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1.

図書
図書
1. Introduction to plasmonics : advances and applications (: hardcover)
edited by Sabine Szunerits, Rabah Boukherroub
出版情報: Singapore : Pan Stanford Publishing, c2015  xix, 358 p. ; 24 cm
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Foreword
Preface
Propagating Surface Plasmon Polaritons / Atef Shalabney1：
Introduction / 1.1：
Surface Plasmons on Smooth Surfaces / 1.2：
Surface Plasmon at Single Interface / 1.2.1：
Surface Plasmon in Multilayer Systems / 1.2.2：
Electromagnetic Energy Confinement and Field Enhancement / 1.2.3：
Excitation of Surface Plasmon Polaritons / 1.2.4：
Applications / 1.3：
Surface Plasmon Resonance-Based Sensors / 1.3.1：
Enhanced Spectroscopy and Emissive Processes / 1.3.2：
Concluding Remarks / 1.4：
Different Strategies for Glycan Immobilization onto Plasmonic Interfaces / Sabine Szunerits ; Rabah Boukherroub2：
Carboxymethylated Dextran Layers: The BiAcore Chip / 2.1：
Self-Assembled Monolayers Based on Thiolated Functional Groups / 2.3：
Polymer Films / 2.4：
Lamellar SPR Structures / 2.5：
Conclusion
Biophysics of DNA: DNA Melting Curve Analysis with Surface Plasmon Resonance Imaging / Arnaud Buhot ; Julia Pingel ; Jean-Bernard Fiche ; Roberto Calemczuk ; Thierry Livache3：
Temperature Regulation of SPRi for DNA Melting Curves Analysis / 3.1：
SPRi Apparatus with Temperature Regulation / 3.2.1：
Equilibrium versus Out-of-Equilibrium Melting Curves / 3.2.2：
Stability of Grafting Chemistries at High Temperatures / 3.2.3：
Electro-copolymerization of poly-pyrrole / 3.2.3.1：
Thiol self-assembling monolayer / 3.2.3.2：
Physico-Chemistry of DNA Melting at a Surface / 3.3：
Effects of Denaturant Molecules / 3.3.1：
Effects of Salt Concentration / 3.3.2：
Detection of Single Point Mutation from Melting Curve Analysis / 3.4：
Detection with Oligonucleotides Targets / 3.4.1：
Detection Limit of Somatic Mutations / 3.4.2：
Homozygous and Heterozygous Detection of PCR Products / 3.4.3：
Plasmon Waveguide Resonance Spectroscopy: Principles and Applications in Studies of Molecular Interactions within Membranes / Isabel D. Alves3.5：
Plasmon Spectroscopy / 4.1：
Description of Surface Plasmons / 4.2.1：
Types of Surface Plasmon Resonances / 4.2.2：
Conventional surface plasmon resonance / 4.2.2.1：
Plasmon-waveguide resonance / 4.2.2.2：
PWR Spectral Analysis / 4.2.3：
PWR Applications / 4.3：
Lipid Bilayers / 4.3.1：
Solid-supported lipid bilayers / 4.3.1.1：
Membranes composed of cellular membrane fragments / 4.3.1.2：
GPCR Insertion into Membranes, Activation and Signaling / 4.3.2：
Role of Lipids in GPCR Activation, Signaling, and Partition into Membrane Microdomains / 4.3.3：
Interaction of Membrane Active Peptides with Lipid Membranes / 4.3.4：
PWR Ongoing Developments / 4.4：
Surface-Wave Enhanced Biosensing / Wolfgang Knoll ; Amal Kasry ; Chun-Jen Huang ; Yi Wang ; Jakub Dostalek5：
Surface Plasmon Field-Enhanced Fluorescence Detection / 5.1：
Long-Range Surface Plasmon Fluorescence Spectroscopy / 5.3：
Optical Waveguide Fluorescence Spectroscopy / 5.4：
Conclusions / 5.5：
Infrared Surface Plasmon Resonance / Stefan Franzen ; Mark Losego ; Misun Kang ; Edward Sachet ; Jon-Paul Maria6：
The Hypothesis That Surface Plasmon Resonance Will Be Observed in Free Electron Conductors / 6.1：
Confirmation of the Hypothesis That Conducting Metal Oxides Can Support Surface Plasmon Resonance / 6.3：
The Effect of Carrier Concentration / 6.4：
The Effect of Mobility / 6.5：
Hybrid Plasmons: Understanding the Relationship between Localized LSPR and SPR / 6.6：
The Effect of Materials Properties on the Observed Surface Plasmon Polaritons / 6.7：
Detection of Mid-Infrared Surface Plasmon Polaritons / 6.8：
The Search for High Mobility Conducting Metal Oxides / 6.9：
