Evidence map›Paper›PMID 39771406›Full record

ArticlePolymers2024

Characterization and Evaluation of Zero-Order Release System Comprising Glycero-(9,10-trioxolane)-trialeate and PLA: Opportunity for Packaging and Biomedicine Applications.

Olga V Alexeeva, Marina L Konstantinova, Valentina Siracusa, Vyacheslav V Podmasterev, Levon Yu Martirosyan, Olga K Karyagina, Sergey S Kozlov, Sergey M Lomakin, Ilya V Tretyakov, Tuyara V Petrova and 1 more

Abstract read
In one paragraph

Article in Polymers, 2024. 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
–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

1 citing paper in PubMed.

  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

11 authors.

Olga V AlexeevaEmanuel Institute of Biochemical Physics of Russian Academy of Sciences, 119334 Moscow, Russia.ORCID 0000-0001-8982-3959
Marina L KonstantinovaEmanuel Institute of Biochemical Physics of Russian Academy of Sciences, 119334 Moscow, Russia.
Valentina SiracusaDepartment of Chemical Science (DSC), University of Catania, Viale A. Doria 6, 95125 Catania, Italy.ORCID 0000-0001-9055-5082
Vyacheslav V PodmasterevEmanuel Institute of Biochemical Physics of Russian Academy of Sciences, 119334 Moscow, Russia.
Levon Yu MartirosyanEmanuel Institute of Biochemical Physics of Russian Academy of Sciences, 119334 Moscow, Russia.ORCID 0000-0003-1769-6377
Olga K KaryaginaEmanuel Institute of Biochemical Physics of Russian Academy of Sciences, 119334 Moscow, Russia.
Sergey S KozlovEmanuel Institute of Biochemical Physics of Russian Academy of Sciences, 119334 Moscow, Russia.ORCID 0000-0002-8660-5646
Sergey M LomakinEmanuel Institute of Biochemical Physics of Russian Academy of Sciences, 119334 Moscow, Russia.ORCID 0000-0003-3191-8415
Ilya V TretyakovN.N. Semenov Federal Research Center for Chemical Physics Russian Academy of Sciences, 119991 Moscow, Russia.
Tuyara V PetrovaN.N. Semenov Federal Research Center for Chemical Physics Russian Academy of Sciences, 119991 Moscow, Russia.
Alexey L IordanskiiN.N. Semenov Federal Research Center for Chemical Physics Russian Academy of Sciences, 119991 Moscow, Russia.ORCID 0000-0003-0771-0825

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Glycerol-(9,10-trioxolane) trioleate (OTOA) is a promising material that combines good plasticizing properties for PLA with profound antimicrobial activity, which makes it suitable for application in state-of-the-art biomedical and packaging materials with added functionality. On the other hand, application of OTOA in PLA-based antibacterial materials is hindered by a lack of knowledge on kinetics of the OTOA release. In this work, the release of glycero-(9,10-trioxolane) trioleate (OTOA) from PLA films with 50% OTOA content was studied during incubation in normal saline solution, and for the first time, the kinetics of OTOA release from PLA film was evaluated. Morphological, thermal, structural and mechanical properties of the PLA + 50% OTOA films were studied during incubation in normal saline and corresponding OTOA release using differential scanning calorimetry (DSC), X-ray diffraction (XRD), Fourier-transform infrared (FTIR) spectroscopy and mechanical tests. It was confirmed by DSC and XRD that incubation in the saline solution and corresponding OTOA release from PLA film does not lead to significant changes in the structure of the polymer matrix. Thus, the formation of more disturbed α' crystalline phase of PLA due to partial hydrolysis of amorphous zones and/or most unstable crystallites in the PLA/OTOA semi-crystalline structure was observed. The degree of crystallinity of PLA + OTOA film was also slightly increased at the prolonged stages of OTOA release. PLA + 50% OTOA film retained its strength properties after incubation in normal saline, with a slight increase in the elastic modulus and tensile strength, accompanied by a significant decrease in relative elongation at break. The obtained results showed that PLA + 50% OTOA film could be characterized by sustained OTOA release with the amount of released OTOA exceeding 50% of the initial content in the PLA film. The OTOA release profile was close to zero-order kinetics, which is beneficial in order to provide stable drug release pattern. Developed PLA + 50% OTOA films showed a strong and stable antibacterial effect against

Indexed as

drug releasefilmsozonidepolylactic acidtrioleate

Identifiers

PMID39771406
PMCPMC11679401

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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.