Self-nanoemulsifying performance of two grades of Lauroglycol (Lauroglycol-90 and Lauroglycol-FCC) in the presence of mixed nonionic surfactants

References

• Shakeel F, Haq N, Elbadry M, et al. Ultra fine super self-nanoemulsifying drug delivery system enhanced solubility and dissolution of indomethacin. J Mol Liq 2013;180:89–94
   Web of Science ®Google Scholar
• Abdelbary G, Amin M, Salah S. Self-nanoemulsifying simvastatin based tablets: design and in vitro/in vivo evaluation. Pharm Develop Technol. doi: 10.3109/10837450.2012.672989
   Google Scholar
• Zhu S, Hong M, Liu C, Pei Y. Application of Box--Behnken design in understanding the quality of genistein self-nanoemulsifyied drug delivery systems and optimizing its formulations. Pharm Develop Technol 2009;14:642–649
   PubMed Web of Science ®Google Scholar
• Thomas N, Holm R, Mullertz A, Rades T. In vitro and in vivo performance of novel super saturated self-nanoemulsifying drug delivery systems (super-SNEDDS). J Controlled Rel 2012;160:25–32
   PubMed Web of Science ®Google Scholar
• Thomas N, Mullertz A, Graf A, Rades T. Influence of lipid composition and drug load on the in vitro performance of self-nanoemulsifying drug delivery systems. J Pharm Sci 2012;101:1721–1731
   PubMed Web of Science ®Google Scholar
• Shanmugam S, Baskaran R, Balakrishnan P, et al. Solid self-nanoemulsifying drug delivery system (S-SNEDDS) containing phosphatidycholine for enhanced bioavailability of highly lipophilic bioactive carotenoid lutein. Eur J Pharm Biopharm 2011;79:250–257
   PubMed Web of Science ®Google Scholar
• Yoo JH, Shanmugam S, Thapa P, et al. Novel self-nanoemulsifying drug delivery system for enhanced solubility and dissolution of lutein. Arch Pharm Res 2010;33:417–426
   PubMed Web of Science ®Google Scholar
• Singh AK, Chaurasiya A, Singh M, et al. Exemestane loaded self-microemulsifying drug delivery system (SMEDDS): development and optimization. AAPS Pharm Sci Tech 2008;9:628–634
   PubMed Web of Science ®Google Scholar
• Singh AK, Chaurasiya A, Awasthi A, et al. Oral bioavailability enhancement of exemestane from self-microemulsifying drug delivery system (SMEDDS). AAPS Pharm Sci Tech 2009;10:906–916
   PubMed Web of Science ®Google Scholar
• Sarpal K, Pawar YB, Bansal AK. Self-emulsifying drug delivery systems: a strategy to improve bioavailability. Curr Res Infor Pharm Sci 2010;11:42–49
   Google Scholar
• Wadhwa J, Nair A, Kumria R. Emulsion forming drug delivery system for lipophilic drugs. Acta Pol Pharm 2012;69:179–191
   PubMed Web of Science ®Google Scholar
• Nanovskaya T, Nekhayeva I, Hankins G, Ahmed M. Effect of human serum albumin on transplacental transfer of glyburide. Biochem Pharmacol 2006;72:632–639
   PubMed Web of Science ®Google Scholar
• Wais M, Samad A, Khale A, et al. Investigation of nanoemulsions system for transdermal delivery of glibenclamide. Int J Pharm Pharm Sci 2012;4:482–487
   Google Scholar
• Bachhav YG, Patravale VB. SMEDDS of glyburide: formulation, in vitro evaluation and stability studies. AAPS Pharm Sci Tech 2009;10:482–487
   PubMed Web of Science ®Google Scholar
• Singh SK, Verma PR, Razdan B. Glibenclamide-loaded self-nanoemulsifying drug delivery system: development and characterization. Drug Develop Ind Pharm 2010;36:933–945
   PubMed Web of Science ®Google Scholar
• Mura P, Valleri M, Cirri M, Mennini N. New solid self-microemulsifying systems to enhance dissolution rate of poorly soluble drugs. Pharm Develop Technol 2012;17:277–284
   PubMed Web of Science ®Google Scholar
• Salazar J, Muller RH, Moschwitzer JP. Application of the combinative particle size reduction technology H 42 to produce fast dissolving glibenclamide tablets. Eur J Pharm Sci 2013;49:565–577
   PubMed Web of Science ®Google Scholar
• Singh SK, Srinivasanr KK, Gowthamarajan K, et al. Influence of formulation parameters on dissolution rate enhancement of glyburide using liquisolid technique. Drug Develop Ind Pharm 2012;38:961–970
