Redox-sensitive Pluronic F127-tocopherol micelles: synthesis, characterization, and cytotoxicity evaluation
Medicine (General)
Magnetic Resonance Spectroscopy
micelles
alpha-Tocopherol
Chemistry Techniques, Synthetic
Poloxamer
02 engineering and technology
Hemolysis
Cell Line
R5-920
Drug Delivery Systems
Drug Stability
International Journal of Nanomedicine
Spectroscopy, Fourier Transform Infrared
Animals
Humans
Particle Size
Micelles
Original Research
Tocopherol
Rats
3. Good health
Redox-sensitive
0210 nano-technology
Hydrophobic and Hydrophilic Interactions
Oxidation-Reduction
Pluronic F127
DOI:
10.2147/ijn.s122746
Publication Date:
2017-04-03T23:39:45Z
AUTHORS (8)
ABSTRACT
Pluronic F127 (F127), an amphiphilic triblock copolymer, has been shown to have significant potential for drug delivery, as it is able to incorporate hydrophobic drugs and self-assemble into nanosize micelles. However, it suffers from dissociation upon dilution owing to the relatively high critical micelle concentration and lack of stimuli-responsive behavior. Here, we synthesized the α-tocopherol (TOC) modified F127 polymer (F127-SS-TOC) via a redox-sensitive disulfide bond between F127 and TOC, which formed stable micelles at relatively low critical micelle concentration and was sensitive to the intracellular redox environment. The particle size and zeta potential of the F127-SS-TOC micelles were 51.87±6.39 nm and -8.43±2.27 mV, respectively, and little changes in both particle size and zeta potential were observed within 7 days at room temperature. With 10 mM dithiothreitol stimulation, the F127-SS-TOC micelles rapidly dissociated followed by a significant change in size, which demonstrated a high reduction sensitivity of the micelles. In addition, the micelles showed a high hemocompatibility even at a high micelle concentration (1,000 μg/mL). Low cytotoxicity of the F127-SS-TOC micelles at concentrations ranging from 12.5 μg/mL to 200 μg/mL was also found on both Bel 7402 and L02 cells. Overall, our results demonstrated F127-SS-TOC micelles as a stable and safe aqueous formulation with a considerable potential for drug delivery.
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