The influence of sodium salts (iodide, chloride and sulfate) on the formation efficiency of sulfamerazine nanocrystals

References

• Lipinski CA. Poor solubility – an industry wide problem in drug discovery. Am Pharm Rev 2002;5:82–85
   Google Scholar
• Shah V, Konecny J, Everett R, et al. In vitro dissolution profile of water-insoluble drug dosage forms in the presence of surfactants. Pharm Res 1989;6:612–618
   PubMed Web of Science ®Google Scholar
• Leuner C, Dressman J. Improving drug solubility for oral delivery using solid dispersions. Eur J Pharm Biopharm 2000;50:47–60
   PubMed Web of Science ®Google Scholar
• Kobayashi Y, Ito S, Itai S, Yamamoto K. Physicochemical properties and bioavailability of carbamazepine polymorphs and dihydrate. Int J Pharm 2000;193:137–146
   PubMed Web of Science ®Google Scholar
• Challa R, Ahuja A, Ali J, Khar R. Cyclodextrins in drug delivery: an updated review. AAPS PharmSciTech 2005;6:329–357
   PubMed Web of Science ®Google Scholar
• Berge S, Bighley L, Monkhouse D. Pharmaceutical salts. J Pharm Sci 1977;66:1–19
   PubMed Web of Science ®Google Scholar
• Neslihan GR, Benita S. Self-emulsifying drug delivery systems (SEDDS) for improved oral delivery of lipophilic drugs. Biomed Pharmacother 2004;58:173–182
   PubMed Web of Science ®Google Scholar
• Keck CM, Müller RH. Drug nanocrystals of poorly soluble drugs produced by high pressure homogenisation. Eur J Pharm Biopharma 2006;62:3–16
   PubMed Web of Science ®Google Scholar
• Hecq J, Deleers M, Fanara D, et al. Preparation and characterization of nanocrystals for solubility and dissolution rate enhancement of nifedipine. Int J Pharm 2005;299:167–177
   PubMed Web of Science ®Google Scholar
• Shegokar R, Müller RH. Nanocrystals: industrially feasible multifunctional formulation technology for poorly soluble actives. Int J Pharm 2010;399:129–139
   PubMed Web of Science ®Google Scholar
• Hu J, Johnston K, Williams R. Nanoparticle engineering processes for enhancing the dissolution rates of poorly water soluble drugs. Drug Dev Ind Pharm 2004;30:233–245
   PubMed Web of Science ®Google Scholar
• Zhang D, Tan T, Gao L, et al. Preparation of azithromycin nanosuspensions by high pressure homogenization and its physicochemical characteristics studies. Drug Dev Ind Pharm 2007;33:569–575
   PubMed Web of Science ®Google Scholar
• Gao L, Zhang D, Chen M, et al. Preparation and characterization of an oridonin nanosuspension for solubility and dissolution velocity enhancement. Drug Dev Ind Pharm 2007;33:1332–1339
   PubMed Web of Science ®Google Scholar
• Jiang T, Han N, Zhao B, et al. Enhanced dissolution rate and oral bioavailability of simvastatin nanocrystal prepared by sonoprecipitation. Drug Dev Ind Pharm 2012;38:1230–1239
   PubMed Web of Science ®Google Scholar
• Peltonen L, Hirvonen J. Pharmaceutical nanocrystals by nanomilling: critical process parameters, particle fracturing and stabilization methods. J Pharm Pharmacol 2010;62:1569–1579
   PubMed Web of Science ®Google Scholar
• Van Eerdenbrugh B, Vermant J, Martens JA, et al. A screening study of surface stabilization during the production of drug nanocrystals. J Pharm Sci 2009;98:2091–2103
   PubMed Web of Science ®Google Scholar
• Sepassi S, Goodwin DJ, Drake AF, et al. Effect of polymer molecular weight on the production of drug nanoparticles. J Pharm Sci 2007;96:2655–2666
   PubMed Web of Science ®Google Scholar
