| Literature DB >> 31403246 |
T M Ebaston1, Alex Rozovsky1, Alisa Zaporozhets1, Andrii Bazylevich1, Helena Tuchinsky2, Vered Marks1, Gary Gellerman1, Leonid D Patsenker1.
Abstract
Targeted drug delivery (TDD) is an efficient strategy for cancer treatment. However, the real-time monitoring of drug delivery is still challenging because of a pronounced lack of TDD systems capable of providing a near-infrared (NIR) fluorescence signal for the detection of drug-release events. Herein, a new TDD system, comprising a turn-on NIR fluorescent reporter attached to an anticancer drug and targeting peptide, is reported. This system provides both TDD and NIR fluorescence monitoring of drug-release events in target tissue. In this TDD system, a new carboxy-derivatized xanthene-cyanine (XCy) dye is attached to an anticancer drug, chlorambucil (CLB), through a hydrolytically cleavable ester linker and coupled to a targeting peptide, octreotide amide (OCTA), which is specific to somatostatin receptors SSTR-2 and STTR-5 overexpressed on many tumor cells. This OCTA-G-XCy-CLB (G: γ-aminobutyric acid) conjugate exhibits no detectable fluorescence, whereas, upon the hydrolytic cleavage of the ester linker, a bright NIR fluorescence appears at λ≈710 nm; this signals release of the drug. Real-time TDD monitoring is demonstrated for the example of the human pancreatic cancer cell line overexpressing SSTR-2 and STTR-5, in comparison with the noncancerous Chinese hamster ovary cell line, which contains a reduced number of these receptors.Entities:
Keywords: cancer; drug delivery; dyes/pigments; fluorescence; peptides
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Year: 2019 PMID: 31403246 DOI: 10.1002/cmdc.201900464
Source DB: PubMed Journal: ChemMedChem ISSN: 1860-7179 Impact factor: 3.466