Title : Enzyme-Catalytic Self-Triggered Release of Drugs from a Nanosystem for Efficient Delivery to Nuclei of Tumor Cells.

Pub. Date : 2019 Nov 20

PMID : 31664812






4 Functional Relationships(s)
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1 Herein, a core crosslinked pullulan-di-(4,1-hydroxybenzylene)diselenide nanosystem, which could generate abundant exogenous-stimulant reactive oxygen species (ROS) via tumor-specific NAD(P)H:quinone oxidoreductase-1 (NQO1) catalysis, was constructed by the encapsulation of beta-lapachone. Reactive Oxygen Species NAD(P)H quinone dehydrogenase 1 Homo sapiens
2 Herein, a core crosslinked pullulan-di-(4,1-hydroxybenzylene)diselenide nanosystem, which could generate abundant exogenous-stimulant reactive oxygen species (ROS) via tumor-specific NAD(P)H:quinone oxidoreductase-1 (NQO1) catalysis, was constructed by the encapsulation of beta-lapachone. Reactive Oxygen Species NAD(P)H quinone dehydrogenase 1 Homo sapiens
3 Herein, a core crosslinked pullulan-di-(4,1-hydroxybenzylene)diselenide nanosystem, which could generate abundant exogenous-stimulant reactive oxygen species (ROS) via tumor-specific NAD(P)H:quinone oxidoreductase-1 (NQO1) catalysis, was constructed by the encapsulation of beta-lapachone. Reactive Oxygen Species NAD(P)H quinone dehydrogenase 1 Homo sapiens
4 Herein, a core crosslinked pullulan-di-(4,1-hydroxybenzylene)diselenide nanosystem, which could generate abundant exogenous-stimulant reactive oxygen species (ROS) via tumor-specific NAD(P)H:quinone oxidoreductase-1 (NQO1) catalysis, was constructed by the encapsulation of beta-lapachone. Reactive Oxygen Species NAD(P)H quinone dehydrogenase 1 Homo sapiens