核桃提取物纳米载体的设计与表征及其对骨癌的影响

Samanah Aboeepoor, M. Dehghani Ashkezari, F. Aboee-Mehrizi, B. Haghiralsadat, Narges Nikoonahad Lotfabadi
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引用次数: 2

摘要

目的在现代药物给药系统中,niosome被认为是靶向给药的载体。伊朗Nepta (Nepta属)具有独特的生物学特性;因此,本研究以该植物为研究对象,制备了含提取物的纳米体的优化配方,并对其细胞毒性进行了评价。方法与材料初步制备伊朗胡桃树提取物。然后,以胆固醇和Span-60为原料,设计并合成了含提取物的纳米乳质体体系。用FTIR和SEM对体系的理化性质进行了表征。采用MTT法[3-(4,5-二甲基噻唑-2-基)-2,5-二苯基溴化四唑]测定了Nepta提取物及其纳米体系对骨癌细胞(MG63)的毒性。结果以胆固醇与Span-60的比例为80:20,得到了最佳配方。该配方的提取物释放量在很长一段时间内保持稳定的斜率。MG63细胞对100 μg/mL果仁提取物和乳质体提取物的存活率分别为22%和8.88%。结论猕猴桃提取物具有一定的抗癌作用,niosome可提高其抗癌作用。因此,它可以作为一种合适的载体,将提取物输送到目标组织。
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Designing and Characterizing Nano-carriers Containing Nepeta Persica Extract and Their Effect on Bone Cancer
Aims Niosomes have been considered as carriers for targeted delivery of drugs in modern drug delivery systems. The Iranian Nepta (Nepta genus) has unique biological properties; thus, this plant was used in this study to prepare the optimized formulation of niosomes containing extract, and to evaluate its cytotoxicity. Methods & Materials Initially, the extract of Iranian Nepta (N. persica) was prepared. Then, the nano-niosomal system, containing the extract was designed and synthesized using cholesterol and Span-60. The physicochemical properties of the system were evaluated by FTIR and SEM. MTT assay [3-(4,5-Dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide] was used to determine the toxicity of the Nepta extract and nano-system containing it against bone cancer cells (MG63). Findings An optimized formulation was obtained using cholesterol and Span-60 with a ratio of 80:20. The amount of extract release from this formulation continued with a steady slope over a long period of time. The survival rate of MG63 cells against 100 μg/mL of the free form of N. persica extract and its niosomal form were 22% and 8.88%, respectively. Conclusion The present research results suggested that N. persica extract exert anti-cancer effects and niosome could improve its anti-cancer efficiency. Therefore, it could be used as a proper carrier to deliver the extract to the target tissue.
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