机械化学诱导的莱沃弗洛克萨辛固态转化
Lena Kadri1,2, Maria Carta3, Giulio Lampronti4
1School of Pharmacy and Pharmaceutical Sciences, Trinity College Dublin, College Green, Dublin 2 D02 PN40, Ireland.
Molecular pharmaceutics
|April 25, 2024
概括
球磨可以部分无形化levovofloxacin半水合物 (LVXh),在完全无形的levovofloxacin (LVXam) 之前形成一个中间无水形式. 喷雾干燥也实现了LVXam,表明无形化取决于机制和工艺.
科学领域:
- 制药科学 制药科学
- 固态化学 固态化学
- 材料科学 材料科学 材料科学
背景情况:
- 列沃素半酸盐 (LVXh) 是一种复杂的化诺,具有多种固体形式.
- 了解固态转换对于药物配方和稳定性至关重要.
研究的目的:
- 通过球磨来研究LVXh的无形化能力和固态转换.
- 为了比较球磨与喷雾干燥对于无形的levovofloxacin (LVXam) 形成.
- 通过机械处理阐明LVXam形成的机制.
主要方法:
- 采用球磨和喷雾干燥来准备样品.
- 粉末X射线衍射,热分析,红外光谱学,瑞特维尔德精细化和动态蒸汽吸附被用于表征.
- 动力学和相位定量是通过瑞特维尔德的精细化来确定的.
主要成果:
- 球磨部分无形的LVXh,通过无水的中间形式 (LVXγ) 进行LVXam.
- 开发了一种使用机械力形成LVXγ和LVXam的新方法.
- 从水中喷雾干燥实现了完整的LVXam形成,玻璃过渡温度为80°C.
结论:
- LVXam的形成取决于所使用的机制和特定的过程.
- 球磨和喷雾干燥方法都产生了具有相似稳定的LVXam,结晶为半水合物形式.
- 这项研究增强了使用可持续制造方法对化诺固态转换的理解.
更多相关视频
相关概念视频
Drug Biotransformation: Overview
2.4K
Pharmaceutical substances known as xenobiotics are predominantly lipophilic and nonionized. This enables them to permeate lipid bilayers, such as cell membranes, and interact with intracellular target receptors. Lipophilic drugs have an advantage in crossing biological barriers and reaching their intended sites of action. However, lipophilic drugs often have a restricted capacity for renal expulsion or elimination from the body. When these drugs enter the kidneys and undergo glomerular...
2.4K
Electrophilic Aromatic Substitution: Fluorination and Iodination of Benzene
6.0K
Bromination and chlorination of aromatic rings by electrophilic aromatic substitution reactions are easily achieved, but fluorination and iodination are difficult to achieve. Fluorine is so reactive that its reaction with benzene is difficult to control, resulting in poor yields of monofluoroaromatic products. To address this, Selectfluor reagent is used as a fluorine source in which a fluorine atom is bonded to a positively charged nitrogen.
6.0K
Acid Halides to Carboxylic Acids: Hydrolysis
2.6K
Hydrolysis of acid halides is a nucleophilic acyl substitution reaction in which acid halides react with water to give carboxylic acids. The reaction occurs readily and does not require acid or a base catalyst.
As shown below, the mechanism involves a nucleophilic attack by water at the carbonyl carbon to form a tetrahedral intermediate. This is followed by the reformation of the carbon–oxygen π bond along with the departure of a halide ion. A final proton transfer step yields carboxylic...
As shown below, the mechanism involves a nucleophilic attack by water at the carbonyl carbon to form a tetrahedral intermediate. This is followed by the reformation of the carbon–oxygen π bond along with the departure of a halide ion. A final proton transfer step yields carboxylic...
2.6K
Factors Affecting Dissolution: Polymorphism, Amorphism and Pseudopolymorphism
301
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...
Some polymorphic crystals possess lower aqueous solubility than their amorphous counterparts, leading to incomplete absorption. For instance, the oral suspension of Chloramphenicol, which...
301
Diazonium Group Substitution with Halogens and Cyanide: Sandmeyer and Schiemann Reactions
1.9K
Arenediazonium substitution reactions occur when the diazonium group is substituted by various functional groups such as halides, hydroxyl, nitrile, etc. For instance, arenediazonium salts react with copper(I) salts of chloride, bromide, or cyanide to form corresponding aryl chlorides, bromides, and nitriles. These reactions are named Sandmeyer reactions. Although the mechanism of this reaction is complicated, as illustrated in Figure 1, they are believed to progress via an aryl copper...
1.9K
Phase I Reactions: Oxidation of Aliphatic and Aromatic Carbon-Containing Systems
191
Phase I biotransformation reactions are integral to drug metabolism, predominantly involving oxidative, reductive, and hydrolytic transformations. Chief among these are oxidative reactions, which enhance the hydrophilicity of xenobiotics and introduce polar functional groups to facilitate their elimination from the body.
Oxidation reactions are fundamental in aromatic carbon-containing systems. An example is the hydroxylation of phenobarbital, a process that transforms it into...
Oxidation reactions are fundamental in aromatic carbon-containing systems. An example is the hydroxylation of phenobarbital, a process that transforms it into...
191


