Abstract
In this report we show that drug incubation temperature, methods used for removing surfactant templates from mesoporous materials and solvents used for placing surface organic functional groups on the materials can improve or affect the adsorption capacity and drug release properties of potentially useful nanoporous silica and organosilica as drug delivery vehicles. This is demonstrated by investigating the adsorption and release properties toward rhodamine 6G (R6G) and an anticancer drug, cisplatin, of various solventextracted and calcined mesoporous silicas (MCM-41 and SBA-15), organic-functionalized mesoporous silicas containing terminal organoamine, organothiol and vinyl groups, and bridging organic-functionalized ethane periodic mesoporous organosilica (ethane PMO) under various conditions. Two different solvents, isopropanol and toluene, were used to graft the terminal organic groups from their corresponding organosilanes, producing materials with slightly different adsorption and release properties. The adsorption capacities of the organicfunctionalized mesoporous silicas that were prepared from a well solvent-extracted MCM-41 increased significantly as the temperature was raised from room temperature to 50 and 75 °C. Furthermore, samples with a higher percent adsorption of R6G and cisplatin also showed higher overall percent release of the adsorbed R6G or cisplatin molecules in a simulated body fluid (SBF) solution. Interestingly, the ethane PMO also showed significantly higher adsorption capacity for both R6G and cisplatin than the control samples, MCM-41 or SBA-15. Raising the temperature improved the adsorption capacity of ethane PMO, for both R6G and cisplatin. The method used to remove the surfactant templates from the parent mesostructured materials was also found to affect the materials' adsorption properties.
| Original language | English |
|---|---|
| Pages (from-to) | 13135-13150 |
| Number of pages | 16 |
| Journal | Journal of Physical Chemistry C |
| Volume | 115 |
| Issue number | 27 |
| DOIs | |
| Publication status | Published - Jul 14 2011 |
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ASJC Scopus subject areas
- Physical and Theoretical Chemistry
- Electronic, Optical and Magnetic Materials
- Surfaces, Coatings and Films
- Energy(all)
Cite this
Improving the adsorption and releasecapacity oforganic-functionalized mesoporous materials to drug molecules with temperature and synthetic methods. / Vathyam, Rajyalakshmi; Wondimu, Elisabeth; Das, Sayantani; Zhang, Chao; Hayes, Stephanie; Tao, Zhimin; Asefa, Teddy.
In: Journal of Physical Chemistry C, Vol. 115, No. 27, 14.07.2011, p. 13135-13150.Research output: Contribution to journal › Article
}
TY - JOUR
T1 - Improving the adsorption and releasecapacity oforganic-functionalized mesoporous materials to drug molecules with temperature and synthetic methods
AU - Vathyam, Rajyalakshmi
AU - Wondimu, Elisabeth
AU - Das, Sayantani
AU - Zhang, Chao
AU - Hayes, Stephanie
AU - Tao, Zhimin
AU - Asefa, Teddy
PY - 2011/7/14
Y1 - 2011/7/14
N2 - In this report we show that drug incubation temperature, methods used for removing surfactant templates from mesoporous materials and solvents used for placing surface organic functional groups on the materials can improve or affect the adsorption capacity and drug release properties of potentially useful nanoporous silica and organosilica as drug delivery vehicles. This is demonstrated by investigating the adsorption and release properties toward rhodamine 6G (R6G) and an anticancer drug, cisplatin, of various solventextracted and calcined mesoporous silicas (MCM-41 and SBA-15), organic-functionalized mesoporous silicas containing terminal organoamine, organothiol and vinyl groups, and bridging organic-functionalized ethane periodic mesoporous organosilica (ethane PMO) under various conditions. Two different solvents, isopropanol and toluene, were used to graft the terminal organic groups from their corresponding organosilanes, producing materials with slightly different adsorption and release properties. The adsorption capacities of the organicfunctionalized mesoporous silicas that were prepared from a well solvent-extracted MCM-41 increased significantly as the temperature was raised from room temperature to 50 and 75 °C. Furthermore, samples with a higher percent adsorption of R6G and cisplatin also showed higher overall percent release of the adsorbed R6G or cisplatin molecules in a simulated body fluid (SBF) solution. Interestingly, the ethane PMO also showed significantly higher adsorption capacity for both R6G and cisplatin than the control samples, MCM-41 or SBA-15. Raising the temperature improved the adsorption capacity of ethane PMO, for both R6G and cisplatin. The method used to remove the surfactant templates from the parent mesostructured materials was also found to affect the materials' adsorption properties.
AB - In this report we show that drug incubation temperature, methods used for removing surfactant templates from mesoporous materials and solvents used for placing surface organic functional groups on the materials can improve or affect the adsorption capacity and drug release properties of potentially useful nanoporous silica and organosilica as drug delivery vehicles. This is demonstrated by investigating the adsorption and release properties toward rhodamine 6G (R6G) and an anticancer drug, cisplatin, of various solventextracted and calcined mesoporous silicas (MCM-41 and SBA-15), organic-functionalized mesoporous silicas containing terminal organoamine, organothiol and vinyl groups, and bridging organic-functionalized ethane periodic mesoporous organosilica (ethane PMO) under various conditions. Two different solvents, isopropanol and toluene, were used to graft the terminal organic groups from their corresponding organosilanes, producing materials with slightly different adsorption and release properties. The adsorption capacities of the organicfunctionalized mesoporous silicas that were prepared from a well solvent-extracted MCM-41 increased significantly as the temperature was raised from room temperature to 50 and 75 °C. Furthermore, samples with a higher percent adsorption of R6G and cisplatin also showed higher overall percent release of the adsorbed R6G or cisplatin molecules in a simulated body fluid (SBF) solution. Interestingly, the ethane PMO also showed significantly higher adsorption capacity for both R6G and cisplatin than the control samples, MCM-41 or SBA-15. Raising the temperature improved the adsorption capacity of ethane PMO, for both R6G and cisplatin. The method used to remove the surfactant templates from the parent mesostructured materials was also found to affect the materials' adsorption properties.
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U2 - 10.1021/jp1108587
DO - 10.1021/jp1108587
M3 - Article
AN - SCOPUS:80053912066
VL - 115
SP - 13135
EP - 13150
JO - Journal of Physical Chemistry C
JF - Journal of Physical Chemistry C
SN - 1932-7447
IS - 27
ER -