Voltammetric determination of lercanidipine in urine, blood plasma, and serum using hollow fiber-based liquid phase microextraction
Language English Country Netherlands Media print-electronic
Document type Journal Article
PubMed
40215720
DOI
10.1016/j.talanta.2025.128038
PII: S0039-9140(25)00528-4
Knihovny.cz E-resources
- Keywords
- Hollow fiber liquid-phase microextraction, Lercanidipine hydrochloride, Sample preparation, Screen-printed boron-doped diamond electrode, Square wave voltammetry,
- MeSH
- Antihypertensive Agents * blood urine MeSH
- Dihydropyridines * blood urine isolation & purification MeSH
- Electrochemical Techniques * methods MeSH
- Electrodes MeSH
- Humans MeSH
- Limit of Detection MeSH
- Liquid Phase Microextraction * methods MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- Antihypertensive Agents * MeSH
- Dihydropyridines * MeSH
- lercanidipine MeSH Browser
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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