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相关概念视频

Recrystallization: Solid–Solution Equilibria01:10

Recrystallization: Solid–Solution Equilibria

1.1K
Recrystallization is a purification technique used to separate impurities from solid compounds. In this technique, no chemical reactions occur. Instead, it exploits physical properties only, specifically, the solubility differences between the desired compound and impurities, either at a single temperature or at different temperatures, and under other selected conditions. The solid-solution equilibrium (solubility equilibrium) of each component in the solution represents a binary phase...
1.1K
Crystal Growth: Principles of Crystallization01:25

Crystal Growth: Principles of Crystallization

2.1K
Crystallization is a phase transformation process in which crystals are precipitated from a supersaturated solution or formed from other sources. During crystallization, atoms or molecules arrange themselves into a well-defined, rigid crystal lattice to minimize energy.
Initiating crystallization involves manipulating the concentration of the solute and the temperature of the solution. Since crystal growth occurs when the ratio of concentration and solubility of the solute in the solvent...
2.1K
Factors Affecting Dissolution: Polymorphism, Amorphism and Pseudopolymorphism01:21

Factors Affecting Dissolution: Polymorphism, Amorphism and Pseudopolymorphism

332
Polymorphism refers to the existence of a drug substance in multiple crystalline forms, known as polymorphs. Recently, this term has been expanded to include solvates (forms containing a solvent), amorphous forms (non-crystalline forms), and desolvated solvates (forms from which the solvent has been removed).
Some polymorphic crystals possess lower aqueous solubility than their amorphous counterparts, leading to incomplete absorption. For instance, the oral suspension of Chloramphenicol, which...
332
Precipitation Processes01:12

Precipitation Processes

484
The experimental conditions in a gravimetric analysis should be optimized to maximize the particle size and purity of the obtained precipitate. Ideally, the concentration of the precipitating reagent should be low with effective stirring to maintain low relative supersaturation for the growth of large crystals. In homogeneous precipitation, the precipitant is slowly generated by a chemical reaction in the solution to avoid local reagent excesses. For example, urea decomposes gradually to...
484
Precipitate Formation and Particle Size Control01:16

Precipitate Formation and Particle Size Control

811
In precipitation gravimetry, the precipitating agent should react specifically or selectively with the analyte. While a specific reagent reacts with the analyte alone, a selective reagent can react with a limited number of chemical species.
The obtained precipitate should be either a pure substance of known composition or easily converted to one by a simple process, such as ignition or drying. In addition, the precipitate should be insoluble and easily filterable. In general, filterability...
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相关实验视频

Updated: Jul 16, 2025

Optimizing the Growth of Endothiapepsin Crystals for Serial Crystallography Experiments
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瑞巴维林溶液的结晶选择性和无形阶段

Fuying Li1,2, Shiying Chen1, Haoxin Hu3

  • 1Fujian Provincial Key Laboratory of Resources and Environment Monitoring & Sustainable Management and Utilization, Sanming University, Sanming 365004, China.

Molecules (Basel, Switzerland)
|September 9, 2023
PubMed
概括

这项研究探讨了利巴维林多态控制中的结晶选择性. 了解固体形式和溶液中的短距离顺序有助于开发强大的合成元稳定相的方法.

关键词:
无形阶段是无形阶段.结晶的选择性结晶的选择性中频拉曼差异光谱利巴维林是一种利巴维林.解决方案 解决方案 解决方案酸盐溶剂的使用方法

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相关实验视频

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科学领域:

  • 固态化学 固态化学
  • 结晶科学是结晶的科学.
  • 制药的多态化物 制药的多态化物

背景情况:

  • 在药物开发中,对多态生物的控制至关重要.
  • 利巴维林表现出多种固体形式,包括形式I,形式II,DMSO溶酸盐和无形状态.
  • 了解结晶选择性是控制这些多态的关键.

研究的目的:

  • 为了研究里巴维林固体制剂中的结晶选择性.
  • 为了比较不同利巴维林固体形式及其溶液的短距离顺序.
  • 解释结晶过程和制备特定溶酸盐的挑战.

主要方法:

  • 利巴维林I型,II型,DMSO溶盐和无形利巴维林的制备.
  • 使用中频拉曼差异光谱 (MFRDS) 来分析短距离顺序.
  • 将固体形式的光谱数据与利巴维林的水和DMSO溶液进行比较.

主要成果:

  • 在固体形式和它们各自的解决方案之间发现了短距离顺序的相似之处.
  • 从无形利巴维林到I型的结晶路径得到了阐明.
  • 解释了从溶液过渡到无形阶段的过程.
  • 提出了制备利巴维林DMSO溶解物的困难的潜在原因.

结论:

  • 这项研究为利巴维林的结晶选择性提供了理由.
  • 这种理解构成了对超稳定制药阶段的强大和方便合成的基础.
  • 这些发现有助于更广泛的多态控制和固态化学领域.