Carbon Quantum Dots Assisted Virus Tracking: From Skin to Brain

Y Yaxiu Feng (Department of Biomedical Sciences City University of Hong Kong Hong Kong SAR 999077 China) X Xiong Wang (Department of Physics, The University of Hong Kong, Pokfulam Road, Hong Kong, Hong Kong SAR, China) C Cien Chen (Department of Biomedical Sciences City University of Hong Kong Hong Kong SAR 999077 China) D Di Wang C Changshun Hou Y Yiran Wang H Huan Hu P Peiran Chen (State Key Laboratory of Bioactive Molecules and Druggability Assessment, The First Affiliated Hospital of Jinan University Guangzhou) L LeiYing Qin (Department of Biomedical Sciences City University of Hong Kong Hong Kong SAR 999077 China) Q Qianya Wan (Department of Biomedical Sciences City University of Hong Kong Hong Kong SAR 999077 China) X Xi Yao M Ming‐Liang He (Department of Biomedical Sciences City University of Hong Kong Hong Kong SAR 999077 China)

Abstract

Abstract Incurable infection by herpes simplex virus 1 (HSV‐1) can cause severe encephalitis and neurodegenerative diseases, e.g., Alzheimer's disease (AD) and amyotrophic lateral sclerosis. How HSV‐1 reaches the brain from the initial infection site remains inconclusive. Here, an innovative approach combining carbon quantum dots (CQDs) with dissolving microneedles (dMN) for real‐time tracking of HSV‐1 from skin to brain is presented. Upon application, CQDs‐HSV‐1 is released from the dMN through the swelling of interstitial fluid (ISF) in skin and subsequently monitored by living imaging. Remarkably, it is observed that HSV‐1 preferentially infects peripheral skin nerves, almost all viruses directly enter to brain via the spinal cord within 10–30 min, while few viruses enter the brain through the bloodstream via tail vein injection at the same time. Spinal cord injury (SCI) significantly delays the HSV‐1 transport from skin to brain but has no effect on the virus's travel from blood to brain. In a microfluid system, HSV‐1 shows preferential neurite infection, then transports to the cell body of differentiated SH‐SY5Y cells, highlighting the viral traffic process in neurons. The integration of CQDs‐virus labelling technology and dMN delivery model presents a promising tool for investigating the in vivo transport routes of neurotropic viruses with initial skin infections.

Article Details

Volume / Issue Vol. 38, Issue 6
Published January 01, 2026
ISSN 0935-9648
Publisher Unknown Publisher

Journal Info

Advanced Materials

Unknown Publisher

ISSN: 0935-9648 Physical Sciences

Authors (12)

Y

Yaxiu Feng

Department of Biomedical Sciences City University of Hong Kong Hong Kong SAR 999077 China

X

Xiong Wang

Department of Physics, The University of Hong Kong, Pokfulam Road, Hong Kong, Hong Kong SAR, China

C

Cien Chen

Department of Biomedical Sciences City University of Hong Kong Hong Kong SAR 999077 China

D

Di Wang

C

Changshun Hou

Y

Yiran Wang

H

Huan Hu

P

Peiran Chen

State Key Laboratory of Bioactive Molecules and Druggability Assessment, The First Affiliated Hospital of Jinan University Guangzhou

L

LeiYing Qin

Department of Biomedical Sciences City University of Hong Kong Hong Kong SAR 999077 China

Q

Qianya Wan

Department of Biomedical Sciences City University of Hong Kong Hong Kong SAR 999077 China

X

Xi Yao

M

Ming‐Liang He

Department of Biomedical Sciences City University of Hong Kong Hong Kong SAR 999077 China