2006
DOI: 10.1016/j.chroma.2005.10.009
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Preparation and evaluation of novel stationary phases for improved chromatographic purification of pneumocandin B0

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Cited by 3 publications
(2 citation statements)
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“…It is possible that the interaction is influenced by the so‐called partitioning mechanism (20–26) . In a follow‐up study to explore the use of silica‐bonded phases (in which the bonded amine group was available for direct interactions) for the purification of pneumocandins, a significant increase in k ' for pneumocandin B 0 as well as for the two structural analogues was observed (29). It is possible that direct interactions of the pneumocandin hydroxyl with the bonded amine resulted in the retention increases.…”
Section: 0 Results and Discussionmentioning
confidence: 99%
“…It is possible that the interaction is influenced by the so‐called partitioning mechanism (20–26) . In a follow‐up study to explore the use of silica‐bonded phases (in which the bonded amine group was available for direct interactions) for the purification of pneumocandins, a significant increase in k ' for pneumocandin B 0 as well as for the two structural analogues was observed (29). It is possible that direct interactions of the pneumocandin hydroxyl with the bonded amine resulted in the retention increases.…”
Section: 0 Results and Discussionmentioning
confidence: 99%
“…Achiral stationary phases evaluated in the study include Chromegabond Diol, Amine, Nitro, and Pyridyl Amide (ES Industries), Kromasil silica (Eka Chemicals), Princeton Benzamide, Pyridine, CPU, PPU, and PhPU (Princeton Chromatography) and an assortment of experimental stationary phases prepared in these laboratories. 10 …”
Section: Stationary Phasesmentioning
confidence: 97%