logging in or signing up PARENTERAL CONTROLLED RELEASE DRUG DELIVERY SYSTEM vnskvarma 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: Embed: Flash iPad Copy Does not support media & animations WordPress Embed Customize Embed URL: Copy Thumbnail: Copy The presentation is successfully added In Your Favorites. Views: 670 Category: Entertainment License: All Rights Reserved Like it (0) Dislike it (0) Added: March 06, 2012 This Presentation is Public Favorites: 1 Presentation Description No description available. Comments Posting comment... Premium member Presentation Transcript Approaches for parenteral controlled drug administration: Approaches for parenteral controlled drug administration Facilitator: DR.HEMANT K S YADAV, Department of Pharmaceutics, JSSCP, Mysore Presented by: N.SANKEERTH KUMAR, Pharmaceutics, JSSCP Mysore 3/6/2012 1Approaches for parenteral controlled drug administration:: Approaches for parenteral controlled drug administration: Several pharmaceutical formulation approaches may be applied to the development of parental controlled release or sustained release formulations. The most commonly used techniques are as follows: Use of viscous, water miscible vehicles such as an aqueous solution of gelatin or poly vinyl pyrrolidine . Formation of thixotropic suspensions. 3/6/2012 2PowerPoint Presentation: Use of water immiscible vehicles such as vegetable oil or water repelling agent such as aluminium mono stearate. Preparation of water insoluble drug derivatives such as salts, complexes and esters. Dispersion in polymeric micro spheres or microcapsules such as lactide glycolide homopolymer or copolymers. Co-administration of vaso constrictors. 3/6/2012 3Depot formulation may be classified on the basis of the process used for controlled drug release as follows: : Depot formulation may be classified on the basis of the process used for controlled drug release as follows: DISSOLUTION CONTROLLED DEPOT FORMULATION : Rate of drug absorption is controlled by the slow dissolution of drug in the formulation or in the tissue fluid surrounding the formulation. 3/6/2012 4PowerPoint Presentation: Two approaches to control dissolution a) Formation of salt or complexes with low aqueous solubility: E.g. Aqueous suspensions of benzathine penicillin G from water soluble alkali salts of acidic pencillin G. b) Suspension of macrocrystals : large crystals are known to dissolve more slowly than small crystals. It is called ‘the macro crystal principle’ and can be applied to control the rate of drug dissolution. Eg : aqueous suspension of testosterone isobutyrate for I.M injection Exception : Penicillin G procaine suspension in gelled peanut oil for I.M. injection . 3/6/2012 5PowerPoint Presentation: The major drawback of these two types of injectables depot formulations is that the release of drug molecules is not of zero order kinetics as expected from the theoretical model defined in the equation. Reasons: surface area of the drug solids diminishes with time because of increased drug release saturation solubility of the drug in the medium cannot be maintained easily because of rapid absorption. 3/6/2012 6PowerPoint Presentation: 2) ADSORPTION TYPE DEPOT FORMULATION: This type of depot preparation is formed by the binding of drug molecule to adsorbents. I n this only the unbound, free species of the drug is available for adsorption. A s soon as the unbound drug molecule are absorbed, a fraction of the bound drug molecule is released to maintain equilibrium. E.g. vaccine preparations. 3/6/2012 7PowerPoint Presentation: 3)ENCAPSULATION TYPE DEPOT FORMULATIONS: This type of depot formulation is prepared by encapsulating drug solids within a permeation barrier or dispersing drug particles in a diffusion matrix. Both of these are made from either bio-degradable or bio-absorbable polymers. Release of drug is controlled by rate of penetration across the diffusion barrier rate of biodegradation of the barrier macro molecules. Eg : naltrexone pamoate releasing biodegradable micro capsules 3/6/2012 8PowerPoint Presentation: 4)ESTERFICATION TYPE DEPOT FORMULATION : This depot preparation is produced by synthesizing the bio-erodible esters of a drug and then making up an injectable formulation. This formulation forms a drug reservoir at the site of injection. Rate of absorption is controlled by interfacial partitioning of drug esters from reservoir to tissue fluid . Rate of bioconversion of drug esters to regenerate active drug molecules. Eg : fluphenazine enanthate , testosterone 17 cypionate in oleaginous solution. 3/6/2012 9References:: References: Novel Drug Delivery Systems by Yie.W . Chien,2 nd edition, Pg. no : 381 to 385. Google search 3/6/2012 10PowerPoint Presentation: 3/6/2012 11 You do not have the permission to view this presentation. In order to view it, please contact the author of the presentation.