Cellular interactions of surface modified nanoporous silicon particles

被引:44
作者
Bimbo, Luis M. [1 ]
Sarparanta, Mirkka [2 ]
Makila, Ermei [3 ]
Laaksonen, Timo [1 ]
Laaksonen, Paivi [4 ]
Salonen, Jarno [3 ]
Linder, Markus B. [4 ]
Hirvonen, Jouni [1 ]
Airaksinen, Anu J. [2 ]
Santos, Helder A. [1 ]
机构
[1] Univ Helsinki, Fac Pharm, Div Pharmaceut Technol, FI-00014 Helsinki, Finland
[2] Univ Helsinki, Dept Chem, Lab Radiochem, FI-00014 Helsinki, Finland
[3] Univ Turku, Dept Phys, Lab Ind Phys, FI-20014 Turku, Finland
[4] VTT Tech Res Ctr Finland, VTT Nanobiomat, Espoo 02044, Finland
基金
芬兰科学院;
关键词
ORAL-DRUG DELIVERY; POROUS SILICON; MESOPOROUS SILICON; TRICHODERMA-REESEI; IN-VITRO; HYDROPHOBIN; MICROPARTICLES; NANOPARTICLES; BIOCOMPATIBILITY; PROTEIN;
D O I
10.1039/c2nr30397c
中图分类号
O6 [化学];
学科分类号
070301 [无机化学];
摘要
In this study, the self-assembly of hydrophobin class II (HFBII) on the surface of thermally hydrocarbonized porous silicon (THCPSi) nanoparticles was investigated. The HFBII-coating converted the hydrophobic particles into more hydrophilic ones, improved the particles' cell viability in both HT-29 and Caco-2 cell lines compared to uncoated particles, and enhanced the particles' cellular association. The amount of HFBII adsorbed onto the particles was also successfully quantified by both the BCA assay and a HPLC method. Importantly, the permeation of a poorly water-soluble drug, indomethacin, loaded into THCPSi particles across Caco-2 monolayers was not affected by the protein coating. In addition, I-125-radiolabelled HFBII did not extensively permeate the Caco-2 monolayer and was found to be stably adsorbed onto the THCPSi nanoparticles incubated in pH 7.4, which renders the particles the possibility for further track-imaging applications. The results highlight the potential of HFBII coating for improving wettability, increasing biocompatibility and possible intestinal association of PSi nanoparticulates for drug delivery applications.
引用
收藏
页码:3184 / 3192
页数:9
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