A simple diffusion cell to monitor drug release from semi-solid dosage forms. Int J Pharm. 1995;120:119-24.Chattaraj SC, Swarbrick J and Kanfer I (1995). A simple diffusion cell to monitor drug release from semi-solid dosage forms. International Journal of Pharmaceutics, 120(1): 119-...
The objective of this study was to determine to what extent bisphenol A (BPA), bisphenol A diglycidyl ether (BADGE) and its derivatives are extractable from epoxy-based coatings of aluminium tubes for pharmaceutical use and to monitor their leaching into different kinds of semi-solid dosage forms...
Design and evaluation of poly-herbal formulation in semisolid dosage form for its antibacterial activity. In ayurveda, most of the drugs were given in the form of powder, kasaya (decoction form) or bhasma. In present study, topical formulations were prepared fo... RB Parmar,AH Baria,SD Fal...
The invention relates to pharmaceutical compositions in the form of semi-solid aqueous gels for use in wound alimentation by application to a wound during healing. The compositions contain in solution each of the essential and semi-essential amino acids and malic acid and have a pH in the range...
[0024] A semisolid dosage form according to the present invention is well known in the art. The term “semisolid” implies a unique type of Theological behavior as described by G. Flynn in “Modern Pharmaceutics”, (G. S. Banker and C. T. Rhodes, ed. Marcel Dekker, Inc., New York...
- 《International Journal of Pharmaceutics》 被引量: 0发表: 2017年 Mucoadhesive Vaginal Drug Delivery Systems To prolong the residence time in the vaginal cavity, bioadhesive therapeutic systems have been developed in the form of semi-solid and solid dosage forms. The most commonly used mucoadhesive...
M Gasˇperlin et al /International Journal of Pharmaceutics 196(2000)37–508 backbone allows all alkyl and glycol substituted groups to be presented at their best (De Smedt et al., 1996). Most semisolid emulsion systems, represented by a large number of pharmaceutical preparations like ointments...
T. M.: „Physical - chemical characterization of semisolid topical dosage from using a new dissolution system.: International Journal of Pharmaceutics1992. 86. 9-15.van Amerongen, I. A.; De Ronde, H. A. G.; Klooster, N. T. M. Physical-chemical characterization of semisolid topical ...
(1995). Release of acyclovir from semi-solid dosage forms; a semi-automated procedure using a simple plexiglass flow-through cell. International Journal of Pharmaceutics, 125, 215-222.Chattaraj, S.C.; Kanfer, I. Release of acyclovir from semisolid dosage forms: a semi-automated procedure ...
FIELD: medicine, pharmaceutics.;SUBSTANCE: composition for medical use contains a solid or semisolid matrix, at least one active ingredient uniformly dispersed therein. The matrix contains at least one pharmaceutically acceptable matrix-forming agent and compound 1,3-bis(lactamyl)butane, especially 1,...