【讨论】Drugs and Pharmaceutical Sciences

推荐以下成套书籍，部分书籍我有。
1. Pharmacokinetics, Milo Gibaldi and Donald Perrier
2. Good Manufacturing Practices for Pharmaceuticals: A Plan for Total Quality Control, Sidney H. Willig,
Murray M. Tuckerman, and William S. Hitchings IV
3. Microencapsulation, edited by J. R. Nixon
4. Drug Metabolism: Chemical and Biochemical Aspects, Bernard Testa and Peter Jenner
5. New Drugs: Discovery and Development, edited by Alan A. Rubin
6. Sustained and Controlled Release Drug Delivery Systems, edited by Joseph R. Robinson
7. Modern Pharmaceutics, edited by Gilbert S. Banker and Christopher T. Rhodes
8. Prescription Drugs in Short Supply: Case Histories, Michael A. Schwartz
9. Activated Charcoal: Antidotal and Other Medical Uses, David O. Cooney
10. Concepts in Drug Metabolism (in two parts), edited by Peter Jenner and Bernard Testa
11. Pharmaceutical Analysis: Modern Methods (in two parts), edited by James W. Munson
12. Techniques of Solubilization of Drugs, edited by Samuel H. Yalkowsky
13. Orphan Drugs, edited by Fred E. Karch
14. Novel Drug Delivery Systems: Fundamentals, Developmental Concepts, Biomedical Assessments, Yie
W. Chien
15. Pharmacokinetics: Second Edition, Revised and Expanded, Milo Gibaldi and Donald Perrier
16. Good Manufacturing Practices for Pharmaceuticals: A Plan for Total Quality Control, Second Edition,
Revised and Expanded, Sidney H. Willig, Murray M. Tuckerman, and William S. Hitchings IV
