4.6 Article

A multifunctional platinum(iv) and cyanine dye-based polyprodrug for trimodal imaging-guided chemo-phototherapy

Journal

JOURNAL OF MATERIALS CHEMISTRY B
Volume 10, Issue 7, Pages 1031-1041

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d1tb02682h

Keywords

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Funding

  1. National Natural Science Foundation of China [51803097, 22107019]
  2. Program for Scientific Research Innovation Team in Colleges and Universities of Jinan [2019GXRC021]
  3. National Key Research & Development Program of China [2020YFA0210800]
  4. Major Project of Science and Technology of Fujian Province [2020HZ06006]

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This work developed an innovative nanoplatform based on a Pt(iv) prodrug and a near-infrared photosensitizer, which can achieve multifunctional cancer therapy and diagnosis. The nanoplatform allows real-time tracking of nanodrugs and has dual effects of photothermal therapy and chemotherapy.
Imaging-guided chemo-phototherapy based on a single nanoplatform has a great significance to improve the efficiency of cancer therapy and diagnosis. However, high drug content, no burst release and real-time tracking of nanodrugs are the three main challenges for this kind of multifunctional nanotheranostics. In this work, we developed an innovative theranostic nanoplatform based on a Pt(iv) prodrug and a near-infrared (NIR) photosensitizer. A Pt(iv) prodrug and a cyanine dye (HOCyOH, Cy) were copolymerized and incorporated into the main chain of a polyprodrug (PCPP), which self-assembled into nanoparticles (NPs) with similar to 27.61% Cy loading and similar to 9.37% Pt loading, respectively. PCPP NPs enabled reduction-triggered backbone cleavage of polyprodrugs and bioactive Pt(ii) release; Cy could be activated under 808 nm laser irradiation to produce local hyperthermia and reactive oxygen species (ROS) for phototherapy. Moreover, PCPP NPs with extremely high Cy and Pt heavy metal contents in the backbone of the polyprodrug could directly track the nanodrugs themselves via near-infrared fluorescence (NIRF) imaging, photothermal imaging, and computed tomography (CT) imaging in vitro and in vivo. As revealed by trimodal imaging, PCPP NPs were found to exhibit excellent tumor accumulation and antitumor efficiency after intravenous injection into H22-tumor-bearing mice. The dual-drug backboned polyprodrug nanoplatform exhibited great potential for bioimaging and combined chemo-phototherapy.

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