Influence of Parameters of Mechanochemical Processing on the Efficacy of Complex Solid Dispersion of Anthelmintics

Q2 Pharmacology, Toxicology and Pharmaceutics Current Bioactive Compounds Pub Date : 2024-06-07 DOI:10.2174/0115734072303357240528095424
A. Varlamova, S. Khalikov, I. Arkhipov, M. Arisov, K. Sadov, Michael M. Ilyin
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Abstract

Due to the fact that animal parasitic diseases often occur in the form of mixed infections, it is necessary to use complex drugs with a combination of active substances that act against different classes of helminths. Fenbendazole has a wide spectrum of nematocidal action and is less effective against cestodes. Considering that sheep are often infected with both gastro-intestinal nematodes and cestodes, a complex drug based on fenbendazole, niclosamide with polyvinylpyrrolidone polymer, was developed using mechanochemical technology in order to increase its solubility and bioavailability and reduce the dosages and side effects. This study aimed to evaluate the influence of mechanochemical technology on the efficacy of complex solid dispersions of anthelmintics against cestodoses and nematodoses. The influence of different types of mills (roller and planetary mills), levels of energy intensity (20, 40, 60 g), and component ratio (2:20:78; 3:30:67; 4:40:56) during mechanochemical processing was studied on the anthelmintic efficacy of complex solid dispersions of fenbendazole, niclosamide, and polyvinylpyrrolidone in laboratory models of trichinellosis and hymenolepiosis of white mice, and on sheep naturally infected with helminths. The efficacy of complex solid dispersions obtained in the planetary mill was higher than the activity of dispersions obtained in a roller mill. It showed 87.5, 96.36, 83.77, and 99.39% efficacy, respectively, against experimental trichinellosis, hymenolepiosis of white mice, gastrointestinal nematode infection and monieziosis of sheep at a ratio of 2:20:78. The basic drug – fenbendazole demonstrated 31.37 and 22.77% activity against experimental trichinellosis and gastro-intestinal nematode infection of sheep. The basic drug, niclosamide, showed 36.37% efficacy against hymenolepiosis in mice and 28.31% against monieziosis in sheep. It was established that with an increase in the energy intensity level of the planetary mill (20, 40, and 60 g), the decrease in the efficacy of solid dispersion occurred from 73.90 to 59.12% against T. spiralis and from 92.73% to 79.81% against H. nana. The use of mechanochemical technology for the production of solid dispersions of fenbendazole and niclosamide with polyvinylpyrrolidone makes it possible to increase the anthelmintic efficacy by 2.7–3 times compared to the activity of basic substances. It was noted that the complex solid dispersions of anthelmintics obtained in a planetary mill had 7.51–10.17% greater activity in comparison with the samples obtained in a roller mill. The most optimal ratio of active substances was 2:20:78 at a 20 g level of energy intensity of the planetary mill.
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机械化学处理参数对复合杀虫剂固体分散体药效的影响
由于动物寄生虫病常常以混合感染的形式出现,因此有必要使用复合药物,将对不同种类蠕虫起作用的活性物质组合在一起。芬苯达唑的杀线虫作用范围很广,但对绦虫的作用较弱。考虑到绵羊经常同时感染胃肠道线虫和绦虫,我们利用机械化学技术开发了一种基于芬苯达唑、烟酰胺和聚乙烯吡咯烷酮聚合物的复方药物,以增加其溶解度和生物利用度,并减少用量和副作用。研究了不同类型的研磨机(辊式研磨机和行星式研磨机)、能量强度水平(20、40、60 克)和机械化学处理过程中的组分比例(2:20:78;3:30:67;4:40:56)对芬苯达唑、烟酰胺和聚乙烯吡咯烷酮复合固体分散体在白鼠旋毛虫病和膜孔虫病实验室模型以及自然感染蠕虫的羊身上的驱虫效力的影响。用行星磨获得的复合固体分散体的效力高于用辊磨获得的分散体。按 2:20:78 的比例计算,它对实验性旋毛虫病、白鼠膜孔虫病、绵羊胃肠道线虫感染和单核细胞增多症的有效率分别为 87.5%、96.36%、83.77%和 99.39%。基本药物芬苯达唑对实验性毛滴虫病和绵羊胃肠线虫感染的活性分别为 31.37% 和 22.77%。基本药物烟酰胺对小鼠膜包虫病的有效率为 36.37%,对绵羊单核细胞增多症的有效率为 28.31%。研究表明,随着行星磨的能量强度水平(20、40 和 60 克)的增加,固体分散体对螺旋蓟马的药效从 73.90% 降至 59.12%,对绵羊花叶病毒的药效从 92.73% 降至 79.81%。使用机械化技术生产芬苯达唑和烟酰胺与聚乙烯吡咯烷酮的固体分散体,可使驱虫效力比基本物质的活性提高 2.7-3 倍。结果表明,用行星磨获得的抗蠕虫药复合固体分散体的活性比用辊磨获得的样品高 7.51-10.17%。在行星式粉碎机的能量强度为 20 克时,活性物质的最佳比例为 2:20:78。
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来源期刊
Current Bioactive Compounds
Current Bioactive Compounds Pharmacology, Toxicology and Pharmaceutics-Pharmacology, Toxicology and Pharmaceutics (all)
CiteScore
1.90
自引率
0.00%
发文量
112
期刊介绍: The journal aims to provide comprehensive review articles on new bioactive compounds with proven activities in various biological screenings and pharmacological models with a special emphasis on stereoeselective synthesis. The aim is to provide a valuable information source of bioactive compounds synthesized or isolated, which can be used for further development of pharmaceuticals by industry and academia. The journal should prove to be essential reading for pharmacologists, natural product chemists and medicinal chemists who wish to be kept informed and up-to-date with the most important developments on new bioactive compounds of natural or synthetic origin, including their stereoeselective synthesis.
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