Evidence map›Paper›PMID 38874114›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2024

Smart Microneedle Arrays Integrating Cell-Free Therapy and Nanocatalysis to Treat Liver Fibrosis.

Yanteng Xu, Yixin Zhang, Hao Tian, Qingguo Zhong, Ke Yi, Fenfang Li, Tiantian Xue, Haixia Wang, Yeh-Hsing Lao, Yingying Xu and 5 more

Abstract read
In one paragraph

Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. Review
  5. Review
  6. Review
  7. Review
  8. Emerging nanomedicine for liver diseases treatment.Journal of nanobiotechnology · 2025
    Review
  9. Article
  10. Review
  11. Article
  12. Review
  13. Article
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.

Yanteng XuLaboratory of Biomaterials and Translational Medicine, Center for Nanomedicine and Department of Ultrasound, The Third Affiliated Hospital, Sun Yat-sen University, Guangzhou, 510630, China.
Yixin ZhangLaboratory of Biomaterials and Translational Medicine, Center for Nanomedicine and Department of Ultrasound, The Third Affiliated Hospital, Sun Yat-sen University, Guangzhou, 510630, China.
Hao TianLaboratory of Biomaterials and Translational Medicine, Center for Nanomedicine and Department of Ultrasound, The Third Affiliated Hospital, Sun Yat-sen University, Guangzhou, 510630, China.
Qingguo ZhongLaboratory of Biomaterials and Translational Medicine, Center for Nanomedicine and Department of Ultrasound, The Third Affiliated Hospital, Sun Yat-sen University, Guangzhou, 510630, China.
Ke YiLaboratory of Biomaterials and Translational Medicine, Center for Nanomedicine and Department of Ultrasound, The Third Affiliated Hospital, Sun Yat-sen University, Guangzhou, 510630, China.
Fenfang LiLaboratory of Biomaterials and Translational Medicine, Center for Nanomedicine and Department of Ultrasound, The Third Affiliated Hospital, Sun Yat-sen University, Guangzhou, 510630, China.
Tiantian XueLaboratory of Biomaterials and Translational Medicine, Center for Nanomedicine and Department of Ultrasound, The Third Affiliated Hospital, Sun Yat-sen University, Guangzhou, 510630, China.
Haixia WangLaboratory of Biomaterials and Translational Medicine, Center for Nanomedicine and Department of Ultrasound, The Third Affiliated Hospital, Sun Yat-sen University, Guangzhou, 510630, China.
Yeh-Hsing LaoDepartment of Pharmaceutical Sciences, University at Buffalo, The State University of New York, Buffalo, NY, 14214, USA.
Yingying XuCenter for Health Research, Guangzhou Institutes of Biomedicine and Health, Chinese Academy of Sciences, Guangzhou, 510530, China.
Yinxiong LiCenter for Health Research, Guangzhou Institutes of Biomedicine and Health, Chinese Academy of Sciences, Guangzhou, 510530, China.
Ling LongDepartment of Neurology, The Third Affiliated Hospital, Sun Yat-sen University, Guangzhou, 510630, China.
Kai LiLaboratory of Biomaterials and Translational Medicine, Center for Nanomedicine and Department of Ultrasound, The Third Affiliated Hospital, Sun Yat-sen University, Guangzhou, 510630, China.
Yu TaoLaboratory of Biomaterials and Translational Medicine, Center for Nanomedicine and Department of Ultrasound, The Third Affiliated Hospital, Sun Yat-sen University, Guangzhou, 510630, China.
Mingqiang LiLaboratory of Biomaterials and Translational Medicine, Center for Nanomedicine and Department of Ultrasound, The Third Affiliated Hospital, Sun Yat-sen University, Guangzhou, 510630, China.ORCID 0000-0002-5178-4138

Funding

China Primary Health Care Foundation 2022-003Guangdong Provincial Pearl River Talents Program 2019QN01Y131National Key Research and Development Program of China 2019YFA0111300National Natural Science Foundation of China 22277155National Natural Science Foundation of China 52373166Natural Science Foundation of Guangdong Province for Distinguished Young Scholar 2024B1515020025Science and Technology Program of Guangzhou 2024A04J6572Thousand Talents Plan
6 · The paper itself

Abstract

Liver fibrosis is a chronic pathological condition lacking specific clinical treatments. Stem cells, with notable potential in regenerative medicine, offer promise in treating liver fibrosis. However, stem cell therapy is hindered by potential immunological rejection, carcinogenesis risk, efficacy variation, and high cost. Stem cell secretome-based cell-free therapy offers potential solutions to address these challenges, but it is limited by low delivery efficiency and rapid clearance. Herein, an innovative approach for in situ implantation of smart microneedle (MN) arrays enabling precisely controlled delivery of multiple therapeutic agents directly into fibrotic liver tissues is developed. By integrating cell-free and platinum-based nanocatalytic combination therapy, the MN arrays can deactivate hepatic stellate cells. Moreover, they promote excessive extracellular matrix degradation by more than 75%, approaching normal levels. Additionally, the smart MN arrays can provide hepatocyte protection while reducing inflammation levels by ≈70-90%. They can also exhibit remarkable capability in scavenging almost 100% of reactive oxygen species and alleviating hypoxia. Ultimately, this treatment strategy can effectively restrain fibrosis progression. The comprehensive in vitro and in vivo experiments, supplemented by proteome and transcriptome analyses, substantiate the effectiveness of the approach in treating liver fibrosis, holding immense promise for clinical applications.

Indexed as

Liver CirrhosisNeedlesAnimalsCell-Free SystemDisease Models, AnimalHumansMaleMicecontrolled releaseliver fibrosismicroneedle arraynanozymestem cell secretome

Identifiers

PMID38874114
PMCPMC11336984

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.