The Unique Characteristics of Localized Surface Plasmon Resonance / Gaetan Leveque ; Abdellatif Akjouj6.10：
Localized Surface Plasmon Resonance of a Single Particle / 7.1：
Single Particle in the Quasi-Static Approximation / 7.1.1：
Case of the spherical particle / 7.1.1.1：
Case of the spheroidal particle / 7.1.1.2：
Beyond the Quasi-Static Approximation / 7.1.2：
Examples of Coupled Plasmonic Systems / 7.2：
Chain of Identical Particles / 7.2.1：
Chain of Different Particles / 7.2.2：
Localized Surface Plasmon for a Periodic Nano structure / 7.3：
Model and Simulation Method / 7.3.1：
Absorption Spectra for Au Nano structures Array / 7.3.2：
Influence of the Thickness of a Diamond Dielectric Overlayer on the LSPR / 7.3.3：
Advances in the Fabrication of Plasmonic Nanostructures: Plasmonics Going Down to the IManoscale / Thomas Maurer7.3.4：
Top-Down Techniques: A Mask-Based Process / 8.1：
Conventional Lithography Techniques: Photolithography and Particle Beam Lithography / 8.2.1：
Photolithography / 8.2.1.1：
Particle beam lithography / 8.2.1.2：
Advanced Lithography Techniques: Masks Coming from Researcher Imagination / 8.2.2：
Multilevel laser interference lithography / 8.2.2.1：
Nanostencil lithography / 8.2.2.2：
Self-assembly techniques for mask fabrication: nanosphere lithorgaphy and block copolymer lithography / 8.2.2.3：
Direct Writing / 8.2.3：
Particle beam-induced etching and particle beam-induced deposition / 8.2.3.1：
Laser ablation / 8.2.3.2：
3D laser lithography / 8.2.3.3：
Printing, Replica Molding and Embossing / 8.2.4：
Printing / 8.2.4.1：
Replica molding / 8.2.4.2：
Embossing / 8.2.4.3：
Conclusion about the Top-Down Strategy / 8.2.5：
Bottom-Up Techniques: Atom by Atom Building / 8.3：
The Bottom-Up Strategy / 8.3.1：
Physical route / 8.3.1.1：
Electrochemical route / 8.3.1.2：
Chemical route / 8.3.1.3：
Self-Organization, the Next Challenge of Plasmonics / 8.3.2：
Laboratory self-assembly techniques / 8.3.2.1：
Mass Production Using Wet Coating Processes / 8.3.3：
Mixing Top-Down and Bottom-Up Routes / 8.4：
Porous Membranes for Ordered Nanowires Growth / 8.4.1：
Copolymer Template Control of Plasmonic Nanoparticle Synthesis via Thermal Annealing / 8.4.2：
Let's Play Your Imagination / 8.4.3：
Conclusion: First, Choose Materials / 8.5：
Colorimetric Sensing Based on Metallic Nanostructures / Daniel Aili ; Borja Sepulveda9：
Introduction and Historical Perspective / 9.1：
Synthesis of Gold Nanoparticles / 9.2：
Optical Properties of Gold Nanoparticles / 9.3：
Colloidal Stability and Surface Chemistry of Gold Nanoparticles / 9.4：
Surface Functionalization / 9.4.1：
Molecular Recognition for Modulation of Nanoparticle Stability / 9.5：
Cross-Linking Assays / 9.5.1：
Redispersion Assays / 9.5.2：
Non-Cross-Linking Assays / 9.5.3：
Outlook and Challenges / 9.6：
Assays with Reversed Sensitivity and Plasmonic ELISA / 9.6.1：
Assays for the Future / 9.6.2：
Surface-Enhanced Raman Scattering: Principles and Applications for Single-Molecule Detection / Diego P. dos Santos ; Marcia I. A. Temperini ; Alexandre G. Brolo10：
Raman Scattering / 10.1：
SERS / 10.3：
SERS Substrates / 10.4：
Single-Molecule SERS / 10.5：
Graphene-Based Plasmonics / Sinan Balci ; Emre Ozan Polat ; Coskun Kocabas10.6：
Introduction: Plasmons in Reduced Dimensions / 11.1：
Optical Properties of Graphene / 11.2：
Synthesis of Graphene / 11.3：
Plasma Oscillations on Graphene-Metal Surface / 11.4：
Graphene Functionalized SPR Sensors / 11.5：
Graphene Passivation for SPR Sensors / 11.6：
Biomolecular Detection Using Graphene Functionalized SPR Sensors / 11.7：
Graphene Oxide Functionalization / 11.8：
Gate-Tunable Graphene Plasmonics / 11.9：
SPR: An Industrial Point of View / Iban Larroulet11.10：
Companies / 12.1：
Future Trends / 12.3：
Index
Foreword
Preface
Propagating Surface Plasmon Polaritons / Atef Shalabney1：
2.

