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Jing Zhang

Researcher at Shandong University

Publications -  23
Citations -  756

Jing Zhang is an academic researcher from Shandong University. The author has contributed to research in topics: Immunotherapy & Drug delivery. The author has an hindex of 12, co-authored 22 publications receiving 421 citations. Previous affiliations of Jing Zhang include Chinese Academy of Sciences.

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Near-infrared mediated quantum dots and paclitaxel co-loaded nanostructured lipid carriers for cancer theragnostic.

TL;DR: It is satisfactorily concluded that co-loaded NLC formulation can be qualified as a splendid parenteral drug delivery system foundation for cancer theragnostic.
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A two-pronged photodynamic nanodrug to prevent metastasis of basal-like breast cancer.

TL;DR: A two-pronged concept combining photodynamic therapy (PDT) and epithelial-mesenchymal transition (EMT) blockade in a minimalist nanoplatform was proposed to combat basal-like breast cancer (BLBC) metastasis as discussed by the authors.
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Site-specific MOF-based immunotherapeutic nanoplatforms via synergistic tumor cells-targeted treatment and dendritic cells-targeted immunomodulation.

TL;DR: Dual tailor-made metal organic framework (MOF) nanoparticles based on zeolitic imidazolate framework-8 (ZIF-8) are designed to comprehensively enhance the immunotherapy via the spatiotemporal cooperation of various therapeutic agents, offering powerful platform against invasive malignancy and rechallenged tumors.
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A Three-in-One Immunotherapy Nanoweapon via Cascade-Amplifying Cancer-Immunity Cycle against Tumor Metastasis, Relapse, and Postsurgical Regrowth.

TL;DR: For the first time, a three-in-one immunotherapy nanoplatform is reported that can simultaneously execute these three phases of the immunotherapy, and is of great interest for designing excellent immunotherapy treatments.
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Cold to Hot: Rational Design of a Minimalist Multifunctional Photo-immunotherapy Nanoplatform toward Boosting Immunotherapy Capability

TL;DR: Li et al. as mentioned in this paper designed an all-rolled-into-one molecule nanoplatform via a molecular engineering strategy, which could self-assemble into nanoparticles with remarkably high dual-therapeutic agent loading.