2015
DOI: 10.1007/s12274-015-0851-6
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Self-assemblies of plasmonic gold/layered double hydroxides with highly efficient antiviral effect against the hepatitis B virus

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Cited by 29 publications
(17 citation statements)
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“…A PEG-stabilized AuNP was found to inhibit the HIV-1 fusion process in a dose-dependent manner through blocking the gp120–CD4 interaction [ 214 ]. AuNPs have also been assembled onto a layered double hydroxide surface to inhibit HBV [ 215 ]. Interestingly, AuNPs have been co-loaded with efaverinz, an NNRTI, into niosomes and then furthered loaded into a thermosensitive gel to create a complex superstructure for sustained release against HIV-1 infections [ 216 ].…”
Section: Nanotechnology Interventionsmentioning
confidence: 99%
“…A PEG-stabilized AuNP was found to inhibit the HIV-1 fusion process in a dose-dependent manner through blocking the gp120–CD4 interaction [ 214 ]. AuNPs have also been assembled onto a layered double hydroxide surface to inhibit HBV [ 215 ]. Interestingly, AuNPs have been co-loaded with efaverinz, an NNRTI, into niosomes and then furthered loaded into a thermosensitive gel to create a complex superstructure for sustained release against HIV-1 infections [ 216 ].…”
Section: Nanotechnology Interventionsmentioning
confidence: 99%
“…[ 19,54 ] Nanomaterials act as replication inhibitors by delivering drugs [ 17,20,55,56 ] or trapping the virus. [ 57,58 ]…”
Section: Nanomaterials For Antivirus Strategiesmentioning
confidence: 99%
“…3.5 nm) organized on the surface of larger layered double hydroxide (LDH) NPs such as MgLDH, ZnLDH, and MgFeLDH (approx. 150 nm) using HBV as a model virus and hepatoma-derived HepG2.2.215 cells for viral replication reduced the amount of viral and subviral particles released from treated cells by up to 80%; in the presence of AuNPs/LDHs the HBV particles were sequestered within the treated cells and the highest antiviral HBV response (>90% inhibition of HBV secretion) was estimated with AuNPs/MgFeLDH (Carja et al 2015). Cu 2 O NPs that were tested on antiviral activity against HCV pronouncedly inhibited the infectivity of HCVcc/Huh7.5.1 at a noncytotoxic concentration, they inhibited the entry of HCV pseudoparticles (HCVpp), including genotypes 1a, 1b, and 2a, while no effect on HCV replication was observed and they were found to stop HCV infection both at the attachment and entry stages suggesting that Cu 2 O NPs could be used in the treatment of patients with chronic hepatitis C (Hang et al 2015).…”
Section: Hepatitis B and C Virusesmentioning
confidence: 99%