Stability indicating ion chromatography method for the simultaneous determination of ibandronate sodium drug substance and its impurities

2011 ◽  
Vol 54 (3) ◽  
pp. 596-601 ◽  
Author(s):  
M. Narendra Kumar ◽  
K.S.R. Pavan Kumar ◽  
Vundavilli Jagadeesh Kumar ◽  
S. John Prasanna ◽  
Hemant Kumar Sharma ◽  
...  
2016 ◽  
Vol 19 (9) ◽  
pp. 1983-1993 ◽  
Author(s):  
Sajad Chamandust ◽  
Mohammad Reza Mehrasebi ◽  
Koorosh Kamali ◽  
Reza Solgi ◽  
Jafar Taran ◽  
...  

2015 ◽  
Vol 7 (2) ◽  
pp. 416-422 ◽  
Author(s):  
Yan Li ◽  
Brett Paull ◽  
Marius N. Müller ◽  
Pavel N. Nesterenko

A new high performance chelation ion chromatography method for the simultaneous determination of trace magnesium and strontium in various calcium carbonate samples was developed.


Author(s):  
Lijun Jiang ◽  
Yan Bao ◽  
Liang Guo ◽  
He Cui ◽  
Qi Wang ◽  
...  

Abstract Background The simultaneous analysis of several anions and carbohydrates by one-dimensional chromatography with a single detector is often complicated by the presence of overlapping peaks. To overcome this problem, analytes are usually analysed separately making analysis long and tedious. Objective A method combining two-dimensional ion chromatography (2 D-IC) and valve switching was developed for the simultaneous determination of anions (F−, Cl−, NO2−, SO42−, NO3−, and PO43−) and carbohydrates (glycerinum, glucosyl glycerol, trehalose, mannose, glucose, galactose, fructose, ribose, and sucrose) in cyanobacteria. Methods Interfering color compounds were removed by first passing the sample through graphitized carbom solid phase extraction (SPE) cartridges. Samples were applied to an AS11-HC column, which was used to separate the anions followed by quantification using a conductance detector. Carbohydrates eluted from the AS11-HC column were trapped and separated on a MA1 column and simultaneously quantified using electrochemical detection in the second dimension with valve switching. Results The following parameters were established: LOD, 0.001–0.030 (mg/L); LOQ, 0.001–0.010 (mg/L); linearity (r), 0.9940; repeatability, 0.39%–3.02%; and spiked recovery, 90.1%–107%. Conclusion The proposed method is adequately linear, accurate, and repeatable. The 2 D-IC method provides fast, high resolution, and completely automated procedure for the simultaneous determination of anions and carbohydrates without co-elution compared to the one dimension ion chromatography method. This study provides application perspectives for use in biotechnology and other research fields. Highlights An accurate and effective 2 D-IC method was developed for determining anions and carbohydrates in cyanobacteria. The method includes pre-treating samples with graphitized carbon SPE cartridges.


Author(s):  
Rohan More ◽  
Dr. Amit Gosar ◽  
Dr. Tabrez Shaikh ◽  
Amit Joglekar

A simple, sensitive, specific, linear and effective Ion chromatography method has been developed and validated for the determination of Isopropylamine content in Metoprolol Succinate. Isopropylamine is possible impurity that may be present in Metoprolol succinate samples. The method was validated as per International Council for Harmonisation (ICH) guidelines, for which limit of detection and limit of quantitation obtained were 29 ppm and 87 ppm respectively. % RSD for System precision observed was 1.38. The regression coefficient found for the linearity study was 0.9997. The % recovery of the spiked Isopropylamine in drug substance obtained was in the range of 83.2 to 100.7 from 50 % to 150 % level ensured the accuracy of the method. The method can be adapted to determine Isopropylamine content in Metoprolol Succinate drug substance (API). Keywords: Ion chromatography (IC), Metoprolol Succinate, Isopropylamine, development, validation.


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