"One-Pot" Fabrication of Highly Versatile and Biocompatible Poly(vinyl alcohol)-porphyrin-based Nanotheranostics.
"One-Pot" Fabrication of Highly Versatile and Biocompatible Poly(vinyl alcohol)-porphyrin-based Nanotheranostics.
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作者:
Luo Y;Wu H;Feng C;Xiao K;Yang X;Liu Q;Lin TY;Zhang H;Walton JH;Ajena Y;Hu Y;Lam KS;Li Y
Nanoparticle-based theranostic agents have emerged as a new paradigm in nanomedicine field for integration of multimodal imaging and therapeutic functions within a single platform. However, the clinical translation of these agents is severely limited by the complexity of fabrication, long-term toxicity of the materials, and unfavorable biodistributions. Here we report an extremely simple and robust approach to develop highly versatile and biocompatible theranostic poly(vinyl alcohol)-porphyrin nanoparticles (PPNs). Through a “one-pot” fabrication process, including the chelation of metal ions and encapsulation of hydrophobic drugs, monodispersenanoparticle could be formed by self-assembly of a very simple and biocompatible building block (poly(vinyl alcohol)-porphyrin conjugate). Using this approach, we could conveniently produce multifunctional PPNs that integrate optical imaging, positron emission tomography (PET), photodynamic therapy (PDT), photothermal therapy (PTT) and drug delivery functions in one formulation. PPNs exhibited unique architecture-dependent fluorescence self-quenching, as well as photodynamic- and photothermal- properties. Near-infrared fluorescence could be amplified upon PPN dissociation, providing feasibility of low-background fluorescence imaging. Doxorubicin (DOX)-loaded PPNs achieved 53 times longer half-life in blood circulation than free DOX. Upon irradiation by near infrared light at a single excitation wavelength, PPNs could be activated to release reactive oxygen species, heat and drugs simultaneously at the tumor sites in mice bearing tumor xenograft, resulting in complete eradication of tumors. Due to their organic compositions, PPNs showed no obvious cytotoxicity in mice via intravenous administration during therapeutic studies. This highly versatile and multifunctional PPN theranostic nanoplatform showed great potential for the integration of multimodal imaging and therapeutic functions towards personalized nanomedicine against cancers.
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影响因子:
17.1
作者:
Gilbert B;Fakra SC;Xia T;Pokhrel S;Mädler L;Nel AE
通讯作者:
Nel AE
影响因子:
8
作者:
Guo Y;Zhang Z;Kim DH;Li W;Nicolai J;Procissi D;Huan Y;Han G;Omary RA;Larson AC
通讯作者:
Larson AC
影响因子:
12.4
作者:
Chen YP;Lv JW;Liu X;Zhang Y;Guo Y;Lin AH;Sun Y;Mao YP;Ma J
通讯作者:
Ma J
影响因子:
17.1
作者:
Bhirde, Ashwinkumar A.;Chikkaveeraiah, Bhaskara V.;Srivatsan, Avinash;Niu, Gang;Jin, Albert J.;Kapoor, Ankur;Wang, Zhe;Patel, Sachin;Patel, Vyomesh;Gorbach, Alexander M.;Leapman, Richard D.;Gutkind, J. Silvio;Walker, Angela R. Hight;Chen, Xiaoyuan
通讯作者:
Chen, Xiaoyuan
影响因子:
12.4
作者:
Jing L;Liang X;Li X;Lin L;Yang Y;Yue X;Dai Z
通讯作者:
Dai Z