Evidence map›Paper›PMID 39140035›Full record

ArticleBiomaterials research2024

Combining Gut Microbiota Modulation and Enzymatic-Triggered Colonic Delivery by Prebiotic Nanoparticles Improves Mouse Colitis Therapy.

Hui Li, Yu Cheng, Luwen Cui, Zizhen Yang, Jingyi Wang, Zixuan Zhang, Kaiwei Chen, Cheng Zhao, Ningning He, Shangyong Li

Abstract read
In one paragraph

Article in Biomaterials research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

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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

10 authors.

Hui LiSchool of Basic Medicine, Qingdao Medical College, Qingdao University, Qingdao, China.ORCID https://orcid.org/0009-0006-1152-5496
Yu ChengSchool of Basic Medicine, Qingdao Medical College, Qingdao University, Qingdao, China.ORCID https://orcid.org/0009-0000-7996-4109
Luwen CuiSchool of Basic Medicine, Qingdao Medical College, Qingdao University, Qingdao, China.ORCID https://orcid.org/0009-0006-7074-7945
Zizhen YangSchool of Basic Medicine, Qingdao Medical College, Qingdao University, Qingdao, China.ORCID https://orcid.org/0009-0000-8455-9749
Jingyi WangSchool of Basic Medicine, Qingdao Medical College, Qingdao University, Qingdao, China.ORCID https://orcid.org/0009-0007-7366-7112
Zixuan ZhangSchool of Basic Medicine, Qingdao Medical College, Qingdao University, Qingdao, China.ORCID https://orcid.org/0009-0001-5951-1206
Kaiwei ChenSchool of Basic Medicine, Qingdao Medical College, Qingdao University, Qingdao, China.ORCID https://orcid.org/0009-0000-8455-9749
Cheng ZhaoDepartment of Abdominal Ultrasound, The Affiliated Hospital of Qingdao University, Qingdao, China.ORCID https://orcid.org/0000-0001-9655-8866
Ningning HeSchool of Basic Medicine, Qingdao Medical College, Qingdao University, Qingdao, China.ORCID https://orcid.org/0000-0001-9453-6911
Shangyong LiSchool of Basic Medicine, Qingdao Medical College, Qingdao University, Qingdao, China.ORCID https://orcid.org/0000-0003-1464-3763

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The efficacy of ulcerative colitis (UC) therapy is closely connected to the composition of gut microbiota in the gastrointestinal tract. Prebiotic-based nanoparticles (NPs) provide a more precise approach to alleviate UC via modulating gut microbiota dysbiosis. The present study develops an efficient prebiotic-based colon-targeted drug delivery system (PCDDS) by using prebiotic pectin (Pcn) and chitosan (Csn) polysaccharides as a prebiotic shell, with the anti-inflammatory drug sulfasalazine (SAS) loaded into a poly(lactic-co-glycolic acid) (PLGA) core to construct SAS@PLGA-Csn-Pcn NPs. Then, we examine its characterization, cellular uptake, and in vivo therapeutic efficacy. The results of our study indicate that the Pcn/Csn shell confers efficient pH-sensitivity properties. The gut microbiota-secreted pectinase serves as the trigger agent for Pcn/Csn shell degradation, and the resulting Pcn oligosaccharides possess a substantial prebiotic property. Meanwhile, the formed PCDDSs exhibit robust biodistribution and accumulation in the colon tissue, rapid cellular uptake, efficient in vivo therapeutic efficacy, and modulation of gut microbiota dysbiosis in a mouse colitis model. Collectively, our synthetic PCDDSs demonstrate a promising and synergistic strategy for UC therapy.

Identifiers

PMID39140035
PMCPMC11321063

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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.