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Engineering silica particles as oral drug delivery vehicles


Reference:

Rigby, S. P., Fairhead, M. and van der Walle, C. F., 2008. Engineering silica particles as oral drug delivery vehicles. Current Pharmaceutical Design, 14 (18), pp. 1821-1831.

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Official URL:

http://dx.doi.org/10.2174/138161208784746671

Abstract

Porous silica particles are emerging as complementary systems to polyester microspheres for the encapsulation and controlled delivery of small-organic drugs. Their recent application in pharmaceutics is strengthened by well-established characterization and synthetic routes from the chemical engineering sciences. Silica is an interesting scaffold material for the encapsulation of organic molecules. It can be formed into hierarchical structures over a wide range of length scales and interconnectivities. Encapsulation can therefore be tailored not only to the drug but the desired release properties. In addition to surfactant-templating of hierarchical silica structures, polypeptides from marine organisms may offer biological routes to novel silica materials. Silica sol-gels have also been evaluated as delivery vehicles, particularly with regard to generating hybrid systems with mesoporous silica or composite xerogels. This review will first focus on the detailed characterisation of pore size and structure of mesoporous silica with regards water penetration and drug diffusion. We then describe the pharmaceutical applications of silica materials with regard to vin oral bioavailability, multiparticulate system for gastroretention or sustained release, composite xerogels and in vivo biocompatibility.

Details

Item Type Articles
CreatorsRigby, S. P., Fairhead, M. and van der Walle, C. F.
DOI10.2174/138161208784746671
DepartmentsFaculty of Engineering & Design > Chemical Engineering
RefereedYes
StatusPublished
ID Code802

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