Controlled drug delivery system based on ordered mesoporous silica matrices of captopril as angiotensin-converting enzyme inhibitor drug.
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G. Mihai | E. Seftel | V. Voicu | R F Popovici | E M Seftel | G D Mihai | E Popovici | V A Voicu | G. Mihai | E. Popovici | R. Popovici
[1] H. Askal. New spectrophotometric methods for determination of captopril bulk drug and tablets. , 1991, Talanta.
[2] Shichao Wang,et al. Salicylidene Schiff Base Assembled with Mesoporous Silica SBA-15 as Hybrid Materials for Molecular Logic Function , 2007 .
[3] K. Hidajat,et al. Functionalized SBA-15 materials as carriers for controlled drug delivery: influence of surface properties on matrix-drug interactions. , 2005, Langmuir : the ACS journal of surfaces and colloids.
[4] Evert Schepers,et al. In vivo tissue response to resorbable silica xerogels as controlled-release materials. , 2005, Biomaterials.
[5] N. Peppas,et al. Mechanisms of solute release from porous hydrophilic polymers , 1983 .
[6] J. Devoisselle,et al. Inclusion of ibuprofen in mesoporous templated silica: drug loading and release property. , 2004, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.
[7] Jenny Andersson,et al. Influences of Material Characteristics on Ibuprofen Drug Loading and Release Profiles from Ordered Micro- and Mesoporous Silica Matrices , 2004 .
[8] Tad Hogg,et al. Nanorobot architecture for medical target identification , 2008 .
[9] F. Marmottini,et al. Role of mesoporous silicates on carbamazepine dissolution rate enhancement , 2008 .
[10] M. Vallet‐Regí,et al. Mesoporous MCM-41 as Drug Host System , 2003 .
[11] G. Giammona,et al. Mesoporous silicate as matrix for drug delivery systems of non-steroidal antinflammatory drugs , 2002 .
[12] Y. Sugahara,et al. Adsorption of taxol into ordered mesoporous silicas with various pore diameters , 1999 .
[13] Chi H. Lee,et al. Drug delivery systems for hormone therapy. , 2006, Journal of controlled release : official journal of the Controlled Release Society.
[14] M. Vallet‐Regí. Ordered Mesoporous Materials in the Context of Drug Delivery Systems and Bone Tissue Engineering , 2006 .
[15] T. Bein,et al. Tuning drug uptake and release rates through different morphologies and pore diameters of confined mesoporous silica , 2009 .
[16] Frederick E. Petry,et al. Principles and Applications , 1997 .
[17] Lawrence X. Yu,et al. A provisional biopharmaceutical classification of the top 200 oral drug products in the United States, Great Britain, Spain, and Japan. , 2006, Molecular pharmaceutics.
[18] Fredrickson,et al. Triblock copolymer syntheses of mesoporous silica with periodic 50 to 300 angstrom pores , 1998, Science.
[19] M. Vallet‐Regí,et al. Mesoporous SBA-15 HPLC evaluation for controlled gentamicin drug delivery. , 2004, Journal of controlled release : official journal of the Controlled Release Society.
[20] M. Vallet‐Regí,et al. Bioceramics and pharmaceuticals: A remarkable synergy , 2007 .
[21] M. Vallet‐Regí,et al. MCM-41 Organic Modification as Drug Delivery Rate Regulator , 2003 .
[22] M. Ondetti,et al. History of the Design of Captopril and Related Inhibitors of Angiotensin Converting Enzyme , 1991, Hypertension.
[23] N. Peppas,et al. A SIMPLE EQUATION FOR SOLUTE RELEASE PART 1. FICKIAN AND NONFICKIAN RELEASE FROM NONSWELLABLE DEVICES IN THE FORM OF SLABS, SPHERES, CYLINDERS OR DISKS , 1987 .
[24] Matthias Epple,et al. Inorganic nanoparticles as carriers of nucleic acids into cells. , 2008, Angewandte Chemie.
[25] N. Peppas. Analysis of Fickian and non-Fickian drug release from polymers. , 1985, Pharmaceutica acta Helvetiae.
[26] María Vallet-Regí,et al. Mesoporous Materials for Drug Delivery , 2008 .
[27] Shilun Qiu,et al. Controlled release of Captopril by regulating the pore size and morphology of ordered mesoporous silica , 2006 .
[28] R. Langer,et al. Drug delivery and targeting. , 1998, Nature.
[29] N. Sultana,et al. In vitro interactions of captopril with NSAID's. , 2006, Pakistan journal of pharmaceutical sciences.
[30] V. Ramaswamy,et al. Structural features of Penicillin acylase adsorption on APTES functionalized SBA-15 , 2008 .
[31] M. Vallet‐Regí,et al. Influence of pore size of MCM-41 matrices on drug delivery rate , 2004 .
[32] Patrick Marroum,et al. Mechanistic analysis of solute transport in an in vitro physiological two‐phase dissolution apparatus , 2012 .
[33] Daliang Zhang,et al. Drug Self-Templated Synthesis of Ibuprofen/Mesoporous Silica for Sustained Release , 2006 .
[34] C Rossi,et al. Improvement of dissolution rate of piroxicam by inclusion into MCM-41 mesoporous silicate. , 2007, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.
[35] C. Brinker,et al. Aerosol-assisted self-assembly of single-crystal core/nanoporous shell particles as model controlled release capsules. , 2006, Journal of the American Chemical Society.
[36] P. Ashok,et al. Design and statistical optimization of glipizide loaded lipospheres using response surface methodology , 2007, Acta pharmaceutica.