Evidence map›Paper›PMID 41784929›Full record

ArticleInflammopharmacology2026

Hydroxytyrosol-encapsulated solid lipid nanoparticles mitigate induced arthritis via modulating the cytokines and MMP-13 expression and downregulating oxidative stress in rats.

Noor Ul Huda, Aftab Ahmad, Muhammad Anjum Zia, Bushra Akhtar

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Article in Inflammopharmacology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

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1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Noor Ul HudaDepartment of Biochemistry, University of Agriculture, Faisalabad, Pakistan.
Aftab AhmadDepartment of Biochemistry, University of Agriculture, Faisalabad, Pakistan. aftab.ahmad@unizwa.edu.om.
Muhammad Anjum ZiaDepartment of Biochemistry, University of Agriculture, Faisalabad, Pakistan.
Bushra AkhtarDepartment of Pharmacy, University of Agriculture, Faisalabad, Pakistan. bushra.akhtar@uaf.edu.pk.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Rheumatoid arthritis is a chronic inflammatory disease characterized by progressive degeneration of joints and systemic complications. This study aimed at the development and evaluation of hydroxytyrosol-loaded solid lipid nanoparticles as a promising therapeutic approach against FCA-induced arthritis in rats. Hydroxytyrosol-loaded nanoparticles were prepared using stearic and lauric acids with Tween 80, showing a mean particle size of 109.7 nm, a zeta potential of − 26.0 mV, and a high encapsulation efficiency (96.5%). In vitro antioxidant and anti-inflammatory activities were performed by total phenolic and flavonoid content, DPPH radical scavenging assay, hemolytic assay, and protein denaturation assay. The developed formulation was subjected to an in vivo study using 35 rats divided into seven groups. HT-NPs at a dose of 40 mg/kg showed a significant reduction in arthritic score (0.78 ± 0.08) when compared to arthritic control (3.78 ± 0.08) and markedly decreased paw swelling (4.68 ± 0.13 vs. 5.92 ± 0.26). The treatment restored the oxidative balance by increased SOD (9.0 ± 0.2 U/mL) and CAT (66 ± 1.0 U/mL) and reduced MDA levels to 2.7 ± 0.10 nmol/mL. Further, HT-NPs treatment showed downregulation of pro-inflammatory and tissue-degrading genes such as TNF-α (1.30 ± 0.07 vs. 5.90 ± 0.16), IL-1β (1.50 ± 0.07 vs. 7.00 ± 0.16), and MMP-13 (2.12 ± 0.02 vs. 5.97 ± 0.08) while upregulating anti-inflammatory cytokines IL-10 and IL-4. The therapeutic potential of HT-NPs at high doses was comparable to methotrexate. These findings suggest that nanoencapsulation significantly enhances hydroxytyrosol’s therapeutic potential and thus support HT-NPs as a promising natural and safer alternative in the management of RA.

Indexed as

Arthritis, ExperimentalArthritis, RheumatoidCytokinesMatrix Metalloproteinase 13NanoparticlesOxidative StressPhenylethyl AlcoholAnimalsAnti-Inflammatory AgentsAntioxidantsDown-RegulationLipidsLiposomesMaleParticle SizeRats3,4-dihydroxyphenylethanolAnti-Inflammatory AgentsAntioxidantsCytokinesLipid NanoparticlesLipidsLiposomesMatrix Metalloproteinase 13Phenylethyl AlcoholArthritic scoreFreund’s Complete AdjuvantHydroxytyrosolRheumatoid arthritisSolid lipid nanoparticles

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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.