Low flow high-performance liquid chromatography solvent delivery system designed for tandem capillary liquid chromatography-mass spectrometry
β Scribed by M.T. Davis; D.C. Stahl; T.D. Lee
- Publisher
- Elsevier Science
- Year
- 1995
- Tongue
- English
- Weight
- 785 KB
- Volume
- 6
- Category
- Article
- ISSN
- 1044-0305
No coin nor oath required. For personal study only.
β¦ Synopsis
A solvent delivery system is described that is designed to increase the efficiency of liquid chromatography-mass spectrometry (LC/MS) analyses. Gradients formed by using two low pressure syringe pumps are stored in a length of narrow bore tubing (gradient loop) mounted on a standard high pressure switching valve. The preformed gradient is pushed through the column by using a high pressure syringe pump. The system is fully automated and can be controlled with either a personal computer or the mass spectrometer data system. Advantages include gradient operation without the use of split flows, pressure programed flow control for rapid sample loading and recycling to initial conditions, and a flow rate range of 0.1-20 pL/min, which is suitable for packed capillary columns 50-500 pm in diameter. The system has been used extensively for rapid molecular weight determinations of intact protein samples, as well as LC/MS and liquid chromatography-tandem mass spectrometry analyses of complex peptide mixtures.
π SIMILAR VOLUMES
A simple packed-capillary high performance liquid chromatography (HPLC) system for the analysis of trace (picogram) mixtures by electrospray mass spectrometry is described in detail. This simple and cost-effective design is constructed from conventional hardware generally available in the modern LC/
Direct injection versus liquid-liquid extraction for post-dose human plasma sample analysis by high performance liquid chromatography with tandem mass spectrometry (LC/MS/MS) have been studied using a drug candidate compound. For the direct-injection method, an Oasis 1 HLB column (1 Γ 50 mm, 30 mm)
We established a highly sensitive LC/MS/MS method for the analysis of the disaccharides produced from keratan sulfates (KS). It was revealed that the disaccharides produced by keratanase II enzymatic digestion of KS could be determined with high sensitivity by the negative-ion mode of multiple react