Yayın tarihi için Farmasötik Teknoloji Anabilim Dalı listeleme
Toplam kayıt 89, listelenen: 1-20
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Comparison of the metachromatic activity of various heparins using azure dyes
(1989)[No abstract available] -
Comparison of the bioavailability of oral and rectal forms of diphenylhydantoin sodium
(Informa Healthcare, 1990)The bioavailabilities of single 100-mg oral and rectal doses of diphenylhydantoin sodium were studied in five healthy volunteers. The rectal form used was prepared at laboratory conditions and the oral form was a commercial ... -
Studies on the fractionation of heparins and the metachromatic and biologic activity determinations on the fractions
(1990)[No abstract available] -
A polarographic study on dipyridamole and its determination in commercial tablets
(1991)The direct current polarographic behaviour of dipyridamole, a coronary vasodilator, in the supporting electrolyte consisting of 0.2 M KC1, 20 % (v/v) ethanol and buffer solutions is described in this study. Morphologically ... -
A Polarographic Study on Dipyridamole and Its Determination in Commercial Tablets
(Marcel Dekker Inc, 1991)The direct current polarographic behaviour of dipyridamole, a coronary vasodilator, in the supporting electrolyte consisting of 0.2 M KCl, 20% (v/v) ethanol and buffer solutions is described in this study. Morphologically ... -
Multiple emulsions
(1993)The purpose of this review is to update the information on multiple emulsions known to be promising delivery systems for both pharmaceuticals and cosmetic materials. The possibility of encapsulating active substances within ... -
Studies on trifluorothymidine ophthalmic formulations and their stability
(1994)[No abstract available] -
Bioavailability of Verapamil Hydrochloride From Nasal Delivery Systems
(Editions De Sante, 1994)… -
Improvement in the dissolution properties of theophylline with ß-cyclodextrin
(1994)An improvement in the dissolution of theophylline with ß-cyclodextrin was achieved by subjecting them to co-grinding and freeze-drying methods. The products obtained were examined by the phase solubility methad, differential ... -
Rapid analysis of verapamil in plasma by reversed phase HPLC
(1995)A modified and simple HPLC procedure has been developed for verapamil in plasma. Plasma samples have been vortex-mixed and centrifuged without any need of extraction. The analysis has been performed on a C20 reversed-phase ... -
Film-coated enteric tablet formulation of ketorolac tromethamine
(Informa Healthcare, 1997)A great majority of polymers used for pharmaceutical film-coating purposes have been derivatives of cellulose or methacrylate copolymers (Eudragit series) in most recent studies. The type and frequency of the ester ... -
Microencapsulation of ketorolac tromethamine by means of a coacervation phase separation technique induced by the addition of non-solvent
(Taylor & Francis LTD, 1998)Ketorolac tromethamine (KT) is a non-steroidal drug with potent analgesic and anti-inflammatory activity and is absorbed rapidly (T-max (1.0h) with an efficiency >87% following oral and intramuscular administration. The ... -
Studies on vaginal bioadhesive tablets of acyclovir
(Govi-Verlag GMBH, 2000)Bioadhesive vaginal tablets were prepared using poly(acrylic acid) (PAA); Methylcellulose (MC), carboxymethyl cellulose (CMC), hydroxypropyl cellulose (HPC) and hydroxypropylmethyl cellulose (HPMC) as bioadhesive polymers ... -
Solid lipid non-particles (SLN) [Kati lipit nanopartiküller (SLN)]
(2000)Colloidal drug delivery systems are one of the subjects investigated intensively in the pharmaceutical field, in recent years. Those systems include microspheres, polymeric nanoparticles, liposomes and fat emulsions. An ... -
Sustained release wax matrix formulations of ketorolac tromethamine with Compritol 888 ATO and HD 5 ATO
(2000)Sustained release wax matrix tablets of ketorolac tromethamine (KT) were prepared with different concentrations of Compritol 888 ATO (Glyceryl behenate) and HD 5 ATO (Glyceryl and Polyethylene glycol behenate). Tablet ... -
Formulation and in vitro-in vivo evaluation of piribedil solid lipid micro- and nanoparticles
(Taylor & Francis LTD, 2001)Modification of the dissolution rate and, thus, the enhancement of the bioavailability of a dopaminergic drug, piribedil, which has a low aqueous solubility and short elimination half-life have been the aim in this study. ... -
Bioavailability file: Piribedil [Biyoyararlanim dosyasi: Piribedil]
(2001)Piribedil is a dopamin agonist with vasodilator activity and whose aqueous solubility is low and elimination half-life is short. It is widely used in cerebral ageing and in Parkinson's disease. Literature on physico-chemical ... -
Preparation and in vitro evaluation of pyridostigmine bromide microparticles
(Elsevier Science BV, 2002)Pyridostigmine bromide (PB) is an anticholinesterase agent whose aqueous solubility is high and which has a short elimination half-life. Its dosage rate in the treatment of myastenia gravis is frequent due to the short ... -
Investigation of certain varieties of carbopol in ketorolac tromethamine hydrophilic matrix tablet formulations and evaluation of the kinetics of its in vitro release
(Osterreichische Apotheker-Verlagsgesellschaft m.b.H., 2002)Matrix tablets of ketorolac tromethamine (KT) were prepared by direct compression technique and Carbopol 934, 940 and 1342 have been used as polymers in different concentrations (5-15%). For the quality control of tablets; ...
