共 47 条
Cellular interactions of surface modified nanoporous silicon particles
被引:44
作者:

Bimbo, Luis M.
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Univ Helsinki, Fac Pharm, Div Pharmaceut Technol, FI-00014 Helsinki, Finland Univ Helsinki, Fac Pharm, Div Pharmaceut Technol, FI-00014 Helsinki, Finland

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Makila, Ermei
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Univ Turku, Dept Phys, Lab Ind Phys, FI-20014 Turku, Finland Univ Helsinki, Fac Pharm, Div Pharmaceut Technol, FI-00014 Helsinki, Finland

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Laaksonen, Paivi
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VTT Tech Res Ctr Finland, VTT Nanobiomat, Espoo 02044, Finland Univ Helsinki, Fac Pharm, Div Pharmaceut Technol, FI-00014 Helsinki, Finland

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Linder, Markus B.
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机构:
VTT Tech Res Ctr Finland, VTT Nanobiomat, Espoo 02044, Finland Univ Helsinki, Fac Pharm, Div Pharmaceut Technol, FI-00014 Helsinki, Finland

Hirvonen, Jouni
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Univ Helsinki, Fac Pharm, Div Pharmaceut Technol, FI-00014 Helsinki, Finland Univ Helsinki, Fac Pharm, Div Pharmaceut Technol, FI-00014 Helsinki, Finland

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Santos, Helder A.
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h-index: 0
机构:
Univ Helsinki, Fac Pharm, Div Pharmaceut Technol, FI-00014 Helsinki, Finland Univ Helsinki, Fac Pharm, Div Pharmaceut Technol, FI-00014 Helsinki, Finland
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
来源:
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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