Comparison of fenofibrate – mesoporous silica drug-loading processes for enhanced drug delivery

Typeset version

 

TY  - JOUR
  - Robert J. Ahern, John P. Hanrahan, Joseph M. Tobin, Katie B. Ryan, Abina M. Crean
  - 2013
  - August
  - European Journal of Pharmaceutical Sciences
  - Comparison of fenofibrate – mesoporous silica drug-loading processes for enhanced drug delivery
  - Published
  - ()
  - 50
  - 2-3
  - 400
  - 409
  - Loading a poorly water-soluble drug onto a high surface area carrier such as mesoporous silica (SBA-15) can increase the drug’s dissolution rate and oral bioavailability. The loading method can influence subsequent drug properties including solid state structure and release rate. The objective of this research was to compare several loading processes in terms of drug distribution throughout the mesoporous silica matrix, drug solid state form and drug release properties. A model poorly water-soluble drug fenofibrate was loaded onto SBA-15 using; (i) physical mixing, (ii) melt, (iii) solvent impregnation, (iv) liquid CO2 and (v) supercritical CO2 methods. Physical mixing resulted in heterogeneous drug-loading, with no evidence of drug in the mesopores and the retention of the drug in its crystalline state. The other loading processes yielded more homogeneous drug-loading; the drug was deposited into the mesopores of the SBA-15 and was non-crystalline. All the processing methods resulted in enhanced drug release compared to the unprocessed drug with the impregnation, liquid and SC-CO2 producing the greatest increase at t=30 min.
  - Science Foundation Ireland
DA  - 2013/08
ER  - 
@article{V228101776,
   = {Robert J. Ahern,  John P. Hanrahan and  Joseph M. Tobin,  Katie B. Ryan and  Abina M. Crean },
   = {2013},
   = {August},
   = {European Journal of Pharmaceutical Sciences},
   = {Comparison of fenofibrate – mesoporous silica drug-loading processes for enhanced drug delivery},
   = {Published},
   = {()},
   = {50},
   = {2-3},
  pages = {400--409},
   = {{Loading a poorly water-soluble drug onto a high surface area carrier such as mesoporous silica (SBA-15) can increase the drug’s dissolution rate and oral bioavailability. The loading method can influence subsequent drug properties including solid state structure and release rate. The objective of this research was to compare several loading processes in terms of drug distribution throughout the mesoporous silica matrix, drug solid state form and drug release properties. A model poorly water-soluble drug fenofibrate was loaded onto SBA-15 using; (i) physical mixing, (ii) melt, (iii) solvent impregnation, (iv) liquid CO2 and (v) supercritical CO2 methods. Physical mixing resulted in heterogeneous drug-loading, with no evidence of drug in the mesopores and the retention of the drug in its crystalline state. The other loading processes yielded more homogeneous drug-loading; the drug was deposited into the mesopores of the SBA-15 and was non-crystalline. All the processing methods resulted in enhanced drug release compared to the unprocessed drug with the impregnation, liquid and SC-CO2 producing the greatest increase at t=30 min.}},
   = {Science Foundation Ireland},
  source = {IRIS}
}
AUTHORSRobert J. Ahern, John P. Hanrahan, Joseph M. Tobin, Katie B. Ryan, Abina M. Crean
YEAR2013
MONTHAugust
JOURNAL_CODEEuropean Journal of Pharmaceutical Sciences
TITLEComparison of fenofibrate – mesoporous silica drug-loading processes for enhanced drug delivery
STATUSPublished
TIMES_CITED()
SEARCH_KEYWORD
VOLUME50
ISSUE2-3
START_PAGE400
END_PAGE409
ABSTRACTLoading a poorly water-soluble drug onto a high surface area carrier such as mesoporous silica (SBA-15) can increase the drug’s dissolution rate and oral bioavailability. The loading method can influence subsequent drug properties including solid state structure and release rate. The objective of this research was to compare several loading processes in terms of drug distribution throughout the mesoporous silica matrix, drug solid state form and drug release properties. A model poorly water-soluble drug fenofibrate was loaded onto SBA-15 using; (i) physical mixing, (ii) melt, (iii) solvent impregnation, (iv) liquid CO2 and (v) supercritical CO2 methods. Physical mixing resulted in heterogeneous drug-loading, with no evidence of drug in the mesopores and the retention of the drug in its crystalline state. The other loading processes yielded more homogeneous drug-loading; the drug was deposited into the mesopores of the SBA-15 and was non-crystalline. All the processing methods resulted in enhanced drug release compared to the unprocessed drug with the impregnation, liquid and SC-CO2 producing the greatest increase at t=30 min.
PUBLISHER_LOCATION
ISBN_ISSN
EDITION
URL
DOI_LINK
FUNDING_BODYScience Foundation Ireland
GRANT_DETAILS