Bionanocomposites based on mesoporous silica and alginate for enhanced drug delivery

被引:39
作者
de Lima, Hugo H. C. [1 ]
Kupfer, Vicente L. [1 ]
Moises, Murilo P. [1 ,4 ]
Guilherme, Marcos R. [2 ]
Rinaldi, Jaqueline de C. [1 ,3 ]
Felisbino, Sergio L. [3 ]
Rubira, Adley F. [2 ]
Rinaldi, Andrelson W. [1 ]
机构
[1] State Univ Maringa UEM, Mat Chem & Sensors Lab LMSen, 5790 Colombo Ave, BR-87020900 Maringa, Parana, Brazil
[2] State Univ Maringa UEM, 5790 Colombo Ave, BR-87020900 Maringa, Parana, Brazil
[3] Sao Paulo Univ UNESP, Lab Extracelular Matrix LabMEc, Botucatu, SP, Brazil
[4] Fed Univ Technol Parana UTFPR, 635 Marcilio Dias St, BR-86812460 Apucarana, PR, Brazil
关键词
Biomaterials; Cytotoxicity; Drug delivery; Hydrogel; Mesoporous silica; Nanotechnology; CORE-SHELL NANOPARTICLES; NANOCOMPOSITE HYDROGELS; GLYCIDYL METHACRYLATE; POLY(ETHYLENE GLYCOL); CELL-ADHESION; PH; SYSTEMS; RELEASE; FUNCTIONALIZATION; PROLIFERATION;
D O I
10.1016/j.carbpol.2018.04.107
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
This work reports the preparation, the characterization and the prednisolone release profile of biocompatible hydrogel nanocomposites containing mesoporous silica (SBA) and alginate as a biomaterial for enhanced drug delivery with reduced burst effect and improved mechanical properties. Such systems, which were prepared using specific SBA/alginate-crosslinking chemistry, exhibited interconnecting pore hybrid network owing to both mesoporous silica and hydrogel characteristics. Activated SBA was shown to be a determinant factor in inhibiting initial burst by nearly 90% and the drug was released with minimal burst kinetics. The nanoparticles reduced the movements of polymer chains, affecting macromolecular relaxation, and the distribution of mesoporous silica within the hydrogel made drug release into surrounding liquid less favorable. The proposed systems are biocompatible with human immortalized RWPE-1 prostatic epithelial cells. This report offers an approach of up-to-date interest for the development of advanced biomaterials for further physiological and pathological applications.
引用
收藏
页码:126 / 134
页数:9
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