Voltammetric determination of lercanidipine in urine, blood plasma, and serum using hollow fiber-based liquid phase microextraction
Jazyk angličtina Země Nizozemsko Médium print-electronic
Typ dokumentu časopisecké články
PubMed
40215720
DOI
10.1016/j.talanta.2025.128038
PII: S0039-9140(25)00528-4
Knihovny.cz E-zdroje
- Klíčová slova
- Hollow fiber liquid-phase microextraction, Lercanidipine hydrochloride, Sample preparation, Screen-printed boron-doped diamond electrode, Square wave voltammetry,
- MeSH
- antihypertenziva * krev moč MeSH
- dihydropyridiny * krev moč izolace a purifikace MeSH
- elektrochemické techniky * metody MeSH
- elektrody MeSH
- lidé MeSH
- limita detekce MeSH
- mikroextrakce kapalné fáze * metody MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- antihypertenziva * MeSH
- dihydropyridiny * MeSH
- lercanidipine MeSH Prohlížeč
This study investigates a synergistic combination of hollow fiber-based liquid phase microextraction (HF-LPME) and voltammetric analysis using screen-printed boron-doped diamond electrodes (SP-BDDE) for the determination of antihypertensive drug lercanidipine (LCN) in urine, blood plasma, and blood serum. Optimum HF-LPME conditions were: dodecane as supported liquid membrane, Britton-Robinson buffer (BRB) pH 7 as donor solution, BRB pH 3 as acceptor solution, and extraction time 30 min. Square-wave voltammetry (SWV) of 10 μL acceptor solution at SP-BDDE was utilized with amplitude 75 mV, frequency 10 Hz, and potential step 4 mV. The calibration dependence of the combined HF-LPME-SWV method was established in the range of 1-1000 nmol L-1, with limits of quantification (LOQ) and detection (LOD) of 3.3 and 1.1 nmol L-1, respectively. The applicability of the developed method was verified by analysis of human urine, blood plasma, and blood serum samples spiked with 20 and 100 nmol L-1 LCN with recoveries ranging from 93.2 to 112.9 % with respective RSDs 1.72-8.5 % (n = 3).
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