EFFECT OF SOLID DISPERSIONS ON THE SOLUBILITY OF METRONIDAZOLE

I. I. Krasnyuk (jr.), S. R. Naryshkin, I. Krasnyuk, A. Belyatskaya, O. I. Stepanova, I. S. Bobrov, V. Yankova, J. Rau, A. Vorobiev
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引用次数: 2

Abstract

The aim of the work is to study the effect of solid dispersions using polyethylene glycols of various molecular weights on the solubility of metronidazole in water. Metronidazole is an antimicrobial and antiprotozoal drug. Its low solubility in water limits the use of metronidazole, causing technological difficulties and reducing its bioavailability. The solubility and release of the active substance from dosage forms can be increased using the solid dispersion methods. Solid dispersions are bi- or multicomponent systems consisting of an active substance and a carrier (a highly dispersed solid phase of the active substance or molecular-dispersed solid solutions) with a partial formation of complexes of variable compositions with the carrier material.Materials and methods. The substance of metronidazole used in the experiment, was manufactured by Hubei Hongyuan Pharmaceutical Technology Co., Ltd. (China). To obtain solid dispersions, polyethylene glycols of various molar masses – 1500, 2000 and 3000 g/mol – were used. The solid dispersions were prepared by “the solvent removal method”: metronidazole and the polymer were dissolved in a minimum volume of 96% ethyl alcohol (puriss. p.a./analytical grade) at 65±2°C, and then the solvent was evaporated under vacuum to the constant weight. A vacuum pump and a water bath were used at the temperature of 40±2°C. The dissolution of the samples was studied using a magnetic stirrer with heating, and a thermostatting device. The concentration of metronidazole was determined on a spectrophotometer using quartz cuvettes at the wavelength of 318±2 nm. To filter the solutions, syringe nozzles were used, the pores were 0.45 μm, the filter was nylon. Microcrystalloscopy was performed using a microscope with a digital camera. The optical properties of the solutions were investigated using a quartz cuvette and a mirror camera (the image exposure – 20 sec).Results. Obtaining solid dispersions increases the completeness and rate of the metronidazole dissolution. The solubility of metronidazole from solid dispersions increases by 14–17% in comparison with the original substance. The complex of physical-chemical methods of the analysis, including UV spectrophotometry, microcrystalloscopy and the study of the optical properties of the obtained solutions, makes it possible to suggest the following. The increase in the solubility of metronidazole from solid dispersions is explained by the loss of crystallinity and the formation of a solid solution of the active substance and the solubilizing effect of the polymer with the formation of colloidal solutions of metronidazole at subsequent dissolution of the solid dispersion in water.Conclusion. The preparation of solid dispersions with polyethylene glycols improves the dissolution of metronidazole in water. The results obtained are planned to be used in the development of rapidly dissolving solid dosage forms of metronidazole with an accelerated release and an increased bioavailability.
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固体分散体对甲硝唑溶解度的影响
本研究的目的是研究不同分子量的聚乙二醇固体分散体对甲硝唑在水中溶解度的影响。甲硝唑是一种抗微生物和抗原虫药物。甲硝唑在水中的低溶解度限制了甲硝唑的使用,造成了技术上的困难,降低了其生物利用度。使用固体分散方法可以增加活性物质在剂型中的溶解度和释放度。固体分散体是由活性物质和载体(活性物质的高度分散的固相或分子分散的固溶体)组成的双组分或多组分体系,与载体材料形成可变组成的部分配合物。材料和方法。实验所用的甲硝唑物质由湖北宏远医药科技有限公司生产。为了得到固体分散体,使用了不同摩尔质量的聚乙二醇——1500、2000和3000 g/mol。采用“溶剂去除法”制备固体分散体:将甲硝唑和聚合物溶解在96%乙醇的最小体积中。p.a./分析级)在65±2°C下,然后在真空下蒸发溶剂至定重。使用真空泵和水浴,温度为40±2℃。采用带加热的磁力搅拌器和恒温装置对样品的溶解进行了研究。在波长318±2 nm处,用石英比色管分光光度计测定甲硝唑浓度。过滤采用注射器喷嘴,孔径为0.45 μm,滤芯为尼龙。显微晶体检查采用带数码相机的显微镜。利用石英比色皿和反光镜(曝光- 20秒)对溶液的光学性质进行了研究。获得固体分散体可提高甲硝唑溶解的完整性和速度。固体分散体中甲硝唑的溶解度比原物质提高了14-17%。综合运用物理化学分析方法,包括紫外分光光度法、微晶体法和对所得溶液光学性质的研究,可以得出以下结论。甲硝唑在固体分散体中溶解度的增加可以解释为:活性物质的结晶度损失和形成固溶体,以及聚合物在固体分散体随后在水中溶解时与甲硝唑形成胶体溶液的增溶作用。用聚乙二醇制备的固体分散体改善了甲硝唑在水中的溶解。所获得的结果计划用于开发快速溶解的甲硝唑固体剂型,具有加速释放和提高生物利用度。
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