Evidence map›Paper›PMID 35225122›Full record

ArticleDrug delivery2022

Delivery of germacrone (GER) using macrophages-targeted polymeric nanoparticles and its application in rheumatoid arthritis.

Tingfei Tan, Qi Huang, Weiwei Chu, Bo Li, Jingjing Wu, Quan Xia, Xi Cao

Open access · goldAbstract read
In one paragraph

Article in Drug delivery, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
5.6field-weighted citation impact, top 3% 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

15 citing papers in PubMed, 39 citations in OpenAlex.

  1. Nanoparticle Delivery Systems in Rheumatoid Arthritis: More Than Vehicles.Sichuan da xue xue bao. Yi xue ban = Journal of Sichuan University. Medical science edition · 2026
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  6. Mechanistic and therapeutic insights into the function of N6-methyladenosine in arthritic diseases.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2025
    Review
  7. Article
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  9. Targeted liposomes for macrophages-mediated pulmonary fibrosis therapy.Drug delivery and translational research · 2024
    Article
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  12. 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

7 authors at 4 institutions in 1 country.

Tingfei TanDepartment of Pharmacy, The First Affiliated Hospital of Anhui Medical University, Hefei, People's Republic of China.
Qi HuangDepartment of Oncology, The Second Affiliated Hospital of Anhui Medical University, Hefei, China.
Weiwei ChuDepartment of Pharmacy, The First Affiliated Hospital of Anhui Medical University, Hefei, People's Republic of China.
Bo LiDepartment of Pharmacy, The First Affiliated Hospital of Anhui Medical University, Hefei, People's Republic of China.
Jingjing WuDepartment of Oncology, The Second Affiliated Hospital of Anhui Medical University, Hefei, China.
Quan XiaDepartment of Pharmacy, The First Affiliated Hospital of Anhui Medical University, Hefei, People's Republic of China.
Xi CaoDepartment of Pharmacy, The First Affiliated Hospital of Anhui Medical University, Hefei, People's Republic of China.
Anhui Medical University · CNState Administration of Traditional Chinese Medicine of the People's Republic of China · CNFirst Affiliated Hospital of Anhui Medical University · CNSecond Hospital of Anhui Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Macrophages can transform into M1 (pro-inflammatory) and M2 (anti-inflammatory) phenotypes, which mediate the immune/inflammatory response in rheumatoid arthritis (RA). Activated M1 phenotype macrophages and overexpression of folate (FA) receptors are abundant in inflammatory synovium and joints and promote the progression of RA. Germacrone (GER) can regulate the T helper 1 cell (Th1)/the T helper 2 cell (Th2) balance to delay the progression of arthritis. To deliver GER to inflammatory tissue cells to reverse M1-type proinflammatory cells and reduce inflammation, FA receptor-targeting nanocarriers loaded with GER were developed. In activated macrophages, FA-NPs/DiD showed significantly higher uptake efficiency than NPs/DiD.

Indexed as

Arthritis, RheumatoidNanoparticlesAnimalsMacrophagesRatsSesquiterpenes, GermacraneTissue DistributiongermacroneSesquiterpenes, GermacraneGermacronemacrophage polarizationmacrophage-targetednanoparticlesrheumatoid arthritis

Identifiers

PMID35225122
PMCPMC8890522
OpenAlexW4214586470

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.