図書
図書
2. Bioinspired and biomimetic polymer systems for drug and gene delivery (:hbk.)
edited by Zhongwei Gu
出版情報: Weinheim : Wiley-VCH, c2015  xxi, 337 p. ; 25 cm
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List of Contributors
Preface
Backbone Degradable and Coiled-Coil Based Macromolecular Therapeutics / Jiyuan Yang ; Jindrich Kopecek1：
Introduction / 1.1：
Water-Soluble Polymers as Carriers of Anticancer Drugs / 1.2：
First Generation Conjugates - Design, Synthesis, and Activity / 1.2.1：
Analysis of Design Factors That Need Attention / 1.2.2：
Design of Conjugates for the Treatment of Noncancerous Diseases / 1.2.2.1：
Combination Therapy Using Polymer-Bound Therapeutics / 1.2.2.2：
New Targeting Strategies / 1.2.2.3：
Relationship Between Detailed Structure of the Conjugates and Their Properties / 1.2.2.4：
Impact of Binding a Drug to a Polymer on the Mechanism of Action / 1.2.2.5：
Mechanism of Internalization and Subcellular Trafficking / 1.2.2.6：
Relationship Between the Molecular Weight of the Carrier and the Efficacy of the Conjugate / 1.2.2.7：
Design of Second Generation Conjugates - Long-Circulating and Backbone Degradable / 1.2.3：
RAFT Copolymerization for the Synthesis of Conjugates / 1.2.3.1：
Click Reactions for Chain Extension into Multiblock Copolymers / 1.2.3.2：
Biological Properties of Long-Circulating Macromolecular Therapeutics / 1.2.3.3：
Summary of Part 2 and Future Prospects / 1.2.4：
Drug-Free Macromolecular Therapeutics - A New Paradigm in Drug Delivery / 1.3：
Biorecognition in Hybrid Polymer Systems / 1.3.1：
Coiled-Coils in Biomedical Systems / 1.3.2：
Coiled-Coil Based Drug-Free Macromolecular Therapeutics: Design, In Vitro, and In Vivo Activity / 1.3.3：
Potential, Limitations, and Future Prospect of Drug-Free Macromolecular Therapeutics / 1.3.4：
General Summary and Outlook / 1.4：
Acknowledgments
References
Dendritic Polymers as Targeting Nanoscale Drug Delivery Systems for Cancer Therapy / Kui Luo ; Zhongwei Gu2：
Functional Dendritic Polymers Based Drug Delivery Vehicles for Targeting Tumor Therapy via EPR Effect / 2.1：
Functional Dendritic Polymers for Encapsulation of Anticancer Drugs / 2.2.1：
Chemical Conjugation Functional Dendritic Polymers as Drug Delivery Systems / 2.2.2：
Tumor Targeting Moieties Functionalized Dendritic Drug Delivery Vehicles for Cancer Therapy / 2.3：
Conclusion / 2.4：
Composite Colloidal Nanosystems for Targeted Delivery and Sensing / Pilar Rivera Gil ; Moritz Nazarenus ; Wolfgang J. Parak3：
Working Toolkit / 3.1：
Engineering a Multifunctional Carrier / 3.1.2：
Objective / 3.2：
Cellular Behavior of the Carrier / 3.3：
Intracellular Fate / 3.3.1：
Biocompatibility / 3.3.2：
Applications / 3.4：
Delivery with Multifunctional PEM Capsules / 3.4.1：
Magnetic Targeting and Magnetofection / 3.4.1.1：
Strategies for Controlled Opening / 3.4.1.2：
Intracellular Ion Sensing / 3.4.2：
Conclusions / 3.5：
Abbreviations
Polymeric Micelles for Cancer-Targeted Drug Delivery / Huabing Chen ; Zhishen Ge ; Kazunori Kataoka4：
Micelle Formulations in Clinical Development / 4.1：
Particle Size of Micelles / 4.3：
