Evidence map›Paper›PMID 28583153›Full record

ArticleBMC infectious diseases2017

In vitro antibacterial activity of poly (amidoamine)-G7 dendrimer.

Mitra Gholami, Rashin Mohammadi, Mohsen Arzanlou, Fakhraddin Akbari Dourbash, Ebrahim Kouhsari, Gharib Majidi, Seyed Mohsen Mohseni, Shahram Nazari

Abstract read
In one paragraph

Article in BMC infectious diseases, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
–field-weighted citation impact
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

24 citing papers in PubMed.

  1. Investigating the cytotoxic effect of polyethyleneimine nanodendrimer on fibroblast cells.International journal of physiology, pathophysiology and pharmacology · 2026
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  8. Regulation ofPharmaceutics · 2023
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  12. Enhanced photocatalytic activity of FeJournal of environmental health science & engineering · 2022
    Article
  13. Polymeric nanoparticles-Promising carriers for cancer therapy.Frontiers in bioengineering and biotechnology · 2022
    Review
  14. Drug delivery carriers with therapeutic functions.Advanced drug delivery reviews · 2021
    Review
  15. Article
  16. Review
  17. Review
  18. Article
  19. Poly (amidoamine) generation 6 functionalized FeJournal of environmental health science & engineering · 2020
    Article
  20. Review
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.

Mitra GholamiDepartment of Environmental Health Engineering, School of public Health, Iran University of Medical Sciences, Tehran, Iran.
Rashin MohammadiDepartment of Life Science Engineering, Faculty of New Science and Technology, University of Tehran, Tehran, Iran.
Mohsen ArzanlouDepartment of Microbiology, School of Medicine, Ardabil University of Medical Sciences, Ardabil, Iran.
Fakhraddin Akbari DourbashDepartment of Materials science and Engineering, Tarbiat Modares University, Tehran, Iran.
Ebrahim KouhsariDepartment of Microbiology, School of Medical, Iran University of Medical Sciences, Tehran, Iran.
Gharib MajidiDepartment of Environmental Health Engineering, School of public Health, Qom University of Medical Sciences, Qom, Iran.
Seyed Mohsen MohseniDepartment of Environmental Health Engineering, School of public Health, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Shahram NazariDepartment of Environmental Health Engineering, Developmental Center for Student Research and Technology Talent, School of Public Health, Iran University of Medical Sciences, Tehran, Iran. shahramnazari73@yahoo.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundNano-scale dendrimers are synthetic macromolecules that frequently used in medical and health field. Traditional anibiotics are induce bacterial resistence so there is an urgent need for novel antibacterial drug invention. In the present study seventh generation poly (amidoamine) (PAMAM-G7) dendrimer was synthesized and its antibacterial activities were evaluated against representative Gram- negative and Gram-positive bacteria.

methodsPAMAM-G7 was synthesized with divergent growth method. The structural and surface of PAMAM-G7 were investigated by transmission electron microscopy, scanning electron microscope and fourier transform infrared. Pseudomonas. aeruginosa (n = 15), E. coli (n = 15), Acinetobacter baumanni (n = 15), Shigella dysenteriae (n = 15), Klebsiella pneumoniae (n = 10), Proteus mirabilis (n = 15), Staphylococcus aureus (n = 15) and Bacillus subtilis (n = 10) have been used for antibacterial activity assay. Additionally, representative standard strains for each bacterium were included. Minimum Inhibitory Concentration (MIC) was determined using microdilution method. Subsequently, Minimum Bactericidal Concentration (MBC) was determined by sub-culturing each of the no growth wells onto Mueller Hinton agar medium. The cytotoxicity of PAMAM-G7 dendrimer were evaluated in HCT116 and NIH 3 T3 cells by MTT assay.

resultsThe average size of each particle was approximately 20 nm. PAMAM-G7 was potentially to inhibit both Gram positive and gram negative growth. The MIC50 and MIC90 values were determined to be 2-4 μg/ml and 4-8 μg/ml, respectively. The MBC50 and MBC90 values were found to be 64-256 μg/ml and 128-256 μg/ml, respectively. The cytotoxity effect of dendrimer on HCT116 and NIH 3 T3 cells is dependent upon exposure time to and concentration of dendrimers. The most reduction (44.63 and 43%) in cell viability for HCT116 and NIH 3 T3 cells was observed at the highest concentration, 0.85 μM after 72 h treatmentm, respectively.

conclusionsThis study we conclude that PAMAM-G7 dendrimer could be a potential candidate as a novel antibacterial agent.

Indexed as

AnimalsAnti-Bacterial AgentsDendrimersDrug Evaluation, PreclinicalEscherichia coliGram-Negative BacteriaGram-Positive BacteriaHCT116 CellsHumansKlebsiella pneumoniaeMiceMicrobial Sensitivity TestsMicroscopy, Electron, TransmissionNIH 3T3 CellsPseudomonas aeruginosaSpectroscopy, Fourier Transform InfraredAnti-Bacterial AgentsDendrimersPAMAM StarburstAntibacterial activityCytotoxicityGram-negative bacteriaGram-positive bacteriaPolyamidoamine-G7

Identifiers

PMID28583153
PMCPMC5460590

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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.