Liquid–liquid extraction procedure for nonvolatile pesticides determination in acacia honey as environmental biomonitor

Author(s):  
Firas Baroudi ◽  
Josephine Al-Alam ◽  
Olivier Delhomme ◽  
Supansa Chimjarn ◽  
Hanine Al-Ghech ◽  
...  
2016 ◽  
Vol 31 (1) ◽  
pp. 319-327 ◽  
Author(s):  
Katy Murphy ◽  
Mark Rehkämper ◽  
Katharina Kreissig ◽  
Barry Coles ◽  
Tina van de Flierdt

During isotopic analysis of Cd by MC-ICP-MS, organic resin residue can perturb instrumental mass fractionation. These organic compounds can be removed by a liquid–liquid extraction procedure using heptane.


2018 ◽  
Vol 101 (3) ◽  
pp. 897-903 ◽  
Author(s):  
Brian T Veach ◽  
Renea Anglin ◽  
Thilak K Mudalige ◽  
Paula J Barnes

Abstract This paper describes a rapid and robust method utilizing a single liquid–liquid extraction for the quantitation and confirmation of chloramphenicol, florfenicol, and nitrofuran metabolites in honey. This methodology combines two previous extraction methods into a single extraction procedure and utilizes matrix-matched calibration standards and stable isotopically labeled standards to improve quantitation. The combined extraction procedure reduces the average extraction time by >50% when compared with previously used procedures. The drug residues were determined using two separate LC-tandem MS conditions. Validation of all the analytes was performed, with average quantitation ranging from 92 to 105% for all analytes and the RSDs for all analytes being ≤12%.


2011 ◽  
Vol 19 (1-2) ◽  
pp. 23-27 ◽  
Author(s):  
Dragan Milicevic ◽  
Milijan Jovanovic ◽  
Vesna Matekalo-Sverak ◽  
Tatjana Radicevic ◽  
Milan Petrovic ◽  
...  

Background: Toxicological investigations of tissues of normally slaughtered chickens were carried out to provide preliminary evaluation of the incidence of OTA in chicken tissues (n=90). Majority of tissue samples were not found to contain measurable amounts of OTA, while in general, the OTA levels found in the analyzed tissue were low. Methods: The presence of OTA in tissue samples was determined by HPLC-FL after liquid-liquid extraction procedure. Method validation was performed according to the Commission Decision 2002/657/EC. Results: Of the 90 liver, kidney and gizzard samples originating from chicken farms located in the different agricultural areas of Serbia, OTA was reported in 23 (38.33%), 17 (28.3%) and 16 (26.6%) samples, respectively, with levels ranging from 0.14 to 3.9 ng/g in liver, 0.1 to 7.02 ng/g in kidneys and 0.25 to 9.94 ng/g in gizzard. None of the tissue samples contained more than the maximum level (10 ng/g) recommended by the European Commission. Conclusion: Low OTA results also suggested that chicken meat available in the retail market is unlikely to pose an adverse health risk to the consumers in respect to OTA toxicity.


INDIAN DRUGS ◽  
2016 ◽  
Vol 53 (06) ◽  
pp. 46-50
Author(s):  
A Faizee ◽  
◽  
S. S Sonawane ◽  
A. S. Patil ◽  
S. J Kshirsagar ◽  
...  

A simple, rapid and accurate RP-HPLC method was developed and validated for the quantification of Erlotinib in spiked human plasma using liquid-liquid extraction. Sufficient recovery was obtained when drug and internal standard (Nabumetone) were extracted using ethyl acetate and 1N NaOH. Chromatographic separation was performed on C18 Phenomenex Hyperclone column (250 × 4.6 mm, 5 μm) using mobile phase acetonitrile: 20 mM ammonium acetate buffer pH 4.6 (60:40%,V/V). Flow rate was kept constant at 1 mL/min and detection was carried out at 331 nm. Calibration curve was found to be linear in the range of 100-3200 ng/mL. During the calibration experiments, it was found that heteroscedasticity can be minimized using weighted regression calibration model with weighing factor of 1/x2.


Sign in / Sign up

Export Citation Format

Share Document