Morphology of Micelles / 4.4：
Targeting Design of Micelles for Enhanced Accumulation and Cell Internalization / 4.5：
Functional Designs of Micelles / 4.6：
Design of Micelles for Gene Delivery / 4.7：
Challenge and Future Perspective 103 / 4.8：
Biomimetic Polymers for in Vivo Drug Delivery / Wenping Wang ; Kinam Park5：
Commonly Used Biomimetic Polymers and Their Applications in DDS / 5.1：
Polylactones and Their Modifications / 5.2.1：
Poly(lactic acid) (PLA) / 5.2.1.1：
Poly(lactic-co-glycolic acid) (PLGA) / 5.2.1.2：
Poly(ε-caprolactone) (PCL) / 5.2.1.3：
Dendrimer / 5.2.2：
Structure and Properties of Dendrimers / 5.2.2.1：
Types of Dendrimers / 5.2.2.2：
Applications of Dendrimers as Carriers in Drug Delivery Systems / 5.2.2.3：
Synthetic Polypeptides / 5.2.3：
Challenges and Perspectives / 5.3：
Drug Delivery from Protein-Based Nanoparticles / Dan Ding ; Xiqun Jiang6：
Preparation of Protein-Based Nanoparticles / 6.1：
Desolvation / 6.2.1：
Emulsification / 6.2.2：
Coacervation / 6.2.3：
Polymer-Monomer Pair Reaction System / 6.2.4：
Drug Delivery from Albumin-Based Nanoparticles / 6.3：
Albumin-Based Nanoparticles as Drug Carriers / 6.3.1：
Targeting Ligand-Functionalized Albumin-Based Nanoparticles / 6.3.2：
Nanoparticle Albumin-Bound (nab) Technology / 6.3.3：
Drug Delivery from Gelatin-Based Nanoparticles / 6.4：
Gelatin-Based Nanoparticles as Drug Carriers / 6.4.1：
Targeting Ligand-Functionalized Gelatin-Based Nanoparticles / 6.4.2：
Site-Specific Drug Delivery System / 6.4.3：
Drug Delivery from Other Protein-Based Nanoparticles / 6.5：
Polymeic Gene Carriers / Xuesi Chen ; Huayu Tian ; Xiuwen Guan7：
Gene Therapy and Gene Carriers / 7.1：
Gene Therapy / 7.1.1：
The Concept of Gene Therapy / 7.1.1.1：
Development and the Present Situation of Gene Therapy / 7.1.1.2：
Methods and Strategies of Gene Therapy / 7.1.1.3：
Research Contents and Challenges of Gene Therapy / 7.1.1.4：
Gene Carriers / 7.1.2：
The Concept of Gene Carrier / 7.1.2.1：
The Necessity of the Gene Carrier / 7.1.2.2：
Requirements of Gene Carrier / 7.1.2.3：
Classification of Gene Carrier / 7.1.2.4：
Polymeric Gene Carriers / 7.2：
Cationic Polymer Gene Carriers / 7.2.1：
Process of the Polycation Vector Mediated Gene Delivery / 7.2.1.1：
Categories and Research Situation of the Cationic Polymer Gene Vector / 7.2.1.2：
PEI Grafting Modification Polymeric Gene Carriers / 7.3：
Amino Acid Derivatives Modified Polymeric Gene Carriers / 7.3.1：
Poly(glutamic acid) Derivatives Modified PEI / 7.3.1.1：
Polyphenyialanine Derivatives Modified PEI / 7.3.1.2：
PEG Modified Hyperbranched PEI / 7.3.2：
Low Molecular Weight (LWM) PEI Base Polymeric Gene Carriers / 7.4：
Crosslinked Polycations / 7.4.1：
Crosslinlced Polycation OEI-CBA / 7.4.1.1：
Crosslinked Polycation OEI-PBLG-PEGDA / 7.4.1.2：
Hexachlorotriphosphazene Crosslinked Polycation / 7.4.1.3：
Grafted Polycations / 7.4.2：
Grafted Cationic Polymer MP-g-OEI / 7.4.2.1：
Graft Cationic Polymer N-PAE-g-OEI / 7.4.2.2：
Graft Cationic Polymer mPEGT-PMCC-g-OEI / 7.4.2.3：
Targeted Shielding System for Polymeric Gene Carriers / 7.5：
Static Shielding System / 7.5.1：
