Evidence map›Paper›PMID 32103939›Full record

ArticleInternational journal of nanomedicine2020

Dual-Ligand Functionalized Core-Shell Chitosan-Based Nanocarrier for Hepatocellular Carcinoma-Targeted Drug Delivery.

Amr Hefnawy, Islam H Khalil, Kholoud Arafa, Marwan Emara, Ibrahim M El-Sherbiny

Open access · goldAbstract read
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. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.4field-weighted citation impact, top 12% 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

19 citing papers in PubMed, 64 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 2 institutions in 1 country.

Amr HefnawyNanomaterials Lab, Center of Material Science (CMS), Zewail City of Science and Technology, Giza 12578, Egypt.ORCID 0000-0002-5340-7571
Islam H KhalilNanomaterials Lab, Center of Material Science (CMS), Zewail City of Science and Technology, Giza 12578, Egypt.ORCID 0000-0002-6804-4144
Kholoud ArafaCenter for Aging and Associated Diseases, Zewail City of Science and Technology, Giza 12578, Egypt.ORCID 0000-0002-1181-3977
Marwan EmaraCenter for Aging and Associated Diseases, Zewail City of Science and Technology, Giza 12578, Egypt.ORCID 0000-0002-9499-1655
Ibrahim M El-SherbinyNanomaterials Lab, Center of Material Science (CMS), Zewail City of Science and Technology, Giza 12578, Egypt.ORCID 0000-0002-8179-437X
Zewail City of Science and Technology · EGMisr University for Science and Technology · EG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionHepatocellular carcinoma represents a major health problem with the related death numbers still increasing. Active targeting is considered an attractive choice for the development of selective therapeutics with limited side effects and improved efficiency. In this study, we report the design, development and evaluation of a novel dual-ligand functionalized core-shell chitosan-based nanocarrier for the selective delivery of doxorubicin (DOX) for treatment of hepatocellular carcinoma (HCC).

methodsFollowing factorial design experiments, DOX was initially complexed with negatively charged carboxymethyl chitosan-g-poly(acrylate) and then the complex was coated with a positively charged dual-ligand (lactobionic acid and glycyrrhetinic acid)-conjugated chitosan. The developed active targeting system was then tested in vitro on Hep-G2 cells using flow cytometry and fluorescence imaging.

resultsThe obtained results proved the ability of the dual-ligand system to enhance the intracellular uptake of the drug by 4-fold and 8-fold after 4 hrs and 24 hrs of incubation, respectively. The efficiency of the dual-ligand functionalized nanoparticles was also tested in vivo on Wistar rats with induced liver tumors. Testing of serum biomarkers (albumin, creatinine, urea, alpha fetoprotein, ALT, AST and ALP) in addition to histopathological microscopic examination of liver, kidney and heart tissues confirmed the enhanced safety of the developed targeted nanocarrier system compared to the conventional DOX. DISCUSSION: The developed targeted system showed improved intracellular drug delivery and uptake as well as enhanced safety profile. The nanoparticles were formed based on electrostatic interactions providing the flexibility that allows their use as a model for delivery of other drugs and other targets.

Indexed as

AnimalsCarcinoma, HepatocellularChitosanDisaccharidesDoxorubicinDrug CarriersDrug Delivery SystemsFemaleGlycyrrhetinic AcidHep G2 CellsHumansLiver Neoplasms, ExperimentalNanoparticlesRats, Wistarcarboxymethyl-chitosanChitosanDisaccharidesDoxorubicinDrug CarriersGlycyrrhetinic Acidlactobionic acidcore-shell nanoparticlesdoxorubicindual targetingliver cancer

Identifiers

PMID32103939
PMCPMC7015065
OpenAlexW3005462413

What OpenQuestion holds

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LicenceCC BY-NC
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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 OpenQuestion graph.