Assessing the effectiveness of fenbendazole supramolecular complexes against schistosomiasis, monieziosis and parabronemosis in sheep

IF 1.4 4区 医学 Q3 PARASITOLOGY
Firuza Akramova , Ulugbek Shakarbaev , Dilbar Paluaniyazova , Abror Akbarov , Salavat Khalikov , Alisher Safarov , Djalaliddin Azimov , Mourad Ben Said
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引用次数: 0

Abstract

Helminth infections pose a significant economic threat to livestock production, causing productivity declines and, in severe cases, mortality. Conventional anthelmintics, exemplified by fenbendazole, face challenges related to low solubility and the necessity for high doses. This study explores the potential of supramolecular complexes, created through mechanochemical modifications, to address these limitations. The study focuses on two key anthelmintics, praziquantel (PZQ) and fenbendazole (FBZ), employing mechanochemical techniques to enhance their solubility and efficacy. Solid dispersions (SD) of PZQ with polymers and dioctyl sulfosuccine sodium (DSS) and fenbendazole with licorice extract (ES) and DSS were prepared. The helminthicidal activity of these complexes was assessed through helminthological dissections of sheep infected with Schistosoma turkestanicum, moniesiasis, and parabronemosis. In the assessment of supramolecular complex of FBZ (SMCF) at doses ranging from 1.0 to 3.0 mg/kg for the active substance (AS), optimal efficacy was observed with the fenbendazole formulation containing arabinogalactan and polyvinylpyrrolidone at a 3.0 mg/kg dosage. At this concentration, the formulation demonstrated a remarkable 100% efficacy in treating spontaneous monieziosis in sheep, caused by Moniezia expansa (Rudolphi, 1810) and M. benedenii (Moniez, 1879). Furthermore, the SMCF, administered at doses of 1.0, 2.0, and 3.0 mg/kg, exhibited efficacy rates of 42.8%, 85.7%, and 100%, respectively, against the causative agent of parabronemosis (Parabronema skrjabini Rassowska, 1924). Mechanochemical modifications, yielding supramolecular complexes of PZQ and FBZ, present a breakthrough in anthelmintic development. These complexes address solubility issues and significantly reduce required doses, offering a practical solution for combating helminth infections in livestock. The study underscores the potential of supramolecular formulations for revolutionizing helminthiasis management, thereby enhancing the overall health and productivity of livestock.

评估芬苯达唑超分子复合物对绵羊血吸虫病、包虫病和副包虫病的疗效。
蠕虫感染对畜牧业生产构成了严重的经济威胁,会导致生产力下降,严重时还会造成死亡。以苯菌唑为代表的传统抗蠕虫药面临着溶解度低和必须使用大剂量的挑战。本研究探讨了通过机械化学修饰产生的超分子复合物在解决这些局限性方面的潜力。研究重点是吡喹酮(PZQ)和芬苯达唑(FBZ)这两种主要的驱虫药,利用机械化学技术提高它们的溶解度和药效。制备了 PZQ 与聚合物和二辛基磺酸钠(DSS)的固体分散体(SD),以及芬苯达唑与精油甘草提取物(ES)和 DSS 的固体分散体(SD)。通过对感染土耳其血吸虫、莫尼丝虫病和副猪嗜血杆菌病的绵羊进行蠕虫学解剖,评估了这些复合物的杀蠕虫活性。在对活性物质(AS)剂量为 1.0 至 3.0 毫克/千克的芬苯达唑超分子复合物(SMCF)进行评估时,观察到含有阿拉伯半乳聚糖和聚乙烯吡咯烷酮的芬苯达唑制剂在 3.0 毫克/千克的剂量下具有最佳药效。在这一浓度下,该制剂对由扩张莫尼茨绦虫(Moniezia expansa,Rudolphi,1810 年)和贝尼登莫尼茨绦虫(Moniez,1879 年)引起的绵羊自发性莫尼茨绦虫病的疗效显著,达到 100%。此外,以 1.0、2.0 和 3.0 毫克/千克的剂量给药 SMCF,对副猪疫病(Parabronema skrjabini Rassowska,1924 年)的病原体的有效率分别为 42.8%、85.7% 和 100%。通过机械化学修饰,产生了 PZQ 和 FBZ 的超分子复合物,为抗蠕虫药的开发带来了突破性进展。这些复合物解决了溶解性问题,大大减少了所需剂量,为防治家畜蠕虫感染提供了切实可行的解决方案。这项研究强调了超分子制剂在彻底改变蠕虫病管理方面的潜力,从而提高牲畜的整体健康水平和生产力。
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来源期刊
Experimental parasitology
Experimental parasitology 医学-寄生虫学
CiteScore
3.10
自引率
4.80%
发文量
160
审稿时长
3 months
期刊介绍: Experimental Parasitology emphasizes modern approaches to parasitology, including molecular biology and immunology. The journal features original research papers on the physiological, metabolic, immunologic, biochemical, nutritional, and chemotherapeutic aspects of parasites and host-parasite relationships.
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