Global ETD Search
Search theses and dissertations gathered from participating repositories worldwide. Every result links back to the library that holds it. No account is needed.
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Showing 1 to 12 of 12 for “"Flurbiprofen"”.
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Factors affecting the disposition of the enantiomers of arylpropionic acids: focus on flurbiprofen
This document only includes an excerpt of the corresponding thesis or dissertation. To request a digital scan of the full text, please contact the Ruth Lilly Medical Library's Interlibrary Loan Department (rlmlill@iu.edu).
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The efficacy of a local action transcutaneous flurbiprofen patch, in the treatment of lateral epicondylitis
Thesis (Masters in Technology: Chiropractic)-, Durban Institute of Technology, Durban, South Africa, 2002.
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Development and formulation of wax-based transdermal drug delivery systems
… determination of the solubility of ibuprofen, flurbiprofen and naproxen in the was using microscopy, Higuchi release kinetics, HyperDSC and mathematical modelling techniques. Correlations between the results obtained via these techniques were noted with additional merits such as provision of …
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Drug-cyclodextrin complexes: an approach to enhance the solubility and dissolution properties of poorly soluble drugs
… olanzapine and methyl-β-cyclodextrin; flurbiprofen and methyl-β-cyclodextrin) in order to enhance the apparent solubility and dissolution properties of drugs. Specifically, the effectiveness of supercritical carbon dioxide processing for the preparation of solid drug-cyclodextrin …
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Improving the solubility and dissolution of poorly soluble drugs by salt formation and the consequent effect on mechanical properties
… carboxylic acid drugs were selected, which were flurbiprofen, etodolac, ibuprofen and gemfibrozil. The drugs were chosen because they are weak acids with poor aqueous solubility and should readily form salts. The counterions used for salt formation were: butylamine, pentylamine, hexylamine, …
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Solubility enhancement of poorly water soluble drugs using liposome technology
… of a range of insoluble drugs including flurbiprofen, indomethacin, sulindac, mefenamic acid, lignocaine and progesterone to investigate the influence of drugs properties and functional group on liposomal loading. The results show that no defined trend could be obtained linking the drug …
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BIORELEVANT RELEASE TESTING OF LONG-ACTING INJECTABLES INTENDED FOR PARENTERAL ADMINISTRATION
… microspheres loaded with naltrexone or flurbiprofen were used as model delivery systems to investigate the impact of interstitial fluid and extracellular matrix components on release behavior under different hydrodynamic conditions. Biorelevant media were developed based on an extensive …
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Regulation of Endogenous Excitatory Neurotransmitters by Isoprostanes
… 8-isoPGE2, eyeballs were pretreated with either flurbiprofen, a nonselective COX inhibitor; NS-398, a selective COX-2 inhibitor or furegrelate, a thromboxane (Tx) synthase inhibitor. All the three enzyme inhibitors had no effect (p>0.05) on the inhibitory effects of 8-isoPGE2 (1μM-100μM) on …
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Improved Estimation of Transport Parameters in the Dermis
… were made for Econazole, Methoxsalen, Flurbiprofen and ketoprofen with adjustments to the diffusivity of the stratum corneum. The revised computational model is able to make predictions for topically applied permeants, yet further work can be done to better improve the predictive …
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Processi di biorefining per l'estrazione di secondary chemical building blocks da sottoprotti dell'agro-industria
… anti-inflammatory drugs such as ibuprofen or flurbiprofen) and polymers (i.e. poly p-vinylphenol, a photosensitive polymer for electronic and optoelectronic applications). European agrifood waste represents a low cost abundant raw material (250 millions tons per year) which does not subtract …
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Effect of Hydrogen Sulfide Donors on Sympathetic Neurotransmission and Intraocular Pressure of the Eye
… endogenous PG synthesis was blocked using flurbiprofen (FBF) which is a PG synthesis inhibitor.|To determine the mechanism of action of the drugs, antagonists were used. These included aminooxyacetic acid (AOA), a cystathionine-β-synthase (CBS) inhibitor and glibenclamide, a KATP channel …