17. Formulation of Veterinary Dosage Forms, edited by Jack Blodinger
18. Dermatological Formulations: Percutaneous Absorption, Brian W. Barry
19. The Clinical Research Process in the Pharmaceutical Industry, edited by Gary M. Matoren
20. Microencapsulation and Related Drug Processes, Patrick B. Deasy
21. Drugs and Nutrients: The Interactive Effects, edited by Daphne A. Roe and T. Colin Campbell
22. Biotechnology of Industrial Antibiotics, Erick J. Vandamme
23. Pharmaceutical Process Validation, edited by Bernard T. Loftus and Robert A. Nash
24. Anticancer and Interferon Agents: Synthesis and Properties, edited by Raphael M. Ottenbrite and
George B. Butler
25. Pharmaceutical Statistics: Practical and Clinical Applications, Sanford Bolton
26. Drug Dynamics for Analytical, Clinical, and Biological Chemists, Benjamin J. Gudzinowicz, Burrows T.
Younkin, Jr., and Michael J. Gudzinowicz
27. Modern Analysis of Antibiotics, edited by Adjoran Aszalos
28. Solubility and Related Properties, Kenneth C. James
29. Controlled Drug Delivery: Fundamentals and Applications, Second Edition, Revised and Expanded,
edited by Joseph R. Robinson and Vincent H. Lee
30. New Drug Approval Process: Clinical and Regulatory Management, edited by Richard A. Guarino
31. Transdermal Controlled Systemic Medications, edited by Yie W. Chien
32. Drug Delivery Devices: Fundamentals and Applications, edited by Praveen Tyle
33. Pharmacokinetics: Regulatory • Industrial • Academic Perspectives, edited by Peter G. Welling and
Francis L. S. Tse
34. Clinical Drug Trials and Tribulations, edited by Allen E. Cato
35. Transdermal Drug Delivery: Developmental Issues and Research Initiatives, edited by Jonathan
Hadgraft and Richard H. Guy
36. Aqueous Polymeric Coatings for Pharmaceutical Dosage Forms, edited by James W. McGinity
37. Pharmaceutical Pelletization Technology, edited by Isaac Ghebre-Sellassie
38. Good Laboratory Practice Regulations, edited by Allen F. Hirsch
39. Nasal Systemic Drug Delivery, Yie W. Chien, Kenneth S. E. Su, and Shyi-Feu Chang
40. Modern Pharmaceutics: Second Edition, Revised and Expanded, edited by Gilbert S. Banker and
Christopher T. Rhodes
41. Specialized Drug Delivery Systems: Manufacturing and Production Technology, edited by Praveen Tyle
42. Topical Drug Delivery Formulations, edited by David W. Osborne and Anton H. Amann
43. Drug Stability: Principles and Practices, Jens T. Carstensen
44. Pharmaceutical Statistics: Practical and Clinical Applications, Second Edition, Revised and Expanded,
Sanford Bolton
45. Biodegradable Polymers as Drug Delivery Systems, edited by Mark Chasin and Robert Langer
46. Preclinical Drug Disposition: A Laboratory Handbook, Francis L. S. Tse and James J. Jaffe
47. HPLC in the Pharmaceutical Industry, edited by Godwin W. Fong and Stanley K. Lam
48. Pharmaceutical Bioequivalence, edited by Peter G. Welling, Francis L. S. Tse, and Shrikant V. Dinghe
49. Pharmaceutical Dissolution Testing, Umesh V. Banakar
50. Novel Drug Delivery Systems: Second Edition, Revised and Expanded, Yie W. Chien
51. Managing the Clinical Drug Development Process, David M. Cocchetto and Ronald V. Nardi
52. Good Manufacturing Practices for Pharmaceuticals: A Plan for Total Quality Control, Third Edition,
edited by Sidney H. Willig and James R. Stoker
53. Prodrugs: Topical and Ocular Drug Delivery, edited by Kenneth B. Sloan
54. Pharmaceutical Inhalation Aerosol Technology, edited by Anthony J. Hickey
55. Radiopharmaceuticals: Chemistry and Pharmacology, edited by Adrian D. Nunn
56. New Drug Approval Process: Second Edition, Revised and Expanded, edited by Richard A. Guarino
57. Pharmaceutical Process Validation: Second Edition, Revised and Expanded, edited by Ira R. Berry and
Robert A. Nash
58. Ophthalmic Drug Delivery Systems, edited by Ashim K. Mitra
59. Pharmaceutical Skin Penetration Enhancement, edited by Kenneth A. Walters and Jonathan Hadgraft
60. Colonic Drug Absorption and Metabolism, edited by Peter R. Bieck
61. Pharmaceutical Particulate Carriers: Therapeutic Applications, edited by Alain Rolland
62. Drug Permeation Enhancement: Theory and Applications, edited by Dean S. Hsieh
63. Glycopeptide Antibiotics, edited by Ramakrishnan Nagarajan
64. Achieving Sterility in Medical and Pharmaceutical Products, Nigel A. Halls
65. Multiparticulate Oral Drug Delivery, edited by Isaac Ghebre-Sellassie
66. Colloidal Drug Delivery Systems, edited by Jörg Kreuter
67. Pharmacokinetics: Regulatory • Industrial • Academic Perspectives, Second Edition, edited by Peter G.
Welling and Francis L. S. Tse
68. Drug Stability: Principles and Practices, Second Edition, Revised and Expanded, Jens T. Carstensen
69. Good Laboratory Practice Regulations: Second Edition, Revised and Expanded, edited by Sandy
Weinberg
70. Physical Characterization of Pharmaceutical Solids, edited by Harry G. Brittain
71. Pharmaceutical Powder Compaction Technology, edited by Göran Alderborn and Christer Nyström
72. Modern Pharmaceutics: Third Edition, Revised and Expanded, edited by Gilbert S. Banker and
Christopher T. Rhodes
73. Microencapsulation: Methods and Industrial Applications, edited by Simon Benita
74. Oral Mucosal Drug Delivery, edited by Michael J. Rathbone
