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Development of a Solid Formulation Containing a Microemulsion of a Novel

机译:研制含有新型微乳液的固体制剂

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摘要

Background: Intestinal nematode infections are usually treated with benzimidazole drugs, but the emergence of resistance to these drugs has led to an increasing demand of new anthelmintic strategies. A new microemulsion formulation (ME) consisting of an Artemisia absinthium extract with proven nematocidal efficacy was previously developed. The aim of our study is to implement a D-optimal mixture design methodology to increase the amount of a silica material (loaded with this ME) in a tablet formulation, considering its tensile strength and disintegration time. Methods: 16 experiments or combinations of the 6 tablet components (loaded silica, microcrystalline cellulose, polyvinylpyrrolidone, croscarmellose, Syloid® 244 FP and magnesium stearate) were assessed. Tensile strength and disintegration time models were developed, and an optimization process was carried out. Results: Tensile strength was improved by increasing the polyvinylpyrrolidone content, while croscarmellose decreased the disintegration time. The optimized powder mixture contains 49.7% w/w of the loaded silica material. A compression force of 12 kN was applied to the powder mixture to form tablets with a tensile strength of 2.0 MPa and a disintegration time of 3.8 min. Conclusions: Our results show that D-optimal mixture designs provide a promising approach to formulate liquid-loaded silica materials.
机译:背景:肠道线虫感染通常用苯并咪唑药物治疗,但对这些药物的抗性的出现导致了对新的新策略的需求越来越大。以先前发育了一种新的微乳液配方(ME),由验证的Nematical疗效组成的Artemisia Absinthium提取物。我们的研究目的是实施一种D-最佳混合的混合设计方法,以提高片剂配方中的二氧化硅材料(加载含量)的量,考虑到其拉伸强度和崩解时间。方法:评估16种片剂组分(加载二氧化硅,微晶纤维素,聚乙烯吡咯烷酮,Croscarmellose,Syloiders 244fp和硬脂酸镁)的16种实验或组合。开发了拉伸强度和崩解时间模型,进行了优化过程。结果:通过增加聚乙烯吡咯烷酮含量提高拉伸强度,而Croscarmellose降低了崩解时间。优化的粉末混合物含有49.7%w / w的负载二氧化硅材料。将12kN的压缩力施加到粉末混合物中以形成2.0MPa的拉伸强度的片剂和3.8分钟的崩解时间。结论:我们的研究结果表明,D-最优混合物设计提供了配制液体加载的二氧化硅材料的有希望的方法。

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