紫外检测方法发展与验证综述

Komal P. Shinde, Akash D. Rajmane
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引用次数: 0

摘要

紫外光谱法是制药工业中一种重要的先进分析仪器,已有35年的历史。分析方法是基于测量光谱近紫外路径(200-400nm)中无色化合物对单色光的吸收。药物分析包括确定这些化合物的“特性、强度、质量和纯度”所需的程序。它还包括药品生产过程中对原料和中间体的分析。覆盖紫外线区域的分光光度计的基本工作原理是,一定波长间隔的光通过带有溶剂的电池,并落在光电电池上,光电电池将辐射能转化为由电流计测量的电能。紫外-可见光谱学用于测定化合物在溶液或固体状态下的吸光度。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Review UV Method Development and Validation
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.
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