PubMed Health⌕ Search

PubMed · 3782317

Parallel column ion exchange for post-separation pH modification in liquid chromatography. Application to barbiturates and miniaturization.

Abstract

A new approach to the UV detection of barbiturates in high-performance liquid chromatography is demonstrated. The analytical system comprises an anion-exchange column inserted parallel to the injection valve and analytical column. One part of the acetate-containing mobile phase flows through the injection valve and analytical column to achieve the separation, the other part flows through the anion-exchange column where the acetate ions cause the release of hydroxide ions from this column. Finally, the alkaline stream from the anion-exchange column is recombined with the analytical column effluent. This results in an alkaline medium which can be favourable for many detection processes. A series of barbiturates, which show enhanced UV detectability at 254 nm in alkaline solution, was chosen to demonstrate the potential of such a method. Applications of this principle to the analysis of urine and plasma samples are described. In the system only one pump is needed for the separation and the post-column pH modification. A critical comparison between conventional scale and narrow-bore systems is made.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

H Jansen, C J Vermunt, U A Brinkman, R W Frei. 1986-09-24. Parallel column ion exchange for post-separation pH modification in liquid chromatography. Application to barbiturates and miniaturization.. https://doi.org/10.1016/s0021-9673(01)93461-2

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related citations

Occurrence and fate of barbiturates in the aquatic environment.

Barbiturates have been widely used as sedative hypnotics in the mid-1960s and since then mainly as veterinary drugs. To monitor their presence and fate in the aquatic environment, a method based on gas chromatography-mass spectrometry (GC-MS) has been developed to quantify butalbital, secobarbital, hexobarbital, aprobarbital, phenobarbital, and pentobarbital, all with a limit of detection (LOD) down to 1 ng/L. From the various investigated waste and surface water samples, barbiturates were only, but regularly detected in the Mulde, a tributary of the river Elbe in Germany at relevant concentrations up to several microg/L. Investigations of groundwater being affected with wastewater infiltration several decades ago also revealed a barbiturate pattern, indicating a strong recalcitrance of these drugs. To confirm this hypothesis, studies were carried out on biotic and abiotic degradation. Both, the biodegradability under aerobic conditions and hydrolysis did not show any degradation, implementing, that the investigated barbiturates, once released into the aquatic environment, show high stability over a long period of time.

Barbiturates↗

True and false reversal of the elution order of barbiturates on a bonded cellulose-based chiral stationary phase.

A set of racemic N-alkylated barbiturates were investigated for their direct enantioselective HPLC separation on a new chiral stationary phase (CSP) containing cellulose tris(3,5-dimethylphenylcarabamate) immobilized onto silica gel (Chiralpak IB) and its coated version (Chiralcel OD). They were online detected by UV and optical rotation detectors to trace the elution order of their enantiomers. Surprisingly, examples of false and true reversal of the elution order of enantiomers of barbiturates were observed and reported.

Barbiturates↗