0000000000174678
AUTHOR
Anna Drapała
Peptides analysis in blood plasma using on-line system of supported liquid membrane and high-performance liquid chromatography
The potential of using supported liquid membrane (SLM) technique, combined with reversed-phase high-performance liquid chromatography (RP-HPLC) has been investigated for the determination of peptides in human blood plasma. The peptides studied were (DL)Leu(DL)Phe, MetLeuPhe, GlyLeuTyr and ValGluProlleProTyr. The carrier (Aliquat 336) was incorporated in membrane phase in order to facilitate the transport of investigated peptides. After extraction, the analyte-enriched acceptor phase was directly injected into an HPLC system for analysis. With SLM, high selectivity and efficiency were achieved for extraction of peptides in aqueous solutions. Lower extraction efficiency was obtained in plasma…
Facilitated SLM extraction of peptides with D2EHPA as a carrier
Abstract The extraction of short peptides through a supported liquid membrane containing di-2-(ethylhexyl)phosphoric acid (D2EHPA) as a carrier was investigated. The extraction was carried out from the aqueous donor phase with pH 3 to amore acidic acceptor phase. The proton gradient between the donor and the acceptor phase was the main driving force of the mass transfer in this system. The influence of various parameters such as diluent of the carrier, pH of the donor and acceptor phase, peptide structure and concentration on the extraction efficiency was presented.
Extraction of short peptides using supported liquid membranes
Studies of extraction of short peptides using supported liquid membranes containing Aliquat 336 as a carrier are presented. The extractions are carried out from an aqueous donor phase with pH ≥ 10 to an acceptor phase containing salt. The mass transfer is driven by the gradient of salt concentration between these phases. The extraction efficiency is dependent on the composition of water phases, the type and concentration of counter-ion in the stagnant acceptor phase and the flow rate of the donor phase. Moreover, it is also influenced by the concentration and structure of the examined peptides.