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相关概念视频

Ultraviolet and Visible (UV–Vis) Spectroscopy: Overview01:02

Ultraviolet and Visible (UV–Vis) Spectroscopy: Overview

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Ultraviolet–visible (UV–visible or UV–Vis) spectroscopy is an analytical technique that investigates the interaction between matter and UV–Vis light within the electromagnetic spectrum. This method is widely used for its versatility, simplicity, and relatively quick data acquisition, making it valuable for both qualitative and quantitative analysis. When UV–Vis radiation passes through a material,  molecules absorb light depending on the energy required for...
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UV–Vis Spectrometers01:14

UV–Vis Spectrometers

1.4K
The absorbance of UV and visible (UV–visible) radiations is measured using a UV–visible spectrophotometer. Deuterium lamps, which emit UV radiation, and tungsten lamps, which produce radiation in the visible region, are used as light sources in UV–visible spectrophotometers. A monochromator or prism is used for diffraction grating, i.e., to split the incoming radiation into different wavelengths. A system of slits is used to focus the desired wavelength on the sample cell.
1.4K
UV–Vis Spectrum01:30

UV–Vis Spectrum

1.2K
When light passes through a substance, a portion of the light is absorbed while the remaining light is reflected or transmitted. If the molecule absorbs light between the wavelengths of 180–400 nm range, the UV spectrum is obtained, and if it absorbs light in the 400–780 nm wavelength range, the visible spectrum is obtained.     
The UV–Vis spectrum of a molecule is the plot of its absorbance versus wavelength. The plot is drawn by taking molar...
1.2K
UV–Vis Spectroscopy: Woodward–Fieser Rules01:29

UV–Vis Spectroscopy: Woodward–Fieser Rules

24.6K
UV–Visible absorption spectra of conjugated dienes arise from the lowest energy π → π* transitions. The light-absorbing part of the molecule is called the chromophore, and the substituents directly attached to the chromophore are called auxochromes. A strong correlation exists between the absorption maxima, λmax, and the structure of a conjugated π system. The Woodward–Fieser rules predict the value of λmax for a given...
24.6K
UV–Vis Spectroscopy: Beer–Lambert Law01:09

UV–Vis Spectroscopy: Beer–Lambert Law

3.1K
The Beer-Lambert law describes the relationship between absorbance and concentration, which combines the principles established by scientists Johann Heinrich Lambert and August Beer. Lambert's law states that when light passes through a medium, the loss in intensity is directly proportional to the original intensity and the path length of the light. Beer's law proposed that the transmittance of a solution remains constant if the product of concentration and path length is constant. The...
3.1K
Atomic Absorption Spectroscopy: Interference01:25

Atomic Absorption Spectroscopy: Interference

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Interference leads to systematic error in atomic absorption (AA) measurements by enhancing or diminishing the analytical signal or the background. These interferences can be grouped into three main categories: spectral interference, chemical interference, and physical interference.
Spectral interference occurs when signals from other elements or molecules overlap with the analyte signal, falsely elevating or masking the analyte's absorbance. This interference can be corrected using Zeeman,...
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相关实验视频

Updated: Jul 18, 2025

Author Spotlight: Exploring Light-Driven Chemical Reactions and Energy-Harnessing Devices in Photochemical Research
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为基线文物纠正紫外线可见光谱

Andrew J Basalla1, Brent S Kendrick2

  • 1KBI Biopharma, Inc., Louisville, CO, USA; First Principles Biopharma, LLC, Louisville, CO, USA.

Journal of pharmaceutical sciences
|August 24, 2023
PubMed
概括

精确的蛋白质度测量非常重要. 这项研究引入了一种新的曲线拟合方法,用于纠正紫外线光谱学中的光散射误差,提高各种样品的测量可靠性.

科学领域:

  • 分析化学 分析化学
  • 生物化学 生物化学
  • 频谱学是一种光谱学.

背景情况:

  • 颗粒和蛋白质聚合物的光散射会干扰紫外线光谱学度测量.
  • 现有的校正方程式可能会因样本组合变化或偏离其开发基础而失败.

研究的目的:

  • 开发和验证一种可靠的方法来纠正UV光谱中的光散射器件.
  • 为了提高在分散剂的存在下蛋白质度测定的准确性.

主要方法:

  • 开发了一种曲线匹配基线减法方法,集成了基本的雷利和米散射原理.
  • 该方法将仪器基线人工物纳入纠正模型.
  • 验证涉及多种控制:蛋白质尺寸标准,强制降解聚合物,晶体病毒和聚烯纳米圈.

主要成果:

  • 建议的雷利-米校正方法在各种散射场景中表现出有效的准确性.
  • 该方法成功地解决了由颗粒物,可溶性蛋白质聚合物和大型蛋白质引起的错误.
  • 验证证实了该方法与各种生物和合成散射剂的可靠性.

结论:

  • 曲线适配雷利-米校正为准确的紫外线光谱度测量提供了比现有方法更可靠的替代方案.
关键词:
生物制药特征的表征纠正的纠正 纠正的纠正在曲线上适应曲线.微光散射是一种光散射.雷利光散射是雷利光的散射.紫外线 (UV) 光谱学

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  • 这种方法提高了在复杂样本中量化蛋白质和类似大分子的精度.
  • 经过验证的方法为生物制药分析和研究提供了宝贵的工具.