Cover image for Update on Polymers for Ocular Drug Delivery.
Update on Polymers for Ocular Drug Delivery.
Title:
Update on Polymers for Ocular Drug Delivery.
Author:
Mundada, Atish S.
ISBN:
9781847355645
Personal Author:
Edition:
1st ed.
Physical Description:
1 online resource (210 pages)
Contents:
9781847355645 _Front Cover.pdf -- 9781847355645 _Content.pdf -- Update on Polymers for Ocular Drug Delivery -- Dedication and Acknowledgements -- Contents -- Preface -- 1 Introduction: Overview of Ocular Drug Delivery -- 1.1 Drug Delivery and Polymer Science -- 1.2 Ocular Drug Delivery -- 1.2.1 Anatomy and Physiology of the Eye -- 1.2.2 Pharmacokinetics of Drugs Delivered through the Ocular Route -- References -- 2 Conventional Ocular Drug Delivery -- 2.1 Introduction -- 2.2 Eye Drops -- 2.2.1 Aqueous Solutions -- 2.2.2 Ophthalmic Suspensions -- 2.3 Semisolids -- 2.4 Summary and Conclusion -- References -- 3 Hydrogels and Viscosity Modifiers -- 3.1 Introduction -- 3.2 Hydrogels -- 3.2.1 Sodium Hyaluronate -- 3.2.2 Cellulose Derivatives -- 3.2.3 Polyvinyl Alcohol -- 3.2.4 Carbomers -- 3.2.5 Miscellaneous Polymers -- 3.3 Viscosity Enhancing Agents -- 3.3.1 Cellulose Derivatives -- 3.3.2 Acrylates -- 3.3.3 Hyaluronic Acid -- 3.3.4 Chitosan -- 3.3.5 Thiomers -- 3.3.6 Others -- 3.4 Summary and Conclusion -- References -- 4 Ocular Inserts -- 4.1 Introduction -- 4.2 Ocular Inserts as Drug Delivery Systems -- 4.2.1 Soluble Ocular Drug Inserts -- 4.2.1.1 Inserts Based on Natural Polymers -- 4.2.1.2 Inserts Based on Synthetic and Semisynthetic Polymers -- 4.2.1.3 Inserts Utilising Particular Approaches -- 4.2.1.3.1 The Mucoadhesive Approach -- 4.2.1.3.2 The Prodrug Approach -- 4.2.1.3.3 The Drug Carrier Approach -- 4.2.2 Insoluble Ocular Drug Inserts -- 4.2.2.1 Diffusional Inserts -- 4.2.2.2 Osmotic Inserts -- 4.2.2.3 Contact Lenses -- 4.2.3 Bioerodible Inserts -- 4.3 Summary and Conclusion -- References -- 5 Particulate Drug Delivery -- 5.1 Introduction -- 5.2 Nanoparticles and Polymers used in their Preparation -- 5.2.1 Acrylates -- 5.2.1.1 Polyalkylcyanoacrylate -- 5.2.1.2 Acrylate Derivatives -- 5.2.2 Polyester-based Nanoparticles.

5.2.2.1 Poly-ε-caprolactone -- 5.2.2.2 Poly(D,L-lactic acid) and Poly(D,L-lactide-co-glycolide) -- 5.2.3 Natural Polymer Based Nanoparticles -- 5.2.3.1 Protein Nanoparticles -- 5.2.3.2 Polysaccharide Based Nanoparticles -- 5.2.3.3 Lipid Based Nanoparticles -- 5.2.4 Polymeric Coating to Nanoparticles -- 5.3 Microparticles and Polymers used in their Preparation -- 5.3.1 Ocular Delivery of Drug Loaded Microparticulates -- 5.3.2 Polymers used in the Preparation of Microparticulates -- 5.3.2.1 Acrylates -- 5.3.2.2 Poly(D,L-lactic acid) and Poly (D,L-lactide-co-glycolide) -- 5.3.2.3 Natural Polymers -- 5.3.2.4 Lipids -- 5.4 Summary and Conclusion -- 5.2.4.1 Polysaccharide Coating -- 5.2.4.2 Polyacrylic Coating -- 5.2.4.3 Polyethylene Glycol Coating -- References -- 6 In Situ Gelling Polymers in Ocular Drug Delivery -- 6.1 Introduction -- 6.2 In Situ Gelling Hydrogels -- 6.2.1 Temperature-induced In Situ Gelling Polymeric Carriers -- 6.2.1.1 Poloxamers (Pluronic) and their Analogues -- 6.2.1.2 Xyloglucan -- 6.2.1.3 Cellulose Derivatives -- 6.2.2 pH-induced In Situ Gelling Polymeric Carriers -- 6.2.2.1 Carbomers -- 6.2.2.2 Pseudolatexes -- 6.2.3 Osmotically Induced In Situ Gelling Polymeric Carriers -- 6.2.3.1 Gellan Gum (Gelrite) -- 6.2.3.2 Alginates -- 6.2.4 Dual Mechanism based In Situ Gelling Polymeric Carriers -- 6.2.4.1 Carrageenans and Chitosan -- 6.3 Summary and Conclusion -- References -- 7 Intraocular Implants -- 7.1 Introduction -- 7.2 Polymers used for Intraocular Drug Delivery Implants -- 7.2.1 Nonbiodegradable Solid Implants -- 7.2.1.1 Polyvinyl Alcohol - Ethylene Vinyl Acetate -- 7.2.1.2 Polysulfone Capillary Fibre -- 7.2.2 Biodegradable Solid Implants -- 7.2.2.1 Polylactic Acid, Polyglycolic Acid and Poly(D,L-lactide-co-glycolide) -- 7.2.2.2 Polycaprolactones -- 7.2.2.3 Polyanhydrides -- 7.2.3 Viscous and Injectable Polymers.

7.2.3.1 Polyorthoesters -- 7.3 Summary and Conclusion -- 7.4 Future Directions for Ophthalmic Research -- References -- Abbreviations -- Index -- 9781847355645 _Back Cover.pdf.
Abstract:
The eye is the most easily accessible site for topical administration of a medication. Drugs are commonly applied to the eye for localised action on the surface or in the interior of the eye. A major problem in ocular therapeutics is the attainment of an optimal drug concentration at the site of action. Poor bioavailability of drugs from ocular dosage forms is mainly due to the precorneal loss factors which include tear dynamics, non-productive absorption, transient residence time in the cul-de-sac, and the relative impermeability of the corneal epithelial membrane. Due to these physiological and anatomical constraints only a small fraction of the drug, effectively 1% or even less of the instilled dose is ocularly absorbed. The effective dose of medication administered ophthalmically may be altered by increasing the retention time of medication in contact with the surface of the eye. To date, Pharmaceutical Technologists have tried to develop different novel formulations like gel, ocular inserts, collagen shields, implants, liposomes, nanoparticles, penetration enhancers and in-situ gelling systems, in order to increase the bioavailability and duration of the therapeutic action of ocular drugs and polymers plays an important role in all these approaches. This book provides detailed information regarding all such polymers which have been used and shown to be excellent in improving the bioavailability of ocular drugs.
Local Note:
Electronic reproduction. Ann Arbor, Michigan : ProQuest Ebook Central, 2017. Available via World Wide Web. Access may be limited to ProQuest Ebook Central affiliated libraries.
Electronic Access:
Click to View
Holds: Copies: