Procedure for the Screening of Eggs and Egg Products to Detect Oxolonic Acid, Ciprofloxacin, Enrofloxacin, and Sarafloxacin Using Micellar Liquid Chromatography

A method based on micellar liquid chromatography was developed to determine oxolinic acid, ciprofloxacin, enrofloxacin, and sarafloxacin in eggs and egg products. The antimicrobial drugs were obtained in a micellar solution which was directly injected. The analytes were resolved using a C18 column a...

Full description

Saved in:
Bibliographic Details
Main Authors: Juan Peris-Vicente (Author), Daniel García-Ferrer (Author), Pooja Mishra (Author), Jaume Albiol-Chiva (Author), Abhilasha Durgbanshi (Author), Samuel Carda-Broch (Author), Devasish Bose (Author), Josep Esteve-Romero (Author)
Format: Book
Published: MDPI AG, 2019-11-01T00:00:00Z.
Subjects:
Online Access:Connect to this object online.
Tags: Add Tag
No Tags, Be the first to tag this record!

MARC

LEADER 00000 am a22000003u 4500
001 doaj_4b611c8d22dc4e86a7e96ee9a30794ea
042 |a dc 
100 1 0 |a Juan Peris-Vicente  |e author 
700 1 0 |a Daniel García-Ferrer  |e author 
700 1 0 |a Pooja Mishra  |e author 
700 1 0 |a Jaume Albiol-Chiva  |e author 
700 1 0 |a Abhilasha Durgbanshi  |e author 
700 1 0 |a Samuel Carda-Broch  |e author 
700 1 0 |a Devasish Bose  |e author 
700 1 0 |a Josep Esteve-Romero  |e author 
245 0 0 |a Procedure for the Screening of Eggs and Egg Products to Detect Oxolonic Acid, Ciprofloxacin, Enrofloxacin, and Sarafloxacin Using Micellar Liquid Chromatography 
260 |b MDPI AG,   |c 2019-11-01T00:00:00Z. 
500 |a 2079-6382 
500 |a 10.3390/antibiotics8040226 
520 |a A method based on micellar liquid chromatography was developed to determine oxolinic acid, ciprofloxacin, enrofloxacin, and sarafloxacin in eggs and egg products. The antimicrobial drugs were obtained in a micellar solution which was directly injected. The analytes were resolved using a C18 column and a mobile phase of 0.05 M sodium dodecyl sulfate-7.5% 1-propanol-0.5% triethylamine, buffered at pH 3 with phosphate salt, running under the isocratic mode. The signal was monitored by fluorescence. Validation was successfully performed according to the EU Commission Decision 2002/657/EC in terms of specificity, calibration range (LOQ to 1 mg/kg), linearity (<i>R</i><sup>2</sup> > 0.9991), limit of detection and decision limit (0.01-0.05 mg/kg), limit of quantification (0.025-0.150 mg/kg), detection capability (<0.4 times decision limit), trueness (−14.2% to +9.8%), precision (<14.0%), robustness, and stability. The procedure was environmentally friendly, safe, easy-to-conduct, inexpensive, and had a high sample throughput, thus it is useful for routine analysis as a screening method in a laboratory for food residue control. 
546 |a EN 
690 |a food safety 
690 |a fluorescence 
690 |a laying hen 
690 |a optimization 
690 |a solid-to-liquid extraction 
690 |a validation 
690 |a Therapeutics. Pharmacology 
690 |a RM1-950 
655 7 |a article  |2 local 
786 0 |n Antibiotics, Vol 8, Iss 4, p 226 (2019) 
787 0 |n https://www.mdpi.com/2079-6382/8/4/226 
787 0 |n https://doaj.org/toc/2079-6382 
856 4 1 |u https://doaj.org/article/4b611c8d22dc4e86a7e96ee9a30794ea  |z Connect to this object online.