An Advanced In Situ Magnetic Resonance Imaging and Ultrasonic Theranostics Nanocomposite Platform: Crossing the Blood-Brain Barrier and Improving the Suppression of Glioblastoma Using Iron-Platinum Nanoparticles in Nanobubbles

被引:55
作者
Chan, Ming-Hsien [1 ]
Chen, William [2 ]
Li, Chien-Hsiu [1 ]
Fang, Chih-Yeu [1 ]
Chang, Yu-Chan [3 ]
Wei, Da-Hua [4 ,5 ]
Liu, Ru-Shi [6 ]
Hsiao, Michael [1 ,7 ]
机构
[1] Acad Sinica, Genom Res Ctr, Taipei 11529, Taiwan
[2] Taipei Amer Sch, Upper Sch, Taipei 11152, Taiwan
[3] Natl Yang Ming Chiao Tung Univ, Dept Biomed Imaging & Radiol Sci, Taipei 11221, Taiwan
[4] Natl Taipei Univ Technol, Grad Inst Mfg Technol, Taipei 10608, Taiwan
[5] Natl Taipei Univ Technol, Dept Mech Engn, Taipei 10608, Taiwan
[6] Natl Taiwan Univ, Dept Chem, Taipei 10617, Taiwan
[7] Kaohsiung Med Univ, Kaohsiung 80708, Taiwan
关键词
glioblastoma treatment; blood-brain barrier; nanobubbles; FePt nanoparticles; magnetic resonance imaging; FEPT NANOPARTICLES; DRUG-DELIVERY; THERAPY; CHEMOTHERAPY; DISRUPTION; SYSTEM; VITRO; ACID; VIVO;
D O I
10.1021/acsami.1c04990
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Glioblastoma (GBM) is one of the deadliest and most invasive brain cancers/gliomas, and there is currently no established way to treat this disease. The treatment of GBM typically involves intracranial surgery followed by chemotherapy. However, the blood-brain barrier (BBB) impedes the delivery of the chemotherapeutic drug, making the treatment challenging. In this study, we embedded a chemotherapeutic drug and other nanomaterials into a nanobubble (NB), utilized active tracking and other guidance mechanisms to guide the nanocomposite to the tumor site, and then used high-intensity focused ultrasound oscillation to burst the nanobubbles, generating a transient cavitation impact on the BBB and allowing the drug to bypass it and reach the brain. FePt enhances the resolution of T2-weighted magnetic resonance imaging images and has magnetic properties that help guide the nanocomposite to the tumor location. FePt nanoparticles were loaded into the hydrophobic core of the NBs along with doxorubicin to form a bubble-based drug delivery system (Dox-FePt@NB). The surface of the NBs is modified with a targeting ligand, transferrin (Dox-FePt@NB-Tf), giving the nanocomposite active tracking abilities. The Dox-FePt@NB-Tf developed in the present study represents a potential breakthrough in GBM treatment through improved drug delivery and biological imaging.
引用
收藏
页码:26759 / 26769
页数:11
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