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An acidic pH-triggered polymeric micelle for dual-modality MR and optical imaging
40
Citations
21
References
2010
Year
Ethylene GlycolEngineeringSmart PolymerMicroscopyResponsive PolymersBiomedical EngineeringBlock CopolymerMagnetic Resonance ImagingTherapeutic NanomaterialsBioimagingMolecular ImagingBiophysicsNovel Imaging MethodMicelleBiopolymersBiophotonicsSolution Nmr SpectroscopyOptical ImagingBiomolecular EngineeringBiomedical DiagnosticsBiomedical ImagingBiomedical PhotonicsDrug Delivery SystemsAmphiphilic SystemDual-modality MrMedicine
A dual-modality imaging probe was developed for magnetic resonance imaging (MRI) and optical imaging, based on a Fe3O4-encapsulated pH-responsive block copolymer, which was conjugated with a red fluorescent dye Sulforhodamine 101 (SR101). The block copolymer, containing methoxy poly(ethylene glycol) (PEG) as a hydrophilic segment and poly(β-amino ester) (PAE) with ionizable tertiary amine groups on its backbone as a pH-responsive segment, can be dissolved in response to an acidic pH environment, or form self-assembled micelles in aqueous media at the physiological pH (∼pH 7.4) due to the hydrophobic deionized PAE segment acting as a micellar core. The polymeric micelle conjugated with SR101 was found to have a red-fluorescent emission at 612 nm, a sharp pH transition of pH 6.8–7.0, indicating that it can be an ideal pH-triggered carrier in response to the acidic biological environment. Subsequently, the Fe3O4-encapsulated micelle was evaluated by dynamic light scattering (DLS), cryogenic transmission electron microscope (cryo-TEM), and pH-dependent Fe3O4 release. The confocal laser scanning microscopy (CLSM) observation demonstrated the cellular uptake of SR101-labeled polymeric micelles by breast cancer cells.
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