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Obtenção de sistemas microemulsionados e estudo de simulação por dinâmica molecular de sistemas micelares objetivando a veiculação de produtos naturais bioativos

机译:针对生物活性天然产物的传递,获得微乳化体系并通过胶束体系的分子动力学模拟研究

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摘要

Among the new drugs launched into the market since 1980, up to 30% of them belong to the class of natural products or they have semisynthetic origin. Between 40-70% of the new chemical entities (or lead compounds) possess poor water solubility, which may impair their commercial use. An alternative for administration of poorly water-soluble drugs is their vehiculation into drug delivery systems like micelles, microemulsions, nanoparticles, liposomes, and cyclodextrin systems. In this work, microemulsion-based drug deliverysystems were obtained using pharmaceutically acceptable components: a mixture Tween 80 and Span 20 in ratio 3:1 as surfactant, isopropyl mirystate or oleic acid as oil, bidistilledwater, and ethanol, in some formulations, as cosurfactants. Self-Microemulsifying Drug Delivery Systems (SMEDDS) were also obtained using propylene glycol or sorbitol as cosurfactant. All formulations were characterized for rheological behavior, droplet size and electrical conductivity. The bioactive natural product trans-dehydrocrotonin, as well some extracts and fractions from Croton cajucara Benth (Euphorbiaceae), Anacardium occidentale L. (Anacardiaceae) e Phyllanthus amarus Schum. & Thonn. (Euphorbiaceae) specimens, weresatisfactorily solubilized into microemulsions formulations. Meanwhile, two other natural products from Croton cajucara, trans-crotonin and acetyl aleuritolic acid, showed poor solubility in these formulations. The evaluation of the antioxidant capacity, by DPPH method, of plant extracts loaded into microemulsions evidenced the antioxidant activity of Phyllanthusamarus and Anacardium occidentale extracts. For Phyllanthus amarus extract, the use of microemulsions duplicated its antioxidant efficiency. A hydroalcoholic extract from Crotoncajucara incorporated into a SMEDDS formulation showed bacteriostatic activity against colonies of Bacillus cereus and Escherichia coli bacteria. Additionally, Molecular Dynamicssimulations were performed using micellar systems, for drug delivery systems, containing sugar-based surfactants, N-dodecylamino-1-deoxylactitol and N-dodecyl-D-lactosylamine.The computational simulations indicated that micellization process for N-dodecylamino-1- deoxylactitol is more favorable than N-dodecyl-D-lactosylamine system.
机译:自1980年以来投放市场的新药中,多达30%属于天然产品类别或具有半合成来源。 40-70%的新化学实体(或铅化合物)具有较差的水溶性,这可能会损害其商业用途。水溶性差的药物的替代给药方法是将其溶入药物输送系统中,例如胶束,微乳剂,纳米颗粒,脂质体和环糊精系统。在这项工作中,使用药学上可接受的成分获得了基于微乳剂的药物递送系统:比例为3:1的吐温80和Span 20的混合物作为表面活性剂,异丙基丙三酸酯或油酸作为油,双蒸馏水和乙醇,在某些制剂中作为助表面活性剂。还使用丙二醇或山梨糖醇作为助表面活性剂获得了自微乳化药物递送系统(SMEDDS)。所有配方的流变行为,液滴尺寸和电导率均经过表征。具有生物活性的天然产物反式脱氢巴豆素,以及巴豆(Broton cajucara Benth(Euphorbiaceae),Anacardium occidentale L.(Anacardiaceae)e Phyllanthus amarus Schum)的一些提取物和馏分。 &Thonn。 (大戟科)样品被令人满意地溶解成微乳液制剂。同时,来自巴豆角豆的另外两种天然产物,反式巴豆素和乙酰丙二酸,在这些制剂中显示出较差的溶解性。通过DPPH法对微乳液中提取的植物提取物的抗氧化能力进行了评估,证明了毛竹兰和西洋参提取物的抗氧化活性。对于苦竹叶提取物,微乳液的使用复制了其抗氧化效率。结合到SMEDDS配方中的巴豆花的水醇提取物表现出对蜡状芽孢杆菌和大肠杆菌细菌菌落的抑菌活性。此外,使用胶束系统对包含糖基表面活性剂,N-十二烷基氨基-1-脱氧乳糖醇和N-十二烷基-D-乳糖苷胺的胶束系统进行了分子动力学模拟,计算模拟表明N-十二烷基氨基-1的胶束化过程。 -脱氧乳糖醇比N-十二烷基-D-乳糖苷胺体系更有利。

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