PEER-REVIEWED PUBLICATION

2026

Novel Vascular-Adaptive Liquid Metal Microspheres Enable Visualized Arterial Embolization Therapy

A tensile test divider icon

Shen C, Chen J, et al.

Advanced Science

CAS Center for Excellence in Nanoscience, National Center for Nanoscience and Technology of China, Chinese PLA General Hospital, Tangshan Gongren Hospital, Beihang University, Peking University First Hospital, University of Pennsylvania

RESEARCH SUMMARY
This study developed radiopaque gallium-based liquid metal microspheres for arterial embolization and chemoembolization. The authors formed gallium microspheres by ultrasonically disrupting liquid gallium and then grafted doxorubicin-loaded DSPE-PEG2000-SH micelles onto the particle surface to create X-MEN, a drug-loaded embolic microsphere with an external solid shell and liquid core. In vitro, X-MEN showed sustained doxorubicin release, strong radiopacity comparable to iohexol on CT, good blood compatibility, and favorable immunocompatibility. In rabbit ear and VX2 tumor models, GaMs and X-MEN produced more durable vessel occlusion and lower blood-flow recovery than Embosphere, while X-MEN also reduced tumor burden more effectively than PBS, free Dox-m, or GaMs alone; tumor volume fell to 118.7 ± 76.36 mm3 by day 21 in the X-MEN group. In a rabbit liver tumor model, X-MEN achieved stepwise filling of tumor-feeding vessels and complete disappearance of tumor staining after embolization. In dogs, gallium microspheres remained stable in the prostate for at least 6 months, reduced prostate volume from 36.0 ± 3.7 to 12.4 ± 4.6 cm3 at 2 months, and showed good long-term biosafety. Overall, the work demonstrates a persistent, image-visible embolic platform that combines embolization, visualization, and drug delivery for transcatheter arterial embolization therapy.
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CELLSCALE INSTRUMENT USED

MicroTester

A CellScale MicroTester G2 was used to quantify the micro-scale mechanical behavior of the embolic microspheres and to compare X-MEN and unloaded gallium microspheres (GaMs) against the commercial embolic control Embosphere. Before testing, samples were filtered through a 70 µm cell strainer to obtain uniformly sized microspheres. The sample chamber was filled with deionized water and maintained at 37°C. For compression testing, a single microsphere was isolated on the iron sample stage and compressed with a 0.5588 mm diameter cylindrical probe to 20% of its original diameter while images, load, displacement, and diameter were recorded throughout loading and recovery. The resulting data were used to calculate compressive modulus with a spherical model, evaluate maximum compression ratio, and assess recovery behavior. For tensile/stretch testing, a single microsphere was first compressed to 20% of its original diameter and then the same 0.5588 mm probe was lifted vertically by 100 µm to initiate stretching; images and load-displacement data were collected during the deformation. These MicroTester G2 measurements showed that GaMs and X-MEN had markedly higher compressive modulus than Embosphere, exhibited hysteresis during compression-recovery, recovered rapidly after compression, and could be stretched under the probe whereas Embosphere could not. The CellScale data supported the authors’ core conclusion that the liquid-core gallium microspheres possess deformability, viscoelasticity, viscosity, and catheter-delivery-friendly mechanics that help them pack tightly and embolize vessels more effectively.
AUTHORS

Chenyu Shen, Junge Chen, Gang Zhang, Zhusheng Liu, Yichen Wan, Lei Lei, Weiyan Ren, Yanyu Zhao, Bozhang Xia, Zhiqiang Yi, Jinjin Wang, Jingwang Gao, Gen Mu, Xing-Jie Liang, Zhijun Wang.

PUBLICATION DETAILS
JOURNAL

Advanced Science

YEAR

2026

INSTITUTIONS

CAS Center for Excellence in Nanoscience, National Center for Nanoscience and Technology of China, Chinese PLA General Hospital, Tangshan Gongren Hospital, Beihang University, Peking University First Hospital, University of Pennsylvania

COUNTRIES

China, United States

INSTRUMENT USED

MicroTester

TESTING METHODS

Compression TestingHydrated and Temperature Controlled TestingMicro-Mechanical TestingTensile TestingUltra Low Force Testing

RESEARCH APPLICATIONS

Drug Screening & Drug Delivery MechanicsInjectable & Regenerative Biomaterials

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