Comprehensive study for the development of rectal suppositories with diosmin and hesperidin

Q3 Pharmacology, Toxicology and Pharmaceutics ScienceRise: Pharmaceutical Science Pub Date : 2022-02-28 DOI:10.15587/2519-4852.2022.253518
Yelyzaveta Borko, Kovalevska Inna, V. Grudko, N. Kononenko, M. Velya
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引用次数: 3

Abstract

The aim. To conduct a comprehensive study of biphasic-type suppositories that contain diosmin and hesperidin. Materials and methods. Samples of biphasic-type suppositories with a mass of 4.0 were objects of the study. Pharmacological, technological and analytical research methods were used to directly or indirectly analyze the strength and completeness of the drug activity. Thus, in this work we combined the study of the specificity of the pharmacological action of the drug, experimental verification of the quantitative content of API, analysis of the structural properties of suppositories and study of the profile of the release of active pharmaceutical ingredients. Results. Therefore, based on the obtained data, the most effective dose was 75 mg / kg (in terms of a human dose of 300 mg per suppository). The drug in the selected dose showed a significant therapeutic effect, which significantly exceeded that of the test sample at a lower dose and the reference agent. According to the results of technological studies, it was determined that all samples of suppositories had satisfactory structural and mechanical properties. Studies of the histological structure of the mucous membrane of rats proved that there is a positive effect of treatment with suppositories with diosmin and hesperidin due to the improvement of the normal condition of the mucous membrane, the absence of edema and ulcerative defect. Research of the release profile of active pharmaceutical ingredients showed that the best percentage of release is characteristic of sample 2 (99.8 %) Conclusions. Therefore, suppositories with diosmin and hesperidin in therapeutically dose of 75 mg/kg of animal weight can be used for further research and will be of interest in the treatment of hemorrhoids of both acute and chronic forms
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薯蓣皂苷、橙皮苷直肠栓剂研制的综合研究
的目标。对含薯蓣皂苷和橙皮苷的双相型栓剂进行综合研究。材料和方法。以质量为4.0的双相型栓剂为研究对象。采用药理学、工艺和分析等研究方法,直接或间接地分析了药物活性的强度和完整性。因此,在本工作中,我们将药物药理作用的特异性研究、原料药定量含量的实验验证、栓剂结构性质的分析和有效药物成分释放谱的研究相结合。结果。因此,根据获得的数据,最有效剂量为75 mg / kg(按每个栓剂300 mg的人体剂量计算)。在所选剂量下的药物表现出显著的治疗效果,明显超过低剂量的被试样品和参比剂。根据工艺研究结果,确定所有栓剂样品具有令人满意的结构和力学性能。对大鼠粘膜组织结构的研究证实,地奥司明、橙皮苷栓剂治疗大鼠粘膜正常状态改善,无水肿、溃疡性缺损,具有积极作用。对其有效成分的释放曲线进行了研究,发现其最佳释放率为样品2(99.8%)。因此,治疗剂量为75 mg/kg动物体重的薯蓣皂苷和橙皮苷的栓剂可用于进一步研究,并将对治疗急性和慢性痔疮有兴趣
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来源期刊
ScienceRise: Pharmaceutical Science
ScienceRise: Pharmaceutical Science Pharmacology, Toxicology and Pharmaceutics-Pharmacology, Toxicology and Pharmaceutics (all)
CiteScore
1.70
自引率
0.00%
发文量
39
审稿时长
6 weeks
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