Pregled bibliografske jedinice broj: 711235
HPLC–DAD–FLD determination of veterinary pharmaceuticals in pharmaceutical industry wastewater with precolumn derivatization using fluorescamine
HPLC–DAD–FLD determination of veterinary pharmaceuticals in pharmaceutical industry wastewater with precolumn derivatization using fluorescamine // Chromatographia, 77 (2014), 15-16; 1059-1066 doi:10.1007/s10337-014-2685-x (međunarodna recenzija, članak, znanstveni)
CROSBI ID: 711235 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
HPLC–DAD–FLD determination of veterinary pharmaceuticals in pharmaceutical industry wastewater with precolumn derivatization using fluorescamine
Autori
Ašperger, Danijela ; Tišler, Vesna ; Zrnčić, Mirta ; Mutavdžić Pavlović, Dragana ; Babić, Sandra ; Horvat, Alka J. M. ; Kaštelan-Macan, Marija
Izvornik
Chromatographia (0009-5893) 77
(2014), 15-16;
1059-1066
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
High-performance liquid chromatography ; Fluorescence detection ; Derivatization ; Fluorescamine ; Pharmaceuticals ; Wastewater
Sažetak
A simple and robust method suitable for routine analysis of pharmaceuticals from different classes in pharmaceutical industry wastewater samples is presented. Seven veterinary pharmaceuticals (antibiotics and anesthetic) were simultaneously isolated from a highly complex wastewater matrix. Target compounds were three sulfonamide antibiotics (sulfaguanidine, sulfadiazine, and sulfamethazine), three fluoroquinolone antibiotics (ciprofloxacin, enrofloxacin, norfloxacin), and one anesthetic, procaine. The investigated compounds were simultaneously pre-concentrated and cleaned up by solid-phase extraction using Strata-X extraction cartridges. The analysis was performed using liquid chromatography (LC) with diode array and fluorescence detectors connected in series to the chromatographic system. LC separation was performed on a C18 modified column (Phenomenex) with a gradient elution of mobile phase (0.1 % acetic acid in water and 0.1 % acetic acid in acetonitrile) in 25 min at 30 °C. Recoveries ranged from 86.9 to 110 % with relative standard deviations below 10.1 %. Method limits of quantification were in the range of 0.005–0.1 μg L−1 depending on the fluorescence intensity after precolumn derivatization by fluorescamine.
Izvorni jezik
Engleski
Znanstvena područja
Kemija
POVEZANOST RADA
Projekti:
MZOS-125-1253008-1350 - Razvoj naprednih analitičkih metoda za određivanje farmaceutika u okolišu (Babić, Sandra, MZOS ) ( CroRIS)
Ustanove:
Fakultet kemijskog inženjerstva i tehnologije, Zagreb
Profili:
Dragana Mutavdžić Pavlović
(autor)
Sandra Babić
(autor)
Mirta Čizmić
(autor)
Marija Kaštelan-Macan
(autor)
Alka Horvat
(autor)
Danijela Ašperger
(autor)
Citiraj ovu publikaciju:
Časopis indeksira:
- Current Contents Connect (CCC)
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus
Uključenost u ostale bibliografske baze podataka::
- CA Search (Chemical Abstracts)