logging in or signing up TB : IMA: NCP Abhi2master Download Post to : URL : Related Presentations : Share Add to Flag Embed Email Send to Blogs and Networks Add to Channel Uploaded from authorPOINT lite Insert YouTube videos in PowerPont slides with aS Desktop Copy embed code: (To copy code, click on the text box) Embed: URL: Thumbnail: WordPress Embed Customize Embed The presentation is successfully added In Your Favorites. Views: 43 Category: Education License: All Rights Reserved Like it (0) Dislike it (0) Added: March 03, 2011 This Presentation is Public Favorites: 0 Presentation Description No description available. Comments Posting comment... Premium member Presentation Transcript Slide 1: WEL – COME To Seminar on AntiTubercular Drugs ANTI TUBERCULAR DRUGS : ANTI TUBERCULAR DRUGS Presented by : Abhijith.P 1st yr M Pharm Pharmaceutical Analysis Under the Guidance of B.Gopinath, Pharmaceutical Analysis ANTI TUBERCULAR DRUGS : ANTI TUBERCULAR DRUGS CYCLOSERINE : CYCLOSERINE Chemical name : 4-Amino-3-Isoxazolidone Chemical formula : C3H6N2O2 Chemical structure : Mol. Wt. : 102.09 Physical properties : Physical properties It is a White to slightly Yellow , Odourless Crystalline powder. It is Insoluble in common organic solvents, but readily Soluble in Water. It’s Melting point range’s b/w 1540C - 1560C Analytical Methods : Analytical Methods Spectrophotometry. Colorimetry Paper Chromatography. Thin Layer Chromatography SPECTROPHOTOMETRIC METHOD : SPECTROPHOTOMETRIC METHOD Cycloserine has been determined by a Spectrophotometric method based on the complex formation with chloranil. The method involves addition of cycloserine solution to chloranil reagent in borate buffer of pH 9; and heating at 65°C for 45 min. The complex formed exhibits absorption maximum of 348 nm COLORIMETRY : COLORIMETRY This method is mainly used for determination of Cycloserine in Biological fluids such as Blood ,Urine & CSF . Cycloserine reacts with Sodium-nitropentacyano- ferrate in a slightly acidic aqueous soln to give an intense Blue colour complex which is quantitatively measured at 625nm PAPER CHROMATOGRAPHY : PAPER CHROMATOGRAPHY THIN LAYER CHROMATOGRAPHY : THIN LAYER CHROMATOGRAPHY Detecting Agent : Ninhydrin spray reagent ETHAMBUTOL HYDROCHLORIDE : ETHAMBUTOL HYDROCHLORIDE Chemical name : N, N1-di-isopropyl - -ethylenediamine Chemical formula : C10H24O2N2 (2HCl) Chemical structure : .2HCl Mol. Wt. : 277.5 Physical properties : Physical properties It is a White, Odourless, Bitter Tasting, Thermostable -Crystalline Powder. It is Soluble in Water & Ethanol. Analytical Methods : Analytical Methods 1. Colorimetry 2. Non-Aqueous Titration COLORIMETRIC METHOD : COLORIMETRIC METHOD Take the sample solution Add bromothymol blue Complex will form Give yellow color Determined at 520 nm NON AQUEOUS TITRATION : NON AQUEOUS TITRATION Take the sample dissolve CH3COOH Mercuric acetate add Crystal violate Titrate with 0.1M HClO4 add RIFAMPIN : RIFAMPIN Chemical name : 2,7-(epoxypentadeca [1,11,13] trienimino)naphtho [2,1-b]furan-1,11(2H)-dione 5,6,9,17,19,21-hexahydroxy-23-methoxy-2,4,12,16,18,20,22-heptamethyl-8-[N-(4-methyl-1-perazinyl)formimidoyl]-21-acetate. Chemical Structure : Chemical formula : C43H58N4O12 Mol. Wt. : 822.95 Physical properties : Physical properties It is a Red-Orange, Odourless Crystalline Powder. It’s Melting point range’s b/w 1830C - 1880C Analytical Methods : Analytical Methods 1. Paper Chromatography 2. Thin Layer Chromatography 3. Column Chromatography 4. Fluorometric Method 