Reverse-phase high performance liquid chromatographic determination of Tizanidine and Valdecoxib in tablets

2006 ◽  
Vol 68 (4) ◽  
pp. 514 ◽  
Author(s):  
CS Ramaa ◽  
DK Deshpande ◽  
AR Shirode ◽  
VV Wamorkar ◽  
AB Kakad ◽  
...  
Keyword(s):  
High Performance ◽  
Chromatographic Determination ◽  
High Performance Liquid Chromatographic ◽  
Reverse Phase ◽  
Liquid Chromatographic Determination ◽  
Liquid Chromatographic

Rapid Method for Extraction and Reverse Phase Liquid Chromatographic Determination of Paraquat Residues in Water

1983 ◽  
Vol 66 (3) ◽  
pp. 663-666
Author(s):  
Ijaz Ahmad
Keyword(s):  
High Performance ◽  
Chromatographic Determination ◽  
High Performance Liquid Chromatographic ◽  
Reverse Phase ◽  
Ultraviolet Detection ◽  
Liquid Chromatographic Determination ◽  
Phase Liquid ◽  
Low Levels ◽  
Liquid Chromatographic

Abstract A simple and fast analytical method is described for the quantitative determination of low levels of paraquat residues in water. The method involves extraction and concentration of paraquat in water by using a C18 Sep-Pak cartridge followed by reverse phase high performance liquid chromatographic determination with ultraviolet detection at 257 nm. Recoveries of paraquat from spiked samples were above 93% with a coefficient of variation of 6.1%. The method can be used for water samples with paraquat concentrations as low as 0.05 ppm.

High Performance Liquid Chromatographic Determination of Methapyrilene Hydrochloride in Feed and Sleep Aid Tablets

1981 ◽  
Vol 64 (4) ◽  
pp. 889-892
Author(s):  
Badaruddin Shaikh ◽  
Margarette R Hallmark
Keyword(s):  
High Performance ◽  
Ammonium Carbonate ◽  
Chromatographic Determination ◽  
High Performance Liquid Chromatographic ◽  
Reverse Phase ◽  
Phase Partition ◽  
Coefficients Of Variation ◽  
Liquid Chromatographic Determination ◽  
Liquid Chromatographic

Abstract Methapyrilene hydrochloride (MP·HCl) was extracted from feed with methanol and determined by reverse phase partition chromatography in less than 15 min, using isocratic elution with acetonitrile-1.1% ammonium carbonate (1 + 1) as the mobile phase. This procedure was tested on feed treated with MP·HCl at levels of 125,500, and 2000 ppm. Recoveries were 104,95, and 96% with coefficients of variation of 2.4,1.6, and 0.6%, respectively. MP·HCl in feed was stable for 14 days. This method was also successfully used to determine MP·HCl in 3 sleep aid tablets.

Reverse Phase High Performance Liquid Chromatographic Determination of Phenprocoumon in Tablets

1982 ◽  
Vol 65 (3) ◽  
pp. 753-756
Author(s):  
Walter F Schmidt
Keyword(s):  
High Performance ◽  
Internal Standard ◽  
Chromatographic Determination ◽  
High Performance Liquid Chromatographic ◽  
Reverse Phase ◽  
Assay Procedure ◽  
Chromatographic Procedure ◽  
Liquid Chromatographic Determination ◽  
Liquid Chromatographic

Abstract A high performance liquid chromatographic procedure has been developed for the assay of phenprocoumon in tablets. In comparison to the present official USP assay procedure, it is equivalent in precision and accuracy and is faster and more specific. A mobile phase consisting of a 1% solution of acetic acid in acetonitrile-water (4 + 3) separates phenprocoumon from warfarin internal standard on a 6 μm octadecylsilane (ODS) column with UV detection at 311 nm. The method enables the concurrent determination of phenprocoumon and possible contaminants such as salicylic acid.

High Performance Liquid Chromatographic Determination of Dielofop-Methyl

1983 ◽  
Vol 66 (5) ◽  
pp. 1207-1208
Author(s):  
Rodger W Stringham ◽  
Brian R Bennett
Keyword(s):  
Acetic Acid ◽  
High Performance ◽  
Standard Addition ◽  
Chromatographic Determination ◽  
High Performance Liquid Chromatographic ◽  
Reverse Phase ◽  
Matrix Interferences ◽  
Liquid Chromatographic Determination ◽  
Liquid Chromatographic

Abstract Diclofop-methyl is diluted in acetonitrile-2% acetic acid (70 + 30) and chromatographed on a reverse phase C-18 column. The anaìyte is eluted by an acetonitrile- 2% acetic acid mobile phase and detected at 280 nm. The method was validated by testing precision, linearity, and recovery. Precision and linearity were excellent (% RSD = 0.55, r2 = 0.9997). A multiple standard addition to a pool of formulation samples showed the method to have excellent recovery (99%) and to be free of matrix interferences

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