Flyer

International Journal of Drug Development and Research

  • ISSN: 0975-9344
  • Journal h-index: 51
  • Journal CiteScore: 46.50
  • Journal Impact Factor: 26.99
  • Average acceptance to publication time (5-7 days)
  • Average article processing time (30-45 days) Less than 5 volumes 30 days
    8 - 9 volumes 40 days
    10 and more volumes 45 days
Awards Nomination 20+ Million Readerbase
Indexed In
  • Genamics JournalSeek
  • China National Knowledge Infrastructure (CNKI)
  • CiteFactor
  • Scimago
  • Directory of Research Journal Indexing (DRJI)
  • OCLC- WorldCat
  • Publons
  • MIAR
  • University Grants Commission
  • Euro Pub
  • Google Scholar
  • J-Gate
  • SHERPA ROMEO
  • Secret Search Engine Labs
  • ResearchGate
  • International Committee of Medical Journal Editors (ICMJE)
Share This Page

Development and in-house validation of an analytical method for multi residue determination of 202 pesticides residues in tomato, orange and tea using QuEChERS-LC-MS/MS

9th Edition of International Conference on Mass Spectrometry
March 04-05, 2019 Berlin, Germany

Adil Chahid

ONSSA, Morocco

Posters & Accepted Abstracts: Int J Drug Dev & Res

Abstract:

A simple, efficient, sensitive, accurate and reliable multi-residue analytical method was developed and validated for the determination of 202 residual pesticides in three matrices: tomato, orange and tea using modified QuEChERS method with liquid chromatography coupled to triple quadrupole mass spectrometer (LC-MS/MS) for qualitative and quantitative analysis according to the international standard concepts. The optimization and validation method of the mass spectrometry parameters was performed by injecting pesticide standard solutions into the electrospray ion (ESI) source according to the European SANTE/11813/2017 guideline. The specificity of the developed method is considered satisfactory. Good linearity (R2>0.99) was obtained for all pesticide matrix calibration curves within the range of 0.005–0.15 μg.kg−1. The limit of quantification (LOQ) of this method is far lower than the non-detectable level (0.01 mg/ kg) recommended by the regulation. Mean recoveries of all target analyte was within the acceptable range of 70–120%; the relative standard deviations were less than 20%.

Biography :

E-mail:

chahidadilster@gmail.com