References
- Attama AA, Reichl S, Müller-Goymann CC. (2008). Diclofenac sodium delivery to the eye: in vitro evaluation of novel solid lipid nanoparticle formulation using human cornea construct. Int J Pharm 355:307–13
- Basu SK, Adhiyaman R. (2008). Preparation and characterization of nitrndipine-loaded Eudragit RL 100 microspheres by an emulsion-solvent evaporation method. Trop J Pharm Res 7:1033–41
- Berchane NS, Carson KH, Rice-Ficht AC, et al. (2007). Effect of mean diameter andpolydispersity of PLG microspheres on drug release: experiment and theory. Int J Pharm 337:118–26
- Bipul N, Lila K, Pradeep K. (2011). Preparation and in vitro dissolution profile of zidovudine loaded microspheres made of Eudragit RS 100, RL 100 and their combinations. Acta Poloniae Pharmaceutica n Drug Res 68:415--422
- Davies NM, Sharkey KA, Asfaha S, et al. (1997). Aspirin causes rapid up-regulation of cyclooxygenase-2 expression in the stomach of rats. Aliment Pharmacol Ther 11:1101–8
- Desai JV, Patil JS, Kulkarni RV, et al. (2009). Alginate-based microparticulate oral drug delivery system for rifampicin. Res J Pharm Tech 2:301–3
- Freiberg S, Zhu XX. (2004). Polymer microspheres for controlled drug release. Int J Pharm 2:1–18
- Haznedar S, Dortunç B. (2004). Preparation and in vitro evaluation of Eudragit microspheres containing acetazolamide. Int J Pharm 269:131–40
- John LW, Linda V. (2008). NSAID-induced gastrointestinal damage and the design of GI-sparing NSAIDs. Curr Opin Invest Drugs 9:1151–6
- Kidane A, Bhatt PP. (2005). Recent advances in small molecule drug delivery. Curr Opin Chem Biol 9:347–51
- Kishori LD, Nilima AT, Paraag SG. (2013). Formulation and development of tinidazole microspheres for colon targeted drug delivery system. J Pharm Res 5:158–60
- Marshal K. (1987). Compression and consolidation of powdered solids. In: Lachman L, Lieberman HA, Kanig JL, eds. Theory and practice of industrial pharmacy, 3rd ed. (Indian ed.), Bombay: Varghese Publishing House, 66–7
- Ofokansi KC, Adikwu MU. (2007). Formulation and evaluation of microspheres based on gelatin-mucin admixtures for the rectal delivery of cefuroxime sodium. Trop J Pharm Res 6:825–32
- Sunit KS, Abdul AM, Barik BB, et al. (2005). Formulation and in vitro evaluation of Eudragit microspheres of stavudine. Trop J Pharm Res 4:369–75
- Sinye AB, Salome AC, Anthony AA, et al. (2013). In vitro and in vivo characterisation of piroxicam-loaded dika wax lipospheres. Trop J Pharm Res 12:33–8
- Staniforth, J. (2003). Particle-size analysis. In: Aulton ME, ed. The science of dosage form design, 2nd ed. Toronto: Churchill Livingstone, 152–65
- Tanwar YS, Naruka PS, Ojha GR. (2007). Development and evaluation of floating microspheres of verpamil hydrochloride. Braz J Pharm Sci 43:529–34
- Ttrivedi P, Verma AML, Garud N. (2008). Preparation and characterization of aceclofenac microspheres. Asian J Pharm 2008:110–5
- Zuniga JR, Phillips CL, Shugars D, et al. (2004). Analgesic safety and efficacy of diclofenac sodium softgels on postoperative third molar extraction pain. J Oral Maxillofac Surg 62:806–15