Biomimetic Delivery with Micro- and Nanoparticles

被引:153
作者
Balmert, Stephen C. [1 ,2 ]
Little, Steven R. [1 ,2 ]
机构
[1] Univ Pittsburgh, Dept Immunol, Dept Bioengn, Dept Chem Engn, Pittsburgh, PA 15261 USA
[2] Univ Pittsburgh, McGowan Inst Regenerat Med, Pittsburgh, PA 15261 USA
基金
美国国家科学基金会;
关键词
biomimetic; particulates; controlled release; anisotropy; biological communication; ANTIGEN-PRESENTING CELLS; GROWTH-FACTOR DELIVERY; SEQUENTIAL BMP-2/BMP-7 DELIVERY; CYTOTOXIC T-LYMPHOCYTES; TARGETED DRUG-DELIVERY; CONTROLLED-RELEASE; IMMUNE-RESPONSES; DENDRITIC CELLS; INTRACELLULAR DELIVERY; POLYMER MICROSPHERES;
D O I
10.1002/adma.201200224
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The nascent field of biomimetic delivery with micro- and nanoparticles (MNP) has advanced considerably in recent years. Drawing inspiration from the ways that cells communicate in the body, several different modes of delivery (i.e., temporospatial presentation of biological signals) have been investigated in a number of therapeutic contexts. In particular, this review focuses on (1) controlled release formulations that deliver natural soluble factors with physiologically relevant temporal context, (2) presentation of surface-bound ligands to cells, with spatial organization of ligands ranging from isotropic to dynamically anisotropic, and (3) physical properties of particles, including size, shape and mechanical stiffness, which mimic those of natural cells. Importantly, the context provided by multimodal, or multifactor delivery represents a key element of most biomimetic MNP systems, a concept illustrated by an analogy to human interpersonal communication. Regulatory implications of increasingly sophisticated and cell-like biomimetic MNP systems are also discussed.
引用
收藏
页码:3757 / 3778
页数:22
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