Affiliations 

  • 1 School of Chemical Sciences, Universiti Sains Malaysia, Penang, Malaysia; Centre for Global Sustainability Studies, Universiti Sains Malaysia, Penang, Malaysia. Electronic address: normaliza@usm.my
  • 2 School of Chemical Sciences, Universiti Sains Malaysia, Penang, Malaysia; Fundamental & Applied Sciences Department, Universiti Teknologi Petronas, Perak, Malaysia. Electronic address: bahruddin.saad@utp.edu.my
  • 3 Department of Chemistry, University of Saskatchewan, Saskatoon, Saskatchewan, Canada
  • 4 Anti-Doping Laboratory Qatar, Doha, Qatar
J Chromatogr A, 2018 Mar 30;1543:23-33.
PMID: 29478831 DOI: 10.1016/j.chroma.2018.02.032

Abstract

Sorbents were prepared by cross-linking β-cyclodextrin (β-CD) using two different types of cross-linker units at variable reactant mole ratios. The resulting polymers containing β-CD were evaluated as sorbents in micro-solid phase extraction (μ-SPE) format for the extraction of the endogenous steroids testosterone (T), epitestosterone (E), androsterone (A), etiocholanolone (Etio), 5α-androstane-3α,17β-diol (5αAdiol) and 5β-androstane-3α,17β-diol (5βAdiol). The best sorbent (C1; cyclodextrin polymer) showed superior extraction characteristics compared with commercial sorbents (C18 and Bond Elut Plexa). Parameters influencing the extraction efficiency of the C1 sorbent such as extraction and desorption times, desorption solvent and volume of sample were investigated. The extracts were separated using a Hypersil Gold column (50 × 2.1 mm, 1.9 μm) under gradient elution coupled to a LC-MS/MS. The compounds were successfully separated within 8 min. The method offers good repeatability (RSD  0.995) were within the range of 1-200 ng mL-1 for T and E, 250-4000 ng mL-1 for A and Etio and 25-500 ng mL-1 for 5αAdiol and 5βAdiol, respectively. The method was applied for the determination of steroid profile of urine from volunteers.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.

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