Poly(glutamine acid) Shielding System and PEGylations / 7.5.1.1：
Sulfonamides Related Shielding System / 7.5.1.2：
Other Design Strategies of Cationic Gene Carrier / 7.5.2：
pH-Sensitive Polymeric Nanoparticles as Carriers for Cancer Therapy and Imaging / Yi Li ; Guang Hui Gao ; Ick Chan Kwon ; Doo Sung Lee7.6：
pH-Sensitive Polymers / 8.1：
pH-Sensitive Anionic Polymers / 8.2.1：
pH-Sensitive Cationic Polymers / 8.2.2：
pH-Sensitive Neutral Polymers / 8.2.3：
pH-Sensitive Polymers as Drug Carriers / 8.3：
pH-Sensitive Polymer-Drug Conjugates / 8.3.1：
pH-Sensitive Polymeric Micelles / 8.3.2：
pH-Sensitive Polymersomes / 8.3.3：
pH-Sensitive Polymer-Inorganic Hybrid Nanoparticles / 8.3.4：
pH-Sensitive Dendrimers / 8.3.5：
pH-Sensitive Polymers for Bioimaging / 8.4：
Charge-Reversal Polymers for Biodelivery / Bo Zhan ; Kai Wang ; Jingxing Si ; Meihua Sui ; Youqing Shen8.5：
Applications of Cationic Polymers in Biodelivery / 9.1：
Barriers for Cationic Polymers in In vitro and In vivo Applications / 9.2：
Characteristic pH Gradients in Tumor Interstitium and Endo/Lyso somes / 9.3：
Chemistry of Charge-Reversal Polymers Based on Acid-Labile Amides / 9.4：
pHe-Triggered Charge-Reversal / 9.4.1：
pHL-Triggered Charge-Reversal / 9.4.2：
Applications of Charge-Reversal Polymers in Biodelivery Systems / 9.5：
Charge-Reversal in Cancer Drug Delivery / 9.5.1：
Charge-Reversal in Gene Delivery / 9.5.2：
Charge-Reversal in Protein Delivery / 9.5.3：
Charge-Reversal Incorporated with Inorganic Materials / 9.5.4：
Perspectives / 9.6：
Phenylbaronic Acid-Containing Glucose-Responsive Polymer Materials: Synthesis and Applications in Drug Delivery / Rujiang Ma ; Linqi Shi10：
PBA-Containing Polymers Operating Under Physiological Conditions / 10.1：
Chemically Crosslinked PBA-Based Gels / 10.3：
Self-Assembled PBA-Based Polymer Micelles / 10.4：
Self-Assembled PBA-Based Polymersomes / 10.5：
Extracellular pH-Activated Nanocarriers for Enhanced Drug Delivery to Tumors / You-Yong Yuan ; Cheng-Qiong Mao ; Jin-Zhi Du ; Xian-Zhu Yang ; Jun Wang10.6：
Passive and Active Tumor Targeting / 11.1：
Targeting the Extracellular pH (pHe) in Tumors / 11.3：
Extracellular pH-Induced Drug Delivery to Tumors / 11.4：
Ligand Exposure by a Shielding/Deshielding Method / 11.5：
Surface Charge Reversing Nanoparticles / 11.6：
Enhanced Cellular Uptake by Surface Charge Reversing Nanoparticles / 11.6.1：
Overcoming MDR by Surface Charge Reversing Nanoparticles / 11.6.2：
Enhanced Delivery of siRNA by Surface-Charge Reversing Nanoparticles / 11.6.3：
Stimulation-Sensitive Drug Delivery Systems / Xintao Shuai ; Du Cheng11.7：
pH-Sensitive Delivery Systems / 12.1：
pH-Sensitive Micellar Delivery Systems / 12.2.1：
pH-Sensitive Liposomes / 12.2.2：
Thermo-Sensitive Delivery Systems / 12.3：
Biomolecule-Sensitive Delivery Systems / 12.4：
Enzyme-Sensitive Nanocarriers / 12.4.1：
Reduction-Responsive Conjugates / 12.4.2：
Other Environmentally Sensitive Nanocarriers / 12.5：
Outlook / 12.6：
Index
List of Contributors
Preface
Backbone Degradable and Coiled-Coil Based Macromolecular Therapeutics / Jiyuan Yang ; Jindrich Kopecek1：
3.

