Engineering Phototheranostic Nanoscale Metal–Organic Frameworks for Multimodal Imaging-Guided Cancer Therapy

吲哚青绿 光热治疗 体内 材料科学 药物输送 透明质酸 纳米技术 光动力疗法 生物医学工程 癌症研究 化学 医学 病理 有机化学 生物技术 解剖 生物
作者
Wen Cai,Haiyan Gao,Chengchao Chu,Xiaoyong Wang,Junqing Wang,Pengfei Zhang,Gan Lin,Wengang Li,Gang Liu,Xiaoyuan Chen
出处
期刊:ACS Applied Materials & Interfaces [American Chemical Society]
卷期号:9 (3): 2040-2051 被引量:349
标识
DOI:10.1021/acsami.6b11579
摘要

Many photoresponsive dyes have been utilized as imaging and photodynamic/photothermal therapy agents. Indocyanine green (ICG) is the only near-infrared region (NIR) organic dye for clinical applications approved by the United States Food and Drug Administration; however, the clinical application of ICG is limited by its poor aqueous solubility, low cancer specificity, and low sensitivity in cancer theranostics. To overcome these issues, a multifunctional nanoplatform based on hyaluronic acid (HA) and ICG-engineered metal-organic framework MIL-100(Fe) nanoparticles (MOF@HA@ICG NPs) was successfully developed for imaging-guided, anticancer photothermal therapy (PTT). The synthesized NPs showed a high loading content of ICG (40%), strong NIR absorbance, and photostability. The in vitro and in vivo imaging showed that the MOF@HA@ICG NPs exhibited greater cellular uptake in CD44-positive MCF-7 cells and enhanced tumor accumulation in xenograft tumors due to their targeting capability, compared to MOF@ICG NPs (non-HA-targeted) and free ICG. The in vitro photothermal toxicity and in vivo PTT treatments demonstrated that MOF@HA@ICG NPs could effectively inhibit the growth of MCF-7 cells/xenograft tumors. These results suggest that MOF@HA@ICG NPs could be served as a new promising theranostic nanoplatform for improved anticancer PTT through cancer-specific and image-guided drug delivery.
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