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  • Sensitivity enhancement in direct coupling of supported liquid membrane extractions to capillary electrophoresis by means of transient isotachophoresis and large electrokinetic injections.

Sensitivity enhancement in direct coupling of supported liquid membrane extractions to capillary electrophoresis by means of transient isotachophoresis and large electrokinetic injections.

Journal of chromatography. A (2015-03-10)
Pavla Pantůčková, Pavel Kubáň, Petr Boček
ABSTRACT

Enhanced sensitivity for determination of basic drugs in body fluids was achieved by in-line coupling of extraction across supported liquid membrane (SLM) to large electrokinetic injection and transient isotachophoresis-capillary zone electrophoresis (tITP-CZE) in commercial CZE instrument. Twelve cm long tITP plug of 300mM ammonium acetate was formed in the separation capillary just before the electrokinetic injection of acceptor solution containing nortriptyline, haloperidol and loperamide extracted across the SLM. The tITP plug ensured efficient stacking and preconcentration of the injected basic drugs due to the tITP action of ammonium and the drugs were then separated by CZE using 5.2M acetic acid as background electrolyte. No interferences were observed from highly-abundant body fluid species (NaCl and human serum albumin) due to the excellent clean-up properties of SLMs and analytical sensitivity increased up to 340 times compared to SLM extractions coupled in-line to CZE with standard hydrodynamic injections. The SLM-tITP-CZE method was characterized by good repeatability (RSDs of peak areas below 7.8%), linearity over two orders of magnitude (r(2) better than 0.994) and limits of detection (defined as 3×S/N) between 3 and 45μg/L. Interfacing of SLM extractions to CZE instrumentation was achieved by low-cost, disposable micro-extraction devices, which can be routinely prepared in every analytical laboratory. These devices eliminated sample carry-over, minimized the need for manual sample handling and ensured fully automated determination (including extraction, injection, preconcentration and separation) of the three basic drugs in 20μL of untreated body fluids.

MATERIALS
Product Number
Brand
Product Description

Sigma-Aldrich
Acetic acid, glacial, puriss., 99-100%
Sigma-Aldrich
Acetic acid, glacial, puriss., meets analytical specification of Ph. Eur., BP, USP, FCC, 99.8-100.5%
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Acetic acid, glacial, ReagentPlus®, ≥99%
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Acetic acid, glacial, puriss. p.a., ACS reagent, reag. ISO, reag. Ph. Eur., ≥99.8%
Sigma-Aldrich
Acetic acid solution, suitable for HPLC
Sigma-Aldrich
Ammonium acetate, ≥99.99% trace metals basis
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Acetic acid, glacial, ≥99.99% trace metals basis
USP
Haloperidol, United States Pharmacopeia (USP) Reference Standard
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Ethanol, JIS first grade, 94.8-95.8%
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Acetic acid, ≥99.7%, suitable for amino acid analysis
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Sodium chloride, SAJ first grade, ≥99.0%
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Acetic acid, 99.5-100.0%
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Sodium chloride, JIS special grade, ≥99.5%
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Sodium chloride solution, 1 M
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Acetic acid, SAJ first grade, ≥99.0%
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Acetic acid, ≥99.7%
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Acetic acid solution, 1 M, 1 N
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Haloperidol for system suitability, European Pharmacopoeia (EP) Reference Standard
Sigma-Aldrich
Sodium chloride solution, 0.85%
Supelco
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USP
Nortriptyline hydrochloride, United States Pharmacopeia (USP) Reference Standard
Nortriptyline hydrochloride, European Pharmacopoeia (EP) Reference Standard