Emerging Nanotechnologies in Immunology : The Design, Applications and Toxicology of Nanopharmaceuticals and Nanovaccines /

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Bibliographic Details
Imprint:Amsterdam : Elsevier, 2018.
Description:1 online resource.
Language:English
Subject:
Format: E-Resource Book
URL for this record:http://pi.lib.uchicago.edu/1001/cat/bib/11655036
Hidden Bibliographic Details
Other authors / contributors:Shegokar, Ranjita, editor.
Souto, Eliana B., editor.
ISBN:9780323401135
0323401139
9780323400169
0323400167
Notes:Includes bibliographical references and index.
Online resource; title from PDF title page (EBSCO, viewed May 23, 2018).
Summary:Emerging Nanotechnologies in Immunology: The Design, Applications and Toxicology of Nanopharmaceuticals and Nanovaccines aims to deliver a systematic and comprehensive review of data concerning the nature of interaction and nano-related risks between the nanopharmaceuticals currently in the pipeline of S&T development for skin, ocular and nasal drug delivery, including absorption, toxicity, and the ability to distribute after systemic exposure. The book's contributors address a representative set of the broad spectrum of nanopharmaceutics presently being used, including cationic lipid nanoparticles, polymeric PLGA, PLA nanoparticles, biomacromolecules-based nanoparticles, and other scaffolds tissue-engineered skin substitutes. In addition, regulation and risk are also covered since the safety of these nanopharmaceuticals still represents a barrier to their wide and innovative use.
Other form:Print version: 0323400167 9780323400169

MARC

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245 0 0 |a Emerging Nanotechnologies in Immunology :  |b The Design, Applications and Toxicology of Nanopharmaceuticals and Nanovaccines /  |c edited by Ranjita Shegokar, Eliana B. Souto. 
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300 |a 1 online resource. 
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505 0 |a Front Cover; Emerging Nanotechnologies in Immunology; Copyright Page; Contents; List of Contributors; Biography; Preface; Key Features; 1 Nanopharmaceuticals in immunology: What's new in research?; 1.1 Introduction; 1.2 Application of Nanopharmaceuticals for Disease Treatment; 1.3 Evolution of Nanopharmaceuticals for Disease Treatment; 1.3.1 Cancer; 1.3.2 Immunotherapy; 1.3.3 Vaccines; 1.3.4 HIV/AIDS; 1.3.5 Tuberculosis and Malaria; 1.4 Conclusion; References; 2 Skin delivery of antimicrobial peptides; Abbreviations; 2.1 Introduction; 2.2 AMPs -- Chemistry, Antimicrobial and Antitumor Effects 
505 8 |a 2.3 Human AMPs and Proteins2.3.1 Defensins; 2.3.2 Cathelicidins; 2.3.3 Psoriasin; 2.4 AMPs From Non-human Vertebrates and From Invertebrates; 2.4.1 Magainins and Temporins - AMPs From Frogs; 2.4.2 AMPs From Insects; 2.5 AMPs Regulate Homeostasis in Healthy and Diseased Skin; 2.6 Atopic Dermatitis; 2.6.1 Atopic Dermatitis and the AMPs; 2.6.2 Reconstructed Atopic Skin - AMPs and Bacterial Growth; 2.7 Psoriasis; 2.8 Acne; 2.9 Wound Healing/Keloid Formation; 2.10 Topical Use of AMPs; 2.11 Nanoparticle-Enhanced Peptide Penetration Into the Skin; 2.12 Penetration Enhancers for Protein Delivery 
505 8 |a 2.13 Nanoparticle Enforced Peptide Effects2.13.1 Antibacterial Effects; 2.13.2 Nanoparticles for Improved Antipsoriatic Therapy; 2.14 Conclusion; References; Further Reading; 3 Skin penetration of nanoparticles; 3.1 Introduction; 3.2 Skin Structure and Function; 3.2.1 Skin Structure; 3.2.1.1 Epidermis; 3.2.1.2 Dermis; 3.2.1.3 Hypodermis (subcutis); 3.2.2 Derivative Structure of the Skin; 3.2.2.1 Hair; 3.2.2.2 Nails; 3.2.2.3 Sebaceous glands; 3.2.2.4 Sweat glands; 3.3 Skin Functions; 3.3.1 Mechanism of Skin Penetration; 3.3.1.1 Transappendageal route; 3.3.1.2 Transepidermal route 
505 8 |a 3.3.1.3 Translocation3.4 Sources of NPs; 3.4.1 Significance of Skin Penetration Studies of NPs; 3.4.1.1 Designing novel topical and transdermal nanocarriers and biomedical diagnostic agents; 3.4.1.2 Understanding NPs health hazards; 3.4.2 Factors Affecting Skin Penetration of NPs; 3.4.2.1 Physicochemical properties of the penetrant; 3.4.2.1.1 Penetrant formulation; 3.4.2.1.2 Size and surface properties of penetrant; 3.4.2.1.3 Penetrant surface polarity; 3.4.2.1.4 Penetrant shape; 3.4.2.2 Vehicle effects; 3.4.2.2.1 Microemulsions; 3.4.2.2.2 Nanoemulsions 
505 8 |a 3.4.2.2.3 Solid Lipid NPs and Nanostructured Lipid Carriers3.4.2.2.4 Liposomes; 3.4.2.2.5 Niosomes; 3.4.2.2.6 Transfersomes and ethosomes; 3.4.2.3 Surface area, dose, duration, and frequency of exposure; 3.4.2.4 Distribution; 3.4.2.5 Subanatomical pathways (skin appendages); 3.4.2.6 Skin surface condition; 3.4.2.6.1 Skin health and integrity; 3.4.2.6.2 Hydration; 3.4.2.6.3 Occlusion; 3.4.2.6.4 Temperature; 3.4.2.6.5 Other parameters; 3.4.2.7 Additional factors of skin penetration and permeation; 3.4.2.7.1 Different body regions and hair follicle volume and distribution; 3.4.2.7.2 Flexed skin 
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