75. Clinical Research in Pharmaceutical Development, edited by Barry Bleidt and Michael Montagne
76. The Drug Development Process: Increasing Efficiency and Cost Effectiveness, edited by Peter G.
Welling, Louis Lasagna, and Umesh V. Banakar
77. Microparticulate Systems for the Delivery of Proteins and Vaccines, edited by Smadar Cohen and
Howard Bernstein
78. Good Manufacturing Practices for Pharmaceuticals: A Plan for Total Quality Control, Fourth Edition,
Revised and Expanded, Sidney H. Willig and James R. Stoker
79. Aqueous Polymeric Coatings for Pharmaceutical Dosage Forms: Second Edition, Revised and
Expanded, edited by James W. McGinity
80. Pharmaceutical Statistics: Practical and Clinical Applications, Third Edition, Sanford Bolton
81. Handbook of Pharmaceutical Granulation Technology, edited by Dilip M. Parikh
82. Biotechnology of Antibiotics: Second Edition, Revised and Expanded, edited by William R. Strohl
83. Mechanisms of Transdermal Drug Delivery, edited by Russell O. Potts and Richard H. Guy
84. Pharmaceutical Enzymes, edited by Albert Lauwers and Simon Scharpé
85. Development of ***aceutical Parenteral Dosage Forms, edited by John A. Bontempo
86. Pharmaceutical Project Management, edited by Tony Kennedy
87. Drug Products for Clinical Trials: An International Guide to Formulation • Production • Quality Control,
edited by Donald C. Monkhouse and Christopher T. Rhodes
88. Development and Formulation of Veterinary Dosage Forms: Second Edition, Revised and Expanded,
edited by Gregory E. Hardee and J. Desmond Baggot
89. Receptor-Based Drug Design, edited by Paul Leff
90. Automation and Validation of Information in Pharmaceutical Processing, edited by Joseph F. deSpautz
91. Dermal Absorption and Toxicity Assessment, edited by Michael S. Roberts and Kenneth A. Walters
92. Pharmaceutical Experimental Design, Gareth A. Lewis, Didier Mathieu, and Roger Phan-Tan-Luu
93. Preparing for FDA Pre-Approval Inspections, edited by Martin D. Hynes III
94. Pharmaceutical Excipients: Characterization by IR, Raman, and NMR Spectroscopy, David E. Bugay
and W. Paul Findlay
95. Polymorphism in Pharmaceutical Solids, edited by Harry G. Brittain
96. Freeze-Drying/Lyophilization of Pharmaceutical and Biological Products, edited by Louis Rey and Joan
C. May
97. Percutaneous Absorption: Drugs–Cosmetics–Mechanisms–Methodology, Third Edition, Revised and
Expanded, edited by Robert L. Bronaugh and Howard I. Maibach
98. Bioadhesive Drug Delivery Systems: Fundamentals, Novel Approaches, and Development, edited by
Edith Mathiowitz, Donald E. Chickering III, and Claus-Michael Lehr
99. Protein Formulation and Delivery, edited by Eugene J. McNally
100. New Drug Approval Process: Third Edition, The Global Challenge, edited by Richard A. Guarino
101. Peptide and Protein Drug Analysis, edited by Ronald E. Reid
102. Transport Processes in Pharmaceutical Systems, edited by Gordon L. Amidon, Ping I. Lee, and
Elizabeth M. Topp
103. Excipient Toxicity and Safety, edited by Myra L. Weiner and Lois A. Kotkoskie
104. The Clinical Audit in Pharmaceutical Development, edited by Michael R. Hamrell
105. Pharmaceutical Emulsions and Suspensions, edited by Francoise Nielloud and Gilberte Marti-Mestres
106. Oral Drug Absorption: Prediction and Assessment, edited by Jennifer B. Dressman and Hans
Lennernäs
107. Drug Stability: Principles and Practices, Third Edition, Revised and Expanded, edited by Jens T.
Carstensen and C. T. Rhodes
108. Containment in the Pharmaceutical Industry, edited by James P. Wood
109. Good Manufacturing Practices for Pharmaceuticals: A Plan for Total Quality Control from Manufacturer
to Consumer, Fifth Edition, Revised and Expanded, Sidney H. Willig
110. Advanced Pharmaceutical Solids, Jens T. Carstensen
111. Endotoxins: Pyrogens, LAL Testing, and Depyrogenation, Second Edition, Revised and Expanded,
Kevin L. Williams
112. Pharmaceutical Process Engineering, Anthony J. Hickey and David Ganderton
113. Pharmacogenomics, edited by Werner Kalow, Urs A. Meyer and Rachel F. Tyndale
114. Handbook of Drug Screening, edited by Ramakrishna Seethala and Prabhavathi B. Fernandes
115. Drug Targeting Technology: Physical • Chemical • Biological Methods, edited by Hans Schreier
116. Drug–Drug Interactions, edited by A. David Rodrigues
117. Handbook of Pharmaceutical Analysis, edited by Lena Ohannesian and Anthony J. Streeter
118. Pharmaceutical Process Scale-Up, edited by Michael Levin
119. Dermatological and Transdermal Formulations, edited by Kenneth A. Walters
120. Clinical Drug Trials and Tribulations: Second Edition, Revised and Expanded, edited by Allen Cato,
Lynda Sutton, and Allen Cato III
121. Modern Pharmaceutics: Fourth Edition, Revised and Expanded, edited by Gilbert S. Banker and
Christopher T. Rhodes
122. Surfactants and Polymers in Drug Delivery, Martin Malmsten
123. Transdermal Drug Delivery: Second Edition, Revised and Expanded, edited by Richard H. Guy and
Jonathan Hadgraft
124. Good Laboratory Practice Regulations: Second Edition, Revised and Expanded, edited by Sandy
Weinberg
125. Parenteral Quality Control: Sterility, Pyrogen, Particulate, and Package Integrity Testing: Third Edition,
Revised and Expanded, Michael J. Akers, Daniel S. Larrimore, and Dana Morton Guazzo
