Evidence map›Paper›PMID 33800115›Full record

ArticleMolecules (Basel, Switzerland)2021

Preparation and Optimization of PEGylated Nano Graphene Oxide-Based Delivery System for Drugs with Different Molecular Structures Using Design of Experiment (DoE).

Mohammad Hossain Shariare, Abdullah-Al Masum, Sultan Alshehri, Fars K Alanazi, Jamal Uddin, Mohsin Kazi

Open access · goldAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.0field-weighted citation impact, top 28% 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

9 citing papers in PubMed, 17 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

6 authors at 3 institutions in 3 countries.

Mohammad Hossain ShariareDepartment of Pharmaceutical Sciences, North South University, Dhaka 1229, Bangladesh.ORCID 0000-0001-5176-3647
Abdullah-Al MasumDepartment of Pharmaceutical Sciences, North South University, Dhaka 1229, Bangladesh.
Sultan AlshehriDepartment of Pharmaceutics, College of Pharmacy, King Saud University, Riyadh 11451, Saudi Arabia.ORCID 0000-0002-0922-9819
Fars K AlanaziDepartment of Pharmaceutics, College of Pharmacy, King Saud University, Riyadh 11451, Saudi Arabia.
Jamal UddinCenter for Nanotechnology, Department of Natural Sciences, Coppin State University, Baltimore, MD 21216, USA.ORCID 0000-0002-6714-9286
Mohsin KaziDepartment of Pharmaceutics, College of Pharmacy, King Saud University, Riyadh 11451, Saudi Arabia.ORCID 0000-0002-5611-0378
King Saud University · SANorth South University · BDCoppin State University · US

Funding

Deanship of Scientific Research, King Saud University 1435-017
6 · The paper itself

Abstract

Graphene oxide (GO), due to its 2D planar structure and favorable physical and chemical properties, has been used in different fields including drug delivery. This study aimed to investigate the impact of different process parameters on the average size of drug-loaded PEGylated nano graphene oxide (NGO-PEG) particles using design of experiment (DoE) and the loading of drugs with different molecular structures on an NGO-PEG-based delivery system. GO was prepared from graphite, processed using a sonication method, and functionalized using PEG 6000. Acetaminophen (AMP), diclofenac (DIC), and methotrexate (MTX) were loaded onto NGO-PEG particles. Drug-loaded NGO-PEG was then characterized using dynamic light scattering (DLS), Fourier transform infrared (FTIR), scanning electron microscopy (SEM), differential scanning calorimetry (DSC), XRD. The DLS data showed that the drug-loaded NGO-PEG suspensions were in the size range of 200 nm-1.3 µm. The sonication time and the stirring rate were found to be the major process parameters which affected the average size of the drug-loaded NGO-PEG. FTIR, DSC, XRD, and SEM demonstrated that the functionalization or coating of the NGO occurred through physical interaction using PEG 6000. Methotrexate (MTX), with the highest number of aromatic rings, showed the highest loading efficiency of 95.6% compared to drugs with fewer aromatic rings (diclofenac (DIC) 70.5% and acetaminophen (AMP) 65.5%). This study suggests that GO-based nano delivery systems can be used to deliver drugs with multiple aromatic rings with a low water solubility and targeted delivery (e.g., cancer).

Indexed as

AcetaminophenCalorimetry, Differential ScanningDiclofenacDrug CarriersDrug Delivery SystemsGraphiteMethotrexateMicroscopy, Electron, ScanningMolecular StructureNanoparticlesParticle SizePolyethylene GlycolsSolubilitySpectroscopy, Fourier Transform InfraredX-Ray DiffractionAcetaminophenDiclofenacDrug Carriersgraphene oxideGraphiteMethotrexatePolyethylene Glycol 6000Polyethylene Glycolsacetaminophenaromatic ringdiclofenacgraphene oxide (GO)loading efficiencymethotrexatenano graphene oxide (NGO)NGO-PEG

Identifiers

PMID33800115
PMCPMC7962195
OpenAlexW3133852781

What OpenQuestion holds

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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.