ARTICLE;
DISSOLUTION;
DRUG DELIVERY SYSTEM;
DRUG DISTRIBUTION;
DRUG FORMULATION;
DRUG RELEASE;
DRUG SCREENING;
DRUG SYNTHESIS;
IN VITRO STUDY;
KINETICS;
MICROCAPSULE;
MICROENCAPSULATION;
PRIORITY JOURNAL;
SCANNING ELECTRON MICROSCOPY;
TABLET FORMULATION;
TABLET HARDNESS;
Treatment of mild hypertension with low once-daily doses of a sustained-release capsule formulation of verapamil
Davis PJ, Fagan TC, Topmiller MJ, et al. Treatment of mild hypertension with low once-daily doses of a sustained-release capsule formulation of verapamil. J Clin Pharmacol. 1995;35:52-58.
Comparative efficacy, safety and pharmacokinetics of verapamil SR vs verapamil IR in hypertensive patients
Fuenmayor NT, Faggine BM, Cubeddu LX. Comparative efficacy, safety and pharmacokinetics of verapamil SR vs verapamil IR in hypertensive patients. Drugs. 1992;44:1-11.
Evaluation of microcapsules of ASA prepared with CAP, EC or their mixtures by non-solvent addition technique
Nokodchi A, Zakeri-Milan P, Valizadeh H, et al. Evaluation of microcapsules of ASA prepared with CAP, EC or their mixtures by non-solvent addition technique. Ars Pharmaceut. 2002;43:135-147.
Mechanism of sustained-action medication-theoretical analysis of rate of release of solid drugs dispersed in solid matrices
Higuchi T. Mechanism of sustained-action medication-theoretical analysis of rate of release of solid drugs dispersed in solid matrices. J Pharm Sci. 1963;52:1145-1149.
Microencapsulation of theophylline using ethykellulose: In vitro drug release and kinetic modeling
Lavasanifar A, Ghalandari R, Ateai R, et al. Microencapsulation of theophylline using ethykellulose: in vitro drug release and kinetic modeling. J Microencapsul. 1997;14: 91-100.