MnCO3-mineralized polydopamine nanoparticles as an activatable theranostic agent for dual-modality imaging-guided photothermal therapy of cancers

被引:14
作者
Lee, Kyung Kwan [1 ,2 ]
Lee, Jae-Hyung [3 ]
Lee, Sang Cheon [4 ]
Lee, Chang-Soo [1 ,5 ]
机构
[1] Bionanotechnol Res Ctr, Korea Res Inst Biosci & Biotechnol KRIBB, Daejeon 34141, South Korea
[2] Kyung Hee Univ, Grad Sch, Dept Life & Nanopharmaceut Sci, Seoul 02447, South Korea
[3] Kyung Hee Univ, Sch Dent, Dept Oral Microbiol, Seoul 02447, South Korea
[4] Kyung Hee Univ, Sch Dent, Dept Maxillofacial Biomed Engn, Seoul 02447, South Korea
[5] Univ Sci & Technol UST, Dept Biotechnol, Daejeon 34113, South Korea
基金
新加坡国家研究基金会;
关键词
cancer; fluorescent polydopamine nanoparticles; mineralization; dual-modality imaging; photothermal therapy; theranostics; MANGANESE OXIDE; CARBON DOTS; MR; FLUORESCENT; MNCO3; DELIVERY; FACILE;
D O I
10.7150/thno.77060
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Background: Single imaging modality is still insufficient to evaluate the biological and anatomical structures of tumors with high accuracy and reliability. Generation of non-specific contrast, leading to a low target-to-background signal ratio, results in low imaging resolution and accuracy. Tumor environment-specific activatable multifunctional contrast agents need to maximize the contrast signals, representing a dual imaging-guided photothermal therapy (PTT) at target tumor sites. Methods: Cellular uptake, cytotoxicity assay, and in vitro photothermal conversion efficiency of MnCO3-mineralized fluorescent polydopamine nanoparticles (MnCO3-FPNPs) were evaluated using 4T1 breast cancer cells. In vivo dual-modality imaging was performed using IVIS imaging and a 4.7 T animal MRI systems after injection into 4T1 tumor-bearing nude mice. The effects of photothermal therapeutic through PTT were measured after irradiation with an 808 nm laser (1.5 W/cm2) for 10 min, measuring the size of the tumors every 2 days. Results: At physiological pH (7.4), MnCO3-FPNP is efficiently quenched. Conversely, at acidic pH (5.4), the strong fluorescence (FL) is recovered due to the dissociation of Mn2+ from the FPNPs. At pH 7.4, MnCO3-FPNP activity is silenced to enhance water proton relaxation due to unionized MnCO3 maintenance; conversely, at acidic pH (5.4), MnCO3-FPNPs efficiently release Mn2+ ions, thereby resulting in T1-weighted magnetic resonance (MR) contrast enhancement. MnCO3-FPNPs display a promising diagnostic ability for 4T1 breast cancer xenograft models, as well as exhibit a high photothermal conversion efficiency. A successful tumor treatment via their photothermal activity is accomplished within 14 days. Conclusions: Our studies exhibited unique "OFF-ON" activation abilities in FL/MR dual imaging and PTT functions. This approach suggests that the MnCO3-FPNPs may serve as a useful platform for various mineralization-based multimodal imaging-guided PTT models for many cancer theranostic applications.
引用
收藏
页码:6762 / 6778
页数:17
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