TY - JOUR
T1 - Hybrid theranostic microbubbles for ultrasound/photoacoustic imaging guided starvation/low-temperature photothermal/hypoxia-activated synergistic cancer therapy
AU - Tian, Feng
AU - Zhong, Xingjian
AU - Zhao, Jun Kai
AU - Gu, Yutian
AU - Fan, Yadi
AU - Shi, Fan
AU - Zhang, Yu
AU - Tan, Youhua
AU - Chen, Wen
AU - Yi, Changqing
AU - Yang, Mo
N1 - Funding Information:
This work was supported by the National Natural Science Foundation of China (NSFC) (Grant No. 31771077), the Hong Kong Research Council Collaborative Research Grant (C5011-19G), Innovation and Technology Fund, Guangdong-Hong Kong Cooperation Scheme (GHP-039-18GD), the Hong Kong Research Council General Research Fund (PolyU 15216917) and the Hong Kong Polytechnic University Internal Fund (1-ZE1E).
Publisher Copyright:
© The Royal Society of Chemistry 2021.
PY - 2021/12/7
Y1 - 2021/12/7
N2 - Constructing a theranostic agent for high-contrast multimodality imaging-guided synergistic therapy with long-term tumor retention and minimum systemic side effects still remains a major challenge. Herein, a hybrid microbubble-based theranostic platform was developed for dual-modality ultrasound (US) and enhanced photoacoustic (PA) imaging-guided synergistic tumor therapy by combining starvation therapy, low-temperature photothermal therapy (PTT), and hypoxia-activated therapy, based on polydopamine (PDA) doped poly(vinyl alcohol) microbubbles loaded with glucose oxidase (GOx) (PDA-PVAMBs@GOx) and hypoxia-activated prodrug (HAP) tirapazamine (TPZ). For dual-modality US/enhanced PA imaging, PDA-PVAMBs provided 6.5-fold amplified PA signals relative to freely dispersed PDA nanoparticles (PDA NPs). For synergistic cancer therapy, oxygen (O2) carried by PDA-PVAMBs@GOx was first released to promote starvation therapy by loaded GOx. Then, moderate near-infrared (NIR) laser irradiation triggered PTT and improved enzymatic activity of GOx with its optimal activity around 47 °C. Subsequently, GOx-mediated tumor starvation depleted O2and exacerbated the hypoxia environment, thereby activating the toxicity of TPZ in the tumor site. Through dual-modality US/PA imaging monitoring, PDA-PVAMBs@GOx with long-term retention (∼7 days) combined with PTT and TPZ significantly inhibited the growth of solid tumors with minimum systemic side effects, which might be a powerful tool for effective tumor treatment.
AB - Constructing a theranostic agent for high-contrast multimodality imaging-guided synergistic therapy with long-term tumor retention and minimum systemic side effects still remains a major challenge. Herein, a hybrid microbubble-based theranostic platform was developed for dual-modality ultrasound (US) and enhanced photoacoustic (PA) imaging-guided synergistic tumor therapy by combining starvation therapy, low-temperature photothermal therapy (PTT), and hypoxia-activated therapy, based on polydopamine (PDA) doped poly(vinyl alcohol) microbubbles loaded with glucose oxidase (GOx) (PDA-PVAMBs@GOx) and hypoxia-activated prodrug (HAP) tirapazamine (TPZ). For dual-modality US/enhanced PA imaging, PDA-PVAMBs provided 6.5-fold amplified PA signals relative to freely dispersed PDA nanoparticles (PDA NPs). For synergistic cancer therapy, oxygen (O2) carried by PDA-PVAMBs@GOx was first released to promote starvation therapy by loaded GOx. Then, moderate near-infrared (NIR) laser irradiation triggered PTT and improved enzymatic activity of GOx with its optimal activity around 47 °C. Subsequently, GOx-mediated tumor starvation depleted O2and exacerbated the hypoxia environment, thereby activating the toxicity of TPZ in the tumor site. Through dual-modality US/PA imaging monitoring, PDA-PVAMBs@GOx with long-term retention (∼7 days) combined with PTT and TPZ significantly inhibited the growth of solid tumors with minimum systemic side effects, which might be a powerful tool for effective tumor treatment.
UR - http://www.scopus.com/inward/record.url?scp=85119985403&partnerID=8YFLogxK
U2 - 10.1039/d1tb01735g
DO - 10.1039/d1tb01735g
M3 - Journal article
C2 - 34726226
AN - SCOPUS:85119985403
SN - 2050-750X
VL - 9
SP - 9358
EP - 9369
JO - Journal of Materials Chemistry B
JF - Journal of Materials Chemistry B
IS - 45
ER -