図書
図書
3. Peptide chemistry and drug design (: hardback)
edited by Ben M. Dunn
出版情報: Hoboken, N.J. : Wiley, c2015  xvi, 318 p., [8] p. of colored plates ; 25 cm
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Preface
List of Contributors
Peptide Therapeutics / Nader Fotouhi1：
History of Peptides as Drugs / 1.1：
Factors Limiting the Use of Peptides in the Clinic / 1.2：
Advances that have Stimulated the Use of Peptides as Drugs / 1.3：
Development of Peptide Libraries / 1.4：
Modification of Peptides to Promote Stability and Cell Entry / 1.5：
Targeting Peptides to Specific Cells / 1.6：
Formulations to Improve Peoperties / 1.7：
References
Methods for the Peptide Synthesis and Analysis / Judit Tulla-Puche ; Ayman El-Faham ; Athanassios S. Galanis ; Eliandre de Oliveira ; Aikaterini A. Zompra ; Fernando Albericio2：
Introduction / 2.1：
Solid Supports / 2.2：
Linkers / 2.3：
Protecting Groups / 2.4：
The Special Case of Cysteine / 2.4.1：
Methods for Peptide Bond Formation / 2.5：
Peptide-Bond Formation from Carbodiimide-Mediated Reactions / 2.5.1：
Peptide-Bond Formation from Preformed Symmetric Anhydrides / 2.5.2：
Peptide-Bond Formation from Acid Halides / 2.5.3：
Peptide-Bond Formatiion from Phosphonium Salt-Mediated Reactions / 2.5.4：
Peptide-Bond Formation from Aminium/Uronium Salt-Mediated Reactions / 2.5.5：
Solid-Phase Stepwise Synthesis / 2.6：
Long Peptides / 2.6.1：
Synthesis in Solution / 2.7：
Nα Protection of the N-Terminal Amino Acid Derivative or Fragment / 2.7.1：
Carboxy-Group Protection of the C-terminal Amino-Acid Derivative or Fragment / 2.7.2：
Peptide Bond Formation / 2.7.3：
Hybrid Synthesis-Combination of Solid and Solution Synthesis / 2.8：
Classical Segment Condensation / 2.8.1：
Native Chemical Ligation / 2.8.2：
Cyclic Peptides / 2.9：
Depsipeptides / 2.10：
Separation and Purification of Peptides / 2.11：
Gel-Filtration Chromatography / 2.11.1：
Ion-Exchange Chromatography / 2.11.2：
Reverse-Phase High Performance Liquid Chromatography / 2.11.3：
Characterization of Peptides Through Mass Spectrometry / 2.12：
Ionization Source / 2.12.1：
Mass Analysers / 2.12.2：
Peptide Fragmentation / 2.12.3：
Quantification by MS / 2.12.4：
Conclusions / 2.13：
Acknowledgments
Abbreviations
Peptide Design Strategies for G-Protein Coupled Receptors (GPCRs) / Anamika Singh ; Carrie Haskell-Luevano3：
Classification of GPCRs / 3.1：
Catalog of Peptide-Activated G-Protein Coupled Receptors / 3.3：
Structure of GPCRs: Common Features / 3.4：
Crystal Structures / 3.4.1：
GPCR Activation / 3.5：
Ligand (Peptide) Binding and Receptor Activation / 3.5.1：
Common Structural Changes among GPCRs / 3.5.2：
G-Protein Coupled Intracellular Signaling Pathwayws / 3.5.3：
Structure and Function of Peptide Hormones / 3.6：
Design Approaches for GPCR Selective Peptide Ligands / 3.7：
Structure-Activity Relationship (SAR) Studies / 3.7.1：
Chimeric Peptide Analogs / 3.7.2：
Combinatorial Libraries / 3.7.3：
Three-Dimensional (3D) GPCR Homology Molecular Modeling / 3.7.4：
Peptide-Resed Inhibitors of Enzymes / Anna Knapinska ; Sabrina Amar ; Trista K. Robichaud ; Gregg B. Fields3.8：
Angiotensin-Converting Enzyme and Neprilysin/Neutral Endopeptidase / 4.1：
