Evidence map›Paper›PMID 39355301›Full record

ArticleBeilstein journal of nanotechnology2024

Synthesis, characterization and anticancer effect of doxorubicin-loaded dual stimuli-responsive smart nanopolymers.

Ömür Acet, Pavel Kirsanov, Burcu Önal Acet, Inessa Halets-Bui, Dzmitry Shcharbin, Şeyda Ceylan Cömert, Mehmet Odabaşı

Abstract read
In one paragraph

Article in Beilstein journal of nanotechnology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. Review
  3. 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

7 authors.

Ömür AcetVocational School of Health Science, Pharmacy Services Program, Tarsus University, Tarsus, Turkey.ORCID https://orcid.org/0000-0003-1864-5694
Pavel KirsanovInstitute of Biophysics and Cell Engineering of the National Academy of Sciences of Belarus, Minsk, Belarus.
Burcu Önal AcetFaculty of Arts and Science, Chemistry Department, Aksaray University, Aksaray, Turkey.
Inessa Halets-BuiInstitute of Biophysics and Cell Engineering of the National Academy of Sciences of Belarus, Minsk, Belarus.ORCID https://orcid.org/0000-0003-2614-9914
Dzmitry ShcharbinInstitute of Biophysics and Cell Engineering of the National Academy of Sciences of Belarus, Minsk, Belarus.ORCID https://orcid.org/0000-0002-1414-4465
Şeyda Ceylan CömertFaculty of Arts and Science, Chemistry Department, Aksaray University, Aksaray, Turkey.
Mehmet OdabaşıFaculty of Arts and Science, Chemistry Department, Aksaray University, Aksaray, Turkey.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Nanopolymers represent a significant group of delivery vehicles for hydrophobic drugs. In particular, dual stimuli-responsive smart polymer nanomaterials might be extremely useful for drug delivery and release. We analyzed the possibility to include the known antitumor drug doxorubicin (DOX), which has antimitotic and antiproliferative effects, in a nanopolymer complex. Thus, doxorubicin-loaded temperature- and pH-sensitive smart nanopolymers (DOX-SNPs) were produced. Characterizations of the synthesized nanostructures were carried out including zeta potential measurements, Fourier-transform infrared spectroscopy, and scanning electron microscopy. The loading capacity of the nanopolymers for DOX was investigated, and encapsulation and release studies were carried out. In a final step, the cytotoxicity of the DOX-nanopolymer complexes against the HeLa cancer cell line at different concentrations and incubation times was studied. The DOX release depended on temperature and pH value of the release medium, with the highest release at pH 6.0 and 41 °C. This effect was similar to that observed for the commercial liposomal formulation of doxorubicin Doxil. The obtained results demonstrated that smart nanopolymers can be efficiently used to create new types of doxorubicin-based drugs.

Indexed as

cancer cell line HeLacytotoxicitydoxorubicindrug deliverysmart nanopolymerstemperature- and pH-sensitive nanopolymer

Identifiers

PMID39355301
PMCPMC11443663

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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.