Y1-receptor-ligand-functionalized ultrasmall upconversion nanoparticles for tumor-targeted trimodality imaging and photodynamic therapy with low toxicityElectronic supplementary information (ESI) available. See DOI: 10.1039/c8nr02387e

Achieving efficient photodynamic therapy (PDT) in deeper biological tissue is still the biggest bottleneck that limits its widespread application in clinic. Although deeper biological tissue PDT could be realized through a combination of upconversion nanoparticles with a photosensitizer, issues with...

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Hauptverfasser: Yu, Zhangsen, Xia, Yuanzhi, Xing, Jie, Li, Zihou, Zhen, Jianjun, Jin, Yinhua, Tian, Yuchen, Liu, Chuang, Jiang, Zhenqi, Li, Juan, Wu, Aiguo
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Zusammenfassung:Achieving efficient photodynamic therapy (PDT) in deeper biological tissue is still the biggest bottleneck that limits its widespread application in clinic. Although deeper biological tissue PDT could be realized through a combination of upconversion nanoparticles with a photosensitizer, issues with particle-size-induced upconversion fluorescence (UF) reduction and the related in vivo toxicity still cannot be solved properly. In this study, we synthesized Y 1 Rs-ligand [Pro 30 , Nle 31 , Bpa 32 , Leu 34 ]NPY(28-36) (NPY)-modified and photosensitizer MC540-loaded LiLuF 4 :Yb,Er@nLiGdF 4 @mSiO 2 multifunctional nanocomposites (MNPs) with a core-multishell structure and ultrasmall size. Their in vitro and in vivo breast tumor targeting, trimodality imaging performance, PDT therapeutic efficacy, and acute toxicity were evaluated. Our results demonstrated that the core-multishell MNPs(MC540) could achieve excellent UF imaging, and that doping with Gd 3+ and Lu 3+ rare earth ions could enhance the MR and CT imaging performance. In addition, the mSiO 2 shell provided a higher loading rate for the photosensitizer MC540, and the DSPE-PEG thin layer coating outside the MNPs(MC540) further improved the water solubility and biocompatibility, reducing the acute toxicity of the nanocomposites. Finally, the NPY modification enhanced the targetability of MNPs(MC540)/DSPE-PEG-NPY to breast tumors, improving the trimodality UF, CT, and MR imaging performance and PDT efficacy for Y 1 -receptor-overexpressed breast cancer. In general, our developed multifunctional nanocomposites can serve as a theranostic agent with low toxicity, providing great potential for their use in clinical breast cancer diagnosis and therapy. We design and synthesize an ultrasmall and low toxicity MNPs(MC540)/DSPE-PEG-NPY nanocomposite with the multifunctions of targeted trimodality imaging and PDT.
ISSN:2040-3364
2040-3372
DOI:10.1039/c8nr02387e