Comparative efficacy of transdermal forms for alopecia therapy

Q3 Pharmacology, Toxicology and Pharmaceutics
U. V. Nogaeva, D. Ivkin, G. A. Plisko, E. Flisyuk, V. E. Kovanskov, Y. Shtyrlin, K. O. Sidorov
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Abstract

Introduction. Alopecia is a polyetiological disorder characterized by hair loss and reducing their number per unit area. Baldness causes psychological and social discomfort to patients, in connection with what an important task is to develop formulations that are more effective than the reference agents.Aim. Investigate the possibility of applying the original substance Y in several dosage forms for the treatment of alopecia in comparison with reference drugs: minoxidil and burdock oil.Materials and methods. The research subject was the original substance Y, for which several dosage forms were made: gel, alcohol and oil compositions. The study on the effectiveness and safety of the developed formulations was carried out on 9 groups of male C57BL/6 mice. Depilation with further assessment of the percentage of hair follicles in the growth and resting phases was tested as a pre-clinical model of alopecia. In the study of the mechanism of action of substance Y, chemiluminescent assay was performed compared with natural antioxidant quercetin in the system luminol – 2,2'-azo-bis(2-amidinopropane)dihydrochloride, in potassium-phosphate buffer medium (pH = 7.4). Statistical processing of the results was carried out using two-way ANOVA using GraphPad Prism 8.0.2, USA software at the level of statistical significance of differences p < 0.05 and p < 0.005.Results and discussion. Based on the results of histological analysis and visual changes, it was found that the effectiveness of the topical forms of substance Y decreases in the following order: gel, alcohol form, oil composition. The use of a combination of the gel base with the test substance Y resulted to the appearance of a larger number of hair follicles in the growth phase than when using the reference preparation – 2 % minoxidil solution (the differences are statistically significant). Chemiluminescent assessment of antioxidant activity showed the lack of antioxidant effect in substance Y.Conclusion. The study combines two pharmaceutical profiles: technological and pharmacological. In the course of the experiments, the prospects of the gel form of the original substance Y for topical therapy of alopecia were shown. In the near future, it is planned to study the mechanism of action of substance Y, as well as registration of patent protection for a new drug.
透皮形式治疗脱发的比较疗效
介绍脱发是一种多发病性疾病,其特征是脱发和单位面积脱发数量减少。秃头会给患者带来心理和社会不适,这与开发比参考制剂更有效的配方有关。目标与参考药物米诺地尔和牛蒡油相比,研究以几种剂型应用原始物质Y治疗脱发的可能性。材料和方法。研究对象是原始物质Y,为其制备了几种剂型:凝胶、酒精和油成分。在9组雄性C57BL/6小鼠上对所开发的制剂的有效性和安全性进行了研究。脱毛并进一步评估生长期和休息期毛囊的百分比,作为脱发的临床前模型进行了测试。在研究Y物质的作用机制时,在磷酸钾缓冲介质(pH=7.4)中,将Y物质与天然抗氧化剂槲皮素在鲁米诺–2,2'-偶氮双(2-氨基丙烷)二盐酸盐体系中进行了化学发光测定,美国软件在统计学水平上的显著性差异p<0.05和p<0.005。结果与讨论。根据组织学分析和视觉变化的结果,发现局部形式的Y物质的有效性按以下顺序降低:凝胶、酒精形式、油成分。与使用2%米诺地尔溶液的对照制剂相比,凝胶基质与测试物质Y的组合使用导致生长期出现更多毛囊(差异具有统计学意义)。抗氧化活性的化学发光评估显示Y物质缺乏抗氧化作用。结论:该研究结合了两个药物概况:技术和药理学。在实验过程中,显示了原始物质Y的凝胶形式用于脱发局部治疗的前景。在不久的将来,计划研究Y物质的作用机制,以及一种新药的专利保护注册。
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来源期刊
Drug Development and Registration
Drug Development and Registration Pharmacology, Toxicology and Pharmaceutics-Pharmaceutical Science
CiteScore
1.20
自引率
0.00%
发文量
61
审稿时长
8 weeks
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