Lemon‐Derived Extracellular Vesicles Engineered Oral Capsules for Enhanced Colorectal Cancer Chemotherapy by Mechanical Stress‐Induced Intestinal Epithelial Barrier Opening

X Xiangrong Hao (Cancer Research Institute School of Basic Medical Sciences Southern Medical University Guangzhou P. R. China) Y Ying Li H Houwang Zhou (Cancer Research Institute School of Basic Medical Sciences Southern Medical University Guangzhou P. R. China) J Jingwen Lin M Mengchang Xu (Department of Biochemistry and Molecular Biology School of Basic Medical Sciences Southern Medical University Guangzhou P. R. China) L Lun Li C Chao Fan (State Key Laboratory and Institute of Elemento-Organic Chemistry, College of Chemistry, Frontiers Science Center for New Organic Matter) J Jiawei Huang L Linyun He (Cancer Research Institute School of Basic Medical Sciences Southern Medical University Guangzhou P. R. China) X Xiaole Bai (Department of Gastroenterology Shenzhen Hospital Southern Medical University Shenzhen Guangdong P. R. China) B Biao Zhang M Mingxuan Sun (Cancer Research Institute School of Basic Medical Sciences Southern Medical University Guangzhou P. R. China) Y Ying Wang J Jun‐Bing Fan (Cancer Research Institute School of Basic Medical Sciences Southern Medical University Guangzhou P. R. China)

Abstract

ABSTRACT The effectiveness of colorectal cancer (CRC) treatment remains constrained due to the limited drug delivery efficiency resulting from the intestinal epithelial barriers. Although solid nanoparticle‐mediated drug delivery systems can enhance drug penetration, most of them are digested and excreted from the body, with only a small portion successfully crossing the intestinal epithelial barrier. Herein, we demonstrated lemon‐derived extracellular vesicles (EVs)‐engineered oral capsules loaded with capecitabine (EVOC), enabling them to trigger temporary opening of the intestinal epithelial barrier as a result of mechanical stress and thereby greatly enhancing the drug delivery efficiency. The EVOC enabled them to induce cellular stress responses within the intestinal epithelial barrier due to their much larger dimensions than cells, resulting in cytoskeleton relaxation and thereby breaking the original balance of tight junctions among cells. This cellular stress response could temporarily open the intestinal epithelial barrier, allowing highly efficient drug penetration into tumor tissues. The concentration of 5‐fluorouracil (metabolite of capecitabine) accumulated in tumor tissues within the EVOC group was approximately 13‐fold higher than that in the free capecitabine group and 6‐fold higher than that in the capecitabine@EV nanodrugs. As expected, the EVOC group significantly enhanced the chemotherapy efficiency of CRC.

Article Details

Volume / Issue Vol. 38, Issue 25
Published May 01, 2026
ISSN 0935-9648
Publisher Unknown Publisher

Journal Info

Advanced Materials

Unknown Publisher

ISSN: 0935-9648 Physical Sciences

Authors (14)

X

Xiangrong Hao

Cancer Research Institute School of Basic Medical Sciences Southern Medical University Guangzhou P. R. China

Y

Ying Li

H

Houwang Zhou

Cancer Research Institute School of Basic Medical Sciences Southern Medical University Guangzhou P. R. China

J

Jingwen Lin

M

Mengchang Xu

Department of Biochemistry and Molecular Biology School of Basic Medical Sciences Southern Medical University Guangzhou P. R. China

L

Lun Li

C

Chao Fan

State Key Laboratory and Institute of Elemento-Organic Chemistry, College of Chemistry, Frontiers Science Center for New Organic Matter

J

Jiawei Huang

L

Linyun He

Cancer Research Institute School of Basic Medical Sciences Southern Medical University Guangzhou P. R. China

X

Xiaole Bai

Department of Gastroenterology Shenzhen Hospital Southern Medical University Shenzhen Guangdong P. R. China

B

Biao Zhang

M

Mingxuan Sun

Cancer Research Institute School of Basic Medical Sciences Southern Medical University Guangzhou P. R. China

Y

Ying Wang

J

Jun‐Bing Fan

Cancer Research Institute School of Basic Medical Sciences Southern Medical University Guangzhou P. R. China