   PubMed Web of Science ®Google Scholar
• Ghosh LK, Thakur RS, Sharma PK, et al. Development and evaluation of an ideal formulation of glibenclamide using solid dispersion techniques. Boll Chim Pharm 1998;137:26–29
   PubMedGoogle Scholar
• Shakeel F, Shafiq S, Haq N, et al. Nanoemulsions as potential vehicles for transdermal and dermal delivery of hydrophobic compounds: an overview. Expert Opin Drug Deliv 2012;9:953–974
   PubMed Web of Science ®Google Scholar
• Bali V, Ali M, Ali J. Nanocarrier for the enhanced bioavailability of a cardiovascular agent: in vitro, pharmacodynamics, pharmacokinetic and stability assessment. Int J Pharm 2011;403:46–56
   PubMed Web of Science ®Google Scholar
• Shafiq S, Shakeel F, Talegaonkar S, et al. Development and bioavailability assessment of ramipril nanoemulsion formulation. Eur J Pharm Biopharm 2007;66:227–243
   PubMed Web of Science ®Google Scholar
• Shakeel F, Ramadan W. Transdermal delivery of anticancer drug caffeine from water-in-oil nanoemulsions. Coll Surf B 2010;75:356–362
   PubMed Web of Science ®Google Scholar
• Kawakami K, Yoshikawa T, Hayashi T, et al. Microemulsion formulation for enhanced absorption of poorly soluble drugs: II. in vivo studies. J Controlled Rel 2002;81:75–82
   PubMed Web of Science ®Google Scholar
• Patel N, Prajapati HN, Dalrymple DM, Serajuddin ATM. Development of solid SEDDS: II. Application of Acconon-C14 and Gelucire-44/14 as solidifying agents for self-emulsifying drug delivery systems of medium chain triglycerides. J Excp Food Chem 2012;3:54–66
   Google Scholar
• Djekic L, Primorac M, Jockovic J. Phase behavior, microstructure and ibuprofen solubilization capacity of pseudo-ternary nonionic microemulsions. J Mol Liq 2011;160:81–87
   Web of Science ®Google Scholar
• Fanun M. Conductivity, viscosity, NMR and diclofenac solubilization capacity studies on mixed nonionic surfactants microemulsions. J Mol Liq 2007;135:5–13
   Web of Science ®Google Scholar
• Fanun M. Properties of microemulsions based on mixed nonionic surfactants and mixed oils. J Mol Liq 2009;150:25–32
   Google Scholar
• Brusewitz C, Schendler A, Funke A, et al. Novel poloxamer-based nanoemulsions to enhance the intestinal absorption of active compounds. Int J Pharm 2007;329:173–181
   PubMed Web of Science ®Google Scholar
• Ujhelyi Z, Fenyvesi F, Varadi J, et al. Evaluation of cytotoxicity of surfactants used in self-microemulsifying drug delivery systems and their effects on paracellular transport in caco-2 cell monolayer. Eur J Pharm Sci 2012;47:564–573
   PubMed Web of Science ®Google Scholar
• Barakat NS. Enhanced oral bioavailability of etodolac by self-emulsifying systems: in-vitro and in-vivo evaluation. J Pharm Pharmacol 2010;62:173–180
   PubMed Web of Science ®Google Scholar
• Rao SV, Shao J. Self-nanoemulsifying drug delivery systems (SNEDDS) for oral delivery of protein drugs: I. Formulation development. Int J Pharm 2008;362:2–9
   PubMed Web of Science ®Google Scholar
• Ruan J, Liu J, Zhu D, et al. Preparation and evaluation of self-nanoemulsified drug delivery systems (SNEDDSs) of matrine based on drug--phospholipid complex technique. Int J Pharm 2010;386:282–290
   PubMed Web of Science ®Google Scholar
• Yu H, Huang Q. Improving the oral bioavailability of curcumin using novel organogel-based nanoemulsions. J Agr Food Chem 2012;60:5373–5379
   PubMed Web of Science ®Google Scholar
• Furlanetto S, Cirri M, Piepel G, et al. Mixture experiment methods in the development and optimization of microemulsion formulations. J Pharm Biomed Anal 2011;55:610–617
   PubMed Web of Science ®Google Scholar
• Shafiq S, Shakeel F. Effect of labrasol on self-nanoemulsification efficiency of ramipril nanoemulsion. Pharmazie 2009;64:812–817
   PubMedGoogle Scholar
• Shafiq S, Shakeel F. Stability and self-nanoemulsification efficiency of ramipril nanoemulsion containing labrasol and plurol oleique. Clin Res Reg Affair 2010;27:7–12
   Google Scholar