Evidence map›Paper›PMID 31686814›Full record

ArticleInternational journal of nanomedicine2019

Graphene-based hybrid nanoparticle of doxorubicin for cancer chemotherapy.

Nagaraja SreeHarsha, Rahul Maheshwari, Bandar E Al-Dhubiab, Muktika Tekade, Mukesh Chandra Sharma, Katharigatta N Venugopala, Rakesh Kumar Tekade, Abdullah M Alzahrani

Open access · goldAbstract read
In one paragraph

Article in International journal of nanomedicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
3.0field-weighted citation impact, top 9% 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

12 citing papers in PubMed, 60 citations in OpenAlex.

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  5. Iranian journal of basic medical sciences · 2022
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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

8 authors at 5 institutions in 4 countries.

Nagaraja SreeHarshaDepartment of Pharmaceutical Sciences, College of Clinical Pharmacy, King Faisal University, Al-Ahsa, Saudi Arabia.
Rahul MaheshwariNational Institute of Pharmaceutical Education and Research (NIPER) - Ahmedabad, Gandhinagar, Gujarat 382355, India.
Bandar E Al-DhubiabDepartment of Pharmaceutical Sciences, College of Clinical Pharmacy, King Faisal University, Al-Ahsa, Saudi Arabia.
Muktika TekadeSchool of Pharmacy, Devi Ahilya Vishwavidyalaya, Takshila Campus, Indore, MP 452001, India.
Mukesh Chandra SharmaSchool of Pharmacy, Devi Ahilya Vishwavidyalaya, Takshila Campus, Indore, MP 452001, India.
Katharigatta N VenugopalaDepartment of Pharmaceutical Sciences, College of Clinical Pharmacy, King Faisal University, Al-Ahsa, Saudi Arabia.
Rakesh Kumar TekadeNational Institute of Pharmaceutical Education and Research (NIPER) - Ahmedabad, Gandhinagar, Gujarat 382355, India.
Abdullah M AlzahraniDepartment of Biological Sciences, College of Science, King Faisal University, Al-Ahsa, Saudi Arabia.
King Faisal University · SADevi Ahilya Vishwavidyalaya · INDurban University of Technology · ZANarsee Monjee Institute of Management Studies · INNational Institute of Pharmaceutical Education and Research (NIPER) - Ahmedabad · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundProstate cancer (PC) has the highest prevalence in men and accounts for a high rate of neoplasia-related death. Doxorubicin (DOX) is one of the most widely used anti-neoplastic drugs for prostate cancer among others. However, it has low specificity and many side effects and affects normal cells. More recently, there have been newly developed drug delivery tools which are graphene or graphene-based, used to increase the specificity of the delivered drug molecules. The graphene derivatives possess both π-π stacking and increased hydrophobicity, factors that increase the likelihood of drug delivery. Despite this, the hydrophilicity of graphene remains problematic, as it induced problems with stability. For this reason, the use of a chitosan coating remains one way to modify the surface features of graphene.

methodIn this investigation, a hybrid nanoparticle that consisted of a DOX-loaded reduced graphene oxide that is stabilized with chitosan (rGOD-HNP) was developed.

resultThe newly developed rGOD-HNP demonstrated high biocompatibility and efficiency in entrapping DOX (~65%) and releasing it in a controlled manner (~50% release in 48 h). Furthermore, it was also demonstrated that rGOD-HNP can intracellularly deliver DOX and more specifically in PC-3 prostate cancer cells.

conclusionThis delivery tool offers a feasible and viable method to deliver DOX photo-thermally in the treatment of prostate cancer.

Indexed as

AnimalsApoptosisCell Line, TumorCell SurvivalChitosanDoxorubicinDrug Delivery SystemsDrug LiberationGraphiteHemolysisHumansHydrophobic and Hydrophilic InteractionsKineticsMiceNanoparticlesNeoplasmsChitosanDoxorubicingraphene oxideGraphitechitosangrapheneHNPhybrid nanoparticlesphotothermalprostate cancer

Identifiers

PMID31686814
PMCPMC6751552
OpenAlexW2973117858

What OpenQuestion 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 OpenQuestion graph.