Evidence map›Paper›PMID 39350164›Full record

ArticleJournal of translational medicine2024

Oral colon-targeted pH-responsive polymeric nanoparticles loading naringin for enhanced ulcerative colitis therapy.

Shilong Fan, Yue Zhao, Yinlian Yao, Xin Shen, Xingxing Chai, Jiahui Li, Jiang Pi, Xueqin Huang, Hua Jin, Zhikun Zhou

Abstract read
In one paragraph

Article in Journal of translational medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

  1. Article
  2. Fabrication of vitamin BInternational journal of pharmaceutics: X · 2026
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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.

Shilong FanGuangdong Provincial Key laboratory of research and development of Natural drugs, School of Pharmacology, Guangdong Medical University, Dongguan, 523808, China.
Yue ZhaoGuangdong Provincial Key laboratory of research and development of Natural drugs, School of Pharmacology, Guangdong Medical University, Dongguan, 523808, China.
Yinlian YaoGuangdong Provincial Key laboratory of research and development of Natural drugs, School of Pharmacology, Guangdong Medical University, Dongguan, 523808, China.
Xin ShenGuangdong Provincial Key laboratory of research and development of Natural drugs, School of Pharmacology, Guangdong Medical University, Dongguan, 523808, China.
Xingxing ChaiLaboratory Animal Center, School of Medical Technology, Guangdong Medical University, Dongguan, 523808, China.
Jiahui LiGuangdong Provincial Key laboratory of research and development of Natural drugs, School of Pharmacology, Guangdong Medical University, Dongguan, 523808, China.
Jiang PiLaboratory Animal Center, School of Medical Technology, Guangdong Medical University, Dongguan, 523808, China.
Xueqin HuangLaboratory Animal Center, School of Medical Technology, Guangdong Medical University, Dongguan, 523808, China.
Hua JinGuangdong Provincial Key laboratory of research and development of Natural drugs, School of Pharmacology, Guangdong Medical University, Dongguan, 523808, China. jinhua0413@gdmu.edu.cn.
Zhikun ZhouGuangdong Provincial Key laboratory of research and development of Natural drugs, School of Pharmacology, Guangdong Medical University, Dongguan, 523808, China. zhouzhkun@126.com.ORCID 0009-0001-1149-4531

Funding

Science Fund for Distinguished Young Scholars of Guangdong Province 2022A1515140154
6 · The paper itself

Abstract

An oral colon-targeted drug delivery system holds great potential in preventing systemic toxicity and preserving the therapeutic benefits of ulcerative colitis (UC) treatment. In this study, we developed a negatively charged PLGA-PEG nanoparticle system for encapsulating naringin (Nar). Additionally, chitosan and mannose were coated on the surface of these nanoparticles to enhance their mucosal adsorption and macrophage targeting abilities. The resulting nanoparticles, termed MC@Nar-NPs, exhibited excellent resistance against decomposition in the strong acidic gastrointestinal environment and specifically accumulated at inflammatory sites. Upon payload release, MC@Nar-NPs demonstrated remarkable efficacy in alleviating colon inflammation as evidenced by reduced levels of pro-inflammatory cytokines in both blood and colon tissues, as well as the scavenging of reactive oxygen species (ROS) in the colon. This oral nanoparticle delivery system represents a novel approach to treating UC by utilizing Chinese herbal ingredient-based oral delivery and provides a theoretical foundation for local and precise intervention in specific UC treatment.

Indexed as

Colitis, UlcerativeColonFlavanonesNanoparticlesPolymersAdministration, OralAnimalsCytokinesDrug LiberationHydrogen-Ion ConcentrationMaleMiceReactive Oxygen SpeciesCytokinesFlavanonesnaringinPolymersReactive Oxygen SpeciesColon-targeted nanoparticlesNaringinOral deliveryPro-inflammatory cytokinesReactive oxygen speciesUlcerative colitis

Identifiers

PMID39350164
PMCPMC11440766

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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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.