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Graphene and zeolite as adsorbents in bar-micro-solid phase extraction of pharmaceutical compounds of diverse polarities.
Jajuli, Maizatul Najwa; Herzog, Grégoire; Hébrant, Marc; Poh, Ng Eng; Rahim, Afidah Abdul; Saad, Bahruddin; Hussin, M Hazwan.
Afiliación
  • Jajuli MN; Department of Chemistry, Faculty of Science and Mathematics, Sultan Idris Education University 35900 Tanjong Malim Perak Malaysia najwa@fsmt.upsi.edu.my.
  • Herzog G; Université de Lorraine, CNRS, LCPME F-54000 Nancy France.
  • Hébrant M; Université de Lorraine, CNRS, LCPME F-54000 Nancy France.
  • Poh NE; Université de Lorraine, CNRS, LCPME F-54000 Nancy France.
  • Rahim AA; School of Chemistry, Universiti Sains Malaysia 11800 Pulau Pinang Malaysia mhh@usm.my.
  • Saad B; School of Chemistry, Universiti Sains Malaysia 11800 Pulau Pinang Malaysia mhh@usm.my.
  • Hussin MH; Fundamental and Applied Sciences Department, Universiti Teknologi PETRONAS 32610 Seri Iskandar Perak Darul Rizwan Malaysia.
RSC Adv ; 11(27): 16297-16306, 2021 Apr 30.
Article en En | MEDLINE | ID: mdl-35479128
ABSTRACT
A bar micro-solid phase (bar µ-SPE) extraction method using either graphene or zeolite or their mixtures as an adsorbent, coupled with high-performance liquid chromatography (using a C1 column) was developed for the simultaneous determination of pharmaceutical compounds (metformin (MET), buformin (BUF), phenformin (PHEN) and propranolol (PROP)) of diverse polarity (log P from -1.82 to 3.10). Parameters influencing the extraction, such as conditioning solvents, pH of the sample, sample volume, amount of adsorbent, stirring rate, time of extraction, type and volume of desorption solvent and time of desorption were investigated. Under the optimized conditions, the extraction method using graphene (extraction efficiency, % EE, ∼6-15%) resulted in the least amount of extracted drugs. However, the use of zeolite and zeolite/graphene mixtures improves the % EE significantly, i.e. 30% for PHEN and 42% for PROP using zeolite; 22% for MET and 18% for BUF using the adsorbent mixture. Under similar conditions, enrichment factors for these drugs range from 11-15. The validated method was performed for the determination of the drugs that were spiked to urine samples. Good recoveries ranging from 72.8 to 116% were achieved.