Evidence map›Paper›PMID 34269522›Full record

ArticlePharmacology research & perspectives2021

Novel G-CSF conjugated anionic globular dendrimer: Preparation and biological activity assessment.

Seyed Shahaboddin Mousavi Motlagh, Mohammad Seyedhamzeh, Reza Ahangari Cohan, Mehdi Shafiee Ardestani, Behrouz Vaziri, Kayhan Azadmanesh, Sahar Saberi, Vahideh Masoumi

Open access · goldAbstract read
In one paragraph

Article in Pharmacology research & perspectives, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.1field-weighted citation impact, top 56% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. 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

8 authors at 3 institutions in 1 country.

Seyed Shahaboddin Mousavi MotlaghDepartment of Nanobiotechnology, New Technologies Research Group, Pasteur Institute of Iran, Tehran, Iran.
Mohammad SeyedhamzehFaculty of Pharmacy, Tehran University of Medical Sciences, Tehran, Iran.
Reza Ahangari CohanDepartment of Nanobiotechnology, New Technologies Research Group, Pasteur Institute of Iran, Tehran, Iran.ORCID 0000-0002-0490-4184
Mehdi Shafiee ArdestaniFaculty of Pharmacy, Tehran University of Medical Sciences, Tehran, Iran.
Behrouz VaziriBiotechnology Research Center, Pasteur Institute of Iran, Tehran, Iran.
Kayhan AzadmaneshDepartment of Molecular Virology, Pasteur Institute of Iran, Tehran, Iran.
Sahar SaberiDepartment of Biotechnology, Food and Drug Control Laboratories, National Food and Drug Organization, Tehran, Iran.
Vahideh MasoumiDepartment of Biotechnology, Food and Drug Control Laboratories, National Food and Drug Organization, Tehran, Iran.
Pasteur Institute of Iran · IRIran Nanohealth Committee Food and Drug Organization · IRTehran University of Medical Sciences · IR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The most crucial role of granulocyte colony-stimulating factor (G-CSF) in the body is to increase the strength of immune system. In recent years, research on the use of nanoparticles in pharmaceuticals has been considered, most of which have been for drug-loading purposes. In this study, a novel G-CSF conjugated dendrimer was synthesized and characterized using different techniques. In vitro cytotoxicity was assessed on A549 and L929 cells, while abnormal toxicity was studied in mice. In vitro and in vivo biological activities were assessed in NFS60 cells and rats, respectively. In addition, in vivo distribution, plasma half-life, and histopathological effect were studied in rat. The characterization tests confirmed the successful conjugation. There was no difference between G-CSF cytotoxicity before and after conjugation, and no difference with the control group. No mice showed abnormal toxicity. Although in vitro biological activity revealed both conjugated and free G-CSF promote proliferation cells, biological activity decreased significantly after conjugation about one-third of the unconjugated form. Nonetheless, in vivo biological activity of conjugated G-CSF increased by more than 2.5-fold relative to the unconjugated form, totally. Fortunately, no histopathologic adverse effect was observed in vital rat tissues. Also, in vivo distribution of the conjugate was similar to the native protein with an enhanced terminal half-life. Our data revealed that G-CSF conjugated dendrimer could be considered as a candidate to improve the in vivo biological activity of G-CSF. Moreover, multivalent capability of the dendrimer may be used for other new potentials of G-CSF in future perspectives.

Indexed as

DendrimersGranulocyte Colony-Stimulating FactorAnimalsCell LineHeartHumansKidneyLiverMaleMiceRatsTissue DistributionDendrimersGranulocyte Colony-Stimulating Factorbiodistributionbiological activityconjugatedendrimergranulocyte colony-stimulating factortoxicity

Identifiers

PMID34269522
PMCPMC8283867
OpenAlexW3180617874

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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.