Abstract
Purpose of this article was to know the importance and significance of qualitative and quantitative analysis which has performed in quality control to authenticate the pharmaceutical products. In quality control analytical techniques are used like volumetric analysis which is one of the earlier steps of analysis. Broadly analysis is categorized in three parts- Titrimetric analysis, Chromatographic analysis and Instrumental analysis. Titrimetric analysis further study in three parts- volumetric analysis, Gravimetric analysis and Columnetric analysis. The selection of analytical method depends upon the physical state and nature of analyte. Titration is a quantitative chemical analysis method to estimate the unknown concentration of any substance, such as a raw material, substance or finished good. It is a widely used method that has been included in most of the key international pharmacopoeias and other regulations.
Highlights
In pharmaceutical industry the quality control is the check point for the raw material and as well as finished product
The incoming material in quality control is first checked by titrimetric method
This method result is influenced by the many factor like measuring method Instrument, Electrodes, Handling, Balance, Temperature Change of the volumetric solution because of influence through environmental oxygen, carbon dioxide, microorganism
Summary
Purpose of this article was to know the importance and significance of qualitative and quantitative analysis which has performed in quality control to authenticate the pharmaceutical products. In quality control analytical techniques are used like volumetric analysis which is one of the earlier steps of analysis. Analysis is categorized in three parts- Titrimetric analysis, Chromatographic analysis and Instrumental analysis. Titrimetric analysis further study in three parts- volumetric analysis, Gravimetric analysis and Columnetric analysis. The selection of analytical method depends upon the physical state and nature of analyte. Titration is a quantitative chemical analysis method to estimate the unknown concentration of any substance, such as a raw material, substance or finished good. It is a widely used method that has been included in most of the key international pharmacopoeias and other regulations
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