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Cheng S. Jin

Researcher at Princess Margaret Cancer Centre

Publications -  26
Citations -  2867

Cheng S. Jin is an academic researcher from Princess Margaret Cancer Centre. The author has contributed to research in topics: Photothermal therapy & Photodynamic therapy. The author has an hindex of 17, co-authored 26 publications receiving 2473 citations. Previous affiliations of Cheng S. Jin include University Health Network & University of Toronto.

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Porphysome nanovesicles generated by porphyrin bilayers for use as multimodal biophotonic contrast agents

TL;DR: The development of porphysomes; nanovesicles formed from self-assembled porphyrin bilayers that generated large, tunable extinction coefficients, structure-dependent fluorescence self-quenching and unique photothermal and photoacoustic properties demonstrate the multimodal potential of organic nanoparticles for biophotonic imaging and therapy.
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Ablation of hypoxic tumors with dose-equivalent photothermal, but not photodynamic, therapy using a nanostructured porphyrin assembly.

TL;DR: It is determined that nanostructured porphyrin PTT enhancers are advantageous to overcome hypoxic conditions to achieve effective ablation of solid tumors.
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In situ conversion of porphyrin microbubbles to nanoparticles for multimodality imaging

TL;DR: This work shows the conversion of microbubbles to nanoparticles using low-frequency ultrasound and shows that this conversion is possible in tumour-bearing mice and could be validated using photoacoustic imaging.
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A PEGylation-Free Biomimetic Porphyrin Nanoplatform for Personalized Cancer Theranostics.

TL;DR: 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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Targeting-Triggered Porphysome Nanostructure Disruption for Activatable Photodynamic Therapy

TL;DR: In both in vitro and in vivo studies, folate‐porphysomes can achieve folate receptor‐selective PDT efficacy, which proves the robustness of targeting‐triggered PDT activation of porphysome nanostructure for highly selective tumor ablation.