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基于多阶动态移焦的透皮给药增效研究

龚新越 薛洪惠 宋人杰 郭杨 马勇 屠娟

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基于多阶动态移焦的透皮给药增效研究

龚新越, 薛洪惠, 宋人杰, 郭杨, 马勇, 屠娟

Synergistic effect of ultrasound transdermal drug delivery based on multi-stage dynamic focal-shifting

GONG Xinyue, XUE Honghui, SONG Renjie, GUO Yang, MA Yong, TU Juan
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  • 针对传统超声透皮给药技术中声场聚焦模式单一、药物粒子穿透深度及分布范围受限等关键瓶颈问题, 本研究提出了一种基于超声换能器阵列的多阶动态移焦发射策略, 旨在实现声能量在皮肤深度方向的动态重分布, 从而提升纳米粒子的透皮效率与分布均匀性. 通过调控换能器阵元激励相位, 构建多阶移动的声聚焦作用路径, 并通过在体动物实验与有限元仿真联合验证其透皮给药效果. 结果显示, 与固定焦点模式相比, 动态聚焦显著提升了药物粒子的经皮渗透深度与空间分布均匀性, 其平均渗透深度可提高65.7%, 荧光积分强度提升69.3%, 并在皮肤组织中形成更均匀的沉积带结构. 有限元仿真结果进一步揭示了该模式下粒子扩散演化行为与焦点动态轨迹之间的强耦合机制, 证实动态移焦模式下的“多焦点接力式”驱动效应可在显著优化粒子的经皮渗透效率的同时, 有效降低局部能量沉积引发的潜在风险, 为构建高效、安全、可控的超声透皮递药技术提供了重要的理论基础与技术支撑.
    Ultrasound-assisted transdermal drug delivery (UTDD) is a promising non-invasive strategy to overcome the skin barrier. The traditional fixed-focus ultrasound approaches encounter the problems such as limited penetration depth, localized accumulation, and risk of thermal damage. To address these challenges, we propose a phased-array based dynamic focusing strategy, in which the acoustic focus is shifted sequentially along the depth direction. This approach aims to construct a continuous longitudinal acoustic radiation pathway that can sustain particle migration into deeper skin layers.In vivo experiments are conducted with FITC-labeled nanoparticles on rat dorsal skin under three conditions: natural permeation, fixed focus (~0.5 mm beneath the skin), and dynamic focusing (scanned from the surface to 1 mm). After10-min ultrasound, fluorescence microscopy reveals that fixed focus enhances penetration compared with natural permeation, while dynamic focusing further improves delivery, increasing average depth by 65.7%, maximum depth by 41.2%, and fluorescence intensity by 69.3%. Dynamic focusing also produces a more uniform and continuous deposition band, which is unlike the localized accumulation seen with fixed focus.To elucidate the underlying mechanisms, a two-dimensional finite element model is established in COMSOL Multiphysics. The simulation results reveal that this “multi-focus relay” effect provides a continuous driving force pathway, enabling particles to follow the shifting focal positions. Trajectory analysis confirms that the number of particles reaching deeper layers (up to 5 mm) increases by nearly 14 times under dynamic focusing compared with that in the case of fixed focus, while the width of the lateral distribution extends by 46.1%.In conclusion, both experimental and simulation results demonstrate that phased-array dynamic focusing significantly enhances penetration depth, migration efficiency, and distribution uniformity of nanoparticles in UTDD. By constructing a continuous acoustic radiation pathway in the depth dimension, this approach improves delivery efficiency while mitigating local energy accumulation, providing a safer and more effective strategy for ultrasound-mediated transdermal therapy.
  • 图 1  TDD药物吸收途径示意图

    Fig. 1.  Schematic diagram of TDD drug absorption pathway

    图 2  (a) 实验操作示意图; (b) 粒子渗透示意图, 其中绿色圆球为荧光粒子

    Fig. 2.  (a) Schematic diagram of experimental operation; (b) schematic diagram of particle penetration, where green spheres are fluorescent particles.

    图 3  (a) 聚焦发射的透皮给药原理示意图; (b) 有限元模型结构图

    Fig. 3.  (a) Schematic diagram of transdermal drug delivery principle with focused emission; (b) finite element model structure diagram

    图 4  荧光显微镜下的组织切片 (a)自然渗透组; (b)固定焦点聚焦组; (c)动态聚焦组

    Fig. 4.  Tissue sections under fluorescence microscope: (a) Natural infiltration group; (b) fixed focus group; (c) dynamic focus group in turn.

    图 5  组织切片荧光图像平均渗透深度、最大渗透深度、荧光积分强度三项指标柱状图

    Fig. 5.  Histogram of three indicators: average penetration depth, maximum penetration depth and fluorescence integral intensity of fluorescence images of tissue sections.

    图 6  动态聚焦情况下不同聚焦深度的声场仿真结果 (a)焦点位于皮下1 mm; (b)焦点位于皮下2 mm; (c)焦点位于皮下3 mm

    Fig. 6.  Simulation results of acoustic field with different focusing depths under dynamic focusing: (a) The focus is 1 mm under the skin; (b) the focus is 2 mm under the skin; (c) the focus is 3 mm under the skin.

    图 7  运动至皮下5 mm处的粒子分布情况, 其中分布宽度为运动至皮下5 mm的粒子左右两端的距离(见图2(b))

    Fig. 7.  Distribution of particles moving to 5 mm under the skin. The distribution width is the distance between the left and right ends of particles moving to 5 mm under the skin, as shown in Fig. 2(b).

    图 8  5%, 10%和20%三种占空比条件下, 运动至皮下5 mm处的粒子数量

    Fig. 8.  The number of particles moving to 5 mm under the skin under three duty ratios of 5%, 10% and 20%.

    图 9  三种典型位置粒子在两种声场中的三维运动路径(对应粉、绿、紫曲线), 其中黑色虚线描绘了声场焦点中心的变化 (a)固定焦点聚焦声场; (b)动态移焦声场

    Fig. 9.  The three-dimensional motion paths of particles in three typical positions (corresponding to pink, green and purple curves) in two kinds of acoustic fields: (a) Acoustic field with fixed focus; (b) dynamically focused acoustic field. The black dotted line depicts the change of the focus center of the sound field.

    表 1  不同聚焦深度下的焦域参数

    Table 1.  Focal parameters at different depth of focus.

    预设焦点皮下深度焦点横向宽度/mm焦点纵向长度/mm
    x/mmy/mm
    0.001.000.933.63
    0.002.000.984.13
    0.003.001.054.56
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  • 收稿日期:  2025-07-31
  • 修回日期:  2025-09-07
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