4.8 Article

A PEGylation-Free Biomimetic Porphyrin Nanoplatform for Personalized Cancer Theranostics

期刊

ACS NANO
卷 9, 期 4, 页码 4484-4495

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsnano.5b01077

关键词

porphyrin; nanoparticle; PEGylation; PET imaging; multimodal imaging; fluorescence-guided surgery; photodynamic therapy

资金

  1. Canadian Institutes of Health Research
  2. Ontario Institute for Cancer Research
  3. Natural Sciences and Engineering Research Council of Canada
  4. National Science Foundation of China
  5. US Army Ovarian Cancer Research Program Translational Synergistic Leverage Award
  6. Prostate Cancer Canada
  7. Canada Foundation for Innovation
  8. Princess Margaret Cancer Foundation
  9. Joey and Toby Tanenbaum/Brazilian Ball Chair in Prostate Cancer Research

向作者/读者索取更多资源

PEGylation (PEG) is the most commonly adopted strategy to prolong nanoparticles' vascular circulation by mitigating the reticuloendothelial system uptake. However, there remain many concerns in regards to its immunogenicity, targeting efficiency, etc., which inspires pursuit of alternate, non-PEGylated systems. We introduced here a PEG-free, porphyrin-based ultrasmall nanostructure mimicking nature lipoproteins, termed PLP, that integrates multiple imaging and therapeutic functionalities, including positron emission tomography (PET) imaging, near-infrared (NIR) fluorescence imaging and photodynamic therapy (PDT). With an engineered lipoprotein-mimicking structure, PLP is highly stable in the blood circulation, resulting in favorable pharmacokinetics and biodistribution without the need of PEG. The prompt tumor intracellular trafficking of PLP allows for rapid nanostructure dissociation upon tumor accumulation to release monomeric porphyrins to efficiently generate fluorescence and photodynamic reactivity, which are highly silenced in intact PLP, thus providing an activatable mechanism for low-background NIR fluorescence imaging and tumor-selective PDT. Its intrinsic copper-64 labeling feature allows for noninvasive PET imaging of PLP delivery and quantitative assessment of drug distribution. Using a clinically relevant glioblastoma multiforme model, we demonstrated that PLP enabled accurate delineation of tumor from surrounding healthy brain at size less than 1 mm, exhibiting the potential for intraoperative fluorescence-guided surgery and tumor-selective PDT. Furthermore, we demonstrated the general applicability of PLP for sensitive and accurate detection of primary and metastatic tumors in other clinically relevant animal models. Therefore, PLP offers a biomimetic theranostic nanoplatform for pretreatment stratification using PET and NIR fluorescence imaging and for further customized cancer management via imaging-guided surgery, PDT, or/and potential chemotherapy.

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