基于纳米级二氧化硅的亲疏水伤口护理制备:物理化学和工艺方面

I. Gerashchenko, K. O. Stepanyuk, O. Chepliaka, M. Borysenko, E. Pakhlov, D. G. Klyuchkov, K. G. Vinogradova
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引用次数: 0

摘要

Неaling感染的溃疡和伤口,特别是老年人,是现代外科手术中的一个严重问题。经过多年的努力,我们已经研制出一种具有高吸收、抗炎和伤口愈合能力的创新性创面护理组合物,并已开始临床研究。该组合物的商标为Pathelen®,含有纳米级亲水性二氧化硅(a -300)、疏水性二氧化硅(Aerosil®R972 Pharma)和苯扎氯铵。本工作旨在探索该药物的最佳工业化生产途径,以及质量控制方法。生产中间体和最终产品的检查包括体积密度测量、热分析、红外光谱、化学鉴定方法、吸附能力和微生物污染控制。提出了将苯扎氯铵机械化学固定在疏水二氧化硅表面,并将得到的半成品与亲水性纳米二氧化硅混合的制备途径。因此,提出了一种将亲水性和疏水性纳米材料结合在一种制剂中的技术方法。最终产品符合制定的质量参数。特别是容重分布在50 - 60g /L范围内,每克对蛋白质的吸附量不小于140mg。不存在病原微生物和真菌;非致病性微生物的数量符合欧洲药典对该类产品的要求。所获得的结果可用于组织将来大规模生产所建议的药物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Hydrophilic/hydrophobic wound care preparation based on the nanoscale silica: physicochemical and technological aspects
Неaling of infected ulcers and wounds, particularly in older people, is a serious problem in modern surgery. As a result of many years efforts, we have created an innovative wound care composition that has high absorptive, anti-inflammatory and wound-healing capabilities and are starting the clinical study of it. The composition, which got a trade mark Pathelen®, contains nanoscale hydrophilic silica (A-300), hydrophobic silica (Aerosil® R972 Pharma) and benzalkonium chloride. This work aimed to develop an optimal pathway of industrial production, as well as methods of quality control of the drug. The examination of manufacture intermediates and the final product includes bulk density measurement, thermal analysis, IR spectroscopy, chemical methods of identification, adsorption capacity and microbial contamination control. The pathway of manufacture which consists of mechanochemical immobilization of benzalkonium chloride on hydrophobic silica surface and mixing of obtained semi-product with hydrophilic nanoscale silica is developed. Thus, a technological method is proposed for combining hydrophilic and hydrophobic nanomaterials in one preparation. The final product complies to the elaborated quality parameters. In particular, the bulk density is distributed in a range 50–60 g/L, the adsorption capacity is not less than 140 mg of protein per gram. The absence of pathogenic microorganisms and fungi was demonstrated; the quantity of non-pathogenic microorganisms meets the requirements of the European Pharmacopoeia for products in this category. The results obtained can be useful for the organization a large-scale production of the proposed drug in future.
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