Optimized microemulsions and solid microemulsion systems of simvastatin: characterization and in vivo evaluation.
暂无分享,去创建一个
[1] Roger Leverge,et al. Spray-dried redispersible oil-in-water emulsion to improve oral bioavailability of poorly soluble drugs. , 2003, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.
[2] Raymond C Rowe,et al. Handbook of Pharmaceutical Excipients , 1994 .
[3] Jean Paul Remon,et al. Formulation of a lyophilized dry emulsion tablet for the delivery of poorly soluble drugs , 1998 .
[4] K. Kannan,et al. Oral microemulsions of paclitaxel: in situ and pharmacokinetic studies. , 2009, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.
[5] H. Kristensen,et al. Physical stability of redispersible dry emulsions containing amorphous sucrose. , 2002, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.
[6] M. Nagarsenker,et al. Formulation and In Vivo Evaluation of Self-Nanoemulsifying Granules for Oral Delivery of a Combination of Ezetimibe and Simvastatin , 2008 .
[7] Sami Nazzal,et al. Controlled release of a self-emulsifying formulation from a tablet dosage form: stability assessment and optimization of some processing parameters. , 2006, International journal of pharmaceutics.
[8] Tayade Pralhad,et al. Cyclodextrin complexes of valdecoxib: properties and anti-inflammatory activity in rat. , 2005, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.
[9] M. Nagarsenker,et al. Self-nanoemulsifying granules of ezetimibe: design, optimization and evaluation. , 2008, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.
[10] R. Le Verge,et al. Bupivacaine containing dry emulsion can prolong epidural anesthetic effects in rabbits. , 2004, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.
[11] K. Wasan,et al. Acute P-407 Administration to Mice Causes Hypercholesterolemia by Inducing Cholesterolgenesis and Down-Regulating Low-Density Lipoprotein Receptor Expression , 2006, Pharmaceutical Research.
[12] M. Nagarsenker,et al. Dry Adsorbed Emulsion of Simvastatin: Optimization and In Vivo Advantage , 2007, Pharmaceutical development and technology.
[13] P. Arnaud,et al. In vitro and in vivo evaluation of carbamazepine-PEG 6000 solid dispersions. , 2001, International journal of pharmaceutics.
[14] Chong-Kook Kim,et al. Improvement of bioavailability and photostability of amlodipine using redispersible dry emulsion. , 2006, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.
[15] 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.
[16] F. Podczeck,et al. The influence of formulation variables on the properties of pellets containing a self-emulsifying mixture. , 2001, Journal of pharmaceutical sciences.
[17] Thomas Rades,et al. Silica-lipid hybrid (SLH) microcapsules: a novel oral delivery system for poorly soluble drugs. , 2009, Journal of controlled release : official journal of the Controlled Release Society.
[18] B. Perissutti,et al. Bi-layered self-emulsifying pellets prepared by co-extrusion and spheronization: influence of formulation variables and preliminary study on the in vivo absorption. , 2008, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.
[19] B. Müller,et al. Increasing drug solubility by means of bile salt-phosphatidylcholine-based mixed micelles. , 1998, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.
[20] Karsten Mäder,et al. ESR studies on the influence of physiological dissolution and digestion media on the lipid phase characteristics of SEDDS and SEDDS pellets. , 2009, International journal of pharmaceutics.
[21] Gang Cheng,et al. Development of solid self-emulsifying drug delivery systems: preparation techniques and dosage forms. , 2008, Drug discovery today.
[22] G. Rowley,et al. Comparison of surface modification and solid dispersion techniques for drug dissolution. , 2000, International journal of pharmaceutics.
[23] K. Mäder,et al. Preparation and characterization of a self-emulsifying pellet formulation. , 2007, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.
[24] Harjinder Singh,et al. Microemulsions: A Potential Delivery System for Bioactives in Food , 2006, Critical reviews in food science and nutrition.
[25] M. Lawrence,et al. Microemulsion-based media as novel drug delivery systems. , 2000, Advanced drug delivery reviews.
[26] P. Heard,et al. Dry hybrid lipid-silica microcapsules engineered from submicron lipid droplets and nanoparticles as a novel delivery system for poorly soluble drugs. , 2009, Molecular pharmaceutics.
[27] F. Carli,et al. Ubidecarenone nanoemulsified composite systems. , 2005, International journal of pharmaceutics.
[28] V. Bérard,et al. Dry adsorbed emulsion: 2. Dissolution behaviour of an intricate formulation. , 2002, International journal of pharmaceutics.
[29] Akhtar Siddiqui,et al. Dissolution and powder flow characterization of solid self-emulsified drug delivery system (SEDDS). , 2009, International journal of pharmaceutics.
[30] A. Paradkar,et al. Formulation of a self-emulsifying system for oral delivery of simvastatin: In vitro and in vivo evaluation , 2007, Acta pharmaceutica.
[31] H. Kristensen,et al. Preparation of redispersible dry emulsions by spray drying. , 2001, International journal of pharmaceutics.
[32] Per Holm,et al. Process characteristics and compaction of spray-dried emulsions containing a drug dissolved in lipid. , 2004, International journal of pharmaceutics.
[33] 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.
[34] K. Kawakami,et al. Microemulsion formulation for enhanced absorption of poorly soluble drugs. II. In vivo study. , 2002, Journal of controlled release : official journal of the Controlled Release Society.
[35] K. Franke,et al. Using freezing and drying techniques of emulsions for the microencapsulation of fish oil to improve oxidation stability , 1999 .
[36] D. Thompson,et al. Oral bioavailability of vancomycin solid-state emulsions , 1995 .
[37] P. Dy,et al. Preparation and evaluation of a microemulsion for oral delivery of berberine. , 2008, Die Pharmazie.