Related Experiment Video
Updated: Dec 15, 2025

Contrast Ultrasound Targeted Treatment of Gliomas in Mice via Drug-Bearing Nanoparticle Delivery and Microvascular Ablation
Published on: December 15, 2010
Ultrasound-Augmented Phase Transition Nanobubbles for Targeted Treatment of Paclitaxel-Resistant Cancer
Yi Zhu1,2, Guonan Zhang3, Meiying Li4
1Department of Ultrasound, West China Hospital, Sichuan University, Chengdu 610041, China.
Abstract:
Paclitaxel (PTX) resistance in most epithelial ovarian cancers (EOCs) with increasing membrane expression of mucin 16 (MUC16) is mediated by the Toll-like receptor-myeloid differentiation factor 2/myeloid differentiation factor 88 (TLR4-MD2/MyD88) signaling pathway. 6-Shogaol (6S), an α,β-unsaturated carbonyl compound with lipophilic property, can block PTX-induced formation of the TLR4-MD2 complex that activates the MyD88/NF-κB signaling pathway. Herein, to improve the effectiveness of 6S, augment the sensibility of PTX, and enhance the targeting ability of PTX-resistant cancer therapies, we report a class of 6S-loaded phase transition nanobubbles conjugated with the MUC16 antibody (6S@NBs-MUC16A), which can enhance the sensitivity of PTX to EOC cells through ultrasound-controlled targeted-delivery of 6S. The 6S@NB-MUC16A could enhance the targeting efficiency and organizational distribution of 6S in MyD88+ EOC area, and the 1 MHz ultrasound can be used as an initiator to trigger the "explosion" of nanobubbles and promote the 6S release. Furthermore, in vivo assessment results indicate that ultrasound-augmented 6S@NB-MUC16A can significantly improve the response of EOC to PTX and the inhibition ratio of tumor growth compared to the control-treated with PTX alone, and exhibit less toxicity to the critical organs. The ultrasound-augmented 6S@NB-MUC16A with less cytotoxicity could be a potentially useful nanosystem to surmount PTX resistance in EOC, which provides potential possibilities for the applications in the biological field.
Insights
New nanobubbles loaded with 6-shogaol (6S) and targeted with MUC16 antibodies overcome paclitaxel (PTX) resistance in ovarian cancer. Ultrasound-triggered release of 6S enhances PTX efficacy and reduces toxicity.
Area of Science:
- Biomedical Engineering
- Nanotechnology
- Oncology
Background:
- Paclitaxel (PTX) resistance in epithelial ovarian cancer (EOC) is linked to Mucin 16 (MUC16) and the TLR4-MD2/MyD88 pathway.
- 6-Shogaol (6S) inhibits the TLR4-MD2 complex, potentially sensitizing EOC to PTX.
Purpose of the Study:
- To develop ultrasound-triggered, MUC16-targeted nanobubbles (6S@NBs-MUC16A) for enhanced delivery of 6S.
- To improve PTX sensitivity and therapeutic outcomes in PTX-resistant EOC.
Main Methods:
- Conjugation of MUC16 antibody to 6S-loaded phase transition nanobubbles.
- Ultrasound-controlled targeted delivery of 6S to MyD88+ EOC cells.
- In vivo assessment of therapeutic efficacy and toxicity.
Main Results:
- 6S@NBs-MUC16A demonstrated enhanced targeting and distribution in EOC.
- Ultrasound triggered efficient 6S release, improving PTX response and tumor growth inhibition.
- The nanosystem exhibited reduced toxicity to critical organs.
Conclusions:
- Ultrasound-augmented 6S@NBs-MUC16A is a promising nanosystem for overcoming PTX resistance in EOC.
- This approach offers potential for improved ovarian cancer treatment with reduced side effects.

