Division of Chemistry and Chemical Engineering , California Institute of Technology , Pasadena , California 91125 , United States.
Acc Chem Res. 2019 Sep 17;52(9):2427-2434. doi: 10.1021/acs.accounts.9b00277. Epub 2019 Aug 9.
The precise targeting of cells in deep tissues is one of the primary goals of nanomedicine. However, targeting a specific cellular population within an entire organism is challenging due to off-target effects and the need for deep tissue delivery. Focused ultrasound can reduce off-targeted effects by spatially restricting the delivery or action of molecular constructs to specific anatomical sites. Ultrasound can also increase the efficiency of nanotherapeutic delivery into deep tissues by enhancing the permeability of tissue boundaries, promoting convection, or depositing energy to actuate cellular activity. In this review we focus on the interface between biomolecular engineering and focused ultrasound and describe the applications of this intersection in neuroscience, oncology, and synthetic biology. Ultrasound can be used to trigger the transport of therapeutic payloads into a range of tissues, including specific regions of the brain, where it can be targeted with millimeter precision through intact skull. Locally delivered molecular constructs can then control specific cells and molecular pathways within the targeted region. When combined with viral vectors and engineered neural receptors, this technique enables noninvasive control of specific circuits and behaviors. The penetrant energy of ultrasound can also be used to more directly actuate micro- and nanotherapeutic constructs, including microbubbles, vaporizable nanodroplets, and polymeric nanocups, which nucleate cavitation upon ultrasound exposure, leading to local mechanical effects. In addition, it was recently discovered that a unique class of acoustic biomolecules-genetically encodable nanoscale protein structures called gas vesicles-can be acoustically "detonated" as sources of inertial cavitation. This enables the targeted disruption of selected cells within the area of insonation by gas vesicles that are engineered to bind cell surface receptors. It also facilitates ultrasound-triggered release of molecular payloads from engineered therapeutic cells heterologously expressing intracellular gas vesicles. Finally, focused ultrasound energy can be used to locally elevate tissue temperature and activate temperature-sensitive proteins and pathways. The elevation of temperature allows noninvasive control of gene expression in cells engineered to express thermal bioswitches. Overall, the intersection of biomolecular engineering, nanomaterials and focused ultrasound can provide unparalleled specificity in controlling, modulating, and treating physiological processes in deep tissues.
精确靶向深部组织中的细胞是纳米医学的主要目标之一。然而,由于脱靶效应和深部组织递送的需要,靶向整个生物体中的特定细胞群体具有挑战性。聚焦超声可以通过空间限制分子构建体在特定解剖部位的递送来减少脱靶效应。超声还可以通过增强组织边界的通透性、促进对流或沉积能量来激活细胞活性,从而提高纳米治疗剂递送到深部组织的效率。在本综述中,我们专注于生物分子工程与聚焦超声的界面,并描述了该交点在神经科学、肿瘤学和合成生物学中的应用。超声可用于触发治疗有效载荷向一系列组织(包括大脑的特定区域)的运输,在这些区域,通过完整的颅骨可以以毫米精度靶向它。然后,局部递送的分子构建体可以控制靶向区域内的特定细胞和分子途径。当与病毒载体和工程神经受体结合使用时,该技术可实现对特定回路和行为的非侵入性控制。超声的穿透能量还可用于更直接地激活微纳治疗构建体,包括微泡、可蒸发纳米液滴和聚合物纳米杯,这些构建体在超声暴露时会引发空化,从而导致局部机械效应。此外,最近发现一类独特的声学生物分子——称为气穴的遗传编码纳米级蛋白质结构——可以作为惯性空化的声源被声“引爆”。这使得可以通过工程化以结合细胞表面受体的气穴来靶向破坏照射区域内的选定细胞。它还促进了通过异源表达细胞内气穴的工程治疗细胞从工程治疗细胞中超声触发释放分子有效载荷。最后,聚焦超声能量可用于局部升高组织温度并激活温度敏感蛋白和途径。温度的升高允许非侵入性地控制表达热生物开关的细胞中的基因表达。总体而言,生物分子工程、纳米材料和聚焦超声的交叉可以在控制、调节和治疗深部组织中的生理过程方面提供无与伦比的特异性。