2023
DOI: 10.1016/j.chroma.2023.463873
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A Strategy for assessing peak purity of pharmaceutical peptides in reversed-phase chromatography methods using two-dimensional liquid chromatography coupled to mass spectrometry. Part II: Development of second-dimension gradient conditions

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Cited by 7 publications
(5 citation statements)
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“…The separation of isomers is emphasised, since these compounds with identical m/z are not readily differentiated by MS. The study is divided into two parts: part I is related to selection of columns and mobile phases [current publication] whereas part II is related to the definition of the 2 D gradient elution conditions, and additional proof-of-concept 2D-LC-MS separations that illustrate the power of the strategy [15].…”
Section: Discussionmentioning
confidence: 99%
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“…The separation of isomers is emphasised, since these compounds with identical m/z are not readily differentiated by MS. The study is divided into two parts: part I is related to selection of columns and mobile phases [current publication] whereas part II is related to the definition of the 2 D gradient elution conditions, and additional proof-of-concept 2D-LC-MS separations that illustrate the power of the strategy [15].…”
Section: Discussionmentioning
confidence: 99%
“…An Agilent 1290 Infinity II 2D-LC system was used for the collection of the data shown in Figure 8. A generalised illustration of this system for multiple heart-cutting is provided as supplemental information in Part II ( [15] Figure S1). The first dimension consisted of an autosampler, a binary pump with a 380 µL Jet Weaver mixer, a thermostated column compartment, and a UV absorbance detector with a 6 mm semi-micro flow cell.…”
Section: Methodsmentioning
confidence: 99%
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“…Petersson et al published a study focused on defining the second-dimension chromatographic gradient conditions and demonstrating the 2D-LC-MS methods developed using this approach [62].…”
Section: Two-dimensional Separation Methodsmentioning
confidence: 99%
“…Both, structure and function of proteins are often investigated by means of their enzymatically generated peptide fragments in the so called bottom-up or shotgun proteomics [10][11][12][13]. These peptide fragments are separated and identified by liquid chromatography (LC), 2-DE, and capillary electrophoresis (CE) methods online coupled with MS detection [14][15][16][17][18][19]. In addition, for understanding of both normal and pathological physiological processes, a comprehensive investigation of the whole peptide set (peptidome) of a cell, organ, or organism at given time frame is necessary as well.…”
mentioning
confidence: 99%