References
- Liu P, Grangiulo P, Wang J, Dinh S. A novel method for measuring solubility of a drug in an adhesive polymer. Pharm Res 1997;145:137
- Ma X, Taw J, Chiang C. Control of drug crystallization in transdermal matrix system. Int J Pharm 1996;142:115–119
- Göpferich A, Lee G. Determining the solubility and crystal form clenbuterol in thin films of Eudragit NE30D. Drug Devel Ind Pharm 1992;18:319–331
- Puttipipatkhachorn S, Nunthanid J, Yamamoto K, Peck G. Drug physical state and drug--polymer interaction on drug release from chitosan matrix films. J Cont Rel 2001;75:143–153
- Varinkaval N, Jacob K, Dinh S. Crystallization of beta-estradiol in an acrylic transdermal drug delivery system. J Biomed Mat Res 1999;44:397–406
- Latsch S, Selzer T, Fink L, Kreuter J. Crystallisation of estradiol containing TDDS determined by isothermal microcalorimetry, X-ray diffraction, and optical microscopy. Eur J Pharm Biopharm 2003;52:43–52
- Martin A, Swarbrick J, Cammarota S. Physical pharmacy. 3rd ed. New York: Lea & Febiger; 1983:272--275
- Reismann S, Lee G. Assessment of a five-layer laminate technique to measure the saturation solubility of drug in pressure-sensitive adhesive film. J Pharm Sci 2012;101:2428–2438
- Carslaw H, Jaeger J. Conduction of heat in solids. 2nd ed. Equation 1. Oxford: Oxford University Press; 1988:50
- Hixon S, Crowell J. Dependence of reaction velocity upon surface and agitation: I – theoretical consideration. Ind Eng Chem 1931;23:923–931
- Bäumler K, Bänsch E. A subspace projection method for the implementation of interface conditions in a two-phase flow problem. J Comp Phys 2013;252:438--457
- Nallvri B, Milligan C, Chen J, et al. In vitro release studies of matrix type transdermal drug delivery systems of naltrexone and its acetyl prodrug. Drug Devel Ind Pharm 2005;31:871–877
- Kagayama A, Mustafa R, Akaho E, et al. Mechanism of diffusion of compounds through ethylene vinyl acetate copolymers. 1. Kinetics of diffusion of 1-chloro-4-nitrobenzene, 3,4-dimethylphenol, and 4-hexylresourcinol. Int J Pharm 1984;18:247–258