Development and characterization of curcumin-loaded solid self-emulsifying drug delivery system (SEDDS) by spray drying using Soluplus® as solid carrier

[1]  S. Nazzal,et al.  The rheological and textural characterization of Soluplus®/Vitamin E composites , 2018, International journal of pharmaceutics.

[2]  S. Nazzal,et al.  Development of a new class of sulforaphane-enabled self-emulsifying drug delivery systems (SFN-SEDDS) by high throughput screening: A case study with curcumin. , 2018, International journal of pharmaceutics.

[3]  S. Nazzal,et al.  Novel sulforaphane-enabled self-microemulsifying delivery systems (SFN-SMEDDS) of taxanes: Formulation development and in vitro cytotoxicity against breast cancer cells. , 2018, International journal of pharmaceutics.

[4]  Y. Kawashima,et al.  Improvement in the water solubility of drugs with a solid dispersion system by spray drying and hot‐melt extrusion with using the amphiphilic polyvinyl caprolactam‐polyvinyl acetate‐polyethylene glycol graft copolymer and d‐mannitol , 2018, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.

[5]  Chuan-Yu Wu,et al.  Supersaturable solid self-microemulsifying drug delivery system: precipitation inhibition and bioavailability enhancement , 2017, International journal of nanomedicine.

[6]  F. Sonvico,et al.  Development of a Soluplus budesonide freeze-dried powder for nasal drug delivery , 2017, Drug development and industrial pharmacy.

[7]  A. Concheiro,et al.  α-Lipoic Acid in Soluplus(®) Polymeric Nanomicelles for Ocular Treatment of Diabetes-Associated Corneal Diseases. , 2016, Journal of pharmaceutical sciences.

[8]  Jun Seo Park,et al.  Enhanced dissolution and oral absorption of tacrolimus by supersaturable self-emulsifying drug delivery system , 2016, International journal of nanomedicine.

[9]  Han‐Gon Choi,et al.  Development of Solid Self-Emulsifying Formulation for Improving the Oral Bioavailability of Erlotinib , 2016, AAPS PharmSciTech.

[10]  Hong-Liang Lin,et al.  Thermoanalytical and Fourier transform infrared spectral curve-fitting techniques used to investigate the amorphous indomethacin formation and its physical stability in Indomethacin-Soluplus® solid dispersions. , 2015, International journal of pharmaceutics.

[11]  K. Winnicka,et al.  Development and Evaluation of Liquid and Solid Self-Emulsifying Drug Delivery Systems for Atorvastatin , 2015, Molecules.

[12]  Y. Choi,et al.  Fujicalin®-based solid supersaturable self-emulsifying drug delivery system (S-SEDDS) of tacrolimus for enhanced dissolution rate and oral absorption , 2015, Journal of Pharmaceutical Investigation.

[13]  F. Vrečer,et al.  Development of a solid self-microemulsifying drug delivery system (SMEDDS) for solubility enhancement of naproxen , 2015, Drug development and industrial pharmacy.

[14]  C. Strachan,et al.  Amorphous solid dispersions of piroxicam and Soluplus(®): Qualitative and quantitative analysis of piroxicam recrystallization during storage. , 2015, International journal of pharmaceutics.

[15]  Rajesh Kesarla,et al.  Calcium Alginate-Neusilin US2 Nanocomposite Microbeads for Oral Sustained Drug Delivery of Poor Water Soluble Drug Aceclofenac Sodium , 2015, Journal of drug delivery.

[16]  Xiang Jin,et al.  Soluplus(®) micelles as a potential drug delivery system for reversal of resistant tumor. , 2015, Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie.

[17]  Y. Choi,et al.  Improved oral absorption of dutasteride via Soluplus®-based supersaturable self-emulsifying drug delivery system (S-SEDDS). , 2015, International journal of pharmaceutics.

[18]  S. Majumdar,et al.  Stability-enhanced Hot-melt Extruded Amorphous Solid Dispersions via Combinations of Soluplus® and HPMCAS-HF , 2015, AAPS PharmSciTech.

[19]  Xing Tang,et al.  Investigation of a nanosuspension stabilized by Soluplus® to improve bioavailability. , 2014, International journal of pharmaceutics.

[20]  I. Singh,et al.  Development of Corn Starch-Neusilin UFL2 Conjugate as Tablet Superdisintegrant: Formulation and Evaluation of Fast Disintegrating Tablets , 2014, Journal of drug delivery.

[21]  C. Porter,et al.  Lipid-based formulations solidified via adsorption onto the mesoporous carrier Neusilin® US2: effect of drug type and formulation composition on in vitro pharmaceutical performance. , 2014, Journal of pharmaceutical sciences.

[22]  Y. Choi,et al.  In situ intestinal permeability and in vivo oral bioavailability of celecoxib in supersaturating self-emulsifying drug delivery system , 2014, Archives of pharmacal research.

