Evidence map›Paper›PMID 33198758›Full record

ArticleJournal of nanobiotechnology2020

The double-edged sword effect of macrophage targeting delivery system in different macrophage subsets related diseases.

Yuchuan Yuan, Ling Long, Jiaxing Liu, Yongyao Lin, Cuiping Peng, Yue Tang, Xuemei Zhou, Shuhui Li, Chengyuan Zhang, Xiaohui Li and 1 more

Open access · goldAbstract read
In one paragraph

Article in Journal of nanobiotechnology, 2020. 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
1.5field-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

10 citing papers in PubMed, 36 citations in OpenAlex.

  1. Review
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  6. Green Nanotechnology ofNanotechnology, science and applications · 2023
    Article
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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

11 authors at 3 institutions in 1 country.

Yuchuan YuanDepartment of Pharmaceutics, College of Pharmacy, Army Medical University, Chongqing, 400038, China.
Ling LongDepartment of Oncology, Xinqiao Hospital, Army Medical University, Chongqing, 400042, China.
Jiaxing LiuDepartment of Pharmaceutics, College of Pharmacy, Army Medical University, Chongqing, 400038, China.
Yongyao LinDepartment of Pharmaceutics, College of Pharmacy, Army Medical University, Chongqing, 400038, China.
Cuiping PengDepartment of Pharmaceutics, College of Pharmacy, Army Medical University, Chongqing, 400038, China.
Yue TangSchool of Pharmacy and Bioengineering, Chongqing University of Technology, Chongqing, 400054, China.
Xuemei ZhouSchool of Pharmacy and Bioengineering, Chongqing University of Technology, Chongqing, 400054, China.
Shuhui LiDepartment of Clinical Biochemistry, College of Pharmacy, Army Medical University, Chongqing, 400038, China.
Chengyuan ZhangSchool of Pharmacy and Bioengineering, Chongqing University of Technology, Chongqing, 400054, China. yjxzcy@163.com.
Xiaohui LiDepartment of Pharmaceutics, College of Pharmacy, Army Medical University, Chongqing, 400038, China. lpsh008@aliyun.com.
Xing ZhouSchool of Pharmacy and Bioengineering, Chongqing University of Technology, Chongqing, 400054, China. diszhou@126.com.ORCID http://orcid.org/0000-0003-0852-0687
Army Medical University · CNChongqing University · CNChongqing University of Technology · CN

Funding

National Key Research and Development of China(CN) 2018YFC1313400Natural Science Foundation Project of Chongqing, Chongqing Science and Technology Commission cstc2019jcyj-msxmX0603Scientific Startup Fund of CQUT (CN) 2019ZD88
6 · The paper itself

Abstract

backgroundMonocyte/macrophage-targeting delivery systems (MTDSs) have been focused upon as an emerging routine for delivering drugs to treat various macrophage-related diseases. However, the ability of MTDSs to distinguish different macrophage-related diseases and their impact on macrophage function and disease progression have not been systematically revealed, which is important for actively targeted therapeutic or diagnostic strategies.

resultsHerein, we used dextran-modified polystyrene nanoparticles (DEX-PS) to demonstrate that modification of nanoparticles by dextran can specifically enhance their recognition by M2 macrophages in vitro, but it is obstructed by monocytes in peripheral blood according to in vivo assays. DEX-PS not only targeted and became distributed in tumors, an M2 macrophage-related disease, but was also highly distributed in an M1 macrophage-related disease, namely acute peritonitis. Thus, DEX-PS acts as a double-edged sword in these two different diseases by reeducating macrophages to a pro-inflammatory phenotype.

conclusionsOur results suggest that MTDSs, even those designed based on differential expression of receptors on specific macrophage subtypes, lack the ability to distinguish different macrophage subtype-related diseases in vivo. In addition to the potential impact of these carrier materials on macrophage function, studies of MTDSs should pay greater attention to the distribution of nanoparticles in non-target macrophage-infiltrated disease sites and their impact on disease processes.

Indexed as

Drug Delivery SystemsAnimalsCells, CulturedCytokinesMacrophagesMaleMiceMice, Inbred BALB CMonocytesNanoparticlesPolystyrenesRAW 264.7 CellsCytokinesPolystyrenesDextran modificationMacrophageMacrophage related diseaseTargeted delivery systemTargeting mechanism

Identifiers

PMID33198758
PMCPMC7667812
OpenAlexW3104065869

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.