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Results 1 to 25 of 28

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Microemulsions as carriers for drugs and nutraceuticalsSPEMATH, Aviram; ASERIN, Abraham.Advances in colloid and interface science. 2006, Vol 128-130, pp 47-64, issn 0001-8686, 18 p.Article

A novel plug-controlled colon-specific pulsatile capsule with tablet of curcumin-loaded SMEDDSYUANRUI HUANG; RUI TIAN; WENJING HU et al.Carbohydrate polymers. 2013, Vol 92, Num 2, pp 2218-2223, issn 0144-8617, 6 p.Article

In vitro and in vivo studies of pharmacokinetics and antitumor efficacy of D07001-F4, an oral gemcitabine formulationHAO, Wei-Hua; WANG, Jong-Jing; HSUEH, Shu-Ping et al.Cancer chemotherapy and pharmacology. 2013, Vol 71, Num 2, pp 379-388, issn 0344-5704, 10 p.Article

Rational formulation development and in vitro assessment of SMEDDS for oral delivery of poorly water soluble drugsSPRUNK, Angela; STRACHAN, Clare J; GRAF, Anja et al.European journal of pharmaceutical sciences. 2012, Vol 46, Num 5, pp 508-515, issn 0928-0987, 8 p.Article

Bioavailability of seocalcitol. II Development and characterisation of self-microemulsifying drug delivery systems (SMEDDS) for oral administration containing medium and long chain triglyceridesGROVE, Mette; MÜLLERTZ, Anette; NIELSEN, Jeanet Løgsted et al.European journal of pharmaceutical sciences. 2006, Vol 28, Num 3, pp 233-242, issn 0928-0987, 10 p.Article

Bioavailability of seocalcitol. III. Administration of lipid-based formulations to minipigs in the fasted and fed stateGROVE, Mette; MÜLLERTZ, Anette; PEDERSEN, Gitte P et al.European journal of pharmaceutical sciences. 2007, Vol 31, Num 1, pp 8-15, issn 0928-0987, 8 p.Article

Examination of oral absorption and lymphatic transport of halofantrine in a triple-cannulated canine model after administration in self-microemulsifying drug delivery systems (SMEDDS) containing structured triglyceridesHOLM, René; PORTER, Christopher J. H; EDWARDS, Glenn A et al.European journal of pharmaceutical sciences. 2003, Vol 20, Num 1, pp 91-97, issn 0928-0987, 7 p.Article

The influence of cosurfactants and oils on the formation of pharmaceutical microemulsions based on PEG-8 caprylic/capric glyceridesDJEKIC, Ljiljana; PRIMORAC, Marija.International journal of pharmaceutics. 2008, Vol 352, Num 1-2, pp 231-239, issn 0378-5173, 9 p.Article

What determines dmg solubility in lipid vehicles : Is it predictable?RANE, Sagar S; ANDERSON, Bradley D.Advanced drug delivery reviews. 2008, Vol 60, Num 6, pp 638-656, issn 0169-409X, 19 p.Conference Paper

Stable drug encapsulation in micelles and microemulsionsNARANG, Ajit S; DELMARRE, David; UAO, Danchen et al.International journal of pharmaceutics. 2007, Vol 345, Num 1-2, pp 9-25, issn 0378-5173, 17 p.Article

Controlled release of paclitaxel from microemulsion containing PLGA and evaluation of anti-tumor activity in vitro and in vivoBOK KI KANG; SE KANG CHON; SEON HWA KIM et al.International journal of pharmaceutics. 2004, Vol 286, Num 1-2, pp 147-156, issn 0378-5173, 10 p.Article

Lyotropic, liquid crystalline nanostructures of aqueous dilutions of SMEDDS revealed by small-angle X-ray scattering: Impact on solubility and drug releaseGODDEERIS, Caroline; GODERIS, Bart; VAN DEN MOOTER, Guy et al.European journal of pharmaceutical sciences. 2010, Vol 40, Num 2, pp 110-117, issn 0928-0987, 8 p.Article

Development and evaluation of self-microemulsifying liquid and pellet formulations of curcumin, and absorption studies in ratsSETTHACHEEWAKUL, Saipin; MAHATTANADUL, Sirima; PHADOONGSOMBUT, Narubodee et al.European journal of pharmaceutics and biopharmaceutics. 2010, Vol 76, Num 3, pp 475-485, issn 0939-6411, 11 p.Article