5. UV-Spectroscopy PAPER CHROMATOGRAPHY : PAPER CHROMATOGRAPHY Here …….Descending- Paper-Chromatography is Carried out. Stationary Phase : Whatmann-3mm-Filter Paper. Mobile Phase : Methanol : n-Octanol (4:1) (PH : 6). Detection : The intensity of Red-Orange spots was measured by an Analytrol Photodensiotometer (Mod : R13-450nm filter) THIN LAYER CHROMATOGRAPHY : THIN LAYER CHROMATOGRAPHY TLC is mainly developed for the analysis of Rifampin & it’s Metabolites in Body fluids. The colour spot was eluted & measured Spectrophotometrically. COLUMN CHROMATOGRAPHY : COLUMN CHROMATOGRAPHY This method is mainly used for Determination of Rifampin & it’s Metabolites in Urine, Bile & Serum by extraction with Chloroform & by Column chromatography followed by Spectrophotometry. The Lq-Solid Chromatography was carried out using a Glass Column of 7cm(4mm.i.d)long. The Column is packed with Silica gel-G, buffered at PH=6 & Chloroform Conti……. : Conti……. Chloroform-Methanol is used as Solvent, which is used in Progressively in increasing amount.(i.e..5%, 10% and 16.6%) Flow rate : 0.15min/ml. Rifampin & it’s Metabolites were than quantitated by reading the absorbance of the elutes at 475nm. FLUOROMETRY : FLUOROMETRY Rifampin was determined Fluorometrically by transforming it with Hydrogen peroxide into a Fluorescent product The maximum fluorescence develop in an Aq.Carbonate-bicarbonate buffer at PH=9.2 at 480nm The excitation wave length is 370nm. The Fluorescence intensity is linear in the conc. range from 0.1-10mcg. REFERENCES : REFERENCES Text Book of Pharmacology by Triphati Analytical Profiles of Drug Substances by Klaus Florey Text Book of Pharmaceutical Analysis by Higuchi Internet Source Slide 25: THANK YOU You do not have the permission to view this presentation. In order to view it, please contact the author of the presentation.
TB : IMA: NCP Abhi2master Download Post to : URL : Related Presentations : Share Add to Flag Embed Email Send to Blogs and Networks Add to Channel Uploaded from authorPOINT lite Insert YouTube videos in PowerPont slides with aS Desktop Copy embed code: (To copy code, click on the text box) Embed: URL: Thumbnail: WordPress Embed Customize Embed The presentation is successfully added In Your Favorites. Views: 43 Category: Education License: All Rights Reserved Like it (0) Dislike it (0) Added: March 03, 2011 This Presentation is Public Favorites: 0 Presentation Description No description available. Comments Posting comment... Premium member Presentation Transcript Slide 1: WEL – COME To Seminar on AntiTubercular Drugs ANTI TUBERCULAR DRUGS : ANTI TUBERCULAR DRUGS Presented by : Abhijith.P 1st yr M Pharm Pharmaceutical Analysis Under the Guidance of B.Gopinath, Pharmaceutical Analysis ANTI TUBERCULAR DRUGS : ANTI TUBERCULAR DRUGS CYCLOSERINE : CYCLOSERINE Chemical name : 4-Amino-3-Isoxazolidone Chemical formula : C3H6N2O2 Chemical structure : Mol. Wt. : 102.09 Physical properties : Physical properties It is a White to slightly Yellow , Odourless Crystalline powder. It is Insoluble in common organic solvents, but readily Soluble in Water. It’s Melting point range’s b/w 1540C - 1560C Analytical Methods : Analytical Methods Spectrophotometry. Colorimetry Paper Chromatography. Thin Layer Chromatography SPECTROPHOTOMETRIC METHOD : SPECTROPHOTOMETRIC METHOD Cycloserine has been determined by a Spectrophotometric method based on the complex formation with chloranil. The method involves addition of cycloserine solution to chloranil reagent in borate buffer of pH 9; and heating