Evidence map›Paper›PMID 42884962›Full record

ArticlePolymers2026

Biocomposite Microparticles Incorporating Ibuprofen and ZnO Nanoparticles for Controlled Drug Delivery and Antimicrobial Therapy.

Delia Mihaela Rata, Gisela Trifas, Raluca Somoghi, Anca Niculina Cadinoiu, Doina Simona Matiut, Cosmin Teodor Mihai, Oana-Maria Daraba, Ketan Kuperkar, Leonard Ionut Atanase

Abstract read
In one paragraph

Article in Polymers, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

9 authors.

Delia Mihaela RataFaculty of Medicine, "Apollonia" University of Iasi, 700511 Iasi, Romania.ORCID 0000-0002-4917-9406
Gisela Trifas"Cristofor Simionescu" Faculty of Chemical Engineering and Environmental Protection, "Gheorghe Asachi" Technical University of Iasi, 700050 Iasi, Romania.
Raluca SomoghiFaculty of Petroleum Refining and Petrochemistry, Petroleum-Gas University of Ploiesti, 100680 Ploiesti, Romania.ORCID 0000-0002-7648-3147
Anca Niculina CadinoiuFaculty of Medicine, "Apollonia" University of Iasi, 700511 Iasi, Romania.ORCID 0000-0002-3708-3992
Doina Simona MatiutMedical Investigations Praxis SRL, 700376 Iasi, Romania.
Cosmin Teodor MihaiMedical Investigations Praxis SRL, 700376 Iasi, Romania.ORCID 0000-0002-0945-5437
Oana-Maria DarabaFaculty of Medicine, "Apollonia" University of Iasi, 700511 Iasi, Romania.
Ketan KuperkarDepartment of Chemistry, Sardar Vallabhbhai National Institute of Technology (SVNIT), Ichchhanath, Surat 395007, Gujarat, India.
Leonard Ionut AtanaseFaculty of Medicine, "Apollonia" University of Iasi, 700511 Iasi, Romania.ORCID 0000-0002-3657-1492

Funding

Ministry of Research, Innovation, and Digitization PN-IV-P7-7.1-PED-2024-1065
6 · The paper itself

Abstract

Preparation of complex biomaterials capable of providing both controlled drug delivery and an increased antimicrobial effect without affecting healthy cells remains a major challenge in pharmaceutical and biomedical applications. This study reports the successful preparation of biocomposite microparticles based on carboxymethyl chitosan and poly (vinyl alcohol), co-loaded with zinc oxide nanoparticles with antimicrobial effect and Ibuprofen with anti-inflammatory, antipyretic, and analgesic effect. An environmentally friendly water-in-oil emulsion method using DL-limonene as a biocompatible oil phase was used to obtain these microparticles. FTIR analysis confirmed the formation of intermolecular ester and amide bonds and the successful incorporation of zinc oxide nanoparticles into the polymeric matrix. The obtained microparticles exhibited diameters ranging from 533 to 1054 nm and provided a biphasic Ibuprofen release profile, characterized by an initial burst release within the first 3 h followed by sustained diffusion-controlled release, achieving cumulative drug release of 84-100%. Biocomposite microparticles presented excellent hemocompatibility, with hemolysis values between 0.41% and 2.47%. Moreover, after 24 h of exposure to microparticles, human dermal fibroblasts exhibited a cellular viability ranging from 82.24% to 94.22% whereas prolonged treatment for 48 h resulted in a slight decrease of cell viability until 74.88%. Biocomposite microparticles exhibited notable antimicrobial activity against

Indexed as

antimicrobial activitycell viabilitydrug deliveryhemocompatibilitypolymeric microparticles

Identifiers

PMID42884962
PMCPMC13666744

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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.