Peptide Inhibitors of the HIV-1 Viral Life Cycle / 4.3：
Matrix Metalloproteinases / 4.4：
Antrax Lethal Factor Inhibition by Defensins / 4.5：
Kinases / 4.6：
Glycosyltransferases (Oligosaccharyltransferases) / 4.7：
Telomerase Inhibitors / 4.8：
Tyrosinase / 4.9：
Peptidyl-Prolyl Isomerase / 4.10：
Histone Modifying Enzymes / 4.11：
Histone Deacetylase / 4.11.1：
Histone Methyl-Transferase / 4.11.2：
Putting it all Together: Peptide Inhibitor Applications in Skin Care / 4.12：
Strategies for the Discovery of Novel Peptide Inhibitors / 4.13：
Discovery of Peptide Drugs as Enzyme Inhibitors and Activators / Jeffrey-Tri Nguyen ; Yoshiaki Kiso5：
Peptide Residue Nomenclature / 5.1：
Common Methods of Drug Design / 5.1.2：
Phases of Drug Development / 5.1.3：
Enzyme Types That Process Peptides / 5.2：
Enzymes as Chemicals in Consumer and Medical Products / 5.2.1：
Nonspecific Enzyme Inhibitors / 5.2.2：
Amino Acid Drugs / 5.3：
Thyroid Hormones / 5.3.1：
An Ornithine Decarboxylase Inhibitor / 5.3.2：
Catecholamines / 5.3.3：
Serine Proteases and Blood Clotting / 5.4：
Blood Coagulating Agents / 5.4.1：
Enzymes as Blood Anticoagulants / 5.4.2：
Direct Thrombin Inhibitors as Blood Anticoagulants / 5.4.3：
Diabetes Mellitus / 5.5：
Peptide Hormones and Blood Glucose Regulation / 5.5.1：
Glucagon-Like Peptide-1 and Analogs / 5.5.2：
Dipeptidyl Peptidase-4 Inhibitors / 5.5.3：
Renin-Angiotensin-Aldosterone System / 5.6：
ACE Inhibitors / 5.6.1：
Renin Inhibitors / 5.6.2：
Penicillin and Cephalosporin Antibiotics / 5.7：
HIV Protease / 5.8：
HIV-Specific Protease Inhibitors / 5.8.1：
Peptide Drugs Under Development / 5.9：
Cathepsins / 5.9.1：
Cysterine Proteases / 5.9.2：
Secretases in Alzheimer's Disease / 5.9.3：
Trypsin-Like Serine Proteases / 5.9.4：
Zinc Metalloproteases / 5.9.5：
Non-Mammalian Proteases / 5.9.6：
Discussion / 5.10：
Discovery of Peptide Drugs from Natural Sources / Sónia T Henriques ; David J Craik6：
Peptides are Involved in the Host Defense Mechanism of Living Organisms / 6.1：
Cationic AMPs from Eukaryotes, Peptides that Target the Membrane / 6.2.1：
Peptides and the Host Defense in Bacteria-Bacteriocins / 6.2.2：
Cyclotides, Ultra-Stable Peptides that are Part of Plant Defense Mechanism / 6.2.3：
Animal Venoms, a Rich Source of Peptides with Therapeutic Potential / 6.3：
Conotoxins, a Naturally Occurring Combinatorial Peptide Library / 6.3.1：
Optimization of Peptides for Drug Development / 6.4：
Chemical Modifications to Improve Activity / 6.4.1：
Modification of Peptides of Limit Metabolism / Isuru R. kumarasinghe ; Victor J. Hruby6.5：
Introduction of Unnatural Amino Acids / 7.1：
Cyclization of Linear Peptides to Improve Stability Toward Blood and Brain Protease Degradation / 7.3：
Introduction of D-Amino Acids into Peptides Improves Stability Toward Blood and Brain Protease Degradation / 7.4：
Introduction of β-Amino Acids Increases the Stability Toward Blood and Brain Protease Degradation / 7.5：
INtroduction of Peptide Bond Isosteres / 7.6：
Introduction of a N-Methylation of the Amide Bond of Peptides can Improve the Stability Toward Blood and Brain Protease Degradation / 7.7：
Use of Unnatural Amino Acids-Use of Topographically Constrained Amino Acid / 7.8：
