Technology of dry extract from the Filipendula ulmaria (L.) Maxim. and preliminary assessment of its safety profile

E. Avdeeva, M. Skorokhodova, V. V. Sheikin, T. V. Kadyrova, M. V. Belousov
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Abstract

Introduction. Medicines of natural origin have advantages over synthetic drugs and occupy a significant share in the assortment of pharmacies. Filipendula ulmaria (L.) Maxim., characterized by a chemical composition rich in phenolic compounds and various types of biological activity has the potential in terms of the development of new herbal medicines. In an in vivo experiment, F. ulmaria extract showed immunomodulatory, anti-inflammatory, osteogenic activity and effectively stimulated myelopoiesis in conditions of microbial damage of bone tissue.Aim. Development of an optimal technology for obtaining dry extract of F. ulmaria by remaceration and investigation of its аcute toxicity.Materials and methods. The technology of extract was developed in a laboratory reactor equipped with a water heater jacket and a stirrer. The content of flavonoids was determined by differential spectrometry. Flowability was determined on a flowability tester for powders and granules, bulk density was determined on a bulk density tester for powders and granules, moisture content was developed on a moisture content analyzer. Acute toxicity was determined on Wistar rats.Results and discussion. The dry extract of F. ulmaria, obtained using 70 % ethanol by remaceration, is effective in conditions of microbial damage of bone tissue and bone marrow, which determined the choice of extragent and the type of extract. The optimal parameters for obtaining the extract were determined (three-fold maceration at a water jacket temperature of 80 °C, the ratio of raw materials to extragent 1 : 14, time 30 min), its main technological characteristics were determined and a wet granulation method for improving them was proposed. In the study of acute toxicity of the extract, according to the results of toxicometry for 14 days after administration and necropsy data, the studied extract was classified as low-toxic substance.Conclusion. The dry extract of F. ulmaria, obtained by remaceration using 70 % ethanol, has specific activity in conditions of microbial damage to bone tissue. Optimal extraction parameters allow to increase the yield of target components, it is advisable to improve the technological parameters of the extract by wet granulation. The assessment of the safety profile of the dry extract from F. ulmaria, along with its high biological activity, provides a perspective for its further study and implementation into medical practice.
Filipendula ulmaria (L.) Maxim.干提取物的技术及其安全性初步评估
导言。天然药物比合成药物更有优势,在药房的品种中占有很大份额。Filipendula ulmaria (L.) Maxim.的化学成分中含有丰富的酚类化合物,具有多种生物活性,具有开发新草药的潜力。在一项体内实验中,F. ulmaria 提取物显示出免疫调节、抗炎和成骨活性,并在骨组织受到微生物破坏的情况下有效刺激骨髓造血。开发一种最佳技术,通过重熔法获得溃疡草干提取物,并研究其急性毒性。萃取技术是在实验室反应器中开发的,该反应器配备有热水器夹套和搅拌器。黄酮类化合物的含量通过差分光谱法测定。粉末和颗粒的流动性由流动性测试仪测定,体积密度由粉末和颗粒的体积密度测试仪测定,含水量由含水量分析仪测定。对 Wistar 大鼠进行了急性毒性测定。用 70% 的乙醇通过重熏法获得的溃疡苣苔干提取物对骨组织和骨髓的微生物损伤有效,这决定了外加剂的选择和提取物的类型。确定了获得提取物的最佳参数(水套温度为 80 °C,三次浸渍,原料与外加剂的比例为 1:14,时间为 30 分钟),确定了其主要技术特征,并提出了改进这些特征的湿法造粒方法。在提取物的急性毒性研究中,根据给药后 14 天的毒性测定结果和尸体解剖数据,所研究的提取物被归类为低毒物质。用 70% 的乙醇重熏蒸获得的溃疡苣苔干提取物在骨组织受到微生物破坏的情况下具有特殊活性。最佳提取参数可提高目标成分的产量,建议通过湿法造粒改进提取物的技术参数。对溃疡苣苔干提取物安全性及其高生物活性的评估,为进一步研究该提取物并将其应用于医疗实践提供了前景。
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