2009
DOI: 10.1016/j.powtec.2008.04.088
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Chemical hydrophobisation of silica-based porous particles with n-Octadecyltrichlorosilane (ODTCS) by a solventless process in a fluidised-bed reactor

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Cited by 3 publications
(3 citation statements)
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“…The dominant functional groups of the silica surfaces are siloxane (Si-O-Si) and silanol (-Si-OH) groups, which render these materials highly hygroscopic, and the presence of surface silanol groups also implies functionality to allow the better control of drug loading and release [12][13][14]. By functionalizing the surface, the new functional groups can develop strong interactions, which may lead to drug release retardation [15][16][17]. However, in an utterly different approach, the contribution of attractive drug-surface interactions is not necessarily increased, but the hydrophilicity of the silica carrier is decreased.…”
Section: Introductionmentioning
confidence: 99%
“…The dominant functional groups of the silica surfaces are siloxane (Si-O-Si) and silanol (-Si-OH) groups, which render these materials highly hygroscopic, and the presence of surface silanol groups also implies functionality to allow the better control of drug loading and release [12][13][14]. By functionalizing the surface, the new functional groups can develop strong interactions, which may lead to drug release retardation [15][16][17]. However, in an utterly different approach, the contribution of attractive drug-surface interactions is not necessarily increased, but the hydrophilicity of the silica carrier is decreased.…”
Section: Introductionmentioning
confidence: 99%
“…Finally, we choose to use carboxy‐terminal domains of collagen exposing hydroxyl groups usable for silanization 13, 14. For silanization we used either octadecyltrichlorosilane (OTS), which has been previously investigated for the chemical hydrophobization of silica surfaces, or octadecyltriethoxysilane (OTES) 15, 16. Silanization was first performed with OTS in dichloromethane (DCM); then silanization was repeated with other, more biocompatible solvents, such as ethanol for OTES and ethyl acetate or acetone for OTS.…”
Section: Introductionmentioning
confidence: 99%
“…13,14 For silanization we used either octadecyltrichlorosilane (OTS), which has been previously investigated for the chemical hydrophobization of silica surfaces, or octadecyltriethoxysilane (OTES). 15,16 Silanization was first performed with OTS in dichloromethane (DCM); then silanization was repeated with other, more biocompatible solvents, such as ethanol for OTES and ethyl acetate or acetone for OTS. The effects of different surface modifications were investigated by contact angle measurement, Fourier transform infrared (FTIR) spectroscopy, and scanning electron microscopy (SEM).…”
Section: Introductionmentioning
confidence: 99%