Abstract
BackgroundTumor phototherapy especially photodynamic therapy (PDT) or photothermal therapy (PTT), has been considered as an attractive strategy to elicit significant immunogenic cell death (ICD) at an optimal tumor retention of PDT/PTT agents. Heptamethine cyanine dye (IR-780), a promising PDT/PTT agent, which can be used for near-infrared (NIR) fluorescence/photoacoustic (PA) imaging guided tumor phototherapy, however, the strong hydrophobicity, short circulation time, and potential toxicity in vivo hinder its biomedical applications. To address this challenge, we developed mesoporous polydopamine nanoparticles (MPDA) with excellent biocompatibility, PTT efficacy, and PA imaging ability, facilitating an efficient loading and protection of hydrophobic IR-780.ResultsThe IR-780 loaded MPDA (IR-780@MPDA) exhibited high loading capacity of IR-780 (49.7 wt%), good physiological solubility and stability, and reduced toxicity. In vivo NIR fluorescence and PA imaging revealed high tumor accumulation of IR-780@MPDA. Furthermore, the combined PDT/PTT of IR-780@MPDA could induce ICD, triggered immunotherapeutic response to breast tumor by the activation of cytotoxic T cells, resulting in significant suppression of tumor growth in vivo.ConclusionThis study demonstrated that the as-developed compact and biocompatible platform could induce combined PDT/PTT and accelerate immune activation via excellent tumor accumulation ability, offering multimodal tumor theranostics with negligible systemic toxicity.Graphical
Highlights
Several anti-tumor nanomedicine strategies have been successfully developed, and among those, phototherapeutic tumor killing by photothermal therapy (PTT) or photodynamic therapy (PDT) has attracted significant attention [1,2,3,4,5,6,7]
The surface zeta potential shifted from − 24.5 ± 0.6 to 4.55 ± 0.1 mV for IR-780@mesoporous polydopamine nanoparticles (MPDA), which is attributed to the surface modification of MPDA by positively charged IR-780 (Fig. 1F)
In summary, we established “Two in One” tumor collaborative therapy by mesoporous polydopamine delivery nanoplatform loaded with NIR dye IR-780 (IR-780@ MPDA)
Summary
Several anti-tumor nanomedicine strategies have been successfully developed, and among those, phototherapeutic tumor killing by photothermal therapy (PTT) or photodynamic therapy (PDT) has attracted significant attention [1,2,3,4,5,6,7]. Tumor phototherapy especially photodynamic therapy (PDT) or photothermal therapy (PTT), has been considered as an attractive strategy to elicit significant immunogenic cell death (ICD) at an optimal tumor retention of PDT/PTT agents. Heptamethine cyanine dye (IR-780), a promising PDT/PTT agent, which can be used for near-infrared (NIR) fluorescence/photoacoustic (PA) imaging guided tumor phototherapy, the strong hydrophobicity, short circulation time, and potential toxicity in vivo hinder its biomedical applications. To address this challenge, we developed mesoporous polydopamine nanoparticles (MPDA) with excellent biocompatibility, PTT efficacy, and PA imaging ability, facilitating an efficient loading and protection of hydrophobic IR-780
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