Evidence map›Paper›PMID 36406639›Full record

ArticleInternational journal of nanomedicine2022

Macrophage-Targeted Berberine-Loaded β-Glucan Nanoparticles Enhance the Treatment of Ulcerative Colitis.

Yuying Xu, Jintao Huang, Yapei Fan, Haiyue Long, Minting Liang, Qunjie Chen, Zhiping Wang, Chaoxi Wu, Yifei Wang

Open access · goldAbstract read
In one paragraph

Article in International journal of nanomedicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
3.0field-weighted citation impact, top 8% 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

8 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Berberine: A Negentropic Modulator for Multi-System Coordination.International journal of molecular sciences · 2026
    Review
  5. Review
  6. Can Nature Overcome Invasive Gastrointestinal Infections?International journal of molecular sciences · 2025
    Review
  7. Article
  8. Article
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 at 2 institutions in 1 country.

Yuying Xu *Department of Cell Biology, College of Life Science and Technology, Jinan University, Guangzhou, People's Republic of China.
Jintao Huang *Guangdong Provincial Engineering Center of Topical Precise Drug Delivery System, School of Pharmacy, Guangdong Pharmaceutical University, Guangzhou, People's Republic of China.
Yapei FanDepartment of Cell Biology, College of Life Science and Technology, Jinan University, Guangzhou, People's Republic of China.
Haiyue LongDepartment of Cell Biology, College of Life Science and Technology, Jinan University, Guangzhou, People's Republic of China.
Minting LiangDepartment of Cell Biology, College of Life Science and Technology, Jinan University, Guangzhou, People's Republic of China.
Qunjie ChenDepartment of Cell Biology, College of Life Science and Technology, Jinan University, Guangzhou, People's Republic of China.
Zhiping WangGuangdong Provincial Engineering Center of Topical Precise Drug Delivery System, School of Pharmacy, Guangdong Pharmaceutical University, Guangzhou, People's Republic of China.ORCID 0000-0002-2367-0491
Chaoxi WuDepartment of Cell Biology, College of Life Science and Technology, Jinan University, Guangzhou, People's Republic of China.ORCID 0000-0002-6689-3716
Yifei WangDepartment of Cell Biology, College of Life Science and Technology, Jinan University, Guangzhou, People's Republic of China.
Jinan University · CNGuangdong Pharmaceutical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Aim: This study focuses on constructing of an anti-inflammatory drug delivery system by encapsulation of berberine in the β-glucan nanoparticles and evaluates its effect on treating ulcerative colitis. Methods: β-Glucan and the anti-inflammatory drug berberine (BER) are self-assembled into nanoparticles to construct a drug delivery system (GLC/BER). The interaction between the drug and the carrier was characterized by circular dichroism, ultraviolet-visible spectroscopy, and dynamic light scattering. The anti-inflammatory effect of the GLC/BER was evaluated through a lipopolysaccharide (LPS)-induced RAW264.7 macrophage inflammation model and a sodium sulfate (DSS)-induced C57BL/6 mouse ulcerative colitis model. Results: The GLC/BER nanoparticles have a particle size of 80-120 nm and a high encapsulation efficiency of 37.8±4.21%. In the LPS-induced RAW264.7 macrophage inflammation model, GLC/BER significantly promoted the uptake of BER by RAW264.7 cells. RT-PCR and ELISA assay showed that it could significantly inhibit the inflammatory factors including IL-1β, IL-6 and COX-2. Furthermore, GLC/BER shows inhibiting effect on the secretion of pro-inflammatory factors such as IL-1β and IL-6, down-regulating the production of nitrite oxide; in animal studies, GLC/BER was found to exert a relieving effect on mice colitis. Conclusion: The study found that GLC/BER has an anti-inflammatory effect in vitro and in vivo, and the GLC carrier improves the potency and bioavailability of BER, providing a new type of nanomedicine for the treatment of colitis.

Indexed as

Berberinebeta-GlucansColitisColitis, UlcerativeNanoparticlesAnimalsAnti-Inflammatory AgentsInflammationInterleukin-6LipopolysaccharidesMacrophagesMiceMice, Inbred C57BLAnti-Inflammatory AgentsBerberinebeta-GlucansInterleukin-6Lipopolysaccharidesanti-inflammationchiraldrug carrierimmunoregulationβ-glucan

Identifiers

PMID36406639
PMCPMC9673505
OpenAlexW4309043446

What OpenQuestion holds

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LicenceCC BY-NC
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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.