Abstract
Drug delivery from polymer micelles has been widely studied, but methods to precisely tune rates of drug release from micelles are limited. Here, the mobility of hydrophobic micelle cores was varied to tune the rate at which a covalently bound drug was released. This concept was applied to cysteine-triggered release of hydrogen sulfide (H 2 S), a signaling gas with therapeutic potential. In this system, thiol-triggered H 2 S donor molecules were covalently linked to the hydrophobic blocks of self-assembled polymer amphiphiles. Because release of H 2 S is triggered by cysteine, diffusion of cysteine into the hydrophobic micelle core was hypothesized to control the rate of release. We confirmed this hypothesis by carrying out release experiments from H 2 S-releasing micelles in varying compositions of EtOH/H 2 O. Higher EtOH concentrations caused the micelles to swell, facilitating diffusion in and out of their hydrophobic cores and leading to faster H 2 S release from the micelles. To achieve a similar effect without addition of organic solvent, we prepared micelles with varying core mobility via incorporation of a plasticizing comonomer in the core-forming block. The glass transition temperature (T g ) of the core block could therefore be precisely varied by changing the amount of the plasticizing comonomer in the polymer. In aqueous solution under identical conditions, the release rate of H 2 S varied over 20-fold (t 1/2 = 0.18-4.2 h), with the lowest T g hydrophobic block resulting in the fastest H 2 S release. This method of modulating release kinetics from polymer micelles by tuning core mobility may be applicable to many types of physically encapsulated and covalently linked small molecules in a variety of drug delivery systems.
Original language | English |
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Pages (from-to) | 1104-1111 |
Number of pages | 8 |
Journal | Macromolecules |
Volume | 52 |
Issue number | 3 |
DOIs | |
State | Published - Feb 12 2019 |
Externally published | Yes |
Funding
This work was supported by the National Science Foundation (DMR-1454754), the National Institutes of Health (R01GM123508), and the Dreyfus Foundation. NBS was supported by an NSF-funded REU program (1560240). We thank Prof. Tim Long and Prof. Rick Davis for use of instruments.
Funders | Funder number |
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NSF-funded | 1560240 |
National Science Foundation | DMR-1454754 |
National Institutes of Health | R01GM123508 |
Camille and Henry Dreyfus Foundation | |
National Bureau of Statistics of China |