Journal
SMALL
Volume 19, Issue 22, Pages -Publisher
WILEY-V C H VERLAG GMBH
DOI: 10.1002/smll.202206053
Keywords
activatable; coordination self-assembly; second near-infrared window; synergistic tumor treatments; tumor microenvironments
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This study presents a tumor microenvironment (TME) activated near-infrared window (NIR-II) phototheranostic nanoplatform. The nanoplatform, called Ag2S-Fe(III)-DBZ Pdots (AFD NPs), utilizes the principle of Forster resonance energy transfer (FRET). In normal tissues, the AFD NPs remain in an off state due to FRET between Ag2S QDs and DBZ Pdots. However, the NIR-II fluorescence signal of AFD NPs can be rapidly turned on in tumor tissues by the overexpressed GSH, achieving a superior tumor-to-normal tissue (T/NT) signal ratio. The AFD NPs also provide NIR-II photothermal therapy (PTT) and chemodynamic therapy (CDT) for cancer treatment.
The phototheranostics in the second near-infrared window (NIR-II) have proven to be promising for the precise cancer theranostics. However, the non-responsive and always on imaging mode lacks the selectivity, leading to the poor diagnosis specificity. Herein, a tumor microenvironment (TME) activated NIR-II phototheranostic nanoplatform (Ag2S-Fe(III)-DBZ Pdots, AFD NPs) is designed based on the principle of Forster resonance energy transfer (FRET). The AFD NPs are fabricated through self-assembly of Ag2S QDs (NIR-II fluorescence probe) and ultra-small semiconductor polymer dots (DBZ Pdots, NIR-II fluorescence quencher) utilizing Fe(III) as coordination nodes. In normal tissues, the AFD NPs maintain in off state, due to the FRET between Ag2S QDs and DBZ Pdots. However, the NIR-II fluorescence signal of AFD NPs can be rapidly turn on by the overexpressed GSH in tumor tissues, achieving a superior tumor-to-normal tissue (T/NT) signal ratio. Moreover, the released Pdots and reduced Fe(II) ions provide NIR-II photothermal therapy (PTT) and chemodynamic therapy (CDT), respectively. The GSH depletion and NIR-II PTT effect further aggravate CDT mediated oxidative damage toward tumors, achieving the synergistic anti-tumor therapeutic effect. The work provides a promising strategy for the development of TME activated NIR-II phototheranostic nanoprobes.
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