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Development and Evaluation of a Nanoemulsion Containing Ursolic Acid: a Promising Trypanocidal Agent

机译:含熊酸纳米乳液的开发和评价:一种有前途的胰蛋白酶

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Over a hundred years after the discovery of Chagas disease, this ailment continues to affect thousands of people. For more than 40 years, only two drugs have been available to treat it. Ursolic acid is a naturally occurring terpene that has shown a good trypanocidal action. However, the hydrophobicity of this compound presents a challenge for the development of proper delivery systems. Nanostructured systems are a prominent in delivering lipophilic drugs. Thus, a nanoemulsion containing ursolic acid was developed and had its trypanocidal activity and cytotoxicity evaluated. Pseudo-ternary phase diagrams and hydrophilic-lipophilic balance (HLB) system were used in the development. The system was stable throughout 90 days of testing, as evidenced by turbidimetry analysis and measurements of the droplet size (57.3 nm) and polydispersity index (0.24). Fourier transform infrared spectroscopy and mass spectrometry evidenced drug's integrity in the formulation. An in vitro dissolution profile showed 75% of ursolic acid release after 5 min from the nanoemulsion into the alkaline dissolution medium, while only 20% could be released from a physical mixture after 2 h. Trypanocidal activity and cytotoxicity were evaluated on the CL Brener strain and LLC-MK2 (monkey kidney) fibroblast by chlorophenol red-beta-d-galactoside (CPRG) method. Biological studies showed that the developed formulation was nontoxic and effective against replicant forms of the parasite. A stable and efficient nanoemulsion could be developed to improve the delivery of a promising drug to treat a threatening illness such as Chagas disease.
机译:在发现Chagas病后一百年,这种疾病仍然影响成千上万的人。超过40年,只有两种药物可以治疗它。熊胆酸是一种天然存在的萜烯,其显示出良好的胰蛋白酶作用。然而,该化合物的疏水性呈现出适当的递送系统的开发挑战。纳米结构系统在提供亲脂性药物方面是突出的。因此,开发了含有尿胆酸的纳米乳液并进行其促蛋白酶活性和评估细胞毒性。在开发中使用了伪三元相图和亲水性 - 亲脂性平衡(HLB)系统。该系统在测试后90天稳定,正如液滴尺寸(57.3nm)和多分散指数的测量值(0.24)所证明的速度分析和测量值。傅里叶变换红外光谱和质谱证明了药物在制剂中的完整性。在从纳米乳液到碱性溶解介质中5分钟后,体外溶出曲线显示出75%的尿溶胶释放,而在2小时后,只能从物理混合物中释放20%。通过氯酚红β-D-半乳糖苷(CPRG)法对Cl Brener菌株和LLC-MK2(猴肾)成纤维细胞进行评估胰蛋白酶活性和细胞毒性。生物学研究表明,发育的制剂无毒,对寄生虫的复制剂形式有效。可以开发一种稳定高效的纳米乳液,以改善有希望的药物以治疗危及疾病,如Chagas疾病。

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