Evidence map›Paper›PMID 41359100›Full record

ReviewInflammopharmacology2026

Phytochemicals and nanoformulation strategies for rheumatoid arthritis: mechanistic insights, therapeutic advances, and translational challenges.

Mohsen Rahmanian, Sarah Khosropanah, Sepehr Hoseinzadeh Moghaddam, Abulfazl Vatankhah, Ali Haghbin, Fatemeh Oroojalian, Kasim Sakran Abass, Prashant Kesharwani, Amirhossein Sahebkar

Abstract readReview
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In one paragraph

Review 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.

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. 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

9 authors.

Mohsen RahmanianSchool of Medicine, North Khorasan University of Medical Sciences, Bojnurd, 74877-94149, Iran.
Sarah KhosropanahSchool of Medicine, North Khorasan University of Medical Sciences, Bojnurd, 74877-94149, Iran.
Sepehr Hoseinzadeh MoghaddamSchool of Medicine, North Khorasan University of Medical Sciences, Bojnurd, 74877-94149, Iran.
Abulfazl VatankhahSchool of Medicine, North Khorasan University of Medical Sciences, Bojnurd, 74877-94149, Iran.
Ali HaghbinDepartment of Pediatrics, School of Medicine, North Khorasan University of Medical Sciences, Bojnurd, Iran.
Fatemeh OroojalianCell Therapy and Regenerative Medicine Innovation Center, North Khorasan University of Medical Sciences, Bojnurd, 74877-94149, Iran. f.oroojalian@gmail.com.
Kasim Sakran AbassDepartment of Physiology, Biochemistry, and Pharmacology, College of Veterinary Medicine, University of Kirkuk, Kirkuk, 36001, Iraq.
Prashant KesharwaniNext-Generation Translational Nanomedicine Laboratory, Department of Pharmaceutical Sciences, Dr. Harisingh Gour Vishwavidyalaya, Sagar, Madhya Pradesh, 470003, India. prashantdops@gmail.com.ORCID http://orcid.org/0000-0002-0890-769X
Amirhossein SahebkarBiotechnology Research Center, Pharmaceutical Technology Institute, Mashhad University of Medical Sciences, Mashhad, Iran. amir_saheb2000@yahoo.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Rheumatoid arthritis (RA) is a chronic, progressive autoimmune disease characterized by persistent joint inflammation, cartilage degradation, and systemic complications. Phytochemicals such as curcumin, resveratrol, phenolic acids, flavonoids, lignans, and organosulfur compounds have demonstrated significant disease-modifying potential through modulation of pro-inflammatory cytokines (TNF-α, IL-1β, IL-6) and key signaling pathways (NF-κB, MAPK, PI3K/AKT/mTOR). Curcumin, for example, regulates immune homeostasis by restoring the Th17/Treg balance and inhibiting NF-κB and mTOR signaling, while resveratrol suppresses angiogenesis via VEGF inhibition and induces apoptosis in fibroblast-like synoviocytes. Despite their pharmacological promise, poor aqueous solubility, rapid metabolism, and low systemic bioavailability limit clinical translation. Advances in nanoformulation technologies-including polymeric nanoparticles, liposomes, micelles, solid lipid nanoparticles, and stimuli-responsive carriers-have markedly improved phytochemical stability, pharmacokinetics, targeted delivery, and therapeutic efficacy. Analytical characterization methods such as dynamic light scattering, zeta potential analysis, FTIR, HPLC, and TEM facilitate precise formulation optimization and evaluation of biological interactions. Preclinical studies reveal that nano-curcumin can achieve efficacy comparable to methotrexate, while resveratrol-loaded gold nanoparticles enhance anti-inflammatory effects and joint-specific accumulation. This review integrates mechanistic insights, formulation strategies, and analytical approaches, highlighting the opportunities and regulatory considerations for translating nano-phytochemicals into clinically viable RA therapies.

Indexed as

Antirheumatic AgentsArthritis, RheumatoidNanoparticlesPhytochemicalsAnimalsDrug Delivery SystemsHumansAntirheumatic AgentsPhytochemicalsClinical translationCurcuminNanoformulation strategiesPhytochemical-based therapeuticsPolymeric nanoparticlesResveratrolRheumatoid arthritis

Identifiers

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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.