126. Modified-Release Drug Delivery Technology, edited by Michael J. Rathbone, Jonathan Hadgraft, and
Michael S. Roberts
127. Simulation for Designing Clinical Trials: A Pharmacokinetic-Pharmacodynamic Modeling Perspective,
edited by Hui C. Kimko and Stephen B. Duffull
128. Affinity Capillary Electrophoresis in Pharmaceutics and ***aceutics, edited by Reinhard H. H.
Neubert and Hans-Hermann Rüttinger
129. Pharmaceutical Process Validation: An International Third Edition, Revised and Expanded, edited by
Robert A. Nash and Alfred H. Wachter
130. Ophthalmic Drug Delivery Systems: Second Edition, Revised and Expanded, edited by Ashim K. Mitra
131. Pharmaceutical Gene Delivery Systems, edited by Alain Rolland and Sean M. Sullivan
132. Biomarkers in Clinical Drug Development, edited by John C. Bloom and Robert A. Dean
133. Pharmaceutical Extrusion Technology, edited by Isaac Ghebre-Sellassie and Charles Martin
134. Pharmaceutical Inhalation Aerosol Technology: Second Edition, Revised and Expanded, edited by
Anthony J. Hickey
135. Pharmaceutical Statistics: Practical and Clinical Applications, Fourth Edition, Sanford Bolton and
Charles Bon
136. Compliance Handbook for Pharmaceuticals, Medical Devices, and Biologics, edited by Carmen Medina
137. Freeze-Drying/Lyophilization of Pharmaceutical and Biological Products: Second Edition, Revised and
Expanded, edited by Louis Rey and Joan C. May
138. Supercritical Fluid Technology for Drug Product Development, edited by Peter York, Uday B. Kompella,
and Boris Y. Shekunov
139. New Drug Approval Process: Fourth Edition, Accelerating Global Registrations, edited by Richard A.
Guarino
140. Microbial Contamination Control in Parenteral Manufacturing, edited by Kevin L. Williams
141. New Drug Development: Regulatory Paradigms for Clinical Pharmacology and ***aceutics,
edited by Chandrahas G. Sahajwalla
142. Microbial Contamination Control in the Pharmaceutical Industry, edited by Luis Jimenez
143. Generic Drug Product Development: Solid Oral Dosage Forms, edited by Leon Shargel and Izzy Kanfer
144. Introduction to the Pharmaceutical Regulatory Process, edited by Ira R. Berry
145. Drug Delivery to the Oral Cavity: Molecules to Market, edited by Tapash K. Ghosh and William R.
Pfister
146. Good Design Practices for GMP Pharmaceutical Facilities, edited by Andrew Signore and Terry Jacobs
147. Drug Products for Clinical Trials, Second Edition, edited by Donald Monkhouse, Charles Carney, and
Jim Clark
148. Polymeric Drug Delivery Systems, edited by Glen S. Kwon
149. Injectable Dispersed Systems: Formulation, Processing, and Performance, edited by Diane J. Burgess
150. Laboratory Auditing for Quality and Regulatory Compliance, Donald Singer, Raluca-Ioana Stefan, and
Jacobus van Staden
151. Active Pharmaceutical Ingredients: Development, Manufacturing, and Regulation, edited by Stanley
Nusim
152. Preclinical Drug Development, edited by Mark C. Rogge and David R. Taft
153. Pharmaceutical Stress Testing: Predicting Drug Degradation, edited by Steven W. Baertschi
154. Handbook of Pharmaceutical Granulation Technology: Second Edition, edited by Dilip M. Parikh
155. Percutaneous Absorption: Drugs–Cosmetics–Mechanisms–Methodology, Fourth Edition, edited by
Robert L. Bronaugh and Howard I. Maibach
156. Pharmacogenomics: Second Edition, edited by Werner Kalow, Urs A. Meyer and Rachel F. Tyndale
157. Pharmaceutical Process Scale-Up, Second Edition, edited by Michael Levin
158. Microencapsulation: Methods and Industrial Applications, Second Edition, edited by Simon Benita
159. Nanoparticle Technology for Drug Delivery, edited by Ram B. Gupta and Uday B. Kompella
