ANIMAL EXPERIMENT;
ARTICLE;
DISPERSION;
DRUG ABSORPTION;
DRUG BIOAVAILABILITY;
DRUG BLOOD LEVEL;
DRUG DELIVERY SYSTEM;
IN VIVO STUDY;
MAXIMUM PLASMA CONCENTRATION;
MEAN RESIDENCE TIME;
MICROEMULSION;
NONHUMAN;
PRIORITY JOURNAL;
RAT;
TECHNIQUE;
TIME TO MAXIMUM PLASMA CONCENTRATION;
ABSORPTION;
ADMINISTRATION, ORAL;
ANIMALS;
BETA-LACTAMASES;
CHEMISTRY, PHARMACEUTICAL;
DRUG CARRIERS;
DRUG DELIVERY SYSTEMS;
DRUG DESIGN;
DRUG STABILITY;
EMULSIONS;
MOUTH MUCOSA;
NANOPARTICLES;
OILS;
PARTICLE SIZE;
PROTEIN STABILITY;
RATS;
RATS, SPRAGUE-DAWLEY;
SURFACE-ACTIVE AGENTS;
Oral anhydrous non-ionic nanoemulsions administered in soft gel capsules
Georgakopoulos E., Farah N., and Vergnault G. Oral anhydrous non-ionic nanoemulsions administered in soft gel capsules. Bull. Tech. Gattefosse (1992) 11-19
Bioavailability of seocalcitol. II. Development and characterization of self-microemulsifying drug delivery systems (SMEDDS) for oral administration containing medium and long chain triglycerides
Grove M., Mullertz A., Nielsen J.L., and Pedersen G.P. Bioavailability of seocalcitol. II. Development and characterization of self-microemulsifying drug delivery systems (SMEDDS) for oral administration containing medium and long chain triglycerides. Eur. Int. J. Pharm. 28 (2006) 233-242
Self-emulsifying drug delivery systems (SEDDS) for improved oral delivery of lipophilic drugs
Gursoy N.R., and Benita S. Self-emulsifying drug delivery systems (SEDDS) for improved oral delivery of lipophilic drugs. Biomed. Pharm. 58 (2004) 173-182
Oral delivery of β-lactamase by Lactococcus lactis subsp. Lactis transformed with Plasmid ss80
Kaushal G., and Shao J. Oral delivery of β-lactamase by Lactococcus lactis subsp. Lactis transformed with Plasmid ss80. Int. J. Pharm. 312 (2006) 90-95
Factors limiting the oral bioavailability of N-acetylglucosaminyl-N-acetylmuramyl dipeptide (GMDP) and enhancement of absorption in rats by delivery in a water-in-oil nanoemulsion
Lyons K.C., Charman W.N., Millerm W., and Porter C.J.H. Factors limiting the oral bioavailability of N-acetylglucosaminyl-N-acetylmuramyl dipeptide (GMDP) and enhancement of absorption in rats by delivery in a water-in-oil nanoemulsion. Int. J. Pharm. 1 (2000) 17-28
Preparation and in-vitro characterization of a eutectic based semisolid self-nanoemulsified drug delivery system (SNEDDS) of ubiquinone: mechanism and progress of emulsion formation
Nazzal S., Smalyukh I.I., Lavrentovich O.D., and Khan M.A. Preparation and in-vitro characterization of a eutectic based semisolid self-nanoemulsified drug delivery system (SNEDDS) of ubiquinone: mechanism and progress of emulsion formation. Int. J. Pharm. 235 (2002) 247-265
Self-nanoemulsifying Drug Delivery Systems (SNEDDS) for Oral Delivery of Protein Drugs. II. In-vitro Transport Study
Rao S.V.R., Agarwal P., and Shao J. Self-nanoemulsifying Drug Delivery Systems (SNEDDS) for Oral Delivery of Protein Drugs. II. In-vitro Transport Study. Int. J. Pharm. 362 (2008) 10-15
Self-nanoemulsifying drug delivery systems (SNEDDS) for oral delivery of protein drugs
Venkata Ramana Rao S., and Shao J. Self-nanoemulsifying drug delivery systems (SNEDDS) for oral delivery of protein drugs. Int. J. Pharm. 362 (2008) 2-9