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235 Pages·2016·3.97 MB·English
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Saurabh Bhatia Natural Polymer Drug Delivery Systems Nanoparticles, Plants, and Algae Natural Polymer Drug Delivery Systems Saurabh Bhatia Natural Polymer Drug Delivery Systems Nanoparticles, Plants, and Algae Saurabh Bhatia Assistant Professor School of Medical and Allied Sciences GD Goenka University Gurgaon , India ISBN 978-3-319-41128-6 ISBN 978-3-319-41129-3 (eBook) DOI 10.1007/978-3-319-41129-3 Library of Congress Control Number: 2016944154 © Springer International Publishing Switzerland 2016 T his work is subject to copyright. All rights are reserved by the Publisher, whether the whole or part of the material is concerned, specifi cally the rights of translation, reprinting, reuse of illustrations, recitation, broadcasting, reproduction on microfi lms or in any other physical way, and transmission or information storage and retrieval, electronic adaptation, computer software, or by similar or dissimilar methodology now known or hereafter developed. T he use of general descriptive names, registered names, trademarks, service marks, etc. in this publication does not imply, even in the absence of a specifi c statement, that such names are exempt from the relevant protective laws and regulations and therefore free for general use. T he publisher, the authors and the editors are safe to assume that the advice and information in this book are believed to be true and accurate at the date of publication. Neither the publisher nor the authors or the editors give a warranty, express or implied, with respect to the material contained herein or for any errors or omissions that may have been made. Printed on acid-free paper This Springer imprint is published by Springer Nature The registered company is Springer International Publishing AG Switzerland Author Bio Saurabh Bhatia, is currently working as an Assistant Professor at the School of Medical and Allied sciences, GD Goenka University, Gurgaon, Haryana, India. He has several years of academic experience, teaching such specialized subjects as Natural product science, nanotechnology, biotechnology, parasitology, polymeric sciences, biomaterials. He has promoted several marine algae and their derived polymers throughout India. He has written more than 30 international publications in these areas and has been an active participant of more than 35 national and inter- national conferences. So far he has successfully fi nished nine books in pharma and its allied sciences. His published books include Modern Applications of Plant Biotechnology in Pharmaceutical Sciences , Academic press, Elsevier, 2015; Nanotechnology in Drug Delivery: Fundamentals, Design, and Applications , Apple Academic Press 2016; Leishmaniasis: Biology, Control and New Approaches for Its Treatment , Apple Academic Press 2016; Natural polymer drug delivery systems: Nanoparticles, plants and algae, Springer, 2016, N atural polymer drug delivery systems: Nanoparticles, Mammals and microbes , Springer, 2016. Dr. Bhatia has graduated from Kurushetra University followed by M. Pharm from Bharati Vidyapeeth University, Pune, India. He has received his Ph.D. degree from Jadavpur University, Kolkata, India. v Contents 1 Nanotechnology and Its Drug Delivery Applications ............................. 1 1.1 Introduction ........................................................................................ 1 1.2 Historical Prospects of Nanotechnology ............................................ 2 1.3 Promising Role in Drug Delivery ...................................................... 3 1.3.1 Nanoparticles and Drug Delivery .......................................... 8 1.3.2 Use of NPs Formulation in Drug Delivery ............................ 9 1.3.3 Cellular and Intracellular Targets ........................................... 11 1.3.4 The Brain—The Ultimate Target for Drug Delivery.............. 12 1.4 Innovations in Nanotechnology ......................................................... 14 1.5 Nanotechnology Theory to Applications ........................................... 16 1.6 Nanomedicine/Nanoscience/Nano-Engineering and Relationship with Drug Delivery ................................................ 19 1.6.1 Nanomedicine and Drug Delivery ......................................... 19 1.6.2 Nanoengineering and Drug Delivery ..................................... 21 1.7 Types of Nanodelivery: Natural or Synthetic ..................................... 23 1.7.1 Synthetic Polymers ................................................................ 23 1.7.2 Natural Polymers ................................................................... 23 1.8 Natural and Synthetic Polymeric Nanoparticles ................................ 24 2 Nanoparticles Types, Classification, Characterization, Fabrication Methods and Drug Delivery Applications .......................... 33 2.1 Introduction ........................................................................................ 34 2.2 Classifi cation of Nanoparticles .......................................................... 40 2.3 Characterization of Nanoparticles ...................................................... 40 2.3.1 Particle Size ........................................................................... 40 2.3.2 Surface Charge ....................................................................... 43 2.3.3 Surface Hydrophobicity ......................................................... 44 2.3.4 Drug Release .......................................................................... 44 vii viii Contents 2.4 Preparation of Nanoparticles .............................................................. 44 2.4.1 Solvent Evaporation Method ............................................... 45 2.4.2 Spontaneous Emulsifi cation or Solvent Diffusion Method ................................................................................. 46 2.4.3 Double Emulsion and Evaporation Method ........................ 46 2.4.4 Salting Out Method ............................................................. 46 2.4.5 Emulsions-Diffusion Method .............................................. 47 2.4.6 Solvent Displacement/Precipitation Method ....................... 48 2.4.7 Coacervation or Ionic Gelation Method .............................. 48 2.4.8 Polymerization Method ....................................................... 49 2.4.9 Production of Nanoparticles Using Supercritical Fluid Technology ................................................................. 