References
- Chidambaram N, Burgess DJ. (1999). A novel in vitro release method for submicron-sized dispersed systems. AAPS Pharmsci, 1(3), article 11.
- Washington C. (1990). Drug release from microdisperse systems: A critical review. Int J Pharm, 58:1–12.
- Illum L, Khan MA, Mak E, Davis SS. (1986). Evaluation of carrier capacity and release characteristics for poly(butyl-2-cyanoactylate) nanoparticles. Int J Pharm, 30:17–28.
- Wakiyama N, Juni K, Nakano M. (1981). Preparation and evaluation in vitro of poly lactic acid microspheres containing local anesthetics. Chem Pharm Bull, 29:3363–8.
- D'Souza S, DeLuca P. (2006). Methods to assess in vitro drug release from injectable polymeric particulate systems. Pharm Res, 23:460–74.
- Lamprecht A, Bouligand Y, Benoit JP. (2002). New lipid nanocapsules exhibit sustained release properties for amiodarone. J Control Release, 84:59–68.
- Mukherjee B, Patra B, Layek B, Mukherjee A. (2007). Sustained release of acyclovir from nano-liposomes and nano-niosomes: An in vitro study. Int J Nanomed, 2(2):213–25.
- Nounou M, Elkhordagui L, Khalafallah N, Khalil S. (2006). In vitro release of hydrophilic and hydrophobic drugs from liposomal dispersions and gels. Acta Pharm, 56:311–24.
- Saarinen-Savolainen P, Järvinen T, Taipale H, Urtti A. (1997). Method for evaluating drug release from liposomes in sink conditions. Int J Pharm, 159:27–33.
- Shabbits J, Chiu G, Mayer L. (2002). Development of an in vitro drug release assay that accurately predicts in vivo drug retention for liposome-based delivery systems. J Control Release, 84:161–70.
- Murthy RSR, Harivardhan R. (2007). Poly (alkyl cyanoacrylate) nanoparticles for delivery of anticancer agents. In: Amiji MM, ed. Nanotechnology for cancer therapy. Florida: CRC Press, Taylor & Francis Group, 251–88.
- Leavy MY, Benita S. (1990). Drug release from submicron O/W emulsion: A new in vitro kinetic evaluation model. Int J Pharm, 66:29–37.
- Calvo P, Vila-Jato JL, Alonso MJ. (1996). Comparative in vitro evaluation of several colloidal systems, nanoparticles, nanocapsules and nanoemulsions as ocular drug carriers. J Pharm Sci, 85:530–6.
- Henriksen I, Sande SA, Smistad G, Agren T, Karlsen J. (1995). In vitro evaluation of drug release kinetics from liposomes by fractional dialysis. Int J Pharm, 119:231–8.
- Abdel-Mottaleb MMA, Mortada ND, El-Shamy AA, Awad GA. (2009). Physically cross-linked polyvinyl alcohol for the topical delivery of fluconazole. Drug Dev Ind Pharm, 35:311–20.
- Schultz K, Møllgaard B, Frokjaer S, Larsen C. (1997). Rotating dialysis cell as in vitro release method for oily parenteral depot solutions. Int J Pharm, 157:163–9.
- Yamaguchi Y, Sato H, Sugibayashi K, Morimoto Y. (1996). Drug release test to assess quality of topical formulations in Japanese market. Drug Dev Ind Pharm, 22:569–77.
- Diebold SM. (2005). Physiological parameters relevant to dissolution testing: Hydrodynamic considerations. In: Dressman J, Krämer J, eds. Pharmaceutical dissolution testing. Florida: Taylor & Francis Group, 127–91.
- Li J, Yang L, Ferguson S, Hudson T, Watanabe S, Katsuma M, . (2002). In vitro evaluation of dissolution behavior for a colon-specific drug delivery system (CODES™) in multi-pH media using United States pharmacopeia apparatus II and III. AAPS PharmSciTech, 3(4), article 33.
- Mitsumata T, Kakiuchi Y, Takimoto J. (2008). Fast drug release using rotational motion of magnetic gel beads. Res Lett Phys Chem, 2008, article 671642, 5 pp.
- Vemuri S, Yu C, Pushpala S, Roosdorp N. (1991). Drug release rate method for a liposome preparation. Drug Dev Ind Pharm, 17:183–92.
- Yamauchi M, Tsutsumi K, Abe M, Uosaki Y, Nakakura M, Aoki N. (2007). Release of drugs from liposomes varies with particle size. Biol Pharm Bull, 30(5):963–6.
- Lu Z, Bei J, Wang S. (1999). A method of the preparation of polymeric nanocapsules without stabilizer. J Control Release, 61:107–12.
- Lara MG, Bentley MV, Collett JH. (2005). In vitro drug release mechanism and drug loading studies of cubic phase gels. Int J Pharm, 293:241–50.