Gene therapy is one of the promising solutions in cancer therapeutics. Ultrasound-mediated gene delivery showed great potential as a noninvasive strategy for gene therapy. However, the efficiency of gene transfection and incorporation of multiple functions remain key challenges in the development of gene delivery systems. In this study, we developed perfluoropentane (PFP) and gold nanorods (AuNRs) loading nanodroplets for photothermal-enhanced ultrasound-mediated imaging and gene transfection. The nanodroplet theranostic system was formulated with fluorinated cationic poly(aspartamide) based polymer that encapsulated PFP, AuNRs, and plasmid DNA and was stabilized with a negatively charged poly(glutamic acid)-g-MeO-poly(ethylene glycol) (PGA-g-mPEG) coating. The nanodroplets presented good stability, biocompatibility, and DNA binding stability. Upon treatment with both near-infrared and ultrasound energy, the photothermal and ultrasound-responsive system exerted a synergistic effect, in which strong adsorption of light induced hyperthermia that promoted the phase transition of PFP and the following ultrasound irradiation, generating strong acoustic cavitation and sonoporation, thus leading to enhanced ultrasound contrast imaging and gene transfection efficiency both in vitro and in vivo.
Keyphrases
- magnetic resonance imaging
- gene therapy
- genome wide
- copy number
- photodynamic therapy
- contrast enhanced ultrasound
- dna binding
- ultrasound guided
- cancer therapy
- genome wide identification
- high resolution
- drug delivery
- magnetic resonance
- squamous cell carcinoma
- transcription factor
- dna methylation
- radiation therapy
- single molecule
- risk assessment
- mass spectrometry
- drug release
- gold nanoparticles
- contrast enhanced
- smoking cessation
- squamous cell