[23]  A. Siddiqui,et al.  Powdered self-emulsified lipid formulations of meloxicam as solid dosage forms for oral administration , 2013, Drug development and industrial pharmacy.

[24]  Fernando J Muzzio,et al.  Effects of powder flow properties on capsule filling weight uniformity , 2013, Drug development and industrial pharmacy.

[25]  A. Serajuddin,et al.  Development of Solid SEDDS, IV: Effect of Adsorbed Lipid and Surfactant on Tableting Properties and Surface Structures of Different Silicates , 2013, Pharmaceutical Research.

[26]  A. Serajuddin,et al.  Development of Solid SEDDS, V: Compaction and Drug Release Properties of Tablets Prepared by Adsorbing Lipid-Based Formulations onto Neusilin® US2 , 2013, Pharmaceutical Research.

[27]  L. Wang,et al.  Development of a Mini-Tablet of Co-Grinded Prednisone–Neusilin Complex for Pediatric Use , 2013, AAPS PharmSciTech.

[28]  Y. Choi,et al.  Enhanced dissolution of celecoxib by supersaturating self-emulsifying drug delivery system (S-SEDDS) formulation , 2013, Archives of pharmacal research.

[29]  Tao Yi,et al.  Effects of Spray-Drying and Choice of Solid Carriers on Concentrations of Labrasol® and Transcutol® in Solid Self-Microemulsifying Drug Delivery Systems (SMEDDS) , 2013, Molecules.

[30]  S. Ibrić,et al.  Characterization and evaluation of solid self-microemulsifying drug delivery systems with porous carriers as systems for improved carbamazepine release. , 2012, International journal of pharmaceutics.

[31]  S. Onoue,et al.  Novel solid self-emulsifying drug delivery system of coenzyme Q₁₀ with improved photochemical and pharmacokinetic behaviors. , 2012, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.

[32]  Dong Hoon Oh,et al.  Effects of solid carriers on the crystalline properties, dissolution and bioavailability of flurbiprofen in solid self-nanoemulsifying drug delivery system (solid SNEDDS). , 2012, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

[33]  Beom-Jin Lee,et al.  Comparison of solid self-microemulsifying drug delivery system (solid SMEDDS) prepared with hydrophilic and hydrophobic solid carrier. , 2011, International journal of pharmaceutics.

[34]  Koichi Wada,et al.  Formulation design for poorly water-soluble drugs based on biopharmaceutics classification system: basic approaches and practical applications. , 2011, International journal of pharmaceutics.

[35]  B. Ranjbar,et al.  Differential scanning calorimetry techniques: applications in biology and nanoscience. , 2010, Journal of biomolecular techniques : JBT.

[36]  M. Brewster,et al.  Pharmaceutical applications of cyclodextrins: basic science and product development , 2010, The Journal of pharmacy and pharmacology.

[37]  Cordin Arpagaus,et al.  Nanoparticles by spray drying using innovative new technology: the Büchi nano spray dryer B-90. , 2010, Journal of controlled release : official journal of the Controlled Release Society.

[38]  Jucimary V. Santos,et al.  The Influence of the Compression Force on Zidovudine Release from Matrix Tablets , 2010, AAPS PharmSciTech.

[39]  Han‐Gon Choi,et al.  Enhanced oral bioavailability of dexibuprofen by a novel solid self-emulsifying drug delivery system (SEDDS). , 2009, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

[40]  J. Parikh,et al.  Preparation and Characterization of Co-Grinded Mixtures of Aceclofenac and Neusilin US2 for Dissolution Enhancement of Aceclofenac , 2009, AAPS PharmSciTech.

[41]  Qin Zheng,et al.  The Study on the Entrapment Efficiency and In Vitro Release of Puerarin Submicron Emulsion , 2009, AAPS PharmSciTech.

[42]  Akhtar Siddiqui,et al.  Dissolution and powder flow characterization of solid self-emulsified drug delivery system (SEDDS). , 2009, International journal of pharmaceutics.

[43]  Huibi Xu,et al.  A new solid self-microemulsifying formulation prepared by spray-drying to improve the oral bioavailability of poorly water soluble drugs. , 2008, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

[44]  Jean-David Rodier,et al.  Lipolysis of the semi-solid self-emulsifying excipient Gelucire 44/14 by digestive lipases. , 2008, Biochimica et biophysica acta.

[45]  C. Demetzos.  Differential Scanning Calorimetry (DSC): A Tool to Study the Thermal Behavior of Lipid Bilayers and Liposomal Stability , 2008, Journal of liposome research.

[46]  D. Hauss.  Oral lipid-based formulations. , 2007, Advanced drug delivery reviews.

[47]  A. Bansal,et al.  Analytical techniques for quantification of amorphous/crystalline phases in pharmaceutical solids. , 2006, Journal of pharmaceutical sciences.