| Nanocapsule formation by interfacial polymer deposition following solvent displacement H Fessi, F Puisieux, JP Devissaguet, N Ammoury, S Benita International journal of pharmaceutics 55 (1), R1-R4, 1989 | 2815 | 1989 |
| Self-emulsifying drug delivery systems (SEDDS) for improved oral delivery of lipophilic drugs RN Gursoy, S Benita Biomedicine & pharmacotherapy 58 (3), 173-182, 2004 | 1801 | 2004 |
| Microencapsulation: methods and industrial applications S Benita Crc Press, 2005 | 1169 | 2005 |
| Self-dispersing lipid formulations for improving oral absorption of lipophilic drugs T Gershanik, S Benita European journal of pharmaceutics and biopharmaceutics 50 (1), 179-188, 2000 | 715 | 2000 |
| Targeting of nanoparticles to the clathrin-mediated endocytic pathway O Harush-Frenkel, N Debotton, S Benita, Y Altschuler Biochemical and biophysical research communications 353 (1), 26-32, 2007 | 682 | 2007 |
| Surface charge of nanoparticles determines their endocytic and transcytotic pathway in polarized MDCK cells O Harush-Frenkel, E Rozentur, S Benita, Y Altschuler Biomacromolecules 9 (2), 435-443, 2008 | 476 | 2008 |
| Submicron emulsions as colloidal drug carriers for intravenous administration: comprehensive physicochemical characterization S Benita, MY Levy Journal of pharmaceutical sciences 82 (11), 1069-1079, 1993 | 420 | 1993 |
| A new in vitro technique for the evaluation of drug release profile from colloidal carriers-ultrafiltration technique at low pressure B Magenheim, MY Levy, S Benita International journal of pharmaceutics 94 (1-3), 115-123, 1993 | 371 | 1993 |
| Successfully improving ocular drug delivery using the cationic nanoemulsion, novasorb F Lallemand, P Daull, S Benita, R Buggage, JS Garrigue Journal of drug delivery 2012, 2012 | 356 | 2012 |
| Reversion of multidrug resistance by co-encapsulation of doxorubicin and cyclosporin A in polyalkylcyanoacrylate nanoparticles CE Soma, C Dubernet, D Bentolila, S Benita, P Couvreur Biomaterials 21 (1), 1-7, 2000 | 354 | 2000 |
| Characterization of drug‐loaded poly(d,l‐lactide) microspheres S Benita, JP Benoit, F Puisieux, C Thies Journal of Pharmaceutical Sciences 73 (12), 1721-1724, 1984 | 296 | 1984 |
| Drug release from submicronized o/w emulsion: a new in vitro kinetic evaluation model MY Levy, S Benita International journal of pharmaceutics 66 (1-3), 29-37, 1990 | 276 | 1990 |
| The potential of lipid emulsion for ocular delivery of lipophilic drugs S Tamilvanan, S Benita European Journal of Pharmaceutics and Biopharmaceutics 58 (2), 357-368, 2004 | 237 | 2004 |
| Enhanced oral absorption of paclitaxel in a novel self-microemulsifying drug delivery system with or without concomitant use of P-glycoprotein inhibitors S Yang, RN Gursoy, G Lambert, S Benita Pharmaceutical research 21, 261-270, 2004 | 214 | 2004 |
| Nanoparticle characterization: a comprehensive physicochemical approach B Magenheim, S Benita STP Pharma Sciences 1 (4), 221-241, 1991 | 197 | 1991 |
| Positively and negatively charged submicron emulsions for enhanced topical delivery of antifungal drugs MPY Piemi, D Korner, S Benita, JP Marty Journal of Controlled Release 58 (2), 177-187, 1999 | 190 | 1999 |
| Medicinal emulsions S Benita, M Levy US Patent 5,364,632, 1994 | 171 | 1994 |
| Emulsions and nanosuspensions for the formulation of poorly soluble drugs RH Müller, S Benita, BHL Böhm CRC Press, 1998 | 168 | 1998 |
| Positively charged self-emulsifying oil formulation for improving oral bioavailability of progesterone T Gershanik, S Benita Pharmaceutical Development and Technology 1 (2), 147-157, 1996 | 166 | 1996 |
| Polyacrylate (Eudragit retard) microspheres for oral controlled release of nifedipine. I. Formulation design and process optimization A Barkai, YV Pathak, S Benita Drug Development and Industrial Pharmacy 16 (13), 2057-2075, 1990 | 164 | 1990 |
