Evidence map›Paper›PMID 38127247›Full record

ArticleDrug delivery and translational research2024

Co-delivery of indomethacin and uricase as a new strategy for inflammatory diseases associated with high uric acid.

Jie Liu, Chenshi Lin, Man Wu, Yingjie Wang, Shenyu Chen, Taiwang Yang, Chenlu Xie, Yue Kong, Wenliang Wu, Jiaping Wang and 2 more

Abstract read
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In one paragraph

Article in Drug delivery and translational research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
1.6field-weighted citation impact, top 16% of its field
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

7 citing papers in PubMed, 1 synthesis or guideline pooled it, 8 citations in OpenAlex.

  1. Pooled it
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  3. Article
  4. Review
  5. Review
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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

12 authors at 3 institutions in 3 countries.

Jie Liu *Department of Pharmacy, Jiujiang Hospital of Traditional Chinese Medicine, Jiujiang, Jiangxi, 332000, China.
Chenshi Lin *School of Pharmacy, China Pharmaceutical University, Nanjing, 210009, China.
Man WuDepartment of Pharmacy, Jiujiang Hospital of Traditional Chinese Medicine, Jiujiang, Jiangxi, 332000, China.
Yingjie WangCenter for Translational Imaging, Northeastern University, 360 Huntington Ave., Boston, MA, 02115, USA.
Shenyu ChenInstitute of Environmental Medicine, Karolinska Institute, Stockholm, Sweden.
Taiwang YangDepartment of Pharmacy, Jiujiang Hospital of Traditional Chinese Medicine, Jiujiang, Jiangxi, 332000, China.
Chenlu XieDepartment of Pharmacy, Jiujiang Hospital of Traditional Chinese Medicine, Jiujiang, Jiangxi, 332000, China.
Yue KongDepartment of Pharmacy, Jiujiang Hospital of Traditional Chinese Medicine, Jiujiang, Jiangxi, 332000, China.
Wenliang WuDepartment of Pharmacy, Jiujiang Hospital of Traditional Chinese Medicine, Jiujiang, Jiangxi, 332000, China.
Jiaping WangDepartment of Pharmacy, Jiujiang Hospital of Traditional Chinese Medicine, Jiujiang, Jiangxi, 332000, China.
Xiaonan MaSchool of Pharmacy, China Pharmaceutical University, Nanjing, 210009, China. maxiaonan512@126.com.
Chao TengSchool of Pharmacy, China Pharmaceutical University, Nanjing, 210009, China. chaotengTC@163.com.ORCID 0009-0000-2559-2004
China Pharmaceutical University · CNKarolinska Institutet · SENortheastern University · US

Funding

National Postdoctoral Program for Innovative Talents 1412200075
6 · The paper itself

Abstract

Uric acid is the final metabolite in humans. High level of uric acid chronically induces urate deposition, aggravates kidney damage, and concomitantly causes an increase in inflammatory factors. Alleviating acute inflammation and decreasing uric acid levels are the key points in the treatment of inflammatory diseases associated with high uric acid. However, a drug delivery system that combines anti-inflammatory and uric acid reduction functions at the same time remains a challenge to be settled. Here, we designed a nanocrystal-based co-delivery platform, IND Nplex, characterized by loading of indomethacin (IND) and uricase. Compared with free IND or uricase, IND Nplex possessed a better anti-inflammatory effect by restraining the release of inflammation-related factors in vitro. In addition, pharmacokinetic and biodistribution studies revealed that IND Nplex significantly prolonged the retention time in vivo and was more concentrated in the kidney. In acute gouty arthritis model rats, IND Nplex markedly relieved ankle joint swelling and mitigated synovial inflammation. In acute kidney injury model rats, IND Nplex indicated better biocompatibility and significant amelioration of renal fibrosis. Moreover, IND Nplex showed the effect of anti-inflammatory and improved renal function via determination of inflammatory factors and biochemical markers in the serum and kidney. In conclusion, these results indicate that IND Nplex exerts anti-inflammatory activity and uric acid-lowering effect and could become a promising candidate for the treatment of uric acid-related diseases.

Indexed as

Arthritis, GoutyIndomethacinRats, Sprague-DawleyUrate OxidaseUric AcidAcute Kidney InjuryAnimalsAnti-Inflammatory AgentsAnti-Inflammatory Agents, Non-SteroidalDrug Delivery SystemsHumansInflammationKidneyMaleMiceNanoparticlesAnti-Inflammatory AgentsAnti-Inflammatory Agents, Non-SteroidalIndomethacinUrate OxidaseUric AcidAnti-inflammatoryCo-delivery nanoplatformIndomethacinUric acid reductionUricase

Identifiers

PMID38127247
OpenAlexW4390062085

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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.