Evidence map›Paper›PMID 42738788›Full record

ArticleMolecules (Basel, Switzerland)2026

Anti-Inflammatory Effects of Artocarpin-Loaded Chitosan Microparticles on Inflammatory Chondrocytes.

Piyapan Manklinniam, Ratsada Praphasawat, Arthid Thim-Uam, Grissana Pook-In, Jarupa Viyoch, Atchariya Yosboonruang

Abstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 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

6 authors.

Piyapan ManklinniamDivision of Microbiology and Parasitology, School of Medical Sciences, University of Phayao, Phayao 56000, Thailand.
Ratsada PraphasawatDepartment of Pathology, School of Medicine, University of Phayao, Phayao 56000, Thailand.ORCID 0000-0001-8082-1623
Arthid Thim-UamDivision of Biochemistry, School of Medical Sciences, University of Phayao, Phayao 56000, Thailand.
Grissana Pook-InDivision of Microbiology and Parasitology, School of Medical Sciences, University of Phayao, Phayao 56000, Thailand.
Jarupa ViyochDepartment of Pharmaceutical Technology, Faculty of Pharmaceutical Sciences, Naresuan University, Phitsanulok 65000, Thailand.
Atchariya YosboonruangDivision of Microbiology and Parasitology, School of Medical Sciences, University of Phayao, Phayao 56000, Thailand.ORCID 0000-0001-9869-0529

Funding

Frontier Research and Innovation Cluster Fund, Naresuan University, Thailand University R2569C006National Science, Research and Innovation Fund (NSRF) through the Program Management Unit for Human Resources and Institutional Development, Research and Innovation (PMU-B) under the Postdoctoral/Post-master Fellowship Program B13F680066University of Phayao and the Thailand Science Research and Innovation Fund under the Funda-mental Fund 2026 2368/2568
6 · The paper itself

Abstract

Artocarpin is a promising bioactive compound with anti-inflammatory potential; however, its limited aqueous solubility may restrict its direct biological application. Therefore, artocarpin-loaded chitosan microparticles (CSPs/AE) were prepared as a biocompatible carrier to improve artocarpin delivery. This study aimed to evaluate the cytocompatibility, antioxidant activity, and anti-inflammatory effects of CSPs/AE in lipopolysaccharide (LPS)-stimulated chondrocytes. CSPs/AE maintained high cell viability (>80% at 0.125 and 0.5 mg/mL) and showed significantly lower cytotoxicity than free artocarpin. Morphological and DAPI analyses confirmed preserved cellular and nuclear integrity without marked apoptosis. CSPs/AE at 0.25 mg/mL reduced LPS-induced intracellular ROS accumulation by approximately 79% relative to the LPS group. Western blot results demonstrated inhibition of LPS-induced NF-κB phosphorylation, with CSPs/AE at 0.5 mg/mL reducing p-NF-κB expression to approximately 0.66-fold of that observed in the LPS group. CSPs/AE also partially restored aggrecan and collagen II expression without promoting a fibrocartilage, as indicated by unchanged collagen I. These findings indicate that CSPs/AE attenuate oxidative stress and inflammatory signaling while preserving cartilage matrix components, highlighting their potential for cartilage-protective applications.

Indexed as

Anti-Inflammatory AgentsChitosanChondrocytesInflammationPlant LectinsAnimalsAntioxidantsCell SurvivalHumansLipopolysaccharidesMannose-Binding LectinsNF-kappa BOxidative StressReactive Oxygen SpeciesAnti-Inflammatory AgentsAntioxidantsartocarpin lectinChitosanLipopolysaccharidesMannose-Binding LectinsNF-kappa BPlant LectinsReactive Oxygen Speciesanti-inflammationartocarpinchitosan microparticlechondrocytesosteoarthritis

Identifiers

PMID42738788
PMCPMC13567654

What OpenQuestion holds

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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.