AI Chat Paper
Note: Please note that the following content is generated by AMiner AI. SciOpen does not take any responsibility related to this content.
{{lang === 'zh_CN' ? '文章概述' : 'Summary'}}
{{lang === 'en_US' ? '中' : 'Eng'}}
Chat more with AI
PDF (3.3 MB)
Collect
Submit Manuscript AI Chat Paper
Show Outline
Outline
Show full outline
Hide outline
Outline
Show full outline
Hide outline
Review | Open Access

Advances in microneedle design for the delivery of drugs, proteins, and cells in the treatment of hypertrophic scars

Juntong Guo1,2,‡, Qinghan Tang3,‡, Zhengping Ge1, Qing Xia1, Hanmei Liu4, Huaikai Shi5, Jinlong Huang4, Jun Chen1,2,6, Mark S. Cooper7, Xin Yan8( ), Chenxi Yang2,9( ), Yiwei Wang1,6,8 ( )
School of Pharmacy, Nanjing University of Chinese Medicine, 138 Xianlin Road, Nanjing 210023, PR China
Jiangsu Provincial Engineering Research Center of TCM External Medication Development and Application, Nanjing University of Chinese Medicine, 138 Xianlin Road, Nanjing 210023, PR China
Department of Pharmacy, Nanjing Hospital of Chinese Medicine, 157 Daming Road, Nanjing 210022, Jiangsu, China
Affiliated Hospital of Nanjing University of Chinese Medicine, 155 Hanzhong Road, Nanjing 210000, PR China
Asbestos and Dust Diseases Research Institute, Concord Hospital, Gate 3 Hospital Road, Sydney, NSW 2138, Australia
Jiangsu Collaborative Innovation Center of Chinese Medicinal Resources Industrialization, 138 Xianlin Road, Nanjing University of Chinese Medicine, Nanjing 210023, PR China
Adrenal Steroid Group, ANZAC Research Institute, Concord Hospital, The University of Sydney, Gate 3, Hospital Road, Sydney, NSW 2137, Australia
Department of Burns and Plastic Surgery, Nanjing Drum Tower Hospital, Affiliated Hospital of Medical School, Nanjing University, 321 Zhongshan Road, Nanjing 21000, PR China
Department of Immunology, School of Medicine, Nanjing University of Chinese Medicine, 138 Xianlin Road, Nanjing 210023, PR China

‡Juntong Guo and Qinghan Tang contributed equally.

Show Author Information

Abstract

Hypertrophic scars (HS) represent a significant clinical challenge due to their complex pathophysiology and resistance to conventional therapies, often resulting in persistent symptoms such as itching, pain, and impaired joint mobility that compromise patients’ quality of life. Current treatment modalities, including compression therapy, pharmacological agents, radiation, silicone gel, and laser therapies, have faced limitations primarily due to inadequate drug penetration into the dense fibrotic scar tissue. In this context, microneedle-mediated controlled delivery systems have emerged as a promising pharmaceutical platform to enhance localized and sustained delivery of therapeutic agents, including small-molecule drugs, biologic proteins, small interfering RNA, and living cells, directly into HS. This article critically reviews the biological and formulation-related challenges associated with transdermal delivery in scar tissue and highlights recent innovations in microneedle design, material selection, and drug-loading techniques tailored for controlled release applications. Furthermore, it discusses the integration of proteins and cell-based therapies within microneedle platforms and their potential to modulate scar remodeling and inflammation. By addressing current limitations and exploring cutting-edge technologies, this review article aims to guide the development of effective microneedle-mediated strategies for pharmaceutical intervention in hypertrophic scar management.

Graphical Abstract

References

【1】
【1】
 
 
Burns & Trauma
Article number: tkag025

{{item.num}}

Comments on this article

Go to comment

< Back to all reports

Review Status: {{reviewData.commendedNum}} Commended , {{reviewData.revisionRequiredNum}} Revision Required , {{reviewData.notCommendedNum}} Not Commended Under Peer Review

Review Comment

Close
Close
Cite this article:
Guo J, Tang Q, Ge Z, et al. Advances in microneedle design for the delivery of drugs, proteins, and cells in the treatment of hypertrophic scars. Burns & Trauma, 2026, 14(3): tkag025. https://doi.org/10.1093/burnst/tkag025

2

Views

0

Downloads

0

Crossref

0

Web of Science

0

Scopus

Received: 12 November 2025
Revised: 11 March 2026
Accepted: 16 March 2026
Published: 18 March 2026
© The Author(s) 2026. Published by Oxford University Press.

This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact reprints@oup.com for reprints and translation rights for reprints. All other permissions can be obtained through our RightsLink service via the Permissions link on the article page on our site—for further information please contact journals.permissions@oup.com.