Department of Ultrasound Medicine, Laboratory of Ultrasound Molecular Imaging, The Third Affiliated Hospital of Guangzhou Medical University, Duo Bao Road 63, Guangzhou 510150, China.
Cancer Center, Faculty of Health Sciences, Centre for Cognitive and Brain Sciences, University of Macau, Macau SAR, China.
ACS Biomater Sci Eng. 2020 May 11;6(5):2904-2912. doi: 10.1021/acsbiomaterials.0c00014. Epub 2020 Apr 13.
: Gene therapy is an important therapeutic strategy for cancer. Nanoparticles are used for noninvasive gene delivery, which has great potential in tumor therapy. However, it is a challenge to construct a targeted gene delivery vector with high gene delivery efficiency, good biocompatibility, and multiple functions. : Herein, we designed magnetic mesoporous silica nanoparticle loading microbubbles (M-MSN@MBs) for ultrasound-mediated imaging and gene transfection. The plasmid DNA (pDNA) was encapsulated into the pores of M-MSNs. Also, the pDNA-carrying M-MSNs were loaded in the lipid microbubbles. : The gene vector presented good biocompatibility, DNA binding stability, ultrasound imaging performance, and magnetic responsiveness. The polyethyleneimine (PEI)-modified M-MSNs effectively protected the loaded pDNA from enzyme degradation. The cytotoxicity of M-MSNs was significantly reduced via encapsulating in lipid microbubbles. Upon the magnetic field, M-MSN@MBs were attracted to the tumor area. Then, ultrasound-targeted microbubble destruction (UTMD) not only released loaded M-MSNs but also facilitated M-MSNs delivery to tumor tissue by opening blood-tumor barrier and increasing the cytomembrane permeability, and ultimately improved the pDNA delivery efficiency. : Our findings suggested that the developed ultrasound-responsive gene delivery system was a promising platform for gene therapy, which could noninvasively enhance tumor gene transfection.
基因治疗是癌症的一种重要治疗策略。纳米颗粒可用于非侵入性基因传递,在肿瘤治疗中具有很大的潜力。然而,构建具有高基因传递效率、良好生物相容性和多功能的靶向基因传递载体仍然是一个挑战。
在这里,我们设计了用于超声介导成像和基因转染的磁性介孔硅纳米颗粒负载微泡(M-MSN@MBs)。质粒 DNA(pDNA)被包裹在 M-MSNs 的孔中。此外,携带 pDNA 的 M-MSNs 被装载在脂质微泡中。
该基因载体表现出良好的生物相容性、DNA 结合稳定性、超声成像性能和磁响应性。经过修饰的聚乙烯亚胺(PEI)-修饰的 M-MSNs 有效地保护了负载的 pDNA 免受酶降解。通过将 M-MSNs 包裹在脂质微泡中,M-MSNs 的细胞毒性显著降低。在磁场的作用下,M-MSN@MBs 被吸引到肿瘤区域。然后,超声靶向微泡破坏(UTMD)不仅释放了负载的 M-MSNs,还通过打开血-肿瘤屏障和增加细胞质膜通透性来促进 M-MSNs 递送到肿瘤组织,从而最终提高了 pDNA 的递送效率。
我们的研究结果表明,开发的超声响应性基因传递系统是一种很有前途的基因治疗平台,可无创增强肿瘤基因转染。