Evidence map›Paper›PMID 35798154›Full record

ArticleChemosphere2022

CaZnO-based nanoghosts for the detection of ssDNA, pCRISPR and recombinant SARS-CoV-2 spike antigen and targeted delivery of doxorubicin.

Navid Rabiee, Omid Akhavan, Yousef Fatahi, Amir Mohammad Ghadiri, Mahsa Kiani, Pooyan Makvandi, Mohammad Rabiee, Mohammad Hossein Nicknam, Mohammad Reza Saeb, Rajender S Varma and 4 more

Open access · greenAbstract read
In one paragraph

Article in Chemosphere, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
4.8field-weighted citation impact, top 4% 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

10 citing papers in PubMed, 62 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

14 authors at 11 institutions in 7 countries.

Navid RabieeDepartment of Physics, Sharif University of Technology, P.O. Box 11155-9161, Tehran, Iran; School of Engineering, Macquarie University, Sydney, New South Wales, 2109, Australia; Department of Materials Science and Engineering, Pohang University of Science and Technology (POSTECH), 77 Cheongam-ro, Nam-gu, Pohang, Gyeongbuk, 37673, South Korea. Electronic address: nrabiee94@gmail.com.
Omid AkhavanDepartment of Physics, Sharif University of Technology, P.O. Box 11155-9161, Tehran, Iran.
Yousef FatahiDepartment of Pharmaceutical Nanotechnology, Faculty of Pharmacy, Tehran University of Medical Sciences, Tehran, Iran; Nanotechnology Research Centre, Faculty of Pharmacy, Tehran University of Medical Sciences, Tehran, Iran.
Amir Mohammad GhadiriDepartment of Chemistry, Sharif University of Technology, Tehran, Iran.
Mahsa KianiDepartment of Chemistry, Sharif University of Technology, Tehran, Iran.
Pooyan MakvandiIstituto Italiano di Tecnologia, Centre for Materials Interfaces, Viale Rinaldo Piaggio 34, 56025, Pontedera, Pisa, Italy.
Mohammad RabieeBiomaterial Group, Department of Biomedical Engineering, Amirkabir University of Technology, Tehran, Iran.
Mohammad Hossein NicknamMolecular Immunology Research Center, Tehran University of Medical Sciences, Tehran, Iran; Department of Immunology, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran.
Mohammad Reza SaebDepartment of Polymer Technology, Faculty of Chemistry, Gdánsk University of Technology, G. Narutowicza 11/12, 80-233, Gdánsk, Poland.
Rajender S VarmaRegional Centre of Advanced Technologies and Materials, Czech Advanced Technology and Research Institute, Palacky University, Šlechtitelů 27, 783 71, Olomouc, Czech Republic.
Milad AshrafizadehFaculty of Engineering and Natural Sciences, Sabanci University, Orta Mahalle, Üniversite Caddesi No. 27, Orhanlı, Tuzla, 34956, Istanbul, Turkey.
Ehsan Nazarzadeh ZareSchool of Chemistry, Damghan University, Damghan, 36716-41167, Iran.
Esmaeel SharifiDepartment of Tissue Engineering and Biomaterials, School of Advanced Medical Sciences and Technologies, Hamadan University of Medical Sciences, 6517838736, Hamadan, Iran.
Eder C LimaInstitute of Chemistry, Federal University of Rio Grande Do Sul (UFRGS), Porto Alegre, RS, Brazil. Electronic address: profederlima@gmail.com.
Sharif University of Technology · IRTehran University of Medical Sciences · IRAmirkabir University of Technology · IRDamghan University · IRGdańsk University of Technology · PLHamedan University of Medical Sciences · IRPiaggio (Italy) · ITPohang University of Science and Technology · KRRegional Centre of Advanced Technologies and Materials · CZSabancı Üniversitesi · TRUniversidade Federal do Rio Grande do Sul · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Overexpression of proteins/antigens and other gene-related sequences in the bodies could lead to significant mutations and refractory diseases. Detection and identification of assorted trace concentrations of such proteins/antigens and/or gene-related sequences remain challenging, affecting different pathogens and making viruses stronger. Correspondingly, coronavirus (SARS-CoV-2) mutations/alterations and spread could lead to overexpression of ssDNA and the related antigens in the population and brisk activity in gene-editing technologies in the treatment/detection may lead to the presence of pCRISPR in the blood. Therefore, the detection and evaluation of their trace concentrations are of critical importance. CaZnO-based nanoghosts (NGs) were synthesized with the assistance of a high-gravity technique at a 1,800 MHz field, capitalizing on the use of Rosmarinus officinalis leaf extract as the templating agent. A complete chemical, physical and biological investigation revealed that the synthesized NGs presented similar morphological features to the mesenchymal stem cells (MSCs), resulting in excellent biocompatibility, interaction with ssDNA- and/or pCRISPR-surface, through various chemical and physical mechanisms. This comprise the unprecedented synthesis of a fully inorganic nanostructure with behavior that is similar to MSCs. Furthermore, the endowed exceptional ability of inorganic NGs for detective sensing/folding of ssDNA and pCRISPR and recombinant SARS-CoV-2 spike antigen (RSCSA), along with in-situ hydrogen peroxide detection on the HEK-293 and HeLa cell lines, was discerned. On average, they displayed a high drug loading capacity of 55%, and the acceptable internalizations inside the HT-29 cell lines affirmed the anticipated MSCs-like behavior of these inorganic-NGs.

Indexed as

DNA, Single-StrandedDoxorubicinNanoparticle Drug Delivery SystemSARS-CoV-2Spike Glycoprotein, CoronavirusCalciumHEK293 CellsHeLa CellsHumansZinc OxideCalciumDNA, Single-StrandedDoxorubicinNanoparticle Drug Delivery SystemSpike Glycoprotein, Coronavirusspike protein, SARS-CoV-2Zinc OxideGene deliveryIn-situ biosensorNanoghostspCRISPRSARS-CoV-2ssDNA

Identifiers

PMID35798154
PMCPMC9251674
OpenAlexW4283794624

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.