Coacervate delivery systems for proteins and small molecule drugs

被引:107
作者
Johnson, Noah R. [1 ,2 ]
Wang, Yadong [1 ,2 ,3 ,4 ,5 ]
机构
[1] Univ Pittsburgh, Dept Bioengn, Pittsburgh, PA 15219 USA
[2] McGowan Inst Regenerat Med, Pittsburgh, PA 15219 USA
[3] Univ Pittsburgh, Dept Chem & Petr Engn, Pittsburgh, PA 15219 USA
[4] Univ Pittsburgh, Dept Surg, Pittsburgh, PA 15219 USA
[5] Univ Pittsburgh, Dept Mech Engn & Mat Sci, Pittsburgh, PA 15219 USA
关键词
chitosan; coacervate; controlled release; doxorubicin; drug delivery; elastin; growth factor; heparin; hyaluronic acid; ELASTIN-LIKE POLYPEPTIDE; FIBROBLAST GROWTH FACTOR-2; SOLID TUMORS; STEM-CELLS; DESIGN; TEMPERATURE; EFFICIENT; POLYMERS;
D O I
10.1517/17425247.2014.941355
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Coacervates represent an exciting new class of drug delivery vehicles, developed in the past decade as carriers of small molecule drugs and proteins. This review summarizes several well-described coacervate systems, including: i) elastin-like peptides for delivery of anticancer therapeutics; ii) heparin-based coacervates with synthetic polycations for controlled growth factor delivery; iii) carboxymethyl chitosan aggregates for oral drug delivery; iv) Mussel adhesive protein and hyaluronic acid coacervates. Coacervates present advantages in their simple assembly and easy incorporation into tissue engineering scaffolds or as adjuncts to cell therapies. They are also amenable to functionalization such as for targeting or for enhancing the bioactivity of their cargo. These new drug carriers are anticipated to have broad applications and noteworthy impact in the near future.
引用
收藏
页码:1829 / 1832
页数:4
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