• Choi JY, Yoo JY, Kwak HS, et al. Role of polymeric stabilizers for drug nanocrystal dispersions. Curr Appl Phys 2005;5:472–474
   Web of Science ®Google Scholar
• Na G, Stevens J, Yuan B, Rajagopalan N. Physical stability of ethyl diatrizoate nanocrystalline suspension in steam sterilization. Pharm Res 1999;16:569–574
   PubMed Web of Science ®Google Scholar
• Annapragada A, Adjei A. Numerical simulation of milling processes as an aid to process design. Int J Pharm 1996;136:1–11
   Web of Science ®Google Scholar
• Deng Z, Xu S, Li S. Understanding a relaxation behavior in a nanoparticle suspension for drug delivery applications. Int J Pharm 2008;351:236–243
   PubMed Web of Science ®Google Scholar
• Zhang Y, Furyk S, Bergbreiter DE, Cremer PS. Specific ion effects on the water solubility of macromolecules: PNIPAM and the Hofmeister series. J Am Chem Soc 2005;127:14505–14510
   PubMed Web of Science ®Google Scholar
• Nakano T, Yuasa H. Suppression of agglomeration in fluidized bed coating. IV. Effects of sodium citrate concentration on the suppression of particle agglomeration and the physical properties of HPMC film. Int J Pharm 2001;215:3–12
   PubMed Web of Science ®Google Scholar
• Williams HD, Ward R, Hardy IJ, Melia CD. The effect of sucrose and salts in combination on the drug release behaviour of an HPMC matrix. Eur J Pharm Biopharm 2010;76:433–436
   PubMed Web of Science ®Google Scholar
• Ploehn HJ, Russel WB. Interactions between colloidal particles and soluble polymers. Adv Chem Eng 1990;15:137–228
   Google Scholar
• Lee J, Lee SJ, Choi JY, et al. Amphiphilic amino acid copolymers as stabilizers for the preparation of nanocrystal dispersion. Eur J Pharm Sci 2005;24:441–449
   PubMed Web of Science ®Google Scholar
• Zhang Y, Cremer PS. Interactions between macromolecules and ions: the Hofmeister series. Current Opin Chem Biol 2006;10:658–663
   PubMed Web of Science ®Google Scholar
• Van Eerdenbrugh B, Froyen L, Van Humbeeck J, et al. Drying of crystalline drug nanosuspensions – the importance of surface hydrophobicity on dissolution behavior upon redispersion. Eur J Pharm Sci 2008;35:127–135
   PubMed Web of Science ®Google Scholar
• Wang B, Zhang W, Zhang W, et al. Progress in drying technology for nanomaterials. Dry Technol 2005;23:7–32
   Web of Science ®Google Scholar
• Zhang GGZ, Gu C, Zell MT, et al. Crystallization and transitions of sulfamerazine polymorphs. J Pharm Sci 2002;91:1089–1100
   PubMed Web of Science ®Google Scholar
• Cocchetto DM, Levy G. Absorption of orally administered sodium sulfate in humans. J Pharm Sci 1981;70:331–333
   PubMed Web of Science ®Google Scholar
• Leonardi D, Barrera M, Lamas M, Salomón C. Development of prednisone: polyethylene glycol 6000 fast-release tablets from solid dispersions: solid-state characterization, dissolution behavior, and formulation parameters. AAPS PharmSciTech 2007;8:221–228
   Google Scholar
• Ning X, Sun J, Han X, et al. Strategies to improve dissolution and oral absorption of glimerpiride tablets: solid dispersion versus micronization techniques. Drug Dev Ind Pharm 2011;37:727–736
   PubMed Web of Science ®Google Scholar
• Palanisamy M, Khanam J. Solid dispersion of prednisolone: solid state characterization and improvement of dissolution profile. Drug Dev Ind Pharm 2011;37:373–386
   PubMed Web of Science ®Google Scholar
• Lindfors L, Skantze P, Skantze U, et al. Amorphous drug nanosuspensions. 3. Particle dissolution and crystal growth. Langmuir 2007;23:9866–9874
   PubMed Web of Science ®Google Scholar