2021
DOI: 10.1039/d1bm01002f
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Antibody-functionalized theranostic protein nanoparticles for the synergistic deep red fluorescence imaging and multimodal therapy of ovarian cancer

Abstract: Among women, ovarian cancer is the fifth most frequent type of cancer, and despite benefiting from the current standard treatment plan, 90% of patients relapse in the next 18 months...

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Cited by 4 publications
(3 citation statements)
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“…On the other hand, the 0.23 ns increase in the lifetime decay time of antibody‐decorated NPs compared to undecorated NPs suggests the existence of different intracellular localization and/or internalization pathways of the fluorescent agent when FRα is involved. Although further in vivo investigations are needed, HSA&phthaloNO 2 ‐AB NPs have great optical potential as FRα‐targeted FLI nanosized agents 59 …”
Section: Membrane‐associated Targetsmentioning
confidence: 99%
“…On the other hand, the 0.23 ns increase in the lifetime decay time of antibody‐decorated NPs compared to undecorated NPs suggests the existence of different intracellular localization and/or internalization pathways of the fluorescent agent when FRα is involved. Although further in vivo investigations are needed, HSA&phthaloNO 2 ‐AB NPs have great optical potential as FRα‐targeted FLI nanosized agents 59 …”
Section: Membrane‐associated Targetsmentioning
confidence: 99%
“…[121] Nevertheless, the noteworthy advantages of the EDC/NHS chemistry make it a traditional method for the convenient and stable conjugation between antibodies and nanoparticles. [107,[122][123][124][125][126][127][128][129][130][131][132]…”
Section: -Ethyl-3-(3-dimethylaminopropyl)carbodiimide/n-hydroxysuccin...mentioning
confidence: 99%
“…Cancer remains as one of the most significant diseases that seriously threatens human health all over the world. In order to effectively inhibit malignant tumor and prolong survival, varieties of drug delivery systems and polymer prodrugs have been developed. However, most of them are restricted by their low drug loading capacity, and serious cumulative cytotoxicity. , By comparison, small-molecule prodrugs have the advantage of high loading capacity and easy metabolism for cancer therapeutics. Typically, Yan et al developed an amphiphilic small-molecule prodrug by integrating a hydrophilic anticancer drug and a hydrophobic anticancer drug via a hydrolyzable ester linkage and proposed the concept of amphiphilic drug–drug conjugate (ADDC), which opens up a new way for self-delivery systems.…”
Section: Introductionmentioning
confidence: 99%