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Compound antimalarial ethosomal cataplasm: preparation evaluation and mechanism of penetration enhancement

机译:复方抗疟药物的酶体催化物:渗透增强剂的制备评价和机理

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摘要

Malaria is still a serious public health problem in some parts of the world. The problems of recurrence and drug resistance are increasingly more serious. Thus, it is necessary to develop a novel antimalarial agent. The objectives of this study were to construct a novel compound antimalarial transdermal nanosystem–ethosomal cataplasm, to investigate its characteristics and efficiency, and to systematically explore the penetration-enhancing mechanisms of ethosomal cataplasm. Artesunate-loaded ethosomes and febrifugine-loaded ethosomes were prepared, and their characteristics were evaluated. Drug-loaded ethosomes were incorporated in the matrix of cataplasm to form the compound antimalarial ethosomal cataplasm. With the help of ethosomal technology, the accumulated permeation quantity of artesunate significantly increased at 8 hours after administration, which was 1.57 times as much as that of conventional cataplasm. Soon after administration, the ethosomal cataplasm could make a large quantity of antimalarial drug quickly penetrate through skin, then the remaining drug in the ethosomal cataplasm could be steadily released. These characteristics of ethosomal cataplasm are favorable for antimalarial drugs to kill Plasmodium spp. quickly and prevent the resurgence of Plasmodium spp. As expected, the ethosomal cataplasm showed good antimalarial efficiency in this experiment. The negative conversion rates were 100% and the recurrence rates were 0% at all dosages. The mechanism of penetration enhancement of the ethosomal cataplasm was systematically explored using an optics microscope, polarization microscope, and transmission electron microscopy. The microstructure, ultrastructure, and birefringent structure in skin were observed. Data obtained in this study showed that the application of ethosomal technology to antimalarial cataplasm could improve the transdermal delivery of drug, enhance the efficacy, and facilitate practical application in clinic.
机译:在世界某些地区,疟疾仍然是一个严重的公共卫生问题。复发和耐药性问题越来越严重。因此,有必要开发新型抗疟药。这项研究的目的是构建一种新型的复合抗疟药物透皮纳米系统-核糖体催化物,以研究其特性和效率,并系统地探索增强溶酶体催化物的渗透机制。制备了负载青蒿琥酯的脂质体和替非福定的脂质体,并对其特性进行了评估。将载有药物的脂质体掺入催化基质中,以形成复合的抗疟疾溶酶体催化基质。借助于酶体技术,青蒿琥酯在给药后8小时的累积渗透量显着增加,是常规催化物的1.57倍。服药后不久,内含物就能使大量的抗疟药迅速渗透到皮肤中,从而使内含物中的药物得以稳定释放。溶酶体催化物的这些特征有利于抗疟药杀死疟原虫。快速并防止疟原虫再次流行。如预期的那样,在该实验中,气管内的催化物显示出良好的抗疟疾功效。在所有剂量下,阴性转化率为100%,复发率为0%。使用光学显微镜,偏光显微镜和透射电子显微镜系统地探索了增强气管胞浆的渗透性的机制。观察到皮肤的微观结构,超微结构和双折射结构。这项研究获得的数据表明,将酶体技术应用于抗疟原虫可以改善药物的透皮递送,增强疗效,并有助于临床实际应用。

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