160. Spectroscopy of Pharmaceutical Solids, edited by Harry G. Brittain
161. Dose Optimization in Drug Development, edited by Rajesh Krishna
162. Herbal Supplements-Drug Interactions: Scientific and Regulatory Perspectives, edited by Y. W. Francis
Lam, Shiew-Mei Huang, and Stephen D. Hall
163. Pharmaceutical Photostability and Stabilization Technology, edited by Joseph T. Piechocki and Karl
Thoma
164. Environmental Monitoring for Cleanrooms and Controlled Environments, edited by Anne Marie Dixon
165. Pharmaceutical Product Development: In Vitro-ln Vivo Correlation, edited by Dakshina Murthy Chilukuri,
Gangadhar Sunkara, and David Young
166. Nanoparticulate Drug Delivery Systems, edited by Deepak Thassu, Michel Deleers, and Yashwant
Pathak
167. Endotoxins: Pyrogens, LAL Testing and Depyrogenation, Third Edition, edited by Kevin
L. Williams
168. Good Laboratory Practice Regulations, Fourth Edition, edited by Anne Sandy Weinberg
169. Good Manufacturing Practices for Pharmaceuticals, Sixth Edition, edited by Joseph
D. Nally
170. Oral-Lipid Based Formulations: Enhancing the Bioavailability of Poorly Water-soluble Drugs, edited by
David J. Hauss
171. Handbook of Bioequivalence Testing, edited by Sarfaraz K. Niazi
172. Advanced Drug Formulation Design to Optimize Therapeutic Outcomes, edited by Robert O. Williams
III, David R. Taft, and Jason T. McConville
173. Clean-in-Place for ***aceutical Processes, edited by Dale A. Seiberling
174. Filtration and Purification in the ***aceutical Industry, Second Edition, edited by Maik W. Jornitz
and Theodore H. Meltzer
175. Protein Formulation and Delivery, Second Edition, edited by Eugene J. McNally and Jayne E. Hastedt
176. Aqueous Polymeric Coatings for Pharmaceutical Dosage Forms, Third Edition, edited by James
McGinity and Linda A. Felton
177. Dermal Absorption and Toxicity Assessment, Second Edition, edited by Michael S. Roberts and
Kenneth A. Walters
178. reformulation Solid Dosage Form Development, edited by Moji C. Adeyeye and HarryP
G. Brittain
179. Drug-Drug Interactions, Second Edition, edited by A. David Rodrigues
180. Generic Drug Product Development: Bioequivalence Issues, edited by Isadore Kanfer and Leon
Shargel
181. Pharmaceutical Pre-Approval Inspections: A Guide to Regulatory Success, Second Edition, edited by
Martin D. Hynes III
182. Pharmaceutical Project Management, Second Edition, edited by Anthony Kennedy
183. Modified Release Drug Delivery Technology, Second Edition, Volume 1, edited by Michael J. Rathbone,
Jonathan Hadgraft, Michael S. Roberts, and Majella E. Lane
184. Modified-Release Drug Delivery Technology, Second Edition, Volume 2, edited by Michael J. Rathbone,
Jonathan Hadgraft, Michael S. Roberts, and Majella E. Lane
185. The Pharmaceutical Regulatory Process, Second Edition, edited by Ira R. Berry and Robert P. Martin
186. Handbook of Drug Metabolism, Second Edition, edited by Paul G. Pearson and Larry
C. Wienkers
187. Preclinical Drug Development, Second Edition, edited by Mark Rogge and David R. Taft
188. Modern Pharmaceutics, Fifth Edition, Volume 1: Basic Principles and Systems, edited by Alexander T.
Florence and Jurgen Siepmann
189. Modern Pharmaceutics, Fifth Edition, Volume 2: Applications and Advances, edited by Alexander T.
Florence and Jurgen Siepmann
190. New Drug Approval Process, Fifth Edition: Global Challenges and Solutions, edited by Richard A.
Guarino
191. Drug Delivery Nanoparticulate Formulation and Characterization, edited by Yashwant Pathak and
Deepak Thassu
192. Polymorphism in Pharmaceutical Solids, Second Edition, edited by Harry G. Brittain