Evidence map›Paper›PMID 42381004›Full record

ArticleJournal of nanobiotechnology2026

Neutrophil membrane-mediated biomimetic nanoparticle for co-delivery of icariin and siORMDL3 attenuates asthma exacerbated by respiratory syncytial virus.

Xudong Zhang, Ting Luan, Chenyu Zhao, Li Chen, Fei Wang, Qi Cheng, Tong Zhu, Wanjie Huang

Abstract read
In one paragraph

Article in Journal of nanobiotechnology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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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

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

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4 · The record

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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

8 authors.

Xudong Zhang *Department of Pulmonary and Critical Care Medicine, Shengjing Hospital of China Medical University, Shenyang, 110000, Liaoning, China.
Ting Luan *Department of Critical Care Medicine, Shengjing Hospital of China Medical University, Shenyang, 110000, Liaoning, China.
Chenyu ZhaoDepartment of China, School of Pharmacy, Medical University-The Queen's University of Belfast Joint College, China Medical University, Shenyang, 110001, China.
Li ChenDepartment of Pediatrics, Shengjing Hospital of China Medical University, Shenyang, 110000, Liaoning, China.
Fei WangDepartment of Pediatrics, Shengjing Hospital of China Medical University, Shenyang, 110000, Liaoning, China.
Qi ChengDepartment of Pediatrics, Shengjing Hospital of China Medical University, Shenyang, 110000, Liaoning, China. qcheng@cmu.edu.cn.
Tong ZhuDepartment of Pediatrics, Shengjing Hospital of China Medical University, Shenyang, 110000, Liaoning, China. zhutong19860413@163.com.
Wanjie HuangDepartment of Pediatrics, Shengjing Hospital of China Medical University, Shenyang, 110000, Liaoning, China. wjhuang@cmu.edu.cn.

Funding

Applied Basic Research Program of Department of Science and Technology of Liaoning Province 2023JH2/101600022the General Project of the Department of Science and Technology of Liaoning Province 2024-MSLH-603
6 · The paper itself

Abstract

backgroundAsthma is a chronic inflammatory disorder, and respiratory syncytial virus (RSV) is a major trigger of asthma exacerbation. This study aimed to improve therapeutic efficacy against RSV-exacerbated asthma using neutrophil membrane (NM)-coated nanoparticles (NPs) for co-delivery of orosomucoid-like 3 (ORMDL3)-targeting small interfering RNA (siRNA) and icariin.

methodsA biomimetic dual-drug delivery system (ORMDL3-targeting siRNA [siORMDL3]/Icariin NPs@NM) was developed by coating NM onto poly(lactic-co-glycolic acid) NPs co-loaded with icariin and siORMDL3. The physicochemical properties, biosafety, cellular uptake, biodistribution behavior, and RNA interference efficiency of the NPs were evaluated. Their therapeutic efficacy was further assessed in vitro and in vivo.

resultsThe siORMDL3/Icariin NPs@NM exhibited a core-shell structure with NM camouflage, an average diameter of 141.1 nm, and a negatively charged surface. The NPs demonstrated enhanced lung-targeting delivery efficiency with no apparent adverse effects. In vitro, siORMDL3/Icariin NPs@NM significantly improved the viability of BEAS-2B cells treated with interleukin-4 and RSV, while markedly reducing inflammatory cytokine production and oxidative stress markers. In vivo, the siORMDL3/Icariin NPs@NM effectively alleviated airway resistance and improved the inflammatory microenvironment in mice with RSV-exacerbated asthma, with no observable toxicity in major organs.

conclusionsiORMDL3/Icariin NPs@NM demonstrated potent anti-inflammatory and antioxidative effects and may serve as an effective dual-drug delivery platform for the treatment of RSV-exacerbated asthma through combination therapy.

Indexed as

AsthmaBiomimetic MaterialsFlavonoidsNanoparticlesNeutrophilsRespiratory Syncytial Virus InfectionsRNA, Small InterferingAnimalsDrug Delivery SystemsFemaleHumansLungMiceMice, Inbred BALB CRespiratory Syncytial VirusesFlavonoidsicariinRNA, Small InterferingBiomimetic nanoparticleIcariinNeutrophil membraneORMDL3 siRNARespiratory syncytial virus-exacerbated asthmaTargeted therapy

Identifiers

PMID42381004
PMCPMC13543498

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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.