Moncion Alexander, Lin Melissa, Kripfgans Oliver D, Franceschi Renny T, Putnam Andrew J, Fabiilli Mario L
Applied Physics Program, University of Michigan, Ann Arbor, Michigan, USA; Department of Radiology, University of Michigan Health System, Ann Arbor, Michigan, USA.
Department of Radiology, University of Michigan Health System, Ann Arbor, Michigan, USA.
Ultrasound Med Biol. 2018 Nov;44(11):2323-2335. doi: 10.1016/j.ultrasmedbio.2018.06.011. Epub 2018 Aug 2.
Regenerative processes, such as angiogenesis and osteogenesis, often require multiple growth factors with distinct spatiotemporal patterns and expression sequences. Within tissue engineering, hydrogel scaffolds are commonly used for exogenous growth factor delivery. However, direct incorporation of growth factors within conventional hydrogels does not afford spatiotemporally controlled delivery because release is governed by passive mechanisms that cannot be actively controlled after the scaffold is implanted. We have developed acoustically-responsive scaffolds (ARSs), which are fibrin scaffolds doped with payload-containing, sonosensitive emulsions. Payload release from ARSs can be controlled non-invasively and on demand using focused, megahertz-range ultrasound. In the in vitro study described here, we developed and characterized ARSs that enable sequential release of two surrogate, fluorescent payloads using consecutive ultrasound exposures at different acoustic pressures. ARSs were generated with various combinations and volume fractions of perfluoropentane, perfluorohexane, and perfluoroheptane emulsions. Acoustic droplet vaporization and inertial cavitation thresholds correlated with the boiling point/molecular weight of the perfluorocarbon while payload release correlated inversely. Payload release was longitudinally measured and observed to follow a sigmoidal trend versus acoustic pressure. Perfluoropentane and perfluorohexane emulsions were stabilized when incorporated into ARSs with perfluoroheptane emulsion. These results highlight the potential of using ARSs for sequential, dual-payload release for tissue regeneration.
诸如血管生成和骨生成等再生过程通常需要多种具有不同时空模式和表达序列的生长因子。在组织工程中,水凝胶支架常用于外源性生长因子的递送。然而,将生长因子直接掺入传统水凝胶中并不能实现时空可控的递送,因为释放是由被动机制控制的,在支架植入后无法主动调控。我们开发了声学响应支架(ARSs),它是掺杂了含有效载荷的声敏乳液的纤维蛋白支架。使用聚焦的兆赫兹级超声可以无创且按需控制ARSs中有效载荷的释放。在此处描述的体外研究中,我们开发并表征了ARSs,其能够通过在不同声压下连续进行超声照射来实现两种替代荧光有效载荷的顺序释放。ARSs是由全氟戊烷、全氟己烷和全氟庚烷乳液的各种组合和体积分数生成的。声滴汽化和惯性空化阈值与全氟碳的沸点/分子量相关,而有效载荷释放则与之呈反比。对有效载荷释放进行纵向测量,并观察到其与声压呈S形趋势。当全氟戊烷和全氟己烷乳液与全氟庚烷乳液一起掺入ARSs时能够实现稳定化。这些结果突出了使用ARSs进行组织再生的顺序双有效载荷释放的潜力。