'Mefenamic acid' diaporamas de présentation

A.I.R. Orientation For new staff

A.I.R. Orientation For new staff. Staff Dr. ??? Dr. ??? Dr. ??? (R5). Allergy, Immunology, Rheumatology. Study: Teaching: Morning meeting ( W3 and W5, 7:45 am at 6F MICU meeting room)

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CASE PRESENTATION ( Evidence-based medicine )

CASE PRESENTATION ( Evidence-based medicine ). General Data:. This is a case of M.T, 37 year-old female, married, Christian, right-handed, from Malate , Manila who came in due to stiffening and pain in the neck. History of Present Illness. Patient is a non-diabetic, non-hypertensive.

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Management of Abnormal Vaginal Bleeding

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Synthesis, spectral studies, hydrolysis kinetics and pharmacodynamic profile of mefenamic acid prodrugs

Prodrugs of mefenamic acid with natural compounds eugenol and vanillin have been synthesized by dicyclohexylcarbodimide coupling method. Purified synthesized ester prodrugs were characterized by Melting Point, Thin Layer Chromatography, Fourier Transform Infra Red Spectroscopy, Proton Nuclear Magnetic Resonance Spectroscopy and Mass Sspectroscopy. Prodrugs were also characterized by solubility studies, partition coefficient and hydrolytic studies. The synthesized derivatives are screened for their anti-inflammatory, analgesic and ulcerogenic study which show retention of anti-inflammatory activity with reduced ulcerogenicity.

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Synthesis, spectral studies, hydrolysis kinetics and pharmacodynamic profile of mefenamic acid prodrugs

Prodrugs of mefenamic acid with natural compounds eugenol and vanillin have been synthesized by dicyclohexylcarbodimide coupling method. Purified synthesized ester prodrugs were characterized by Melting Point, Thin Layer Chromatography, Fourier Transform Infra Red Spectroscopy, Proton Nuclear Magnetic Resonance Spectroscopy and Mass Sspectroscopy. Prodrugs were also characterized by solubility studies, partition coefficient and hydrolytic studies. The synthesized derivatives are screened for their anti-inflammatory, analgesic and ulcerogenic study which show retention of anti-inflammatory activity with reduced ulcerogenicity.

82 views • 7 slides