J
Jie Cao
Researcher at Qingdao University
Publications - 72
Citations - 2061
Jie Cao is an academic researcher from Qingdao University. The author has contributed to research in topics: Drug delivery & Micelle. The author has an hindex of 21, co-authored 57 publications receiving 1425 citations. Previous affiliations of Jie Cao include University of Science and Technology of China & Chinese Academy of Sciences.
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Journal ArticleDOI
High-Quality CuInS2/ZnS Quantum Dots for In vitro and In vivo Bioimaging
TL;DR: High-quality CuInS2/ZnS (CIS/SnS) QDs are synthesized without using conventional toxic heavy metals and exhibited improved photoluminescence (PL) properties, and the micelle platform allowed successful formulation of these oil-soluble QDs in water.
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A pH-sensitive doxorubicin prodrug based on folate-conjugated BSA for tumor-targeted drug delivery.
Changli Du,Dawei Deng,Lingling Shan,Shunan Wan,Jie Cao,Junmei Tian,Samuel Achilefu,Yueqing Gu +7 more
TL;DR: The results demonstrate that FA-BSA-CAD prodrug selectively targeted tumor cells and tissue, with associated reduction in non-specific toxicity to the normal cells, and the therapeutic efficacy of the prodrug for FA-positive tumors increased compared to the non-conjuagted DOX.
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Near-infrared light-triggered micelles for fast controlled drug release in deep tissue.
Jie Cao,Shanshan Huang,Yuqi Chen,Siwen Li,Xin Li,Dawei Deng,Zhiyu Qian,Liping Tang,Yueqing Gu +8 more
TL;DR: Results indicate that this system provides an efficient method to surmount the drawback of UV or visible light-responsive polymeric systems for controlled drug release in deep tissues.
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Cell-Inspired All-Aqueous Microfluidics: From Intracellular Liquid–Liquid Phase Separation toward Advanced Biomaterials
TL;DR: An emerging all‐aqueous microfluidic technology derived from micrometer‐scaled manipulation of LLPS is presented and enables the state‐of‐art design of advanced biomaterials with exquisite structural proficiency and diversified biological functions.
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Highly luminescent water-soluble quaternary Zn–Ag–In–S quantum dots for tumor cell-targeted imaging
TL;DR: These highly luminescent ZAIS QDs are less toxic due to the absence of highly toxic cadmium, and can be versatilely modified by a DHLA-PEG-based ligand, and show potential applications in tumor cell imaging as a promising alternative for Cd-based QDs.