Silica-Based Nanoparticles for Protein Encapsulation and Delivery

被引:6
|
作者
Begarani, Filippo [1 ,2 ]
Cassano, Domenico [1 ,2 ]
Margheritis, Eleonora [2 ]
Marotta, Roberto [3 ]
Cardarelli, Francesco [4 ]
Voliani, Valerio [2 ]
机构
[1] Scuola Normale Super Pisa, NEST, I-56100 Pisa, Italy
[2] Ist Italiano Tecnol, Ctr Nanotechnol Innovat, I-56100 Pisa, Italy
[3] Ist Italiano Tecnol, Electron Microscopy Facil, I-00161 Genoa, Italy
[4] CNR, Scuola Normale Super, Ist Nanosci, NEST, I-56100 Pisa, Italy
来源
NANOMATERIALS | 2018年 / 8卷 / 11期
关键词
protein-delivery; silica; biodegradation; liposomes; Lysosomal Storage Disorders (LSDs); NANO-ARCHITECTURES; CELLS;
D O I
10.3390/nano8110886
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Although conceptually obvious, the effective delivery of proteins in therapeutic applications is far from being a routine practice. The major limitation is the conservation of protein physicochemical identity during the transport to the target site. In this regard, nanoparticle-based systems offer new intriguing possibilities, provided that (i) the harsh and denaturating conditions typically used for nanoparticle synthesis are avoided or mitigated; and (ii) nanoparticle biocompatibility and degradation (for protein release) are optimized. Here, we tackle these issues by starting from a nanoparticle architecture already tested for small chemical compounds. In particular, silica-shielded liposomes are produced and loaded with a test protein (i.e., Green Fluorescent Protein) in an aqueous environment. We demonstrate promising results concerning protein encapsulation, protection during intracellular trafficking and final release triggered by nanoparticle degradations in acidic organelles. We believe this proof of principle may open new applications and developments for targeted and efficient protein delivery.
引用
收藏
页数:11
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