阿里利米达米德具有针对血液传播的查加斯病的化学预防的潜力
Bruno Lisboa Timm1, Aline Nefertiti Silva da Gama1, Marcos Meuser Batista1
1Laboratório de Biologia Celular, Instituto Oswaldo Cruz, Fundação Oswaldo Cruz, Rio de Janeiro 21045-900, Brazil.
Pathogens (Basel, Switzerland)
|May 27, 2023
概括
阿里利米达胺 (AIAs) 显示出对血液样本的灭菌有希望,这些血液样本被Trypanosoma cruzi污染,这是导致查加斯病 (CD) 的寄生虫. 一种AIA化合物在输血安全研究中显著改善了动物的生存率.
科学领域:
- 寄生虫学的寄生虫学
- 血液学 血液学 血液学
- 药物发现 药物发现 药物发现
背景情况:
- 查加斯病 (CD) 构成一个重大的全球健康风险,而阳性转移是令人担忧的.
- 水晶紫 (CV),过去的病原体减少剂,有有害的副作用.
- 开发安全有效的血液病原体减少方法对于输血安全至关重要.
研究的目的:
- 评估阿里利米达米德 (AIAs) 作为潜在的杀菌剂的疗效和安全性,用于杀菌被Trypanosoma cruzi.污染的血液样本.
- 为了比较AIAs与Crystal Violet (CV) 在小鼠血液中减少Trypanosoma cruzi寄生病的疗效.
主要方法:
- 实验性污染的小鼠血液样本与Trypanosoma cruzi血流皮虫 (BT).
- 用三个AIA和CV处理的血液样本在非溶血剂量.
- 评估了对小鼠血液细胞的毒性和心脏细胞培养中的体外感染.
- 进行体内测试以评估寄生虫抑制和动物生存率.
主要成果:
- AIAs对小鼠血细胞的毒性没有被证明是高达96μM的.
- 用AIAs进行预治疗损害了Trypanosoma cruzi感染在心脏细胞培养物中的建立.
- 在体内,AIA和CV (96μM) 显著抑制了寄生虫病峰值.
- AIA DB1831实现了90%以上的动物存活率,而用车辆处理的对照组的存活率为0%.
结论:
- 阿里利米达米德显示出作为Trypanosoma cruzi病原体减少血液中的安全和有效药物的潜力.
- 根据AIA DB1831,需要进一步调查血液库的应用程序,以防止查加斯病的传播.
相关概念视频
Physical Properties of Amines
3.3K
Amines with low molecular weight are usually gaseous at room temperature, while those with high molecular weight are liquid or solids in nature. Usually, low molecular weight amines have a rotten fish-like smell. Diamines typically have a pungent smell. For instance, cadaverine and putrescine, depicted in Figure 1, are two molecules responsible for decaying tissue.
3.3K
Aryldiazonium Salts to Azo Dyes: Diazo Coupling
3.0K
The reaction of weakly electrophilic aryldiazonium (also called arenediazonium) salts with highly activated aromatic compounds leads to the formation of products with an —N=N— link, called an azo linkage. This reaction, presented in Figure 1, is known as diazo coupling and occurs without the loss of the nitrogen atoms of the aryldiazonium salt. Highly activated aromatic compounds such as phenols or arylamines favor the diazo coupling reaction. The coupling generally occurs at the...
3.0K
Amines to Amides: Acylation of Amines
2.5K
Various carboxylic acid derivatives (such as acid chlorides, esters, and anhydrides) can be used for the acylation of amines to yield amides. The reaction requires two equivalents of amines. The first amine molecule functions as a nucleophile and attacks the carbonyl carbon to produce a tetrahedral intermediate. This is followed by the loss of the leaving group and restoration of the C=O bond.
Next, the second equivalent of amine serves as a Brønsted base and deprotonates the quaternary...
Next, the second equivalent of amine serves as a Brønsted base and deprotonates the quaternary...
2.5K


