Self-Report Amphiphilic Polymer-Based Drug Delivery System with ROS-Triggered Drug Release for Osteoarthritis Therapy.
Sicheng TangYuhan GaoWenchao WangYijian WangPan LiuZeyu ShouRuhui YangChaofan JinXingjie ZanChenglong WangWujun GengPublished in: ACS macro letters (2023)
The development of drug delivery systems with real-time cargo release monitoring capabilities is imperative for optimizing nanomedicine performance. Herein, we report an innovative self-reporting drug delivery platform based on a ROS-responsive random copolymer ( P1 ) capable of visualizing cargo release kinetics via the activation of an integrated fluorophore. P1 was synthesized by copolymerization of pinacol boronate, PEG, and naphthalimide monomers to impart ROS-sensitivity, hydrophilicity, and fluorescence signaling, respectively. Detailed characterization verified that P1 self-assembles into 11 nm micelles with 10 μg mL -1 CMC and can encapsulate hydrophobic curcumin with 79% efficiency. Fluorescence assays demonstrated H 2 O 2 -triggered disassembly and curcumin release with concurrent polymer fluorescence turn-on. Both in vitro and in vivo studies validated the real-time visualization of drug release and ROS scavenging, as well as the therapeutic effect on osteoarthritis (OA). Overall, this nanotheranostic polymeric micelle system enables quantitative monitoring of drug release kinetics for enhanced treatment optimization across oxidative stress-related diseases.
Keyphrases
- drug release
- drug delivery
- cancer therapy
- dna damage
- cell death
- reactive oxygen species
- oxidative stress
- single molecule
- fluorescent probe
- knee osteoarthritis
- rheumatoid arthritis
- energy transfer
- living cells
- high throughput
- aqueous solution
- sensitive detection
- radiation therapy
- high resolution
- stem cells
- locally advanced
- emergency department
- mass spectrometry
- single cell
- cell therapy
- neural network
- ionic liquid
- heat shock protein
- case control