Multifunctional liposome for photoacoustic/ultrasound imaging-guided chemo/photothermal retinoblastoma therapy

被引:25
|
作者
Li, Meng [1 ,2 ]
Bian, Xintong [1 ,2 ]
Chen, Xu [1 ,3 ]
Fan, Ningke [2 ]
Zou, Hongmi [4 ]
Bao, Yixi [1 ]
Zhou, Yu [4 ]
机构
[1] Chongqing Med Univ, Dept Clin Lab, Affiliated Hosp 2, Chongqing, Peoples R China
[2] Chongqing Med Univ, Coll Lab Med, Key Lab Clin Lab Diagnost, Minist Educ, Chongqing, Peoples R China
[3] Sun Yat Sen Univ, Zhongshan Ophthalm Ctr, State Key Lab Ophthalmol, Guangzhou, Peoples R China
[4] Chongqing Med Univ, Dept Ophthalmol, Affiliated Hosp 2, 74 Linjiang Rd, Chongqing, Peoples R China
基金
中国国家自然科学基金;
关键词
Nanoplatform; dual-modal imaging; doxorubicin; photothermal therapy; retinoblastoma; CONTRAST-ENHANCED ULTRASOUND; DRUG-DELIVERY; INDOCYANINE GREEN; FOLIC-ACID; CANCER; NANOPARTICLES; SURVIVAL; SYSTEM;
D O I
10.1080/10717544.2022.2032876
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Retinoblastoma (RB) is a malignant intraocular neoplasm that occurs in children. Diagnosis and therapy are frequently delayed, often leading to metastasis, which necessitates effective imaging and treatment. In recent years, the use of nanoplatforms allowing both imaging and targeted treatment has attracted much attention. Herein, we report a novel nanoplatform folate-receptor (FR) targeted laser-activatable liposome termed FA-DOX-ICG-PFP@Lip, which is loaded with doxorubicin (DOX)/indocyanine green (ICG) and liquid perfluoropentane (PFP) for photoacoustic/ultrasound (PA/US) dual-modal imaging-guided chemo/photothermal RB therapy. The dual-modal imaging capability, photothermal conversion under laser irradiation, biocompatibility, and antitumor ability of these liposomes were appraised. The multifunctional liposome showed a good tumor targeting ability and was efficacious as a dual-modality contrast agent both in vivo and in vitro. When laser-irradiated, the liposome converted light energy to heat. This action caused immediate destruction of tumor cells, while simultaneously initiating PFP phase transformation to release DOX, resulting in both photothermal and chemotherapeutic antitumor effects. Notably, the FA-DOX-ICG-PFP@Lip showed good biocompatibility and no systemic toxicity was observed after laser irradiation in RB tumor-bearing mice. Hence, the FA-DOX-ICG-PFP@Lip shows great promise for dual-modal imaging-guided chemo/photothermal therapy, and may have significant value for diagnosing and treating RB.
引用
收藏
页码:519 / 533
页数:15
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