Mechanoresponsive materials for drug delivery: Harnessing forces for controlled release

被引:83
作者
Wang, Julia [1 ]
Kaplan, Jonah A. [1 ]
Colson, Yolonda L. [4 ]
Grinstaff, Mark W. [1 ,2 ,3 ]
机构
[1] Boston Univ, Dept Biomed Engn, 590 Commonwealth Ave, Boston, MA 02215 USA
[2] Boston Univ, Dept Chem, 590 Commonwealth Ave, Boston, MA 02215 USA
[3] Boston Univ, Dept Med, 590 Commonwealth Ave, Boston, MA 02215 USA
[4] Brigham & Womens Hosp, Dept Surg, Div Thorac Surg, Boston, MA 02115 USA
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
Drug delivery; Compression; Tension; Shear; Biomaterials; Nanomaterials; INTENSITY FOCUSED ULTRASOUND; SHEAR-STRESS; RESPONSIVE POLYMERS; SENSITIVE HYDROGELS; MUSCLE FORCES; DESIGN; SYSTEM; NANOPARTICLES; PROTEIN; SURFACES;
D O I
10.1016/j.addr.2016.11.001
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Mechanically-activated delivery systems harness existing physiological and/or externally-applied forces to provide spatiotemporal control over the release of active agents. Current strategies to deliver therapeutic proteins and drugs use three types of mechanical stimuli: compression, tension, and shear. Based on the intended application, each stimulus requires specific material selection, in terms of substrate composition and size (e.g., macrostructured materials and nanomaterials), for optimal in vitro and in vivo performance. For example, compressive systems typically utilize hydrogels or elastomeric substrates that respond to and withstand cyclic compressive loading, whereas, tension-responsive systems use composites to compartmentalize payloads. Finally, shear-activated systems are based on nanoassemblies or microaggregates that respond to physiological or externally-applied shear stresses. In order to provide a comprehensive assessment of current research on mechanoresponsive drug delivery, the mechanical stimuli intrinsically present in the human body are first discussed, along with the mechanical forces typically applied during medical device interventions, followed by in-depth descriptions of compression, tension, and shear-mediated drug delivery devices. We conclude by summarizing the progress of current research aimed at integrating mechanoresponsive elements within these devices, identifying additional clinical opportunities for mechanically-activated systems, and discussing future prospects. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:68 / 82
页数:15
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