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张海波

副教授

基本信息 / Basic Information

  • 教师英文名称: Haibo Zhang
  • 教师拼音名称: Zhang Haibo
  • 所在单位: 化学与分子科学学院
  • 职务: 化学国家级实验教学示范中心(武汉大学)副主任
  • 学历: 研究生毕业
  • 性别: 男
  • 在职信息: 在职
  • 毕业院校: 武汉大学
  • 学科: 应用化学 、 化学其他专业

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论文成果

当前位置: 武汉大学张海波 - 科学研究 - 论文成果

An Integrated Microfluidic Chip for Synchronous Drug Loading, Separation and Detection of Plasma Exosomes

发布时间:2025-05-09
点击次数:
发表刊物:
Lab on a Chip
关键字:
Yu-Xin Zhang,‡ Ming Wang,‡ Li-Li Xu, Yi-Jing Chen, Shu-Ting Zhong, Ying Feng, d Hai-Bo Zhang,*Shi-Bo Cheng,* Min Xie* and Wei-Hua Huang, Accepted
摘要:
Exosomes have gained increasing attention as robust, biocompatible carriers for targeted therapy. However, current techniques for exosome drug loading suffer from low drug loading efficiency, substantial exosome loss during repeated purification and quantification processes. Here, we present an integrated microfluidic chip (IMC) that streamlines drug loading, separation, and electrochemical detection of exosomes from plasma in a single device. In this design, the three dimensional (3D) macroporous scaffold and the magnetoresponsive electrode are successfully assembled into the modeling microchip, playing the functions of “3D chaotic flow mixer”, “magnetic separator” and “electrochemical detector”. When plasma, doxorubicin (DOX), boron clusters and immunomagnetic nanoprobes (IMP) are simultaneously injected into the IMC, the exosomes are loaded with DOX-boron cluster (EDB) complexes and synchronously recognized by IMP in the “3D chaotic flow mixer”. Our strategy exhibits high DOX loading efficiency owing to the superchaotropic effect of boron cluster and enhanced immunolabeling efficiency by the thorough mixing of 3D scaffold. Meanwhile, the novel magnetoresponsive electrode enables magnetic separation and real-time, enzyme-linked immunoelectrochemical quantification of exosomes, thereby simplifying the workflow from drug loading to quantification. The resulting EDB in combination with magnetic hyperthermia achieves up to 90% cell-killing efficiency against DOX-resistant breast cancer cells. Overall, our system could simultaneously realize the enhanced DOX loading into exosomes, efficient magnetic immunoseparation of exosomes, and sensitive electrochemical quantification of exosomes, offering a promising approach for autologous exosome-based drug delivery for cancer treatment.
论文类型:
期刊论文
学科门类:
理学
文献类型:
J
是否译文:
发表时间:
2025-05-09
收录刊物:
SCI