Cyclodextrin based polymer sorbents for micro-solid phase extraction followed by liquid chromatography tandem mass spectrometry in determination of endogenous steroids

被引:18
|
作者
Manaf, Normaliza Abdul [1 ,2 ]
Saad, Bahruddin [1 ,3 ]
Mohamed, Mohamed H. [4 ]
Wilson, Lee D. [4 ]
Latiff, Aishah A. [5 ]
机构
[1] Univ Sains Malaysia, Sch Chem Sci, George Town, Malaysia
[2] Univ Sains Malaysia, Ctr Global Sustainabil Studies, George Town, Malaysia
[3] Univ Teknol Petronas, Fundamental & Appl Sci Dept, Perak, Malaysia
[4] Univ Saskatchewan, Dept Chem, Saskatoon, SK, Canada
[5] Antidoping Lab Qatar, Doha, Qatar
关键词
Micro-solid phase extraction; Steroid profile; LC-MS/MS; beta-Cyclodextrin polymer; Endogenous steroids; Molecular selectivity; BETA-CYCLODEXTRIN; REFERENCE RANGES; SCREENING METHOD; WATER SAMPLES; LC-MS/MS; TESTOSTERONE; EPITESTOSTERONE; MICROEXTRACTION; URINE; HORMONES;
D O I
10.1016/j.chroma.2018.02.032
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Sorbents were prepared by cross-linking beta-cyclodextrin (beta-CD) using two different types of cross-linker units at variable reactant mole ratios. The resulting polymers containing beta-CD were evaluated as sorbents in micro-solid phase extraction mu-SPE) format for the extraction of the endogenous steroids testosterone (T), epitestosterone (E), androsterone (A), etiocholanolone (Etio), 5 alpha-androstane-3 alpha,17 beta-diol (5 alpha Adiol) and 5 beta-androstane-3 alpha,17 beta-diol (5 beta Adiol). 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 x 2.1 mm, 1.9 mu m) under gradient elution coupled to a LC-MS/MS. The compounds were successfully separated within 8 min. The method offers good repeatability (RSD < 10%) and linearity (r(2) > 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 5 alpha Adiol and 5 beta Adiol, respectively. The method was applied for the determination of steroid profile of urine from volunteers. (C) 2018 Elsevier B.V. All rights reserved.
引用
收藏
页码:23 / 33
页数:11
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