Journal of Inorganic Materials

   

Degradable Mesoporous Bioglass Microspheres for Chemoembolization Prepared by Microfluidic Method

ZHANG Xiaoliang1, YANG Zili1, TIAN Yuecheng1, LI Dejian2, ZHU Min1   

  1. 1. School of Materials and Chemistry, University of Shanghai for Science and Technology, Shanghai 200093, China;
    2. Fudan University Pudong Medical Center, Department of Orthopedics, Shanghai Pudong Hospital, Shanghai 201399, China
  • Received:2026-03-13 Revised:2026-05-14
  • About author:ZHANG Xiaoliang (1999-), male, Master candidate. E-mail: zxlha0905@163.com
  • Supported by:
    National Natural Science Foundation of China (52072246)

Abstract: Transarterial chemoembolization (TACE) is a widely employed clinical procedure for the treatment of unresectable liver tumors. However, existing embolic microspheres exhibit certain limitations regarding drug loading capacity, sustained drug release, and mechanical adaptability. To address these challenges, in this study, the rigid mesoporous bioactive glass (MBG) microspheres via a one-step microfluidic technique were prepared, yielding particles with a high specific surface area, uniform and controllable size, bimodal pore size distribution with peaks at approximately 5 nm and 8 nm, as well as biodegradability, elevated drug loading efficiency, and sustained drug release profiles. Furthermore, doxorubicin (DOX)-loaded MBG microspheres were encapsulated within sodium alginate (SA) to form MBG-DOX@SA core-shell composite microspheres, which demonstrated pH-responsive and controlled drug release behavior. Drug encapsulation efficiency of this composite system was (81.50±1.93)%. SA shell effectively mitigated the initial burst release of the drug during early embolization and significantly decelerated the cumulative release rate. Under the weakly acidic conditions of the tumor microenvironment (pH 5), the cumulative release after 10 days was only (59.99±1.91)%. Additionally, the SA encapsulation enhanced the surface smoothness and elasticity of the DOX-loaded MBG microspheres, thereby extending the drug diffusion pathway, while also endowing the composite microspheres with improved biocompatibility and safety profiles during treatment. In antitumor tests, the composite microspheres achieved a cell death rate of (36.00±0.03)%. These results indicate that MBG-DOX@SA microspheres represent a promising candidate for application in TACE-based therapies for liver cancer.

Key words: mesoporous bioglass, microsphere, transarterial chemoembolization, drug delivery

CLC Number: