Author(s): Komal P. Shinde, Akash D. Rajmane

Email(s): akash.rajamane4416@gmail.com

DOI: 10.52711/2231-5675.2023.00021   

Address: Komal P. Shinde, Akash D. Rajmane*
Department of Pharmaceutics, D.S.T.S Mandal’s College of Pharmacy, Solapur 413004, Maharashtra, India.
*Corresponding Author

Published In:   Volume - 13,      Issue - 2,     Year - 2023


ABSTRACT:
Ultraviolet spectroscopy is one important and advanced analytical instrument in the Pharmaceutical industry and used for the last 35 years. The method of analysis is based on measuring the absorption of monochromatic light by colorless compounds in the near-ultraviolet path of the spectrum (200-400nm). The pharmaceutical analysis comprises the procedures necessary to determine such compounds' “identity, strength, quality, and purity”. It also includes the analysis of raw materials and intermediates during the manufacturing process of drugs. The fundamental principle of operation of a spectrophotometer covering the UV region consists that light of a definite interval of wavelength passes through a cell with solvent and falls onto the photoelectric cell that transforms the radiant energy into electrical energy measured by a galvanometer. Ultraviolet-visible spectroscopy is used to obtain the absorbance spectra of a compound in solution or as a solid.


Cite this article:
Komal P. Shinde, Akash D. Rajmane. A Review UV Method Development and Validation. Asian Journal of Pharmaceutical Analysis. 2023; 13(2):122-0. doi: 10.52711/2231-5675.2023.00021

Cite(Electronic):
Komal P. Shinde, Akash D. Rajmane. A Review UV Method Development and Validation. Asian Journal of Pharmaceutical Analysis. 2023; 13(2):122-0. doi: 10.52711/2231-5675.2023.00021   Available on: https://ajpaonline.com/AbstractView.aspx?PID=2023-13-2-10


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