Design of Lipid-Based Formulations for Oral Administration of Poorly Water-Soluble Drugs: Precipitation of Drug after Dispersion of Formulations in Aqueous SolutionMOHSIN, Kazi; LONG, Michelle A; POUTON, Colin W et al.Journal of pharmaceutical sciences. 2009, Vol 98, Num 10, pp 3582-3595, issn 0022-3549, 14 p.Article

Self-Emulsifying Drug Delivery Systems (SEDDS): Formulation Development, Characterization, and ApplicationsSINGH, Bhupinder; BANDOPADHYAY, Shantanu; KAPIL, Rishi et al.Critical reviews in therapeutic drug carrier systems. 2009, Vol 26, Num 5, pp 427-521, issn 0743-4863, 95 p.Article

Self-microemulsifying drug delivery systems (SMEDDS) for improving in vitro dissolution and oral absorption of pueraria lobata isoflavoneSHENGMIAO CUI; CHUNSHUN ZHAO; DAWEI CHEN et al.Drug development and industrial pharmacy. 2005, Vol 31, Num 4-5, pp 349-356, issn 0363-9045, 8 p.Article

In vitro evaluation of drug release from self micro-emulsifying drug delivery systems using a biodegradable homolipid from Capra hircusATTAMA, Anthony A; NKEMNELE, Megg O.International journal of pharmaceutics. 2005, Vol 304, Num 1-2, pp 4-10, issn 0378-5173, 7 p.Article

Systèmes microémulsionnables pour actif faiblement soluble et peu biodisponible = Micro-emulsifying systems for a poorly soluble and poorly bioavailable drugBENAMEUR, H; BARTHELEMY, P; FARAH, N et al.STP pharma pratiques. 1999, Vol 9, pp 27-29, issn 1157-1497, HSConference Paper

Improved solubilization of Celecoxib in U-type nonionic microemulsions and their structural transitions with progressive aqueous dilutionGARTI, Nissim; AVRAHAMI, Marganit; ASERIN, Abraham et al.Journal of colloid and interface science. 2006, Vol 299, Num 1, pp 352-365, issn 0021-9797, 14 p.Article

Enhancement of oral absorption of curcumin by self-microemulsifying drug delivery systemsJING CUI; BO YU; YU ZHAO et al.International journal of pharmaceutics (Print). 2009, Vol 371, Num 1-2, pp 148-155, issn 0378-5173, 8 p.Article

Correlation between digestion of the lipid phase of smedds and release of the anti-HIV drug UC 781 and the anti-mycotic drug enilconazole from smeddsGODDEERIS, C; COACCI, J; VAN DEN MOOTER, G et al.European journal of pharmaceutics and biopharmaceutics. 2007, Vol 66, Num 2, pp 173-181, issn 0939-6411, 9 p.Article

Effect of combined use of nonionic surfactant on formation of oil-in-water microemulsionsPING LI; GHOSH, Anasuya; WAGNER, Robert F et al.International journal of pharmaceutics. 2005, Vol 288, Num 1, pp 27-34, issn 0378-5173, 8 p.Article

The fate of paclitaxel during in vitro dispersion testing of different lipid-based formulationsMOHSIN, K; ALANAZI, F.Journal of drug delivery science and technology. 2012, Vol 22, Num 2, pp 197-204, issn 1773-2247, 8 p.Article

Comparison of different in vitro tests to assess oral lipid-based formulations using a poorly soluble acidic drugARNOLD, Y; BRAVO GONZALEZ, R; VERSACE, H et al.Journal of drug delivery science and technology. 2010, Vol 20, Num 2, pp 143-148, issn 1773-2247, 6 p.Article

Self-microemulsifying drug delivery system (SMEDDS) improves anticancer effect of oral 9-nitrocamptothecin on human cancer xenografts in nude miceLU, Juan-Li; WANG, Jian-Cheng; ZHAO, Shu-Xin et al.European journal of pharmaceutics and biopharmaceutics. 2008, Vol 69, Num 3, pp 899-907, issn 0939-6411, 9 p.Article

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