Evidence map›Paper›PMID 36145592›Full record

ArticlePharmaceutics2022

A Novel C@Fe@Cu Nanocomposite Loaded with Doxorubicin Tailored for the Treatment of Hepatocellular Carcinoma.

Mohammed S Saddik, Mahmoud M A Elsayed, Amany A Abdel-Rheem, Mohamed A El-Mokhtar, Eisa S Mosa, Mostafa F Al-Hakkani, Samah A Al-Shelkamy, Ali Khames, Mohamed A Daha, Jelan A Abdel-Aleem

Open access · goldAbstract read
In one paragraph

Article in Pharmaceutics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.0field-weighted citation impact, top 15% 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

13 citing papers in PubMed, 25 citations in OpenAlex.

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  5. GdVOInternational journal of molecular sciences · 2024
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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

10 authors at 5 institutions in 1 country.

Mohammed S SaddikDepartment of Pharmaceutics and Clinical Pharmacy, Faculty of Pharmacy, Sohag University, Sohag 82524, Egypt.ORCID 0000-0001-5236-7419
Mahmoud M A ElsayedDepartment of Pharmaceutics and Clinical Pharmacy, Faculty of Pharmacy, Sohag University, Sohag 82524, Egypt.ORCID 0000-0001-9547-2243
Amany A Abdel-RheemDepartment of Pharmaceutics and Clinical Pharmacy, Faculty of Pharmacy, Sohag University, Sohag 82524, Egypt.
Mohamed A El-MokhtarDepartment of Medical Microbiology and Immunology, Faculty of Medicine, Assiut University, Assiut 71515, Egypt.ORCID 0000-0003-1943-8419
Eisa S MosaMining, Metallurgy and Petroleum Engineering Department, Al-Azhar University, Nasr City, Cairo 11371, Egypt.
Mostafa F Al-HakkaniDepartment of Chemistry, Faculty of Science, Al-Azhar University, Assiut Branch, Assiut 71524, Egypt.ORCID 0000-0003-0004-8939
Samah A Al-ShelkamyDepartment of Physics, Faculty of Science, New Valley University, El-Kharja 72511, Egypt.
Ali KhamesDepartment of Pharmacology and Toxicology, Faculty of Pharmacy, Sohag University, Sohag 82524, Egypt.
Mohamed A DahaProduction Engineering Department, Faculty of Engineering, Alexandria University, El-Chatby, Alexandria 21544, Egypt.ORCID 0000-0002-3443-0514
Jelan A Abdel-AleemDepartment of Industrial Pharmacy, Faculty of Pharmacy, Assiut University, Assiut 71515, Egypt.
Sohag University · EGAl-Azhar University · EGAssiut University · EGAlexandria University · EGSouth Valley University · EG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

High mortality and morbidity rates are related to hepatocellular carcinoma (HCC), which is the most prevalent type of liver cancer. A new vision for cancer treatment and cancer cell targeting has emerged with the application of nanotechnology, which reduces the systemic toxicity and adverse effects of chemotherapy medications while increasing their effectiveness. It was the goal of the proposed work to create and investigate an anticancer C@Fe@Cu nanocomposite (NC) loaded with Doxorubicin (DOX) for the treatment of HCC. Scanning and transmission electron microscopes (SEM and TEM) were used to examine the morphology of the produced NC. The formulation variables (DOX content, C@Fe@Cu NC weight, and stirring speed) were analyzed and optimized using Box-Behnken Design (BBD) and Response Surface Methodology (RSM). Additionally, X-ray diffraction patterns (XRD) and Fourier Transform Infrared (FTIR) were investigated. Doxorubicin and DOX- loaded C@Fe@Cu NC (DOX-C@Fe@Cu NC) were also assessed against HEPG2 cells for anticancer efficacy (Hepatic cancer cell line). The results revealed the formation of C@Fe@Cu NC with a mean size of 7.8 nm. A D-R model with a mean size of 24.1 nm best fits the adsorption behavior of DOX onto the C@Fe@Cu NC surface. DOX-C@Fe@Cu NC has also been demonstrated to have a considerably lower IC50 and higher cytotoxicity than DOX alone in an in vitro investigation. Therefore, DOX-C@Fe@Cu NC is a promising DOX delivery vehicle for the full recovery of HCC.

Indexed as

C@Fe@Cu nanocompositedoxorubicinhepatocellular carcinomaliver cancer

Identifiers

PMID36145592
PMCPMC9505246
OpenAlexW4294168363

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.