Evidence map›Paper›PMID 39238027›Full record

ArticleJournal of nanobiotechnology2024

Hyaluronic acid-coated polypeptide nanogel enhances specific distribution and therapy of tacrolimus in rheumatoid arthritis.

Yuhuan Li, Xin Wang, Yu Gao, Ziyi Zhang, Te Liu, Zhuo Zhang, Yinan Wang, Fei Chang, Modi Yang

Abstract read
In one paragraph

Article in Journal of nanobiotechnology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Review
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  7. Article
  8. Review
  9. Article
  10. Stimuli-Responsive Nanoplatforms for Precision Intervention in Rheumatoid Arthritis.Wiley interdisciplinary reviews. Nanomedicine and nanobiotechnology
    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.

Yuhuan Li *Department of Orthopedics, China-Japan Union Hospital of Jilin University, Changchun, 130033, PR China.
Xin Wang *Department of Orthopedics, The Second Hospital of Jilin University, Changchun, 130041, PR China.
Yu GaoDepartment of Orthopedics, China-Japan Union Hospital of Jilin University, Changchun, 130033, PR China.
Ziyi ZhangDepartment of Orthopedics, China-Japan Union Hospital of Jilin University, Changchun, 130033, PR China.
Te LiuScientific Research Center, China-Japan Union Hospital of Jilin University, Changchun, Jilin, China.
Zhuo ZhangDepartment of Orthopedics, China-Japan Union Hospital of Jilin University, Changchun, 130033, PR China.
Yinan WangDepartment of Biobank, Division of Clinical Research, The First Hospital of Jilin University, Changchun, China.
Fei ChangDepartment of Orthopedics, The Second Hospital of Jilin University, Changchun, 130041, PR China. changfei@jlu.edu.cn.
Modi YangDepartment of Orthopedics, China-Japan Union Hospital of Jilin University, Changchun, 130033, PR China. yangmodi@jlu.edu.cn.

Funding

Funds for Bethune Program of Jilin University 2022B22National Key Research and Development Program of China 2022YFE0107700National Natural Science Foundation of China 3220050753National Natural Science Foundation of China 81701811Natural Science Foundation of Sichuan Province 2023NSFSC1600Science and Technology Development Program of Jilin Province 172410GG010135547Science and Technology Development Program of Jilin Province 20220203120SFScience and Technology Development Program of Jilin Province 20240304072SF
6 · The paper itself

Abstract

Rheumatoid arthritis (RA) involves chronic inflammation, oxidative stress, and complex immune cell interactions, leading to joint destruction. Traditional treatments are often limited by off-target effects and systemic toxicity. This study introduces a novel therapeutic approach using hyaluronic acid (HA)-conjugated, redox-responsive polyamino acid nanogels (HA-NG) to deliver tacrolimus (TAC) specifically to inflamed joints. The nanogels' disulfide bonds enable controlled TAC release in response to high intracellular glutathione (GSH) levels in activated macrophages, prevalent in RA-affected tissues. In vitro results demonstrated that HA-NG/TAC significantly reduced TAC toxicity to normal macrophages and showed high biocompatibility. In vivo, HA-NG/TAC accumulated more in inflamed joints compared to non-targeted NG/TAC, enhancing therapeutic efficacy and minimizing side effects. Therapeutic evaluation in collagen-induced arthritis (CIA) mice revealed HA-NG/TAC substantially reduced paw swelling, arthritis scores, synovial inflammation, and bone erosion while suppressing pro-inflammatory cytokine levels. These findings suggest that HA-NG/TAC represents a promising targeted drug delivery system for RA, offering potential for more effective and safer clinical applications.

Indexed as

Arthritis, ExperimentalArthritis, RheumatoidHyaluronic AcidNanogelsPeptidesTacrolimusAnimalsDrug CarriersDrug Delivery SystemsHumansMacrophagesMaleMiceMice, Inbred DBARAW 264.7 CellsDrug CarriersHyaluronic AcidNanogelsPeptidesTacrolimusActive targetingHyaluronic acidReduction-responsive polypeptide nanogelRheumatoid arthritisTacrolimus

Identifiers

PMID39238027
PMCPMC11378632

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

None linked

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.