PMP catalouge---sep--2011---Final.pmd - BS Publication

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PharmaMed Press Poucher’s Perfumes Cosmetics & Soaps, 10 th Ed. 6 Butler H. Contents : Part I : Historical Background 1. W.A. Poucher’s Influence on the Early Cosmetic Industry 2. Cosmetics Through the Ages Part II : Cosmetics for Everyday Use 3. Antiperspirants and Deodorants 4. Batch and Shower Products 5. Colouring Materials used in Decoratie Cosmetics and Colour Matching 6. Decorative Cosmetics 7. Dental Hygiene 8. Hair Treatments 9. Hair Shampoos 10. Hair Colourants 11. Manicure Preparation 12. Men’s toiletries 13. Pressurized Dispenser 14. Skin Preparations 15. Soap 16. Sun Damage and Sunscreen Preparation Part III : Quality, Stabilitu and Safety Assurance 17. Analytical Methods 18. Efficacy Testing of Cosmetics and Toiletries 19. Emulsion Theory 20. Legislation and Safety Regulations for Cosmetics in the United States, the European Union and Japan 21. Microbiological Control of Cosmetics 22. Safety 23. Stability Testing Part IV : Perfumes, Their Manufacture in Products and Psychology in Use 24. Perfume and the Manufacture of Consumer Products 25. The Psychology of Fragrance and Armatherapy Rpt. 2007 978-81-8128-370-2 782 pages HB Rs. 1750.00 Pharmaceutical Dissolution Testing Jennifer J. Dressman and Johannes Kramer Contents: 1. Historicial Development of Dissolution Testing 2. Compendial Testing Equipment: Qualification, and Sources of Error 3. Compendial Requirements of Dissolution Testing-European Pharmacopoeia, Japanese Pharmacopoeia, United States Pharmacopoeia 4. The Role of Dissolution Testing in the Regulation of Pharmaceuticals: The FDA Perspective 5. Gastrointestinal Transit and Drug Absorption 6. Physiological Parameters Relevant to Dissolution Testing: Hydrodynamic Considerations 7. Development of Dissolution Tests on the Basis of Gastrointestinal Physiology 8. Orally Administered Drug Products: Dissolution Data Analysis with a View to In Vitro-In Vivo Correlation 9. Interpretation of In Vitro-In Vivo Time Profiles in Terms of Extents, Rates, and Shape 10. Study Design Considerations for IVIVC Studies 11. Dissolution Method Development with a View to Quality Control 12. Dissolution Methods Development: An Industry Perspective 13. Design and Qualification of Automated Dissolution Systems 14. Bioavailability of Ingredients in Dietary Supplements: A Practical Approach to the In Vitro Demonstration of the Availability of Ingredients in Dietary Supplements Rpt. <strong>2011</strong> 0-82475-467-0 448 pages HB Rs. 1995.00 Oral Drug Delivery Technology Aukunuru Jithan Contents : 1. New Drug Substances 2. Evaluation of Early Development Candidates- Physical Properties 3. Evaluation of Early Development Candidates-Drug Safety 4. Complimentary Techniques for Solid State Drug Analysis 5. Salt Selection, Characterization and Polymorphism Assessment 6. Dissolution Testing 7. Oral Formulations 8. Novel Drug Delivery Systems 9. Oral Drug Regulatory Departments and Guidelines 10. Pharmaceutical Technology 11. Product Processing and Evaluation 12. Quality Control Investigations 13. Biotechnology Products 14. Gastro-Intestinal Tract Membrane : Drug Transport 15. Oral Pharmacokinetics 16. Biopharmaceutics-A Clinical Trial Perspective 17. Drug Absorption Study Models 18. Drug Absorption Improvement Techniques 19. Prodrugs: Design, Kinetic Study and Synthesis 20. Pharmaceutical Statistics in Oral Drug Development 21. Statistical Methodologies in the Quality Control of the Industrial Processess: An Oral Drug Industry Perspective 2007 81-88449-28-8 637 pages HB Rs. 1495.00 Pharmaceutical Process Scale-Up, 2 nd Ed. Michael Levin Contents : 1. Dimensional Analysis and Scale-up in Theory and Industrial Application 2. Engineering Approaches for Pharmaceutical Process Scale-up, Validation, Optimization, and Control in the PAT Era 3. Parenteral Drug Scale-up 4. Non- Parenteral Liquids and Semi-Solids 5. Scale-up Considerations for Biotechnology Derived Products 6. Batch size increases in Dry Blending and Mixing 7. Batch size increase and Powder Handling 8. Scale-up in the field of Granulation and Drying 9. Scale-up of Roller compaction Process. Rpt. 2007 1-57444-876-5 538 pages HB Rs. 2495.00 Biodegradable Polymers as Drug Delivery Systems Mark Chasin Contents: 1. Controlled release of bioactive agents from lactide/glycolide polymers 2. Polyanhydrides as Drug Delivery Systems 3. Poly-e-caprolactone and its copolymers 4. Poly(ortho esters) 5. Polyphosphazenes as new biomedical and bioactive materials 6. Pseudopoly (amino acids) 7. Natural polymers as drug delivery systems 8. Liposomes Rpt. 2008 0-82478-344-1 368 pages HB Rs.1995.00 Triggered Drug Delivery: Physical Methods and Applications Colin P. McCoy Pharmaceutics NEW Contents: 1. Introduction 2. Light-Triggered Systems 3. Chemically-Triggered Systems 4. Thermally-Triggered Systems 5. Magnetism-Triggered Systems 6. Ultrasound-Triggered Systems 7. Electrically-Triggered Systems 8. Pressure-Triggered Systems <strong>2011</strong> 978-1420099690 296 pages HB £ 82.00 Phone : 040-23445688, 23445605 Fax: 91+40-23445611 e-mail: info@bspbooks.net website: www.bspublications.net Prices are subject to change without prior notice
