Internal biofunctionalization

Szamocki, R., Reculusa, S., Ravaine, S., Bartlett, P.N., Kuhn, A., and Hempelmann, R. (2006) Tailored mesostructuring and biofunctionalization of gold for increase electroactivity. Angewandte Chemie International Edition, 45, 1317-1321. 

Wang Z, Liu S, Guidoin R and Kodama M. Polyurethane vascular grafts with thorough porosity does an internal or an external membrane wrapping improve their in vivo biocompatibility and biofunctionality Art. Cells Blood Subst. Biotech. 32 463-464,2004. 

Traditionally, inorganic silica nanoparticles have been prepared from either TEOS (1) or tetramethoxyorthosilicate (TMOS) (2). When prepared, TEOS nanoparticles are composed internally of a simple silica network (—O—Si—O—), and have silanol groups on their surfaces. However, as they lack any exposed organic residues, both inside and on their surfaces (as shown schemahcally in Figure 4.1), they will require further modification with funchonal residues (e.g. amine or thiol) prior to their surface biofunctionalization. 

The internal biofunctionalization of silica nanoparticles with functional molecules, such as fluorescent dyes and drugs, is also very important for bioassays, imaging and drug delivery. Internally biofunctionalized silica nanoparticles that can provide strong and stable signals for imaging are particularly useful. 

The optimal fusion of surface and internal biofunctionalization of silica nanoparhcles can lead to the creation of useful multifunctional nanoparticles. Although several reviews [8-10] have detailed the advances in biofunctionalization of inorganic siUca nanoparhcles, none of these has summarized recent developments in this area, such as ORMOSIL and funchonal organosilica nanoparhcles. In the following section we describe both surface and internal biofunchonalizahon strategies for various types of inorganic sihca and organosilica nanoparhcles. 

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