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Xuefang Luo

Publications and source records attributed to Xuefang Luo.

2 recordsLinked to original sources
PubMed2006

Single-based resolution for oligodeoxynucleotides and their phosphorothioate modifications by replaceable capillary gel electrophoresis.

A replaceable capillary gel electrophoretic (replaceable CGE) method was developed for the separation of two sets of model compounds of single-stranded oligodeoxynucleotide mixtures (18-20 mers), phosphodiester oligodeoxynucleotides (PO-ODNs) and their phosphorothioate modifications (PS-ODNs), with equal sequences differing in a single base. Polyethylene glycol (PEG) 35000 was chosen as the sieving matrix. It was confirmed that PEG polymer solution less influenced resolutions of the PS-ODNs compared with those of the PO-ODNs, while acetonitrile used as an additive in the system improved the separation significantly. It was also noticed that the effect of temperature on separation was much larger than that of denaturant urea.

Acetonitriles↗
PubMedDate not supplied

Determination of amantadine sulfate in sodium chloride injection by capillary gas chromatography.

This paper describes a new method to determine amantadine sulfate in sodium chloride injection by capillary gas chromatography. The chromatographic conditions of the methods employed a SGE BP-1 capillary column (30 m x 0.53 mm i.d., 1.0-microm film thickness); isothermal elution with N2 at a pressure of 100 KPa; injector, oven, and detector temperatures at 220 degrees C, 110 degrees C, and 220 degrees C, respectively; a split-less mode; and a 1-microL injection volume. Naphthalene was used as the internal standard. Peak purity testing with a Varian Saturn 2200 capillary gas chromatography- mass spectrometry system (Varian, Inc.) equipped with a DB-5 capillary column (30 m x 0.25 mm i.d., 0.25-microm film thickness) was performed for the investigation of specificity. There was a linear relationship between peak area ratios of analyte to the internal standard and concentration of analyte over the concentration range 0.1-2.0 mg/mL. The recovery was 97.8 approximately 100.7%. The relative standard deviation (%) of intermediate precision was less than 0.8. The limits of detection and quantitation were 0.2 microg/mL with a signal-to-noise ratio of 3, and 0.7 microg/mL with a signal-to-noise ratio of 10, respectively. The results of determination were similar to the titration method.

Amantadine↗