Development and in-vitro evaluation of an optimized carvedilol transdermal therapeutic system using experimental design approach

Asian Journal of Pharmaceutical Sciences - Tập 8 - Trang 28-38 - 2013
Namrata Vora1, S. Lin1, P.L. Madan1
1College of Pharmacy and Health Sciences, St. John's University, Queens, NY 11439, USA

Tài liệu tham khảo

Lyons, 2007, Preparation of monolithic matrices for oral drug delivery using a supercritical fluid assisted hot melt extrusion process, Int J Pharm, 329, 62, 10.1016/j.ijpharm.2006.08.028 Wen, 2004, Preparation and study the 1:2 inclusion complex of carvedilol with beta-cyclodextrin, J Pharm Biomed Anal, 34, 517, 10.1016/S0731-7085(03)00576-4 Wen, 2009, Carvedilol ameliorates the decreases in connexin 43 and ventricular fibrillation threshold in rats with myocardial infarction, Tohoku J Exp Med, 218, 121, 10.1620/tjem.218.121 Ubaidulla, 2007, Transdermal therapeutic system of carvedilol: effect of hydrophilic and hydrophobic matrix on in vitro and in vivo characteristics, AAPS PharmSciTech, 8, 2, 10.1208/pt0801002 Feldstein, 1996, Hydrophilic polymeric matrices for enhanced transdermal drug delivery, Int J Pharm, 131, 229, 10.1016/0378-5173(95)04351-9 Wei, 2005, Preparation and evaluation of SEDDS and SMEDDS containing carvedilol, Drug Dev Ind Pharm, 31, 785, 10.1080/03639040500216428 Stamatialis, 2002, Controlled transport of timolol maleate through artificial membranes under passive and iontophoretic conditions, J Control Release, 81, 335, 10.1016/S0168-3659(02)00076-7 Korsmeyer, 1983, Mechanisms of solute release from porous hydrophilic polymers, Int J Pharm, 15, 25, 10.1016/0378-5173(83)90064-9 Hai, 2008, Formulation and biopharmaceutical evaluation of transdermal patch containing benztropine, Int J Pharm, 357, 55, 10.1016/j.ijpharm.2008.01.024 Siepmann, 2001, Modeling of drug release from delivery systems based on hydroxypropyl methylcellulose (HPMC), Adv Drug Deliv Rev, 48, 139, 10.1016/S0169-409X(01)00112-0 Schwarb, 1999, Effect of concentration and degree of saturation of topical fluocinonide formulations on in vitro membrane transport and in vivo availability on human skin, Pharm Res, 16, 909, 10.1023/A:1018890422825 Padula, 2007, Single-layer transdermal film containing lidocaine: modulation of drug release, Eur J Pharm Biopharm, 66, 422, 10.1016/j.ejpb.2006.11.014 Guyot, 2000, Design and in vitro evaluation of adhesive matrix for transdermal delivery of propranolol, Int J Pharm, 204, 171, 10.1016/S0378-5173(00)00494-4 Yamane, 1995, Terpene penetration enhancers in propylene glycol/water co-solvent systems: effectiveness and mechanism of action, J Pharm Pharmacol, 47, 978, 10.1111/j.2042-7158.1995.tb03282.x Hadgraft, 1999, Passive enhancement strategies in topical and transdermal drug delivery, Int J Pharm, 184, 1, 10.1016/S0378-5173(99)00095-2 Thomas, 2003, Transdermal delivery of zidovudine: effect of vehicles on permeation across rat skin and their mechanism of action, Eur J Pharm Sci, 18, 71, 10.1016/S0928-0987(02)00242-7 Melero, 2008, Nortriptyline hydrochloride skin absorption: development of a transdermal patch, Eur J Pharm Biopharm, 69, 588, 10.1016/j.ejpb.2007.11.012 Levang, 1999, Effect of ethanol/propylene glycol on the in vitro percutaneous absorption of aspirin, biophysical changes and macroscopic barrier properties of the skin, Int J Pharm, 181, 255, 10.1016/S0378-5173(99)00055-1 Williams, 2004, Penetration enhancers, Adv Drug Deliv Rev, 56, 603, 10.1016/j.addr.2003.10.025 Pershing, 1990, Mechanism of ethanol-enhanced estradiol permeation across human skin in vivo, Pharm Res, 7, 170, 10.1023/A:1015832903398