کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
5512085 1540219 2017 8 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Antiviral activity of phosphorylated Radix Cyathulae officinalis polysaccharide against Canine Parvovirus in vitro
موضوعات مرتبط
علوم زیستی و بیوفناوری بیوشیمی، ژنتیک و زیست شناسی مولکولی زیست شیمی
پیش نمایش صفحه اول مقاله
Antiviral activity of phosphorylated Radix Cyathulae officinalis polysaccharide against Canine Parvovirus in vitro
چکیده انگلیسی
Phosphorylated Radix Cyathulae officinalis Kuan polysaccharides (pRCPS) was prepared according to three-factors, ratio of STMP (%) and STPP (%), reaction time and reaction temperature, and three level L9(34) orthogonal design. The antiviral activity of nine pRCPS (pRCPS1-9) was systematically evaluated by three methods pre-adding mode, mixed mode, and post-adding mode. Cellular activity was tested by the CCK-8 assay. The results showed that the optimal modification conditions were the ratio of STMP (%) and STPP (%) 1:4, reaction time 2 h and reaction temperature 65 °C. Six pRCPS (pRCPS1-4, pRCPS7, pRCPS9) exhibited significant anti-viral activity in pre-adding mode (P < 0.05). Eight pRCPS (pRCPS1-4, pRCPS5, pRCPS6, pRCPS7, and pRCPS9) showed dramatic anti-viral activity in the mixed mode (P < 0.05). Six pRCPS (pRCPS1-4, pRCPS6, pRCPS9) showed antiviral activity in the post-adding mode (P < 0.05). Taken together, four pRCPS (pRCPS1-4) demonstrated significant antiviral activity in all the test modes (P < 0.05) and their antiviral efficacy were significantly stronger than unmodified RCPS (P < 0.05). Those results indicated that four pRCPS (pRCPS1-4) possessed significant antiviral activity and may have potential as a new CPV therapeutic compound, and phosphorylation could significantly enhance the antiviral effect of RCPS. Moreover, phosphorylation modification technique could be valuable as a method to promote the antiviral activity of polysaccharide.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: International Journal of Biological Macromolecules - Volume 99, June 2017, Pages 511-518
نویسندگان
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