纳米壳聚糖衍生物和链霉素对RD细胞株和热带利什曼原虫的体外作用研究

A. Ahmed, Muna Mohammed Khayri, M. Al-Halbosiy
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引用次数: 0

摘要

研究酸碱法制备的羧甲基纳米壳聚糖包封链霉素对RD横纹肌肉瘤细胞株和热带利什曼原虫的体外抑菌效果。结果表明,100和50 μg/ml包封链霉素比单独使用50和100 μg/ml更有效,孵育24 h后,对RD细胞的抑制率分别为56%和35%,对19.45%和23%。50 μg/ml浓度的羧甲基纳米壳聚糖对RD细胞生长的抑制作用可达20%,而相同浓度的链霉素对RD细胞的抑制作用为19%。链霉素、羧甲基纳米壳聚糖和羧甲基纳米壳聚糖包封的链霉素在100 μg/ml浓度下对热带乳杆菌生长的抑制作用分别为34.4、36和29.5%。因此,羧甲基纳米壳聚糖被认为是热带乳杆菌生长最有效的抑制剂。(DOI: 10.22401 / JUNS.20.4.12)
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In Vitro Evaluation of Nanochitosan Derivatives and Streptomycin on RD Cell Line and Leishmania Tropica
The study aimed to evaluate in vitro the efficiency of the nano-encapsulated streptomycin within carboxymethylnanochitosan synthesized by an acid-base method on Rhabdomyosarcoma RD cell line and Leishmania tropica. Results showed that the concentrations 100 and 50 μg/ml of encapsulated streptomycin were more effective than 50 and 100 μg/ml of streptomycin alone and inhibited the growth of RD cells to 56 and 35 vs. 19.45 and 23% respectively after 24 hrs of incubation. Carboxymethylnanochitosan at a concentration of 50 μg/ml has the anticancer ability since it inhibited the growth of RD cells up to 20% in comparison with 19% for streptomycin at the same concentration. The growth inhibition of L. tropica in the presence of streptomycin, carboxymethylnanochitosan and streptomycin encapsulated within carboxymethylnanochitosan at 100 μg/ml for each was 34.4, 36 and 29.5% respectively. Carboxymethylnanochitosan is then considered the most effective inhibitor of L. tropica growth. [DOI: 10.22401/JUNS.20.4.12]
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