Thermosensitive Polymer Dot Nanocomposites for Trimodal Computed Tomography/Photoacoustic/Fluorescence Imaging-Guided Synergistic Chemo-Photothermal Therapy

ACS Appl Mater Interfaces. 2020 Nov 18;12(46):51174-51184. doi: 10.1021/acsami.0c13252. Epub 2020 Nov 3.

Abstract

Precision delivery of theranostic agents to the tumor site is essential to improve their diagnostic and therapeutic efficacy and concurrently minimize adverse effects during treatment. In this study, a novel concept of near-infrared (NIR) light activation of conjugated polymer dots (Pdots) at thermosensitive hydrogel nanostructures is introduced for multimodal imaging-guided synergistic chemo-photothermal therapy. Interestingly, owing to the attractive photothermal conversion efficiency of Pdots, the Pdots@hydrogel as theranostic agents is able to undergo a controllable softening or melting state under the irradiation of NIR laser, resulting in light-triggered drug release in a controlled way and concurrently hydrogel degradation. Besides, the novel Pdots@hydrogel nanoplatform can serve as the theranostic agent for enhanced trimodal photoacoustic (PA)/computed tomography (CT)/fluorescence (FL) imaging-guided synergistic chemo-photothermal therapy of tumors. More importantly, the constructed intelligent nanocomposite Pdots@hydrogel exhibits excellent biodegradability, strong NIR absorption, bright PA/CT/FL signals, and superior tumor ablation effect. Therefore, the concept of a light-controlled multifunctional Pdots@hydrogel that integrates multiple diagnostic/therapeutic modalities into one nanoplatform can potentially be applied as a smart nanotheranostic agent to various perspectives of personalized nanomedicine.

Keywords: chemo-photothermal therapy; controlled drug release; multimode imaging; photoacoustic imaging; semiconducting polymer nanoparticles.

MeSH terms

  • Animals
  • Biocompatible Materials / chemistry*
  • Biocompatible Materials / pharmacology
  • Cell Line, Tumor
  • Cell Survival / drug effects
  • Contrast Media / chemistry
  • Doxorubicin / chemistry
  • Doxorubicin / metabolism
  • Doxorubicin / therapeutic use
  • Drug Carriers / chemistry
  • Humans
  • Hydrogels / chemistry
  • Infrared Rays
  • Mice
  • Mice, Nude
  • Nanocomposites / chemistry*
  • Neoplasms / diagnostic imaging
  • Neoplasms / drug therapy
  • Optical Imaging*
  • Photoacoustic Techniques*
  • Photothermal Therapy
  • Polymers / chemistry*
  • Thiophenes / chemistry
  • Tomography, X-Ray Computed*

Substances

  • Biocompatible Materials
  • Contrast Media
  • Drug Carriers
  • Hydrogels
  • Polymers
  • Thiophenes
  • Doxorubicin