Premium
Separation and determination of ciprofloxacin in seawater, human blood plasma and tablet samples using molecularly imprinted polymer pipette‐tip solid phase extraction and its optimization by response surface methodology
Author(s) -
Hashemi Sayyed Hossein,
Ziyaadini Morteza,
Kaykhaii Massoud,
Jamali Keikha Ahmad,
Naruie Nasrin
Publication year - 2020
Publication title -
journal of separation science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.72
H-Index - 102
eISSN - 1615-9314
pISSN - 1615-9306
DOI - 10.1002/jssc.201900923
Subject(s) - chromatography , elution , extraction (chemistry) , solid phase extraction , molecularly imprinted polymer , detection limit , central composite design , analyte , column chromatography , solvent , response surface methodology , sorbent , chemistry , seawater , sample preparation , materials science , adsorption , analytical chemistry (journal) , selectivity , biochemistry , oceanography , organic chemistry , geology , catalysis
By synthesizing a molecular imprinted polymer as an efficient adsorbent, ciprofloxacin was micro‐extracted from seawater, human blood plasma and tablet samples by pipette‐tip micro solid phase extraction and determined spectrophotometrically. Response surface methodology was applied with central composite design to build a model based on factors affecting on microextraction of ciprofloxacin; including volume of eluent solvent, number of extraction cycles, number of elution cycles, and pH of sample. Other factors that affect extraction efficiency, such as type of eluent solvent, volume of sample, type, and amount of salt were optimized with one‐variable‐at‐a‐time method. Under optimum extraction condition, pH of sample solution was 7.0, volume of eluent solvent (methanol) was 200 µL, volume of sample solution was 10 mL, and the number of extraction and elution cycles was five and seven, respectively, amount of Na 2 SO 4 (as salt) and MIP (as sorbent) were optimized at 150 and 2 mg, respectively. The linear range of the suggested method under optimum extraction factors was 5–150 µg/L with a limit of detection of 1.50 µg/L for the analyte. Reproducibility of the method (as relative standard deviation) was better than 7%.