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논문 기본 정보

자료유형
학술저널
저자정보
Ghareeb Doaa A. (Alexandria University Egypt) Saleh Samar R. (Alexandria University Egypt) Seadawy Mohamed G. (Chemical Warfare Department MCL Almaza Egypt) Nofal Mohammed S. (Pharmaceutical and Fermentation Industries Development Centre (PFIDC) Egypt) Abdulmalek Shaymaa A. (Alexandria University Egypt) Hassan Salma. F. (Pharmaceutical and Fermentation Industries Development Centre (PFIDC) Egypt) Khedr Shaimaa M. (Pharmaceutical and Fermentation Industries Development Centre (PFIDC) Egypt) AbdElwahab Miral G. (Pharmaceutical and Fermentation Industry Development Center Egypt) Sobhy Ahmed A. (Alexandria University Egypt) Abdel-Hamid Ali saber Ali (Pharmaceutical and Fermentation Industry Development Center Egypt) Yassin Abdelrahman Mohamed (Pharmaceutical and Fermentation Industry Development Center Egypt) Elmoneam Alshimaa A. Abd (Alexandria University Egypt) Masoud Aliaa A. (Alexandria University Egypt) Kaddah Mohamed M. Y. (Pharmaceutical and Fermentation Industries Development Centre (PFIDC) Egypt) El-Zahaby Sally A. (Pharos University in Alexandria Egypt) Al-mahallawi Abdulaziz Mohsen (Cairo University Egypt) El-Gharbawy Alaa M. (Pharmaceutical and Fermentation Industry Development Center Egypt) Zaki Ahmed (Pharmaceutical and Fermentation Industry Development Center Egypt) Seif Inas K. (Alexandria University Egypt) Kenawy Marwa Y. (Advanced Technology and New Materials Research Institute (ATNMRI) Egypt) Amin Magdy (Military Medical Services Egypt) Amer Khaled (Egypt Center for Research and Regenerative Medicine Egypt) El Demellawy Maha Adel (Pharmaceutical and Fermentation Industry Development Center Egypt)
저널정보
한국약제학회 Journal of Pharmaceutical Investigation Journal of Pharmaceutical Investigation 제51권 제6호
발행연도
2021.11
수록면
735 - 757 (23page)
DOI
10.1007/s40005-021-00544-w

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Purpose A novel coronavirus (COVID-19) that has not been previously identified in humans and has no specific treatment has recently spread. Treatment trials using antiviral and immune-modulating drugs such as hydroxychloroquine (HCQ) were used to control this viral outbreak however several side effects have emerged. Berberine (BER) is an alkaloid that has been reported to reveal some pharmacological properties including antioxidant and antimicrobial activities. Additionally, Zinc oxide nanoparticles (ZnO-NPs) possess potent antioxidant and anti-inflammatory properties. Therefore, this study was undertaken to estimate the efficiency of both BER and synthetic ZnO/BER complex as an anti-COVID-19 therapy. Methods First, the ZnO/BER complex was prepared by the facile mixing method. Then in vitro studies on the two compounds were conducted including VeroE6 toxicity, anti-COVID-19 activity, determination of inhibitory activity towards papain-like proteinase (PL pro) and spike protein- and receptor- binding domain (RBD) as well as assessment of drug toxicity on RBCs. Results The results showed that ZnO/BER complex acts as an anti-COVID-19 by inhibiting spike protein binding with angiotensin-converting enzyme II (ACE II), PL pro activity, spike protein and E protein levels, and expression of both E-gene and RNA dependent RNA polymerase (RdRp) at a concentration lower than that of BER or ZnO-NPs alone. Furthermore, ZnO/BER complex had antioxidant and antimicrobial properties where it prevents the auto oxidation of 2,2-Diphenyl- 1-picrylhydrazyl (DPPH) and the culture of lower respiratory system bacteria that affected Covid 19 patients. The ZnO/BER complex prevented as well the HCQ cytotoxic effect on both RBC and WBC (in vitro) and hepatotoxicity, nephrotoxicity and anemia that occurred after HCQ long administration in vivo. Conclusion The ZnO/BER complex can be accounted as promising anti-COVID 19 candidate because it inhibited the virus entry, replication, and assembly. Furthermore, it could be used to treat a second bacterial infection that took place in hospitalized COVID 19 patients. Moreover, ZnO/BER complex was found to eliminate the toxicity of long-term administration of HCQ in vivo.

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