Publication:
Mixed mode monolithic sorbent in pipette tip for extraction of ractopamine and clenbuterol prior to analysis by HPLC-UV and UHPLC-Q Exactive<sup>TM</sup> Plus Orbitrap MS

dc.contributor.authorKesara Ar-sanorken_US
dc.contributor.authorChanpen Karuwanen_US
dc.contributor.authorNakin Surapanichen_US
dc.contributor.authorPrapin Wilairaten_US
dc.contributor.authorDuangjai Nacaprichaen_US
dc.contributor.authorPatcharin Chaisuwanen_US
dc.contributor.otherRajabhat Rajanagarindra Universityen_US
dc.contributor.otherSuranaree University of Technologyen_US
dc.contributor.otherMahidol Universityen_US
dc.contributor.otherThailand National Science and Technology Development Agencyen_US
dc.contributor.otherFlow Innovation-Research for Science and Technology Laboratories (FIRST Labs.)en_US
dc.date.accessioned2022-08-04T08:03:36Z
dc.date.available2022-08-04T08:03:36Z
dc.date.issued2021-12-01en_US
dc.description.abstractThis work developed a fast and simple method for the quantification of two important β-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 ExactiveTM 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 μL washing solvent of 10:90 (v/v) ACN:water and 150 μL 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 μL. The extracts of spiked cattle and swine urines were analyzed by HPLC-UV and UHPLC-Q ExactiveTM 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.en_US
dc.identifier.citationJournal of Analytical Science and Technology. Vol.12, No.1 (2021)en_US
dc.identifier.doi10.1186/s40543-021-00275-5en_US
dc.identifier.issn20933371en_US
dc.identifier.issn20933134en_US
dc.identifier.other2-s2.0-85106265298en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/75937
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85106265298&origin=inwarden_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectChemistryen_US
dc.subjectEnvironmental Scienceen_US
dc.subjectMaterials Scienceen_US
dc.subjectPhysics and Astronomyen_US
dc.titleMixed mode monolithic sorbent in pipette tip for extraction of ractopamine and clenbuterol prior to analysis by HPLC-UV and UHPLC-Q Exactive<sup>TM</sup> Plus Orbitrap MSen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85106265298&origin=inwarden_US

Files

Collections