Integration of Silica Nanorattles with Manganese-Doped In 2 S 3 /InOOH to Enable Ultrasound-Mediated Tumor Theranostics.
Tian ZhangQiang ZhengCongkun XieGonglin FanYifan WangYongjun WuYike FuJie HuangDuncan Q M CraigXiujun CaiXiang LiPublished in: ACS applied materials & interfaces (2023)
As a result of their radiation-free nature and deep-penetration ability, tumor theranostics mediated by ultrasound have become increasingly recognized as a modality with high potential for translation into clinical cancer treatment. The effective integration of ultrasound imaging and sonodynamic therapy (SDT) into one nanoplatform remains an enormous challenge yet to be fully resolved. Here, a novel theranostic system, consisting of rattle-type SiO 2 (r-SiO 2 ) loaded with Mn-doped In 2 S 3 /InOOH (SMISO), was designed and synthesized to enable an improved ultrasound imaging-guided therapy. With Mn-doped In 2 S 3 /InOOH (MISO) and a heterojunction structure, this novel sonosensitizer facilitates the generation of reactive oxygen species (ROS) for SDT. By coupling interfaces between the shell and core in rattle-type SiO 2 , multiple reflections/scattering are generated, while MISO has high acoustic impedance. By integrating r-SiO 2 and MISO, the SMISO composite nanoparticles (NPs) increase the acoustic reflection and provide enhanced contrast for ultrasound imaging. Through the effective accumulation in tumors, which was monitored by B-mode ultrasound imaging in vivo , SMISO composite NPs effectively inhibited tumor growth without adverse side effects under ultrasound irradiation treatment. This work therefore provides a new approach to integrate a novel gas-free ultrasound contrast agent and a semiconductor sonosensitizer for cancer theranostics.
Keyphrases
- magnetic resonance imaging
- reactive oxygen species
- room temperature
- quantum dots
- metal organic framework
- magnetic resonance
- visible light
- contrast enhanced ultrasound
- highly efficient
- ultrasound guided
- photodynamic therapy
- cancer therapy
- magnetic nanoparticles
- drug delivery
- oxide nanoparticles
- squamous cell carcinoma
- contrast enhanced
- cell death
- mesenchymal stem cells
- radiation therapy
- risk assessment
- emergency department
- squamous cell
- young adults
- bone marrow
- radiation induced
- combination therapy
- drug release
- oxidative stress
- human health
- iron oxide