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Performing flow injection chromatography using a narrow open tubular column.
Xiang, Piliang; Yang, Yu; Zhao, Zhitao; Wang, Jianhua; Chen, Mingli; Chen, Apeng; Liu, Shaorong.
Afiliação
  • Xiang P; Department of Chemistry and Biochemistry, University of Oklahoma, Norman, OK, 73019, USA.
  • Yang Y; Department of Chemistry and Biochemistry, University of Oklahoma, Norman, OK, 73019, USA.
  • Zhao Z; Department of Chemistry and Biochemistry, University of Oklahoma, Norman, OK, 73019, USA.
  • Wang J; Department of Chemistry, College of Sciences, Northeastern University, Shenyang, 110819, PR China.
  • Chen M; Department of Chemistry, College of Sciences, Northeastern University, Shenyang, 110819, PR China. Electronic address: chenml@mail.neu.edu.cn.
  • Chen A; Department of Chemistry and Biochemistry, University of Oklahoma, Norman, OK, 73019, USA; Department of Neurological Surgery, University of Pittsburgh, Pittsburgh, PA, 15213, USA. Electronic address: apc55@pitt.edu.
  • Liu S; Department of Chemistry and Biochemistry, University of Oklahoma, Norman, OK, 73019, USA; Department of Chemistry, College of Sciences, Northeastern University, Shenyang, 110819, PR China. Electronic address: Shaorong.liu@ou.edu.
Anal Chim Acta ; 1109: 19-26, 2020 May 01.
Article em En | MEDLINE | ID: mdl-32252901
ABSTRACT
Flow injection chromatography (FIC) or sequential injection chromatography (SIC) is a low-pressure liquid chromatography technique that uses flow injection or sequential injection hardware. Due to the constraints of this hardware, the separation resolution is low; often no more than 3-5 components are resolved. We have recently demonstrated the excellent resolving power of narrow open tubular (OT) columns for various biomolecules, and only moderate elution pressures are needed to carry out these separations. In this paper, we incorporate a narrow OT column with FIC and construct an FIC system using a pressure chamber and two injection valves to implement gradient elution. The resultant system not only improves the resolution but also reduces the system cost. When we use the system to separate peptides from trypsin-digested cytochrome C, we can resolve dozens of peptides (with resolutions of 0.5 or greater) at a speed of 12 samples per hour. When we use this system to separate a mixture containing 3 amino acids, we can base-line resolve these compounds at a speed of 1800 sample per hour.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2020 Tipo de documento: Article