Template-assisted fabrication of protein nanocapsules

被引:11
作者
Dougherty, Shelley A. [1 ]
Liang, Jianyu [1 ]
Kowalik, Timothy F. [2 ]
机构
[1] Worcester Polytech Inst, Dept Mech Engn, Worcester, MA 01609 USA
[2] Univ Massachusetts, Dept Mol Genet & Microbiol, Sch Med, Worcester, MA 01655 USA
关键词
Aluminum oxide; Nanotube; Protein; Enzyme; Gene therapy; Biochemistry; Biomedicine; FUNCTIONALIZED CARBON NANOTUBES; RECEPTOR-MEDIATED ENDOCYTOSIS; ASSEMBLED PEPTIDE NANOTUBES; HUMAN SERUM-ALBUMIN; DRUG-DELIVERY; GENE DELIVERY; NANOPARTICLES; CELLS; SIZE;
D O I
10.1007/s11051-008-9387-y
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Bionanomaterials have recently begun to spark a great amount of interest and could potentially revolutionize biomedical research. Nanoparticles, nanocapsules, and nanotubular structures are becoming attractive options in drug and gene delivery. The size of the delivery vehicles greatly impacts cellular uptake and makes it highly desirable to precisely control the diameter and length of nanocarriers to make uniform nanoparticles at low cost. Carbon nanotubes have shown great potential within the field of drug and gene delivery. However, their insolubility and cytotoxicity could severely delay FDA approval. A desirable alternative would be to fabricate nanostructures from biomaterials such as proteins, peptides, or liposomes, which are already FDA approved. In this article we demonstrate the preparation of protein nanocapsules with both ends sealed using a template-assisted alternate immersion method combined with controlled cleaving. Glucose oxidase nanocapsules with controllable diameter, wall thickness, and length were fabricated and characterized with SEM and TEM. The biochemical activity of glucose oxidase in the form of nanocapsules after processing was confirmed using UV spectrometry. Our future work will explore proteins suitable for drug encapsulation and cellular uptake and will focus on optimizing the cleaving process to gain precise control over the length of the nanocapsules.
引用
收藏
页码:385 / 394
页数:10
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