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Large volume sample stacking of antiepileptic drugs in counter current electrophoresis performed in PAMAPTAC coated capillary
被引:18
|作者:
Tuma, Petr
[1
]
Hlozek, Tomas
[1
,2
]
Sommerova, Blanka
[1
]
Koval, Dusan
[3
]
机构:
[1] Charles Univ Prague, Fac Med 3, Dept Hyg, Ruska 87, Prague 10000 10, Czech Republic
[2] Univ Pardubice, Fac Chem Technol, Dept Analyt Chem, Studentska 573, Pardubice 53210, Czech Republic
[3] Czech Acad Sci, Inst Organ Chem & Biochem, Flemingovo 2, Prague 16610 6, Czech Republic
来源:
关键词:
Antiepileptic;
Capillary electrophoresis;
Coating;
Contactless conductivity detection;
Sample pretreatment;
Serum;
Stacking;
ELECTROOSMOTIC FLOW PUMP;
GAMMA-AMINOBUTYRIC-ACID;
CONDUCTIVITY DETECTION;
SENSITIVE DETERMINATION;
ZONE-ELECTROPHORESIS;
HUMAN SERUM;
PREGABALIN;
GABAPENTIN;
VIGABATRIN;
DERIVATIZATION;
D O I:
10.1016/j.talanta.2020.121626
中图分类号:
O65 [分析化学];
学科分类号:
070302 ;
081704 ;
摘要:
Electrophoretic stacking is developed for sensitive determination of three zwitterionic antiepileptics, namely vigabatrin, pregabalin and gabapentin, in human serum. CE separation is performed in a 25 mu m fused silica capillary covalently coated with the copolymer of acrylamide with 5% content of permanently charged 3-acryl-amidopropyl trimethylammonium chloride (PAMAPTAC). In background electrolyte of 500 mM acetic acid, the 5% PAMAPTAC generates an anodic electm-osmotic flow with a magnitude of (-18.6 +/- 0.5) x 10(-9) m(2)V(-1)s(-1), which acts against the direction of the electrophoretic migration of the analytes. A sample of the antiepileptic prepared in a 25% v/v infusion solution and 75% v/v acetonitrile is injected into the capillary in a large volume attaining a zone length of up to 270 mm. After turning on the separation voltage, the antiepileptics are isotachophoretically focussed behind the zone of Na+ ions with a sensitivity enhancement factor of 78. For the clinical determination of antiepileptics, the human serum is diluted with acetonitrile in a ratio of 1:3 v/v and a zone with a length of 90 mm is injected into the capillary. The method is linear in the 0.025-2.5 mu g/mL concentration range; the attained limit of quantification is in the range 18.3-22.8 nmol/L; the within-day precision for the migration time is 0.8-1.2% and for the peak area 1.5-2.4%.
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