Using Glycosylated Amino Acids to Increase the Resistance of the Proteolytic Degradation / 7.9：
Creation of Peptides as Multiple Antigen Peptide (MAP) Dendrimeric Forms Increases the Stability Toward Blood and Brain Protease Degradation / 7.10：
Halogenations of Aromatic Residues in Peptides can Reduce the Enzymatic Recognition Required for Peptide Hydrolysis / 7.11：
Concluding Discussion / 7.12：
Delivery of Peptide Drugs / 8：
Lipinski's Rule of Five / 8.1：
Molecular Size / 8.2.1：
Lipophilicity / 8.2.2：
Chemical Stability / 8.2.3：
Routes of Administration / 8.2.4：
Approaches to Delivering Peptide Drugs / 8.3：
Enzyme Inhibitors / 8.3.1：
Permeation Enhancers / 8.3.2：
Delivery of Peptide Drugs across the Blood-Brain Barrier / 8.3.3：
Parenteral Peptide Drugs / 8.4：
Topical Peptide Drugs for Local Effects / 8.5：
Cosmeceutical Peptides / 8.5.1：
Intranasal Peptide Drug Delivery / 8.6：
Enteral Peptide Drugs / 8.7：
DIfferent Routes of Administration for Insulin / 8.8：
Index / 8.9：
Preface
List of Contributors
Peptide Therapeutics / Nader Fotouhi1：
4.

図書
図書
4. Essential Japanese kanji. Rev. ed (v. 1 ; v. 2)
Kanji Text Research Group, University of Tokyo
出版情報: Tokyo : Tuttle Publishing, 2015-  2 v. ; 26 cm
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5.

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5. Optical coherence tomography : technology and applications. 2nd ed (: set - v. 3)
Wolfgang Drexler, James G. Fujimoto, editors
出版情報: Cham : Springer Reference, c2015  3 v. (xxx, 2571 p.) ; 24 cm
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6.

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6. Greenfield's neuropathology. 9th ed (: set ; v. 1 ; v. 2)
edited by Seth Love ... [et al.]
出版情報: Boca Raton : CRC Press, c2015  2 v. ; 29 cm
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7. The SAGE encyclopedia of stem cell research. 2nd ed (: [set] - v. 3)
editor, Eric E. Bouhassira ; associate editor, Krishna S. Vyas
出版情報: Los Angeles : SAGE Reference, c2015  3 v. (xli, 1471 p.) ; 29 cm
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8.

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8. 元気でいてよ、R2-D2。
北村薫 [著]
出版情報: 東京 : KADOKAWA, 2015.10  237p ; 15cm
シリーズ名: 角川文庫 ; 19402, [き24-9]
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目次情報: 続きを見る
マスカット・グリーン
腹中の恐怖
微塵隠れのあっこちゃん
三つ、惚れられ
よいしょ、よいしょ
元気でいてよ、R2‐D2。
さりさりさり
ざくろ
スイッチ
マスカット・グリーン
腹中の恐怖
微塵隠れのあっこちゃん
概要: 気心のしれた女同士で飲むお酒は、自分を少し素直にしてくれる...そんな中、思い出すのは、取り返しのつかない色んなこと(「元気でいてよ、R2‐D2。」)。産休中の女性編集者の下に突然舞い込んだ、ある大物作家の原稿。彼女は育児に追われながらも、 … 自ら本作りに乗り出すが...(「スイッチ」)。本人ですら気付かない本心がふと顔を出すとき、世界は崩れ出す。人の本質を巧みに描く、書き下ろしを含む9つの物語。 続きを見る
9.

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9. Dinosaur dinners (: pbk)
written by Lee Davis
出版情報: New York, N.Y. : DK Publishing, 2015  47 p. ; 23 cm
シリーズ名: Dorling Kindersley readers ; 2, Beginning to read alone
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10.

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10. China. 14th ed (: pbk)
Damian Harper ... [et al.]
出版情報: Footscray, Vic. : Lonely Planet, 2015  1053 p. ; 20 cm
シリーズ名: Lonely Planet
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