| Literature DB >> 29195037 |
Dandan Luo1, Shreya Goel, Hai-Jun Liu2, Kevin A Carter1, Dawei Jiang, Jumin Geng1, Christopher J Kutyreff, Jonathan W Engle, Wei-Chiao Huang, Shuai Shao1, Chao Fang2, Weibo Cai, Jonathan F Lovell1.
Abstract
Doxorubicin (Dox)-loaded stealth liposomes (similar to those in clinical use) can incorporate small amounts of porphyrin-phospholipid (PoP) to enable chemophototherapy (CPT). PoP is also an intrinsic and intrabilayer 64Cu chelator, although how radiolabeling impacts drug delivery has not yet been assessed. Here, we show that 64Cu can radiolabel the stable bilayer of preformed Dox-loaded PoP liposomes with inclusion of 1% ethanol without inducing drug leakage. Dox-PoP liposomes labeled with intrabilayer copper behaved nearly identically to unlabeled ones in vitro and in vivo with respect to physical parameters, pharmacokinetics, and CPT efficacy. Positron emission tomography and near-infrared fluorescence imaging visualized orthotopic mammary tumors in mice with passive liposome accumulation following administration. A single CPT treatment with 665 nm light (200 J/cm2) strongly inhibited primary tumor growth. Liposomes accumulated in lung metastases, based on NIR imaging. These results establish the feasibility of CPT interventions guided by intrinsic multimodal imaging of Dox-loaded stealth PoP liposomes.Entities:
Keywords: chemophototherapy; doxorubicin; image-guided drug delivery; liposomes; porphyrin−phospholipid
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Year: 2017 PMID: 29195037 PMCID: PMC6004286 DOI: 10.1021/acsnano.7b06578
Source DB: PubMed Journal: ACS Nano ISSN: 1936-0851 Impact factor: 15.881