Pharmaceutics PharmaMed Press International Stability Testing David J. Mazzo Contents : 1. The ICH Stability Guideline; David J. Mazzo 2. Photostability Testing; Terry G. Beaumont 3. The ICH Stability Guideline for Biological and Biotechnological Products; Manfred Haase 4. Stress Testing Program : Drug Substance Characterization Studies; Elisabeth Pacaud 5. Statistical and Regulatory Aspects of Drug Stability Studies : An FDA Perspective; William R. Fairweather, Tsae-Yun Daphne Lin 6. Matrixing and Bracketing Designs for Stability Studies : An Overview from the European Perspective; Per Helboe 7. Assessment of Preservative Activity During Stability Studies; Norman Hodges 8. Drug Substance Solid-State Characterization and Stability; Ivan Santos 9. Variations and Changes in Europe; Stability Requirements; Anthony C. Cartwright 10. Postapproval FDA Stability Requirements ; Dhiren N. Shah 11. Current Application in Japan of the ICH Stability Guidelines : Does Japanese Registration Require More Than Others Do ?; Sumie Yoshioka – 12. Stability Testing for Australia; Susan Walters 13. The WHO Stability Guideline; Sabine Kopp-Kubel Manuel Zahn 14. Stability Testing Considerations for Some Non-ICH Areas; Terry G. Beaumont Rpt. 2005 1-57491-078-7 332 pages HB Rs. 4495.00 Microencapsulation: Methods and Industrial Applications, 2 nd Ed. Simon Benita Contents : 1. Biodegradable Microsphere : Advances in Production Technology 2. Advances in the Technology for Controlled Release Pesticide Formulations 3. Multiparticulate Pulsatile Drug Delivery for Parenteral Depot Systems and their Application in the Pharmaceutical Industry 5. Coupling Methods to Obtain Ligand-Targeted Liposomes and Nanoparticles 6. Industrial Technologies and Scale up 7 Evaluation and Characterization of Micro- and Nanoparticulate Drug Delivery Systems. Drug Release from Microparticulate Systems. Rpt. 2007 0-8247-2317-1 756 pages HB Rs. 2495.00 Stability of Drugs and Dosage Forms Sumie Yoshioka & Valentino J. Stella Contents : 1. Introduction 2. Chemical Stability of Drugs Substances 3. Physical Stability of Drugs Substances 4. Stability of Dosage Forms 5. Stability of Peptide and Protein Pharmaceuticals 6. Regulations Rpt. 2009 978-81-8128-239-2 268 pages HB Rs. 1250.00 Statistical Design and Analysis of Stability Studies Shein-Chung Chow Contents : 1. Introduction 2. Accelerated Testing 3. Expiration Dating Period 4. Stability Designs 5. Stability Analysis with Fixed Batches 6. Stability Analysis with Random Batches 7. Stability Analysis with a Mixed Effect Model 8. Stability Analysis with Discrete Responses 9. Stability Analysis with Multiple Components 10. Stability Analysis with Frozen Drug Products 11. Stability Testing for Dissolution 12. Current Issues and Recent Developments Rpt. 2010 978-1-584889-05-2 330 pages PB Rs. 895.00 Physical Pharmacy Essentials of Physical Pharmacy, 2 nd Ed. Derle Deeliprao V. and Sai Hanuman Sagar Boddu Contents: 1. States of Matter 2. Physical Properties of Drug Molecules 3. Phase Rule 4. Thermodynamics 5. Rheology 6. Diffusion and Dissolution 7. Colloids 8. Chemical Kinetics 9. Solutions of Non-electrolytes 10. Solutions of Electrolytes 11. Solubility and Distribution Phenomena 12. The Solid State 13. Micromeritics 14. Interfacial Phenomena 15. Units and Measures 16. Buffers and Buffered Isotonic Systems 17. Ionic Equilibria 18. Complexation 19. Coarse Dispersions 20. Electromotive Force and Oxidation-Reduction Systems 21. Some Basic Formulae Useful for Calculations 2010 978-81-910192-5-4 339 pages PB Rs. 210.00 Physical Pharmacy: Practical Text Guru Prasad Mohanta & Prabal Kumar Manna Contents: 1. SI Systems of Units 2. Solubility 3. Distribution Coefficient 4. Density 5. Bulk Density 6. Specific Gravity 7. Flow Properties 7a Carr’s Index 8. Dissociation Constant (pKa) 9. Surface Tension 10. Buffer 11. Micromeritics 12. Viscosity 13. Adsorption Isotherm 14. Physical Stability of Suspension 15. Physical Stability of Emulsion 16. Complexation 17. Rate Kinetics 18. Stability Testing 2009 81-88449-22-9 99 pages PB Rs. 100.00 Phone : 040-23445688, 23445605 Fax: 91+40-23445611 e-mail: info@bspbooks.net website: www.bspublications.net Prices are subject to change without prior notice 7
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