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10.1021/acsami.9b15032

http://scihub22266oqcxt.onion/10.1021/acsami.9b15032
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31633330!7075527!31633330
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suck abstract from ncbi


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pmid31633330      ACS+Appl+Mater+Interfaces 2019 ; 11 (46): 42964-42974
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  • Functional Carbon Quantum Dots as Medical Countermeasures to Human Coronavirus #MMPMID31633330
  • Loczechin A; Seron K; Barras A; Giovanelli E; Belouzard S; Chen YT; Metzler-Nolte N; Boukherroub R; Dubuisson J; Szunerits S
  • ACS Appl Mater Interfaces 2019[Nov]; 11 (46): 42964-42974 PMID31633330show ga
  • Therapeutic options for the highly pathogenic human coronavirus (HCoV) infections are urgently needed. Anticoronavirus therapy is however challenging, as coronaviruses are biologically diverse and rapidly mutating. In this work, the antiviral activity of seven different carbon quantum dots (CQDs) for the treatment of human coronavirus HCoV-229E infections was investigated. The first generation of antiviral CQDs was derived from hydrothermal carbonization of ethylenediamine/citric acid as carbon precursors and postmodified with boronic acid ligands. These nanostructures showed a concentration-dependent virus inactivation with an estimated EC(50) of 52 +/- 8 mug mL(-1). CQDs derived from 4-aminophenylboronic acid without any further modification resulted in the second-generation of anti-HCoV nanomaterials with an EC(50) lowered to 5.2 +/- 0.7 mug mL(-1). The underlying mechanism of action of these CQDs was revealed to be inhibition of HCoV-229E entry that could be due to interaction of the functional groups of the CQDs with HCoV-229E entry receptors; surprisingly, an equally large inhibition activity was observed at the viral replication step.
  • |*Antiviral Agents/pharmacology[MESH]
  • |*Carbon/chemistry/pharmacology[MESH]
  • |*Coronavirus Infections/drug therapy/metabolism/pathology[MESH]
  • |*Quantum Dots/chemistry/therapeutic use[MESH]
  • |Cell Line, Tumor[MESH]
  • |Coronavirus 229E, Human/*physiology[MESH]
  • |Humans[MESH]


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