PREPARATION AND IN VIVO EVALUATION OF EUDRAGIT® L100/EUDRAGIT® NM 30D ENTERIC GRANULES CONTAINING DICLOFANAC SODIUM: ANTI-INFLAMMATORY AND ULCEROGENIC ACTIVITY
暂无分享,去创建一个
M. Çetin | A. Hacımüftüoğlu | E. Çadırcı | B. Polat | E. Demir | H. Süleyman | A. Hacimüftüoğlu | Halis SÜLEYMANElif Çadirci | Beyzagiil Polat
[1] G. Scriba. Sean C. Sweetman (Ed.): Martindale: The Complete Drug Reference , 2011 .
[2] H. Frijlink,et al. Pulsatile drug delivery to ileo-colonic segments by structured incorporation of disintegrants in pH-responsive polymer coatings. , 2008, Journal of controlled release : official journal of the Controlled Release Society.
[3] J. Wallace,et al. NSAID-induced gastrointestinal damage and the design of GI-sparing NSAIDs. , 2008, Current opinion in investigational drugs.
[4] B. S,et al. Hollow microspheres of diclofenac sodium - a gastroretentive controlled delivery system. , 2008, Pakistan journal of pharmaceutical sciences.
[5] S. Chandran,et al. Design and evaluation of pH modulated controlled release matrix systems for colon specific delivery of indomethacin. , 2008, Pharmazie.
[6] G. Van den Mooter,et al. Comparative evaluation of interpolyelectrolyte complexes of chitosan with Eudragit L100 and Eudragit L100-55 as potential carriers for oral controlled drug delivery. , 2008, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.
[7] S. Nazzal,et al. Novel use of Eudragit NE 30D/Eudragit L 30D-55 blends as functional coating materials in time-delayed drug release applications. , 2008, International journal of pharmaceutics.
[8] Alan B. Watts,et al. The manufacture and characterisation of hot-melt extruded enteric tablets. , 2008, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.
[9] P. Mura,et al. Influence of formulation and process variables on in vitro release of theophylline from directly-compressed Eudragit matrix tablets. , 2005, Farmaco.
[10] Shuichi Suzuki,et al. Analgesic Action of a Sustained Release Preparation of Diclofenac Sodium in a Canine Urate-Induced Gonarthritis , 2001 .
[11] Maruf Ahmed,et al. Preparation and Stability Study of Diclofenac Sodium Suppositories , 2000 .
[12] Y. Tando,et al. Pancreatic dysfunction and treatment options. , 1998, Pancreas.
[13] A. Hirschfelder. THE UNITED STATES PHARMACOPEIAL CONVENTION , 1930 .
[14] S. Jayaprakash,et al. Preparation and evaluation of biodegradable microspheres of methotrexate , 2009 .
[15] Xiao-le Qi,et al. [Preparation of tablets containing enteric-coated diclofenac sodium pellets]. , 2008, Yao xue xue bao = Acta pharmaceutica Sinica.
[16] M. D'souza,et al. Formulation and evaluation of albumin microspheres and its enteric coating using a spray-dryer. , 2008, Journal of microencapsulation.
[17] N. Barakat,et al. Diclofenac sodium loaded-cellulose acetate butyrate: effect of processing variables on microparticles properties, drug release kinetics and ulcerogenic activity. , 2008, Journal of microencapsulation.
[18] H. Gul,et al. Anti-inflammatory activity of bis(3-aryl-3-oxo-propyl)methylamine hydrochloride in rat. , 2007, Biological & pharmaceutical bulletin.
[19] Z. Halıcı,et al. Gastroprotective and antioxidant effects of montelukast on indomethacin-induced gastric ulcer in rats. , 2007, Journal of pharmacological sciences.
[20] F. Atyabi,et al. Ion-exchange, an Approach to Prepare an Oral Floating Drug Delivery System for Diclofenac , 2004 .
[21] W. M. Heller,et al. The United States Pharmacopeial Convention, Inc , 1977 .