Evidence map›Paper›PMID 32368050›Full record

ArticleInternational journal of nanomedicine2020

Antiviral Activity of Chitosan Nanoparticles Encapsulating Curcumin Against Hepatitis C Virus Genotype 4a in Human Hepatoma Cell Lines.

Samah A Loutfy, Mostafa H Elberry, Khaled Yehia Farroh, Hossam Taha Mohamed, Aya A Mohamed, ElChaimaa B Mohamed, Ahmed Hassan Ibrahim Faraag, Shaker A Mousa

RetractedErratum issuedOpen access · goldAbstract readRetracted Publication
In one paragraph

Article in International journal of nanomedicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It has been retracted, and should not be counted. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed
6.5field-weighted citation impact, top 2% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

45 citing papers in PubMed, 107 citations in OpenAlex.

  1. Characterization and bioactivity of Fusarium incarnatum Nano-chitosan.Journal, genetic engineering & biotechnology · 2026
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  6. Facile synthesis of FeScientific reports · 2024
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  18. Antiviral and cytotoxic effects of a traditional drugJournal of King Saud University. Science · 2022
    Article
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  20. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 5 institutions in 2 countries.

Samah A LoutfyVirology and Immunology Unit, Cancer Biology Department, National Cancer Institute, Cairo University, Cairo, Egypt.ORCID 0000-0001-5711-2079
Mostafa H ElberryVirology and Immunology Unit, Cancer Biology Department, National Cancer Institute, Cairo University, Cairo, Egypt.
Khaled Yehia FarrohNanotechnology and Advanced Materials Central Lab, Agricultural Research Center, Giza, Egypt.
Hossam Taha MohamedFaculty of Biotechnology, October University for Modern Sciences and Arts, 6th October, Giza, Egypt.ORCID 0000-0003-1989-5783
Aya A MohamedFaculty of Biotechnology, October University for Modern Sciences and Arts, 6th October, Giza, Egypt.
ElChaimaa B MohamedVirology and Immunology Unit, Cancer Biology Department, National Cancer Institute, Cairo University, Cairo, Egypt.
Ahmed Hassan Ibrahim FaraagBotany and Microbiology Department, Bioinformatics Center, Faculty of Science, Helwan University, Cairo, Egypt.ORCID 0000-0002-2568-6059
Shaker A MousaThe Pharmaceutical Research Institute, Albany College of Pharmacy and Health Sciences, Rensselaer, NY, USA.ORCID 0000-0002-9294-015X
Cairo University · EGAgricultural Research Center · EGAlbany College of Pharmacy and Health Sciences · USHelwan University · EGOctober University of Modern Sciences and Arts · EG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeCurrent direct-acting antiviral agents for treatment of hepatitis C virus genotype 4a (HCV-4a) have been reported to cause adverse effects, and therefore less toxic antivirals are needed. This study investigated the role of curcumin chitosan (CuCs) nanocomposite as a potential anti-HCV-4a agent in human hepatoma cells Huh7.

methodsDocking of curcumin and CuCs nanocomposite and binding energy calculations were carried out. Chitosan nanoparticles (CsNPs) and CuCs nanocomposite were prepared with an ionic gelation method and characterized with TEM, zeta size and potential, and HPLC to calculate encapsulation efficiency. Cytotoxicity studies were performed on Huh7 cells using MTT assay and confirmed with cellular and molecular assays. Anti-HCV-4a activity was determined using real-time PCR and Western blot.

resultsThe strength of binding interactions between protein ligand complexes gave scores with NS3 protease, NS5A polymerase, and NS5B polymerase of -124.91, -159.02, and -129.16, for curcumin respectively, and -68.51, -54.52, and -157.63 for CuCs nanocomposite, respectively. CuCs nanocomposite was prepared at sizes 29-39.5 nm and charges of 33 mV. HPLC detected 4% of curcumin encapsulated into CsNPs. IC50 was 8 µg/mL for curcumin and 25 µg/mL for the nanocomposite on Huh7 but was 25.8 µg/mL and 34 µg/mL on WISH cells. CsNPs had no cytotoxic effect on tested cell lines. Apoptotic genes' expression revealed the caspase-dependent pathway mechanism. CsNPs and CuCs nanocomposite demonstrated 100% inhibition of viral entry and replication, which was confirmed with HCV core protein expression.

conclusionCuCs nanocomposite inhibited HCV-4a entry and replication compared to curcumin alone, suggesting its potential role as an effective therapeutic agent.

Indexed as

Antiviral AgentsCell LineChitosanCurcuminDEAD-box RNA HelicasesGenotypeHepacivirusHumansLiver NeoplasmsNanoparticlesNucleoside-TriphosphataseRNA-Dependent RNA PolymeraseSerine EndopeptidasesViral Core ProteinsViral Nonstructural ProteinsViral ProteasesAntiviral AgentsChitosanCurcuminDEAD-box RNA HelicasesNS3 protein, hepatitis C virusNS-5 protein, hepatitis C virusnucleocapsid protein, Hepatitis C virusNucleoside-TriphosphataseRNA-Dependent RNA PolymeraseSerine EndopeptidasesViral Core ProteinsViral Nonstructural ProteinsViral Proteasescaspase-dependent pathwaychitosan curcumin nanocompositedockinghepatitis C virus genotype 4aHuh7

Identifiers

PMID32368050
PMCPMC7184126
OpenAlexW3019909455

What Socratic holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.