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Evaluation of the impact of peak description on the quantitative capabilities of comprehensive two-dimensional liquid chromatography.
Place, Benjamin J; Morris, Mallory J; Phillips, Melissa M; Sander, Lane C; Rimmer, Catherine A.
Affiliation
  • Place BJ; Chemical Sciences Division, Material Measurement Laboratory, National Institute of Standards and Technology, Gaithersburg, MD 20899, United States. Electronic address: benjamin.place@nist.gov.
  • Morris MJ; Chemical Sciences Division, Material Measurement Laboratory, National Institute of Standards and Technology, Gaithersburg, MD 20899, United States; Department of Chemistry & Biochemistry, Florida State University, Tallahassee, FL 32306-4390, United States.
  • Phillips MM; Chemical Sciences Division, Material Measurement Laboratory, National Institute of Standards and Technology, Gaithersburg, MD 20899, United States.
  • Sander LC; Chemical Sciences Division, Material Measurement Laboratory, National Institute of Standards and Technology, Gaithersburg, MD 20899, United States.
  • Rimmer CA; Chemical Sciences Division, Material Measurement Laboratory, National Institute of Standards and Technology, Gaithersburg, MD 20899, United States.
J Chromatogr A ; 1368: 107-15, 2014 Nov 14.
Article in En | MEDLINE | ID: mdl-25441346
ABSTRACT
Comprehensive, two-dimensional liquid chromatography (LC × LC) is a powerful technique for the separation of complex mixtures. Most studies using LC × LC are focused on qualitative efforts, such as increasing peak capacity. The present study examined the use of LC × LC-UV/vis for the separation and quantitation of polycyclic aromatic hydrocarbons (PAHs). More specifically, this study evaluated the impact of different peak integration approaches on the quantitative performance of the LC × LC method. For well-resolved three-dimensional peaks, parameters such as baseline definition, peak base shape, and peak width determination did not have a significant impact on accuracy and precision. For less-resolved peaks, a dropped baseline and the summation of all slices in the peak improved the accuracy and precision of the integration methods. The computational approaches to three-dimensional peak integration are provided, including fully descriptive, select slice, and summed heights integration methods, each with its own strengths and weaknesses. Overall, the integration methods presented quantify each of the PAHs within acceptable precision and accuracy ranges and have comparable performance to that of single dimension liquid chromatography.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Polycyclic Aromatic Hydrocarbons / Chromatography, High Pressure Liquid Type of study: Qualitative_research Language: En Journal: J Chromatogr A Year: 2014 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Polycyclic Aromatic Hydrocarbons / Chromatography, High Pressure Liquid Type of study: Qualitative_research Language: En Journal: J Chromatogr A Year: 2014 Document type: Article