CAO Ze-yu, XIE Xue, NIU Ying, et al. Anti-CoxA16 and EV71 Activity of Components from Reduning Injection[J]. Chinese journal of experimental traditional medical formulae, 2015, 21(14): 106-110.
DOI:
CAO Ze-yu, XIE Xue, NIU Ying, et al. Anti-CoxA16 and EV71 Activity of Components from Reduning Injection[J]. Chinese journal of experimental traditional medical formulae, 2015, 21(14): 106-110. DOI: 10.13422/j.cnki.syfjx.2015140106.
Anti-CoxA16 and EV71 Activity of Components from Reduning Injection
Objective: To study the antiviral effects of components from Reduning injection against coxsachievirus A16 (CoxA16) and enterovirus 71 (EV71) in vitro. Method: African green monkey cell(Vero cells)
infected with 50 times 50% tissue cuture infective dose(TCID50) CoxA16 and EV71
were treated with components (15.625-500 mg · L-1) for 3 days (n=3)
median toxic concentration(TC50) values were clarified. The antiviral activity of components against CoxA16 and EV71 was assessed. Viral load was detected after active components application with optium concentration for 8 h. Result: Firstly
the toxic effects (TC50) of the components (RDN1-19) on Vero cells were investigated
which was from more than 1 000 to 221 mg · L-1. Furthermore
the antivirus and dose-response relationship studies of components showed that RDN7 and RDN18 revealed antiviral activity against CoxA16 with concentration for 50% of maximum effect(EC50) 460
92 mg · L-1
therapeutic index(TI) 1.44
2.40.Meanwhile
RDN6 and RDN17 revealed antiviral activity against EV71 with EC50 395
378 mg · L-1
TI 2.22
1.10.Finally
investigation on viral load indicated that RDN7 reduced CoxA16 copies very significantly in Vero cell (P<0.01). And RDN6
RDN 17 depressed EV71 copies very obviously in Vero cells (P<0.01). However
RDN18 failed to change CoxA16 and EV71 load clearly. Conclusion: The exogenous antiviral activity of components from Reduning injection against CoxA16 and EV71 could be clarified.
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