Author(s):
Sandip A Telavane, Seema Kothari, Manohar V. Lokhande
Email(s):
manohar2210@gmail.com
DOI:
10.52711/2231-5691.2021.00028 
Address:
Sandip A Telavane1, Seema Kothari1, Manohar V. Lokhande2*
1Department of Chemistry, PAHER University, Udaipur-313003, Rajasthan, India.
2Department of Chemistry, Sathaye College, Mumbai – 400057, Maharashtra, India.
*Corresponding Author
Published In:
Volume - 11,
Issue - 3,
Year - 2021
ABSTRACT:
Validation is important technique for detection, progress and estimation of drugs for pharmaceutical analysis. Aim of this article was to check the progress and validation of the method employed for the Residual Solvents in Bisoprolol Fumarate by Gas Chromatographic technique. The objective of this protocol is to validate a GC method of analysis for detection and Quantification of Residual Solvents Methanol, Acetone and Methylene dichloride in Bisoprolol Fumarate. In the pharmaceutical industry, validation policy is more important for documented of validation, types of validation and validation policy. The method was developed accurately and validation parameters are explained. Chromatographic condition was GC- 2014, gas chromatograph equipped with FID detector, column: 30 m x 0.32 mm ID x 1.8 µm DB - 624 capillary column or equivalent and column temperature was 45°C (hold 7 minutes) to 250°C @ 40°C/minutes, hold at 250°C for 3 minutes. The parameters such as Accuracy, Specificity, Precision, Linearity and Range, Limit of detection (LOD), Limit of quantitation (LOQ), ruggedness, robustness and system suitability testing with residual solvent such as Methanol, Acetone and methylene dichloride. All validation parameters are used in the routine and stability analysis.
Cite this article:
Sandip A Telavane, Seema Kothari, Manohar V. Lokhande. Method of Validation for Residual Solvents in Bisoprolol Fumarate by GC Technique. Asian Journal of Pharmaceutical Research. 2021; 11(3):147-5. doi: 10.52711/2231-5691.2021.00028
Cite(Electronic):
Sandip A Telavane, Seema Kothari, Manohar V. Lokhande. Method of Validation for Residual Solvents in Bisoprolol Fumarate by GC Technique. Asian Journal of Pharmaceutical Research. 2021; 11(3):147-5. doi: 10.52711/2231-5691.2021.00028 Available on: https://asianjpr.com/AbstractView.aspx?PID=2021-11-3-2
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