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声响应支架的声滴汽化阈值和有效载荷释放的参数研究。

Parametric Study of Acoustic Droplet Vaporization Thresholds and Payload Release From Acoustically-Responsive Scaffolds.

机构信息

Department of Radiology, University of Michigan Health System, Ann Arbor, USA.

Department of Radiology, University of Michigan Health System, Ann Arbor, USA; Department of Ultrasound, Army Medical University, Chongqing, China.

出版信息

Ultrasound Med Biol. 2019 Sep;45(9):2471-2484. doi: 10.1016/j.ultrasmedbio.2019.05.024. Epub 2019 Jun 22.

Abstract

Hydrogels are commonly used for the delivery of bioactive molecules, especially growth factors and cytokines capable of stimulating tissue regeneration. Regenerative processes are regulated by the concentrations and spatiotemporal presentations of these molecules. With conventional hydrogels, these critical delivery parameters cannot be actively modulated after implantation. We have developed composite hydrogel scaffolds where payload release is non-invasively modulated, in an on-demand manner, using ultrasound (US). These acoustically-responsive scaffolds (ARSs) consist of a fibrin matrix doped with a payload-carrying, perfluorocarbon (PFC) double emulsion. Previously, acoustic droplet vaporization (ADV) was used to trigger release of a pro-angiogenic growth factor, encapsulated in the ARS, which stimulated blood vessel formation in vivo. In the present study, we assess how characteristics of the monodispersed emulsion, fibrin matrix, and US impact ADV thresholds and the release efficiency of a dextran payload. ADV thresholds increased with the molecular weight of the PFC in the emulsion and inversely with the volume fraction of emulsion in the ARS. Payload release from ARSs with perfluoroheptane (C7) or perfluorooctane (C8) emulsions was dependent on the number of z-planes of US used to generate ADV and inversely dependent on the lateral spacing. Conversely, release from ARSs with perfluoropentane (C5) or perfluorohexane (C6) emulsions was less dependent on these US exposure parameters. After ADV, payload diffusion decreased significantly in ARSs with C5 or C6 emulsions compared with ARSs with C7 or C8 emulsions. The expansion of the ARS after ADV decreased with the molecular weight of the PFC. Non-selective release increased with the molecular weight of the PFC and thrombin concentration. Overall, these findings can be used for optimization of ARS properties and US parameters in future therapeutic applications.

摘要

水凝胶常用于生物活性分子的递送,特别是能够刺激组织再生的生长因子和细胞因子。再生过程受这些分子的浓度和时空分布调控。对于传统水凝胶,在植入后这些关键的递送参数无法主动调节。我们开发了复合水凝胶支架,通过超声(US)以非侵入性、按需的方式调节药物释放。这些声响应支架(ARS)由掺入载药的全氟碳(PFC)双重乳液的纤维蛋白基质组成。先前,我们使用声致液滴汽化(ADV)来触发载有促血管生成生长因子的 ARS 释放,该生长因子可刺激体内血管形成。在本研究中,我们评估了单分散乳液、纤维蛋白基质和 US 的特性如何影响 ADV 阈值和葡聚糖载药的释放效率。ADV 阈值随乳液中 PFC 的分子量增加而增加,随 ARS 中乳液的体积分数减小而增加。具有全氟庚烷(C7)或全氟辛烷(C8)乳液的 ARS 的载药释放依赖于用于生成 ADV 的 z 平面数量,且与侧向间距成反比。相反,具有全氟戊烷(C5)或全氟己烷(C6)乳液的 ARS 的释放则较少依赖于这些 US 暴露参数。ADV 后,与具有 C7 或 C8 乳液的 ARS 相比,具有 C5 或 C6 乳液的 ARS 中的载药扩散显著降低。ADV 后 ARS 的扩张随 PFC 分子量的增加而减小。非选择性释放随 PFC 和凝血酶浓度的增加而增加。总体而言,这些发现可用于优化未来治疗应用中 ARS 特性和 US 参数。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/74b1/6689245/52349c3e76ba/nihms-1530940-f0001.jpg

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