基于进口替代型聚氧乙烯醚-Emuxol 的眼用植入物的开发 268

E. Bakhrushina, A. Turaeva, D. Zhalyalova, D. A. Klimov, N. Demina, I. I. Krasnuk
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引用次数: 0

摘要

简介。Emuxol-268(俄罗斯 "NIOPIK "股份公司)是俄罗斯生产的一种嵌段共聚物,其物理化学和生物特性与美国巴斯夫公司生产的聚氧乙烯醚 Kolliphor® P 188(Pluronic F68)相似。然而,以前从未对天然聚合物的特性进行过比较,以评估其剂型的前景。本研究的目的是以开发眼科药物插入剂为例,通过比较弹性、厚度、粘附性、pH 值、生物降解时间和刺激试验(母鸡卵-绒毛膜试验,HET-CAM 试验)等质量参数对剂型进行测试的结果,证明辅助成分的互换性。实验中使用了多羟胺 Emuxol 268(JSC "NIOPIK",俄罗斯)和 Kolliphor® P 188(BASF,德国)、羟乙基纤维素(Natrosol™ 250 HHX,美国亚什兰全球控股公司)和甘油(LLC "Tulskaya Pharmfabrika",俄罗斯)。实验采用了弹性、厚度、粘附性、pH 值、生物降解时间、HET-CAM 试验等筛选方法来确定组合物的优点。实验结果证明,使用国产类似物可以制造出质量参数更高的眼药水。插入物的弹性指数相差 1.3 倍,粘附性相差 1.7 倍,生物降解时间相差 2.5 倍。由此可以推断,基于国产聚合物的药片有助于延长与眼球表面的接触时间,从而延长药物的作用时间并提高其生物利用率。所得结果可能是由于疏水性聚氧丙烯部分的平均分子量不同造成的,Emuxol 268 为 2600 Da,而 Kolliphor 188 为 1800 Da。HET-CAM 方法显示两种复合物的结果相同,都没有刺激作用。综上所述,俄罗斯医药市场上唯一一种 Kolliphor® P 188 的类似物--JSC NIOPIK 公司的 Emuxol-268 是一种很有前途的物质,可在眼科剂型的开发中替代 Kolliphor® P 188。尽管国产嵌段共聚物的理化性质与被替代的 poloxamer 188 相比存在差异,但将其引入安慰剂插页后,在质量指标方面取得了更好的效果,这一点在生物制药分析中得到了证实。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Development of Ocular Inserts Based on Import Substituted Poloxamer Emuxol 268
Introduction. Emuxol-268 (JSC "NIOPIK", Russia) is a block copolymer produced in Russia with similar in physicochemical and biological properties to poloxamer Kolliphor® P 188 (Pluronic F68) manufactured by BASF, USA. However, a comparison of the properties of natural polymers to assess the prospects of their dosage forms has not been carried out before.Aim. The aim of the study was to demonstrate the interchangeability of auxiliary components using the example of the development of an ophthalmic drug insert by comparing the results of testing the dosage form in terms of such quality parameters as elasticity, thickness, mucoadhesion, pH, biodegradation time and irritation test (hen’s egg-chorioallantoic membrane test, HET-CAM test).Materials and methods. Poloxamers Emuxol 268 (JSC "NIOPIK", Russia) and Kolliphor® P 188 (BASF, Germany), hydroxyethyl cellulose (Natrosol™ 250 HHX, Ashland Global Holdings Inc., USA), and glycerol (LLC "Tulskaya Pharmfabrika", Russia) were used in the experiment. Elasticity, thickness, mucoadhesion, pH, biodegradation time, HET-CAM test were used as screening methods to identify the benefits of the composition.Results and discussion. Experiment results proved that the use of a domestic analogue makes it possible to create an ocular insert with improved quality parameters. The difference in the elasticity index of the inserts differs by 1.3 times, mucoadhesion – 1.7 times, biodegradation time – 2.5 times. In this connection, it can be assumed that an insert based on a domestic polymer contributes to an increase in the time of contact with the eye surface, thereby providing a prolonged effect of the drug and improving its bioavailability. The results obtained may be due to the difference in the average molecular weight of the hydrophobic polyoxypropylene part, which is 2600 Da for Emuxol 268 and 1800 Da for Kolliphor 188. The HET-CAM method showed the same results of the two compositions, both compositions do not have an irritating effect.Conclusion. Summing up, the only analogue of Kolliphor® P 188 available on the Russian pharmaceutical market – Emuxol-268 of JSC NIOPIK is a promising substance for replacement in the development of ophthalmic dosage forms. Despite the differences in physicochemical properties of the domestic block copolymer in comparison with the replaced poloxamer 188, its introduction into placebo inserts gave improved results in terms of quality indicators, which was revealed during a biopharmaceutical analysis.
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