Cellulose Nanofibrils of High Immunoaffinity for Efficient Enrichment of Small Extracellular Vesicles

Author:

Wang Zesheng123,Dai Jun2,He Huimin123,Si Tongxu2,Ng Kaki2,Zheng Shuang24,Zhou Xiaoyu123,Zhou Zhihang5,Yuan Huijun6,Yang Mengsu123ORCID

Affiliation:

1. Department of Precision Diagnostic and Therapeutic Technology City University of Hong Kong Shenzhen Futian Research Institute Shenzhen 518000 P. R. China

2. Department of Biomedical Sciences, and Tung Biomedical Sciences Centre City University of Hong Kong Hong Kong 999077 P. R. China

3. Key Laboratory of Biochip Technology Biotech and Health Centre Shenzhen Research Institute of City University of Hong Kong Shenzhen 518057 P. R. China

4. Department of Civil Engineering University of Hong Kong Pokfulam Hong Kong P. R. China

5. Department of Gastroenterology the Second Affiliated Hospital of Chongqing Medical University Chongqing 400010 P. R. China

6. Department of Biochip Center Wuwei Tumor Hospital of Gansu Province Gansu 730000 P. R. China

Abstract

AbstractExtracellular vesicles (EVs), crucial in facilitating the transport of diverse molecular cargoes for intercellular communication, have shown great potential in diagnostics, therapeutics, and drug delivery. The challenge of developing effective preparation methods for EVs is heightened by their intrinsic heterogeneity and complexity. Here, a novel strategy for high EV enrichment is developed by utilizing EV‐affinitive‐modified cellulose nanofibrils. Specifically, modified cellulose with rich carboxyl groups has outstanding dispersing properties, able to be dispersed into cellulose nanofibrils in solution. These cellulose nanofibrils are utilized as scaffolds for the immobilization of EV‐affinitive antibody of CD63 by chemical conjugation. The CD63‐modified nanofibrils demonstrate a superior EV capture efficiency of 86.4% compared with other reported methods. The high performance of this system is further validated by the efficient capture of EVs from biological blood plasma, allowing the detection of bioactive markers from EV‐derived miRNAs and proteins. The authors envision that these modified cellulose nanofibrils of enhanced capability on EV enrichment will open new avenues in various biomedical applications.

Funder

National Basic Research Program of China

Publisher

Wiley

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