Bioactive Nanotherapeutic Ultrasound Contrast Agent for Concurrent Breast Cancer Ultrasound Imaging and Treatment

Author:

Fang Junyue123ORCID,Tan Jiabao12,Lin Li124,Cao Yuan12,Xu Rui12,Lin Chunhao12,He Gui13,Xu Xiaoding12,Xiao Xiaoyun125,Jiang Qiongchao125,Saw Phei Er126ORCID

Affiliation:

1. Guangdong Provincial Key Laboratory of Malignant Tumor Epigenetics and Gene Regulation Medical Research Center Sun Yat‐sen Memorial Hospital Sun Yat‐sen University Guangzhou 510120 P. R. China

2. Guangzhou Key Laboratory of Medical Nanomaterials Sun Yat‐sen Memorial Hospital Sun Yat‐sen University Guangzhou 510120 P. R. China

3. Cellular and Molecular Diagnostics Center Sun Yat‐sen Memorial Hospital Sun Yat‐sen University Guangzhou 510120 P. R. China

4. Department of Dermatology Sun Yat‐sen Memorial Hospital Sun Yat‐sen University Guangzhou 510120 P. R. China

5. Department of Ultrasound Sun Yat‐sen Memorial Hospital Sun Yat‐sen University Guangzhou 510120 P. R. China

6. Department of General Medicine Sun Yat‐sen Memorial Hospital Sun Yat‐sen University Guangzhou 510120 P. R. China

Abstract

AbstractContrast‐enhanced ultrasound (CEUS) plays a crucial role in cancer diagnosis. The use of ultrasound contrast agents (UCAs) is inevitable in CEUS. However, current applications of UCAs primarily focus on enhancing imaging quality of ultrasound contrast rather than serving as integrated platforms for both diagnosis and treatment in clinical settings. In this study, a novel UCA, termed NPs‐DPPA(C3F8), is innovatively prepared using a combination of nanoprecipitation and ultrasound vibration methods. The DPPA lipid possesses inherent antiangiogenic and antitumor activities, and when combined with C3F8, it functions as a theranostic agent. Notably, the preparation of NPs‐DPPA(C3F8) is straightforward, requiring only one hour from raw materials to the final product due to the use of a single material, DPPA. NPs‐DPPA(C3F8) exhibits inherent antiangiogenic and biotherapeutic activities, effectively inhibiting triple‐negative breast cancer (TNBC) angiogenesis and reducing VEGFA expression both in vitro and in vivo. Clinically, NPs‐DPPA(C3F8) enables simultaneous real‐time imaging, tumor assessment, and antitumor activity. Additionally, through ultrasound cavitation, NPs‐DPPA(C3F8) can overcome the dense vascular walls to increase accumulation at the tumor site and facilitate internalization by tumor cells. The successful preparation of NPs‐DPPA(C3F8) offers a novel approach for integrating clinical diagnosis and treatment of TNBC.

Funder

Higher Education Discipline Innovation Project

National Natural Science Foundation of China

Guangzhou Municipal Science and Technology Bureau

Publisher

Wiley

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