Gastroresistant microparticles containing sodium alendronate prevent the bone loss in ovariectomized rats.
暂无分享,去创建一个
[1] S. Guterres,et al. Microencapsulation of sodium alendronate reduces drug mucosal damage in rats , 2010, Drug delivery.
[2] S. Guterres,et al. HIGH ENCAPSULATION EFFICIENCY OF SODIUM ALENDRONATE IN EUDRAGIT S100/HPMC BLEND MICROPARTICLES , 2009 .
[3] S. Guterres,et al. Increasing sodium pantoprazole photostability by microencapsulation: effect of the polymer and the preparation technique. , 2008, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.
[4] R. Handa,et al. Postovariectomy weight gain in female rats is reversed by estrogen receptor alpha agonist, propylpyrazoletriol. , 2008, American journal of obstetrics and gynecology.
[5] C. Franceschi,et al. Calcium metabolism and vitamin D in the extreme longevity , 2008, Experimental Gerontology.
[6] E. Jäger,et al. Rate-modulating PHBHV/PCL microparticles containing weak acid model drugs. , 2007, International journal of pharmaceutics.
[7] S. Haas,et al. Development of HPMC and Eudragit S100 blended microparticles containing sodium pantoprazole. , 2007, Die Pharmazie.
[8] S. Guterres,et al. Microparticles prepared with poly(hydroxybutyrate-co-hydroxyvalerate) and poly(ε-caprolactone) blends to control the release of a drug model , 2007, Journal of microencapsulation.
[9] S. Guterres,et al. Pantoprazole-loaded Eudragit blended microparticles: preparation, characterization, in vitro gastro-resistance and in vivo anti-ulcer evaluation , 2007 .
[10] N. D. da Silveira,et al. Physico-chemical characterization and in vivo evaluation of indomethacin ethyl ester-loaded nanocapsules by PCS, TEM, SAXS, interfacial alkaline hydrolysis and antiedematogenic activity. , 2006, Journal of nanoscience and nanotechnology.
[11] S. Guterres,et al. Preparation, characterization, and in vivo anti-ulcer evaluation of pantoprazole-loaded microparticles. , 2006, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.
[12] E. Comunello,et al. Antiulcerogenic Activity of Crude Extract, Fractions and Populnoic Acid Isolated from Austroplenckia populnea (Celastraceae) , 2006, Zeitschrift fur Naturforschung. C, Journal of biosciences.
[13] N. D. da Silveira,et al. Diffusion and mathematical modeling of release profiles from nanocarriers. , 2006, International journal of pharmaceutics.
[14] J. Cramer,et al. Compliance and persistence with bisphosphonate dosing regimens among women with postmenopausal osteoporosis* , 2005, Current medical research and opinion.
[15] Matthew Roberts,et al. The use of hypromellose in oral drug delivery , 2005, The Journal of pharmacy and pharmacology.
[16] Hyun Jin Park,et al. Encapsulation of vitamin C in tripolyphosphate cross-linked chitosan microspheres by spray drying , 2005, Journal of microencapsulation.
[17] D. Kendler,et al. Pharmaceutical care and community pharmacists’ understanding of bisphosphonate dosing information 1 , 2004, Journal of clinical pharmacy and therapeutics.
[18] I. Hamdan,et al. Spectroscopic and HPLC methods for the determination of alendronate in tablets and urine. , 2004, Talanta.
[19] X. Zhu,et al. Polymer microspheres for controlled drug release. , 2004, International journal of pharmaceutics.
[20] F. Pérez-López,et al. Postmenopausal osteoporosis and alendronate. , 2004, Maturitas.
[21] Mahaveer D. Kurkuri,et al. Poly(vinyl alcohol) and poly(acrylic acid) sequential interpenetrating network pH-sensitive microspheres for the delivery of diclofenac sodium to the intestine. , 2004, Journal of controlled release : official journal of the Controlled Release Society.
[22] K. Nas,et al. Gastrointestinal side effect profile due to the use of alendronate in the treatment of osteoporosis. , 2003, Yonsei medical journal.
[23] P. Lakatos,et al. Mechanisms of action of antiresorptive therapies of postmenopausal osteoporosis. , 2003, Endocrine regulations.
[24] B. Ettinger,et al. Early discontinuation of treatment for osteoporosis. , 2003, The American journal of medicine.
[25] T. Iguchi,et al. Multiple mechanisms are involved in apoptotic cell death in the mouse uterus and vagina after ovariectomy. , 2003, Reproductive toxicology.
[26] C. Nastruzzi,et al. Spray dried Eudragit microparticles as encapsulation devices for vitamin C. , 2002, International journal of pharmaceutics.
[27] D. Baker. Alendronate and risedronate: what you need to know about their upper gastrointestinal tract toxicity. , 2002, Reviews in gastroenterological disorders.
[28] N A Peppas,et al. Modeling of drug release from delivery systems based on hydroxypropyl methylcellulose (HPMC). , 2001, Advanced drug delivery reviews.
[29] W. Jee,et al. Overview: animal models of osteopenia and osteoporosis. , 2001, Journal of musculoskeletal & neuronal interactions.
[30] G. Mundy. Pathogenesis of osteoporosis and challenges for drug delivery. , 2000, Advanced drug delivery reviews.
[31] S. Martelli,et al. Polymers with pH-Dependent Solubility: Possibility of Use in the Formulation of Gastroresistant and Controlled-Release Matrix Tablets , 2000, Drug development and industrial pharmacy.
[32] P. Delmas. Markers of Bone Turnover for Monitoring Treatment of Osteoporosis with Antiresorptive Drugs , 2000, Osteoporosis International.
[33] J. Ford,et al. Thermal analysis of hydroxypropylmethylcellulose and methylcellulose: powders, gels and matrix tablets. , 1999, International journal of pharmaceutics.
[34] F. Castelli,et al. Comparative study of 'in vitro' release of anti-inflammatory drugs from polylactide-co-glycolide microspheres , 1998 .
[35] D. Felsenberg,et al. Placebo-controlled multicenter study of oral alendronate in postmenopausal osteoporotic women. FOSIT-Study-Group. Fosamax International Trial. , 1998, Maturitas.
[36] H. Ammar,et al. Preparation and Evaluation of Sustained-Release Solid Dispersions of Drugs with Eudragit Polymers , 1997 .
[37] P. Geusens,et al. Oral alendronate induces progressive increases in bone mass of the spine, hip, and total body over 3 years in postmenopausal women with osteoporosis. , 1996, Bone.
[38] N. Peppas. Analysis of Fickian and non-Fickian drug release from polymers. , 1985, Pharmaceutica acta Helvetiae.
[39] N. Peppas,et al. Mechanisms of solute release from porous hydrophilic polymers , 1983 .