Zirconium-Based Metal-Organic Frameworks as Acriflavine Cargos in the Battle against Coronaviruses─A Theoretical and Experimental Approach.
SARS-CoV-2
acriflavine
density functional theory calculations
drug delivery
metal−organic frameworks
Journal
ACS applied materials & interfaces
ISSN: 1944-8252
Titre abrégé: ACS Appl Mater Interfaces
Pays: United States
ID NLM: 101504991
Informations de publication
Date de publication:
29 Jun 2022
29 Jun 2022
Historique:
pubmed:
15
6
2022
medline:
2
7
2022
entrez:
14
6
2022
Statut:
ppublish
Résumé
In this study, we present a complementary approach for obtaining an effective drug, based on acriflavine (ACF) and zirconium-based metal-organic frameworks (MOFs), against SARS-CoV-2. The experimental results showed that acriflavine inhibits the interaction between viral receptor-binding domain (RBD) of spike protein and angiotensin converting enzyme-2 (ACE2) host receptor driving viral cell entry. The prepared ACF@MOF composites exhibited low (MOF-808 and UiO-66) and high (UiO-67 and NU-1000) ACF loadings. The drug release profiles from prepared composites showed different release kinetics depending on the local pore environment. The long-term ACF release with the effective antiviral ACF concentration was observed for all studied ACF@MOF composites. The density functional theory (DFT) calculations allowed us to determine that π-π stacking together with electrostatic interaction plays an important role in acriflavine adsorption and release from ACF@MOF composites. The molecular docking results have shown that acriflavine interacts with several possible binding sites within the RBD and binding site at the RBD/ACE2 interface. The cytotoxicity and ecotoxicity results have confirmed that the prepared ACF@MOF composites may be considered potentially safe for living organisms. The complementary experimental and theoretical results presented in this study have confirmed that the ACF@MOF composites may be considered a potential candidate for the COVID-19 treatment, which makes them good candidates for clinical trials.
Identifiants
pubmed: 35700479
doi: 10.1021/acsami.2c06420
pmc: PMC9212192
doi:
Substances chimiques
Metal-Organic Frameworks
0
Phthalic Acids
0
UiO-66
0
Acriflavine
1T3A50395T
Zirconium
C6V6S92N3C
Angiotensin-Converting Enzyme 2
EC 3.4.17.23
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
28615-28627Références
Cell Chem Biol. 2022 May 19;29(5):774-784.e8
pubmed: 35021060
Clin Infect Dis. 2020 Apr 27;:
pubmed: 32338708
ACS Appl Mater Interfaces. 2021 Feb 17;13(6):7004-7020
pubmed: 33554591
Phys Rev B Condens Matter. 1996 Oct 15;54(16):11169-11186
pubmed: 9984901
J Comput Chem. 2010 Jan 30;31(2):455-61
pubmed: 19499576
ChemMedChem. 2022 Apr 20;17(8):e202100721
pubmed: 35157366
ACS Appl Mater Interfaces. 2020 Jan 29;12(4):5147-5156
pubmed: 31904920
Inorg Chem. 2019 May 20;58(10):6983-6992
pubmed: 31041865
ACS Appl Mater Interfaces. 2020 Sep 2;12(35):38989-39004
pubmed: 32805901
Cell Host Microbe. 2020 Dec 9;28(6):867-879.e5
pubmed: 33271067
Environ Int. 2021 Feb;147:106361
pubmed: 33401173
Comput Biol Med. 2022 Jan 26;143:105241
pubmed: 35114443
Angew Chem Int Ed Engl. 2006 Sep 11;45(36):5974-8
pubmed: 16897793
Acta Pharm Sin B. 2020 May;10(5):766-788
pubmed: 32292689
J Am Chem Soc. 2014 Mar 19;136(11):4369-81
pubmed: 24588307
J Control Release. 2000 Nov 3;69(2):261-72
pubmed: 11064133
Molecules. 2019 Sep 16;24(18):
pubmed: 31527488
Comput Struct Biotechnol J. 2022;20:824-837
pubmed: 35126885
J Am Chem Soc. 2008 Oct 22;130(42):13850-1
pubmed: 18817383
Nat Chem. 2019 Jul;11(7):622-628
pubmed: 31086300
Nat Methods. 2019 Jul;16(7):565-566
pubmed: 31217592
ACS Appl Mater Interfaces. 2021 Jan 13;13(1):312-323
pubmed: 33378177
J Am Chem Soc. 2013 Jul 17;135(28):10294-7
pubmed: 23829224
Phys Rev B Condens Matter. 1993 Nov 1;48(17):13115-13118
pubmed: 10007687
J Mol Graph Model. 2022 Jan;110:108045
pubmed: 34688160