Evidence map›Paper›PMID 41608042›Full record

ArticleNational science review2026

Sunlight PDT leveraging NIR-II nanospray: painless, hemostatic, anti-inflammatory therapy towards diabetic wound infections.

Qihang Ding, Lingbo Zhou, Tao Xiong, Jiqiang Liu, Luojia Chen, Jiyoung Yoo, Xiaoyu Xu, Xianglei Jia, Siling Chen, Siyu Chen and 5 more

Abstract read
In one paragraph

Article in National science review, 2026. 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
–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

10 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

15 authors.

Qihang DingDepartment of Chemistry, Korea University, Seoul 02841, Republic of Korea.
Lingbo ZhouDepartment of Neurosurgery, Zhongnan Hospital of Wuhan University, Ministry of Education Key Laboratory of Combinatorial Biosynthesis and Drug Discovery, School of Pharmaceutical Sciences, Wuhan University, Wuhan 430071, China.
Tao XiongCollege of Chemistry and Chemical Engineering, Central South University, Changsha 410083, China.
Jiqiang LiuGuangdong Key Laboratory of Nanomedicine, Chinese Academy of Sciences-Hong Kong Joint Lab for Biomaterials, Chinese Academy of Sciences Key Laboratory of Biomedical Imaging Science and System, Center for Nanomedicine and Nanobiotechnology, Institute of Biomedicine and Biotechnology, Shenzhen Institutes of Advanced Technology, Chinese Academy of Sciences, Shenzhen 518055, China.
Luojia ChenDepartment of Neurosurgery, Zhongnan Hospital of Wuhan University, Ministry of Education Key Laboratory of Combinatorial Biosynthesis and Drug Discovery, School of Pharmaceutical Sciences, Wuhan University, Wuhan 430071, China.
Jiyoung YooDepartment of Chemistry, Korea University, Seoul 02841, Republic of Korea.
Xiaoyu XuDepartment of Neurosurgery, Zhongnan Hospital of Wuhan University, Ministry of Education Key Laboratory of Combinatorial Biosynthesis and Drug Discovery, School of Pharmaceutical Sciences, Wuhan University, Wuhan 430071, China.
Xianglei JiaRenmin Hospital of Wuhan University, Wuhan 430060, China.
Siling ChenDepartment of Neurosurgery, Zhongnan Hospital of Wuhan University, Ministry of Education Key Laboratory of Combinatorial Biosynthesis and Drug Discovery, School of Pharmaceutical Sciences, Wuhan University, Wuhan 430071, China.
Siyu ChenDepartment of Neurosurgery, Zhongnan Hospital of Wuhan University, Ministry of Education Key Laboratory of Combinatorial Biosynthesis and Drug Discovery, School of Pharmaceutical Sciences, Wuhan University, Wuhan 430071, China.
Yifan WangDepartment of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.
Ping GongGuangdong Key Laboratory of Nanomedicine, Chinese Academy of Sciences-Hong Kong Joint Lab for Biomaterials, Chinese Academy of Sciences Key Laboratory of Biomedical Imaging Science and System, Center for Nanomedicine and Nanobiotechnology, Institute of Biomedicine and Biotechnology, Shenzhen Institutes of Advanced Technology, Chinese Academy of Sciences, Shenzhen 518055, China.
Meijia GuDepartment of Neurosurgery, Zhongnan Hospital of Wuhan University, Ministry of Education Key Laboratory of Combinatorial Biosynthesis and Drug Discovery, School of Pharmaceutical Sciences, Wuhan University, Wuhan 430071, China.
Wen JiangDepartment of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.
Jong Seung KimDepartment of Chemistry, Korea University, Seoul 02841, Republic of Korea.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Photodynamic therapy (PDT), which relies on the activation of photosensitizers by specific wavelengths of light to generate reactive oxygen species (ROS) for targeted pathogen or diseased tissue eradication, offers substantial promise for clinical wound management. However, its application in diabetic wound management remains constrained by suboptimal therapeutic efficacy, recurrent infections, treatment-associated pain, scar formation, and dependence on costly specialized equipment. Here, we present a sunlight-activated nanospray formulation comprising chitosan oligosaccharide-coated nanoparticles (SPS), engineered for the rapid and effective management of diabetic wounds in outdoor and resource-limited settings. SPS enables efficient ROS generation under ambient natural light, thereby reducing treatment-associated discomfort while maintaining effective photodynamic antimicrobial action. Additionally, the chitosan oligosaccharide coating confers intrinsic hemostatic, antibacterial, and antioxidative properties that synergistically accelerate wound closure and reduce the risk of scarring. The topical spray delivery circumvents systemic phototoxicity, improving patient compliance and broadening the accessibility of PDT. This strategy effectively overcomes the inherent limitations of conventional PDT by leveraging ambient light for activation and providing a cost-effective, non-invasive, and patient-friendly platform for diabetic wound care, thereby expanding the clinical utility of photodynamic interventions for managing chronic and complex wounds.

Indexed as

antibacterialNIR-IIphotodynamic therapyreactive oxygen speciessunlight

Identifiers

PMID41608042
PMCPMC12839536

What OpenQuestion holds

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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.