49 2.5 Most Favorable Requirements for Designing Therapeutic Nanoparticles ..................................................................................... 50 2.6 Types of Pharmaceutical Nanosystems .............................................. 51 2.6.1 Carbon Based Structures ..................................................... 51 2.6.2 Fullerenes ............................................................................ 53 2.6.3 Quantum Dots ...................................................................... 54 2.6.4 Nanoshells ........................................................................... 56 2.6.5 Nanobubbles ........................................................................ 57 2.6.6 Paramagnetic Nanoparticles ................................................ 58 2.6.7 Nanosomes .......................................................................... 59 2.6.8 Pharmacyte .......................................................................... 59 2.6.9 Dendrimers .......................................................................... 60 2.6.10 Nanopores ............................................................................ 64 2.6.11 Microbivores ........................................................................ 64 2.6.12 Nanocrystals and Nanosuspension ...................................... 65 2.6.13 Solid Lipid Nanoparticles .................................................... 65 2.6.14 Silicon-Based Structures ..................................................... 66 2.6.15 Metallic Nanoparticles ......................................................... 67 2.6.16 Liposomes ............................................................................ 67 2.6.17 Polymeric Micelles .............................................................. 68 2.6.18 Polymer Drug Conjugate ..................................................... 69 2.6.19 Polyplexes/Lipopolyplexes .................................................. 69 2.6.20 Respirocytes......................................................................... 69 2.6.21 Polymeric Nanoparticles ..................................................... 70 2.6.22 Applications of Nanoparticulate Delivery Systems ............. 72 2.6.23 Passive Targeting ................................................................. 73 2.6.24 Active Targeting ................................................................... 73 2.6.25 Tumor Targeting Using Nanoparticulate Delivery Systems ................................................................. 75 2.6.26 Long-Circulating and Target-Specifi c Nanoparticles .......... 76 2.6.27 Nanoparticles for Oral Delivery of Peptides and Proteins ......................................................................... 78 2.6.28 Nanoparticles for Gene Delivery ......................................... 79 Contents ix 2.6.29 Nanoparticles for Drug Delivery into the Brain .................. 80 2.6.30 Anthrax Vaccine Uses Nanoparticles to Produce Immunity ........................................................... 81 2.6.31 Stem Cell Therapy ............................................................... 81 2.6.32 Gold Nanoparticles Detect Cancer ...................................... 82 2.7 Hazards and Toxicity Profi le of Nanoparticles .................................. 84 2.7.1 Health Implication of Nanoparticles ................................... 84 3 Natural Polymers vs Synthetic Polymer ................................................. 95 3.1 Bioengineered Materials: Nano-Engines of Drug Delivery Systems .................................................................. 95 3.2 Polymeric Nanoparticles .................................................................... 96 3.3 Contemporary Methodologies for Fabrication of Polymeric Nanoparticles ................................................................ 97 3.4 Activation-Modulated Drug Delivery: Environmental Activation/Stimuli Responsive Smart Delivery System..................... 98 3.5 Time to Move on Innovative Methods of Administration .................. 100 3.6 History of Drug Delivery from the Ancient to Date .......................... 102 3.6.1 Historical Role of Polymers as Plastics ............................... 105 3.7 Shift from Nature to Synthetic (Including the Merits and Demerits of Synthetic Polymers) ................................................ 106 3.7.1 Natural Polymers and Synthetic Polymers for Scaffolds .... 109 3.7.2 Natural vs Synthetic Polymer (as Biomaterial) ................... 110 3.7.3 Natural vs Synthetic Polymer in Tissue Engineering .......... 112 3.7.4 Natural vs Synthetic Polymer Hydrogels ............................ 113 3.8 Natural Polymers (Reasons for Reverting to Nature) ........................ 114 3.8.1 Need of Natural Polymers ................................................... 115 3.8.2 Disadvantages of Herbal Polymers ...................................... 116 4 Plant Derived Polymers, Properties, Modification & Applications ...... 119 4.1 Introduction ........................................................................................ 119 4.2 Sources of Plant Polymers ................................................................. 121 4.3 Methods of Extractions ...................................................................... 124 4.3.1 Cold Extraction .................................................................... 124 4.3.2 Hot Extraction [Mild Acidic (EHA), Alkaline (EHB) and Radical Hydrolysis (EHR)] ........................................... 125 4.3.3 Radical Hydrolysis (EHR) ................................................... 125 4.3.4 Microwave Assisted Extraction (EM) .................................. 125 4.3.5 Ultrasonic Extraction (EU) .................................................. 126 4.3.6 Enzymatic Hydrolysis (EE) ................................................. 126 4.4 Chemical Composition Analysis ........................................................ 126 4.5 Physical Properties ............................................................................. 126 4.5.1 Determination of Gelling Strength (GS) ............................. 126 4.5.2 Determination of Gelling Temperature (GT) and Melting Temperature (MT) ........................................... 126 4.5.3 Viscosity Measurement (VS) ................................................. 127 4.5.4 Molecular Mass Determination (MM) ................................... 127

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