at 65°C for 45 min. The complex formed exhibits absorption maximum of 348 nm COLORIMETRY : COLORIMETRY This method is mainly used for determination of Cycloserine in Biological fluids such as Blood ,Urine & CSF . Cycloserine reacts with Sodium-nitropentacyano- ferrate in a slightly acidic aqueous soln to give an intense Blue colour complex which is quantitatively measured at 625nm PAPER CHROMATOGRAPHY : PAPER CHROMATOGRAPHY THIN LAYER CHROMATOGRAPHY : THIN LAYER CHROMATOGRAPHY Detecting Agent : Ninhydrin spray reagent ETHAMBUTOL HYDROCHLORIDE : ETHAMBUTOL HYDROCHLORIDE Chemical name : N, N1-di-isopropyl - -ethylenediamine Chemical formula : C10H24O2N2 (2HCl) Chemical structure : .2HCl Mol. Wt. : 277.5 Physical properties : Physical properties It is a White, Odourless, Bitter Tasting, Thermostable -Crystalline Powder. It is Soluble in Water & Ethanol. Analytical Methods : Analytical Methods 1. Colorimetry 2. Non-Aqueous Titration COLORIMETRIC METHOD : COLORIMETRIC METHOD Take the sample solution Add bromothymol blue Complex will form Give yellow color Determined at 520 nm NON AQUEOUS TITRATION : NON AQUEOUS TITRATION Take the sample dissolve CH3COOH Mercuric acetate add Crystal violate Titrate with 0.1M HClO4 add RIFAMPIN : RIFAMPIN Chemical name : 2,7-(epoxypentadeca [1,11,13] trienimino)naphtho [2,1-b]furan-1,11(2H)-dione 5,6,9,17,19,21-hexahydroxy-23-methoxy-2,4,12,16,18,20,22-heptamethyl-8-[N-(4-methyl-1-perazinyl)formimidoyl]-21-acetate. Chemical Structure : Chemical formula : C43H58N4O12 Mol. Wt. : 822.95 Physical properties : Physical properties It is a Red-Orange, Odourless Crystalline Powder. It’s Melting point range’s b/w 1830C - 1880C Analytical Methods : Analytical Methods 1. Paper Chromatography 2. Thin Layer Chromatography 3. Column Chromatography 4. Fluorometric Method 5. UV-Spectroscopy PAPER CHROMATOGRAPHY : PAPER CHROMATOGRAPHY Here …….Descending- Paper-Chromatography is Carried out. Stationary Phase : Whatmann-3mm-Filter Paper. Mobile Phase : Methanol : n-Octanol (4:1) (PH : 6). Detection : The intensity of Red-Orange spots was measured by an Analytrol Photodensiotometer (Mod : R13-450nm filter) THIN LAYER CHROMATOGRAPHY : THIN LAYER CHROMATOGRAPHY TLC is mainly developed for the analysis of Rifampin & it’s Metabolites in Body fluids. The colour spot was eluted & measured Spectrophotometrically. COLUMN CHROMATOGRAPHY : COLUMN CHROMATOGRAPHY This method is mainly used for Determination of Rifampin & it’s Metabolites in Urine, Bile & Serum by extraction with Chloroform & by Column chromatography followed by Spectrophotometry. The Lq-Solid Chromatography was carried out using a Glass Column of 7cm(4mm.i.d)long. The Column is packed with Silica gel-G, buffered at PH=6 & Chloroform Conti……. : Conti……. Chloroform-Methanol is used as Solvent, which is used in Progressively in increasing amount.(i.e..5%, 10% and 16.6%) Flow rate : 0.15min/ml. Rifampin & it’s Metabolites were than quantitated by reading the absorbance of the elutes at 475nm. FLUOROMETRY : FLUOROMETRY Rifampin was determined Fluorometrically by transforming it with Hydrogen peroxide into a Fluorescent product The maximum fluorescence develop in an Aq.Carbonate-bicarbonate buffer at PH=9.2 at 480nm The excitation wave length is 370nm. The Fluorescence intensity is linear in the conc. range from 0.1-10mcg. REFERENCES : REFERENCES Text Book of Pharmacology by Triphati Analytical Profiles of Drug Substances by Klaus Florey Text Book of Pharmaceutical Analysis by Higuchi Internet Source Slide 25: THANK YOU