Evidence map›Paper›PMID 39047093›Full record

ArticleScience advances2024

"Two-birds-one-stone" oral nanotherapeutic designed to target intestinal integrins and regulate redox homeostasis for UC treatment.

Long Huang, Wei Hu, Long Qun Huang, Qin Xuan Zhou, Zheng Yang Song, Heng Yu Tao, Bing Xu, Can Yang Zhang, Yi Wang, Xin-Hui Xing

Abstract read
In one paragraph

Article in Science advances, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed, 1 pooled it
–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

21 citing papers in PubMed, 1 synthesis or guideline pooled it.

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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.

Long HuangInstitute of Biochemical Engineering, Department of Chemical Engineering, Tsinghua University, Beijing 100084, China.ORCID 0009-0005-6069-8732
Wei HuInstitute of Biopharmaceutical and Health Engineering, Shenzhen International Graduate School, Tsinghua University, Shenzhen 518055, China.
Long Qun HuangInstitute of Biochemical Engineering, Department of Chemical Engineering, Tsinghua University, Beijing 100084, China.
Qin Xuan ZhouInstitute of Biopharmaceutical and Health Engineering, Shenzhen International Graduate School, Tsinghua University, Shenzhen 518055, China.ORCID 0000-0002-7953-6304
Zheng Yang SongInstitute of Biopharmaceutical and Health Engineering, Shenzhen International Graduate School, Tsinghua University, Shenzhen 518055, China.
Heng Yu TaoInstitute of Biopharmaceutical and Health Engineering, Shenzhen International Graduate School, Tsinghua University, Shenzhen 518055, China.
Bing XuInstitute of Biomedical Health Technology and Engineering, Shenzhen Bay Laboratory, Shenzhen 518118, China.
Can Yang ZhangInstitute of Biopharmaceutical and Health Engineering, Shenzhen International Graduate School, Tsinghua University, Shenzhen 518055, China.ORCID 0000-0002-6975-5781
Yi WangInstitute of Biochemical Engineering, Department of Chemical Engineering, Tsinghua University, Beijing 100084, China.ORCID 0000-0003-4028-2471
Xin-Hui XingInstitute of Biochemical Engineering, Department of Chemical Engineering, Tsinghua University, Beijing 100084, China.ORCID 0000-0001-6419-4770

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Designing highly efficient orally administrated nanotherapeutics with specific inflammatory site-targeting functions in the gastrointestinal tract for ulcerative colitis (UC) management is a noteworthy challenge. Here, we focused on exploring a specific targeting oral nanotherapy, serving as "one stone," for the directed localization of inflammation and the regulation of redox homeostasis, thereby achieving effects against "two birds" for UC treatment. Our designed nanotherapeutic agent OPNs@LMWH (oxidation-sensitive ε-polylysine nanoparticles at low-molecular weight heparin) exhibited specific active targeting effects and therapeutic efficacy simultaneously. Our results indicate that OPNs@LMWH had high integrin αM-mediated immune cellular uptake efficiency and preferentially accumulated in inflamed tissues. We also confirmed its effectiveness in the treatment experiment of colitis in mice by ameliorating oxidative stress and inhibiting the activation of inflammation-associated signaling pathways while simultaneously bolstering the protective mechanisms of the colonic epithelium. Overall, these findings underscore the compelling dual functionalities of OPNs@LMWH, which enable effective oral delivery to inflamed sites, thereby facilitating precise UC management.

Indexed as

Colitis, UlcerativeHomeostasisIntegrinsNanoparticlesOxidation-ReductionAdministration, OralAnimalsDisease Models, AnimalDrug Delivery SystemsHumansMiceOxidative StressIntegrins

Identifiers

PMID39047093
PMCPMC11268407

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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.