Ultrasound-Responsive Hydrogels for On-Demand Protein Release

被引:1
作者
Arrizabalaga, Julien H. [1 ]
Smallcomb, Molly [2 ]
Abu-Laban, Mohammad [1 ]
Liu, Yiming [1 ]
Yeingst, Tyus J. [1 ]
Dhawan, Aman
Simon, Julianna C. [1 ,2 ]
Hayes, Daniel J. [1 ,3 ,4 ]
机构
[1] Penn State Univ, Dept Biomed Engn, University Pk, PA 16802 USA
[2] Penn State Univ, Grad Program Acoust, University Pk, PA 16802 USA
[3] Penn State Univ, Mat Res Inst, Millennium Sci Complex, University Pk, PA 16802 USA
[4] Penn State Univ, Huck Inst Life Sci, Millennium Sci Complex, University Pk, PA 16802 USA
基金
美国国家卫生研究院;
关键词
chitosan; hydrogels; ultrasound; controlled release; click chemistry; Diels-Alder; CROSS-LINKED HYDROGELS; DRUG-DELIVERY; CLICK CHEMISTRY; CHITOSAN; LINKING; DISRUPTION; CARRIERS; SYSTEMS;
D O I
10.1021/acsabm.2c001923212
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
The development of tunable, ultrasound-responsive hydrogels that can deliver protein payload on-demand when exposed to focused ultrasound is described in this study. Reversible Diels-Alder linkers, which undergo a retro reaction when stimulated with ultrasound, were used to cross-link chitosan hydrogels with entrapped FITC-BSA as a model protein therapeutic payload. Two Diels-Alder linkage compositions with large differences in the reverse reaction energy barriers were compared to explore the influence of linker composition on ultrasound response. Selected physicochemical properties of the hydrogel construct, its basic degradation kinetics, and its cytocompatibility were measured with respect to Diels-Alder linkage composition. Focused ultrasound initiated the retro Diels- Alder reaction, controlling the release of the entrapped payload while also allowing for real-time visualization of the ongoing process. Additionally, increasing the focused ultrasound amplitude and time correlated with an increased rate of protein release, indicating stimuli responsive control.
引用
收藏
页码:3212 / 3218
页数:7
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