane, creating a temporary ion-pair complex between the hydrophilic drug and the carrier. As the model analytes were extracted directly into an aqueous solution, there was no need for evaporation of the extract before injection into LC-MS. Hence, the sample preparation is performed in one step. With optimized conditions, the extraction recoveries were in the range 50-89% from human plasma after 45min extraction. The data from the method evaluation were satisfactory and in line with current guidelines, and revealed an extraction method with substantial potential for high throughput bioanalysis of polar basic drugs.

U2 - 10.1016/j.jchromb.2016.09.019

DO - 10.1016/j.jchromb.2016.09.019

M3 - Journal article

C2 - 27650942

VL - 1043

SP - 25

EP - 32

JO - Journal of Chromatography B: Analytical Technologies in the Biomedical and Life Sciences

JF - Journal of Chromatography B: Analytical Technologies in the Biomedical and Life Sciences

SN - 1570-0232

ER -

ID: 168937327