Mixed mode monolithic sorbent in pipette tip for extraction of ractopamine and clenbuterol prior to analysis by HPLC-UV and UHPLC-Q Exactive Plus Orbitrap MS

被引:7
作者
Ar-sanork, Kesara [1 ]
Karuwan, Chanpen [2 ,3 ]
Surapanich, Nakin [4 ]
Wilairat, Prapin [3 ,5 ,6 ]
Nacapricha, Duangjai [3 ,7 ,8 ]
Chaisuwan, Patcharin [1 ,3 ]
机构
[1] Suranaree Univ Technol, Sch Chem, Inst Sci, 111 Univ Ave, Muang District 30000, Nakhon Ratchasi, Thailand
[2] Natl Sci & Technol Dev Agcy NSTDA, Graphene & Printed Elect Dual Use Applicat Res Di, Pathum Thani 12120, Thailand
[3] Flow Innovat Res Sci Technol Labs FIRST Labs, Bangkok, Thailand
[4] Rajanagarindra Rajabhat Univ, Fac Sci & Technol, Dept Chem, 22 Maruphong Rd, Muang 24000, Chachoengsao, Thailand
[5] Mahidol Univ, Analyt Sci, Rama VI Rd, Bangkok 10400, Thailand
[6] Mahidol Univ, Natl Doping Test Inst, Rama VI Rd, Bangkok 10400, Thailand
[7] Mahidol Univ, Fac Sci, Dept Chem, Rama 6 Rd, Bangkok 10400, Thailand
[8] Mahidol Univ, Fac Sci, Ctr Excellence Innovat Chem, Rama 6 Rd, Bangkok 10400, Thailand
关键词
Micro-solid phase extraction; Monolith; Ractopamine; Clenbuterol; HPLC analysis; BETA-AGONISTS; MASS-SPECTROMETRY; SWINE FEED; TISSUES; URINE; RESIDUES; ELECTROPHORESIS; MICROEXTRACTION; IDENTIFICATION; METABOLITES;
D O I
10.1186/s40543-021-00275-5
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
This work developed a fast and simple method for the quantification of two important beta-agonists, ractopamine (RAC) and clenbuterol (CLEN) in animal urines. The method was based on micro-extraction by a mixed mode monolithic material and analysis by HPLC-UV and UHPLC-Q Exactive Plus Orbitrap mass spectrometer. A mixed functional monolith with nonpolar ester-based structure containing polar carboxylic groups was thermally synthesized in situ in the pipette tips. The material combines both hydrophobic and ionic interactions. Parameters including conditions and composition of reagents for the in-pipette tip monolith synthesis, as well as the extraction process, were investigated and optimized. The procedure for extraction is 800 mu L washing solvent of 10:90 (v/v) ACN:water and 150 mu L eluting solvent of 30:70 (v/v) ACN:200 mM acetate buffer pH 4.0. Extraction efficiencies of 92% and 100% for RAC and CLEN, respectively, were achieved within 5 min with total organic solvent consumption of 395 mu L. The extracts of spiked cattle and swine urines were analyzed by HPLC-UV and UHPLC-Q Exactive Plus Orbitrap mass spectrometer. Good recovery with acceptable precision was observed. The mass spectrometry data confirmed efficient matrix removal by the synthesized extraction sorbent allowing routine analysis by the HPLC-UV method.
引用
收藏
页数:10
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