Development of antifungal gel, composition and technology based on pomiferin metabolite isolated from fruits of Maclura aurantiaca growing in Kazakhstan

Q3 Pharmacology, Toxicology and Pharmaceutics
Serzhan Mombekov, Yerkebulan Orazbekov, Nurila Sadykova, Assel Kozhamzharova, Sarzhan Sharipova, Zhaksylyk Makhatov, Nazym Pushkarskaya
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引用次数: 0

Abstract

The aim. The purpose of this study is to develop the optimal composition and rational gel technology under the conventional name "Kaz-P7" based on the antifungal pomiferin. Materials and methods. The object of the study is the substance pomiferin. Based on the physicochemical properties of the gel (poorly soluble in water) and technological properties structurant - Carbopol Ultrez 20 (swelling) chosen optimal solvent system: DMSO-PG-water (1:4:1) corresponding to the maximum solubility of drug and polymer provides swelling. Following the requirements of GF RK I, vol. 1, 2.2.8, 2.2.10 was determined by rotational viscometric method. Rheological properties of the sample are determined using rotational viscometer "Rheolab QC" (firm "Anton Paar", Austria) with coaxial cylinders CC27/S-SN29766 determined. The rheological parameters were studied at a temperature of 20 °C – 35 °C using the MLM U15c thermostat included in the rheostat. Results. Gel dosage forms provide better bioavailability of the drug substance. In addition, gels are a more modern dosage form, pleasant in terms of organoleptic characteristics. The technology of gel manufacturing consists of two parallel processes: preparation of the drug substance solution and its introduction into the base. From the point of view of biopharmacy, which studies the biological effect of drugs depending on their physical properties, dosage form and preparation technology, the greatest release of the drug substance occurs when it is introduced into the dosage form in dissolved form. Pomiferin administered in the dissolved state has the most therapeutic effect on the gel base. At the same time, active pharmaceutical ingredients (APIs) were dissolved in different solvents with gradual heating. The ratio of solvents DMSO-PG-water (1:4:1) at which the developed dosage form will be more structured, stable, and thixotropic gel is established. Conclusions. Fungal skin diseases are among the most frequently discussed problems in the literature. The relevance of this topic is determined by the high prevalence of pathogens, which account for 37-42 % of all skin diseases. It was experimentally established that for the complete neutralization of one gm of carbopol Ultraz 20 in the DMSO-PG-water solvent system (1:4:1), one gm of triethanolamine (pH 7.0) is consumed. The optimal diluent consisting of DMSO-PG- water in the ratio (1:4:1) was selected by physico-chemical analysis methods, and one gm of triethanolamine (pH 7.0) was selected as the neutralizing agent. The following composition was chosen as the optimal gel model: API-3.0, DMSO-3.0, PG-50.0, Carbopol Ultrez 20-1.0, and Triethanolamine-1.0. The optimal composition and technology of the gel codenamed "Kaz-P7" based on the substance obtained by pomiferin was developed
基于从生长在哈萨克斯坦的 Maclura aurantiaca 果实中分离出的 pomiferin 代谢物的抗真菌凝胶、成分和技术的开发
研究目的本研究的目的是以抗真菌的 pomiferin 为基础,开发常规名称为 "Kaz-P7 "的最佳成分和合理的凝胶技术。材料和方法。研究对象是 pomiferin 物质。根据凝胶的理化特性(难溶于水)和技术特性,选择了最佳溶剂系统--Carbopol Ultrez 20(膨胀):DMSO-PG-水(1:4:1)对应于药物和聚合物的最大溶解度,提供了溶胀性。按照 GF RK I 第 1 卷 2.2.8 和 2.2.10 的要求,用旋转粘度计法测定。样品的流变特性是用同轴圆筒 CC27/S-SN29766 旋转粘度计 "Rheolab QC"(奥地利 "安东帕 "公司)测定的。使用流变仪中的 MLM U15c 恒温器在 20 °C - 35 °C 的温度下对流变参数进行了研究。研究结果凝胶剂型的药物生物利用度更高。此外,凝胶剂型是一种更现代的剂型,在感官特性方面也很舒适。凝胶制造技术包括两个并行的过程:制备药物溶液和将其引入基质。生物药剂学研究药物的生物效应取决于药物的物理特性、剂型和制备技术,从生物药剂学的角度来看,当药物以溶解状态进入剂型时,药物的释放量最大。以溶解状态给药的 Pomiferin 对凝胶基质的治疗效果最好。同时,将活性药物成分(API)溶解在不同的溶剂中并逐渐加热。最终确定了 DMSO-PG- 水(1:4:1)的溶剂比例,在该比例下开发出的剂型将是结构更合理、更稳定、触变性更强的凝胶。结论真菌性皮肤病是文献中讨论最多的问题之一。病原体的高流行率决定了这一主题的相关性,它占所有皮肤病的 37-42%。实验证明,在 DMSO-PG 水溶剂系统(1:4:1)中完全中和 1 克 carbopol Ultraz 20 需要消耗 1 克三乙醇胺(pH 值为 7.0)。通过物理化学分析方法选择了由 DMSO-PG- 水按比例(1:4:1)组成的最佳稀释剂,并选择了一克三乙醇胺(pH 值为 7.0)作为中和剂。选择以下成分作为最佳凝胶模型:API-3.0、DMSO-3.0、PG-50.0、Carbopol Ultrez 20-1.0 和三乙醇胺-1.0。根据波美度素获得的物质,开发了代号为 "Kaz-P7 "的凝胶的最佳成分和技术
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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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