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Chem Commun (Camb) ; 52(15): 3235-8, 2016 Feb 21.
Article in English | MEDLINE | ID: mdl-26812468

ABSTRACT

Design and synthesis of symmetric mannose-functionalized oligothiophenes is reported. Self-organization of these bolaamphiphiles in solution and in the solid state was investigated by optical and AFM experiments. Fluorescence measurements revealed efficient loading and pH-dependent release of the anti-cancer drug doxorubicin. Delivery and release of the active drug into viable A549 cells as well as chirality-dependent cellular toxicity of the bolaamphiphilic transporter were evident from in vitro experiments.


Subject(s)
Antibiotics, Antineoplastic/administration & dosage , Doxorubicin/administration & dosage , Thiophenes/chemistry , Delayed-Action Preparations , Microscopy, Atomic Force , Spectrometry, Fluorescence , Spectrophotometry, Ultraviolet
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