Evidence map›Paper›PMID 36283561›Full record

ArticleInternational journal of biological macromolecules2023

Synthesis of bee venom loaded chitosan nanoparticles for anti-MERS-COV and multi-drug resistance bacteria.

Mohamed E Elnosary, Hesham A Aboelmagd, Manal A Habaka, Salem R Salem, Mehrez E El-Naggar

Open access · greenAbstract read
In one paragraph

Article in International journal of biological macromolecules, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
6.6field-weighted citation impact, top 3% 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

14 citing papers in PubMed, 40 citations in OpenAlex.

  1. Article
  2. Therapeutic Bioactivity Exerted by theMolecules (Basel, Switzerland) · 2025
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  4. Review
  5. Bioactive Compounds fromCurrent pharmaceutical biotechnology · 2025
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  6. Review
  7. Article
  8. Article
  9. Exploring biosurfactant fromFrontiers in bioengineering and biotechnology · 2024
    Article
  10. Frontiers in bioengineering and biotechnology · 2024
    Article
  11. Review
  12. Article
  13. Article
  14. Infection and drug resistance · 2023
    Article
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 3 institutions in 1 country.

Mohamed E ElnosaryAl-Azhar University, Faculty of Science, Botany and Microbiology Department, 11884 Nasr City, Cairo, Egypt. Electronic address: mohamed.elnosary@azhar.edu.eg.
Hesham A AboelmagdAl-Azhar University, Faculty of Science, Botany and Microbiology Department, Assiut 71524, Egypt.
Manal A HabakaMicrobiology and virology Department, Animal Health Research Institute, Zagazig, Sharkia, Egypt.
Salem R SalemDepartment of Biochemistry and Clinical Biochemistry, Military Medical Academy, Egypt.
Mehrez E El-NaggarTextile Research and Technology Institute, National Research Centre, 12622 Dokki, Cairo, Egypt.
Al-Azhar University · EGMilitary Medical Academy · EGNational Research Centre · EG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This study aims to fully exploit the natural compound; bee venom (BV) as a substance that can kill and inhibit the growth of microbes and viruses. For this target, BV was loaded onto a safe, natural, and economically inexpensive polymer; chitosan (Ch) in its nano-size form prepared using ionic gelation method in the presence of chemical crosslinking agent (sodium tripolyphosphate; TPP). The findings illustrated that chitosan nanoparticles (ChNPs) were prepared thru this method and exhibited spherical shape and average hydrodynamic size of 202 nm with a polydispersity index (PDI = 0.44). However, the size was increased to 221 nm with PDI (0.37) when chitosan nanoparticles were loaded with BV (ChNC). In addition, the particles of BV appeared as a core and chitosan nanoparticles as a shell implying the successful preparation of nanocomposite (ChNC). Encapsulation of BV into ChNPs with significantly small size distribution and good stability that protect these formed nanocomposites from agglomeration. The cytopathic effect (CPE) inhibition assay was used to identify potential antivirals for Middle East respiratory syndrome coronavirus (MERS-CoV). The response of the dose study was designed to influence the range of effectiveness for the chosen antiviral, i.e., the 50 % inhibitory concentration (IC

Indexed as

Bee VenomsChitosanMiddle East Respiratory Syndrome CoronavirusNanoparticlesAnti-Bacterial AgentsDrug Resistance, MultipleGram-Negative BacteriaGram-Positive BacteriaParticle SizeAnti-Bacterial AgentsBee VenomsChitosanBee venomChitosan nanoparticlesMDR bacteriaMERS

Identifiers

PMID36283561
PMCPMC9595425
OpenAlexW4307289466

What OpenQuestion holds

Textmetadata
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.