Friday, July 24, 2015
Sunday, August 2, 2009
Play The Game "KAUN BANEGA THE BEST PHARMACIST!"
About the Game and Anchors
This Game is a ditto copy of KAUN BANEGA COREPATI that first anchored by the great actor Amithab Bachan and later Sharookh Khan. But our game " BANEGA THE BEST PHARMACIST!" is anchored by two cartoon characters they are Timon and Pumbaa, may be you know them well coz they are the main part Of Lion King a cartoon from Disney. Wish you all the best.
This game is absolutely free for download, created to promote http://groups.google.co.in/group/variety-mails
Some times the anchor Timon will call you bad words just don’t mind him coz he is our cute gust here. Wishing you all success in this game.
Some times the anchor Timon will call you bad words just don’t mind him coz he is our cute gust here. Wishing you all success in this game.
Before go for downloading the game join here in http://groups.google.co.in/group/variety-mails/
Because the game promoted by variety mails and will receive the updates of the game.
Things that You want to be Carefull while Playing
Here I had uploaded the game as in zip (2011kb) format before playing you want to extract all contents to single folder or to desktop then only the links will work and you can enjoy the game well.
Aftergetting started the game you just don’t press key board, if you selected a wrong answer press ESC key from key board and restart the game
Use your mouse to play, click on the right answer. Once you selected the wrong answer press the "Esc" keys from the key board.
Questions that Going to be asked in the Game
All the questions thats going to be asked in the game is from an Exam conducted by kerala public service commition on 28/07/2009. Simple questions are selected, here qustions are not the matter see the fun with our Anchores.
See Our Anchors
Timon The Anchor
Pumbaa Second Anchor
Download Links You can Use any One
Before go for download just click here http://groups.google.com/group/variety-mails and join over there in the group then only you can download.
Thank You
Wednesday, January 28, 2009
Medical Dictionary
A to Z Drug Facts: Published by Facts and Comparisons
This compact, portable, alphabetically organized drug reference provides quick access to current, reliable information on more than 4,500 commonly prescribed medications. Each drug monograph is divided into pharmacological and patient care considerations, and includes action, indications, contraindications, route/dosage, interactions, lab test interferences, adverse reactions, precautions/warnings, administration/storage, assessment/interventions, and patient/family education. Icons and a second color are used to help readers quickly locate the information they are looking for. A color identification section enables readers to identify drugs by appearance. Coverage includes the newest FDA approvals, investigational and orphan drugs, and indications for labeled, unlabeled, and orphan uses.
Pharmacy
Handbook, Second Edition
It is crucial that pharmacists understand the language of health care professionals and, in turn, can convey the information in an understandable fashion to patients. Procter & Gamble Pharmacist's Handbook, Second Edition facilitates this communication. Now, all in one place, you can have medical terms, abbreviations, and patient counseling principles right at your fingertips. The handbook begins with an Inverted Medical Dictionary to translate lay terminology to more technical vocabulary and an Eponyms section to translate medical terminology to language that is comprehensible to patients. The Dictionary shows how to analyze the medical terms by identifying its root, suffix, and prefix. This examination is supplemented with numerous tables of common roots, suffixes, and prefixes. The book concludes with a glossary of managed care terms that will help you understand the language of the insurance community. Another critical responsibility of a pharmacist is to clearly comprehend a prescription. The sections containing Medical Abbreviations and Terms Used in Prescription Writing will aid in this vital task. Also included in the handbook are general references, such as normal laboratory values, conversion factors, and weights and measures. These features make Procter & Gamble Pharmacist's Handbook, Second Edition a convenient and handy resource for the practicing pharmacist.
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Encyclopedia of Molecular Pharmacology, 2nd edition
An essential text, this is a fully updated second edition of a classic, now in two volumes. It provides rapid access to information on molecular pharmacology for research scientists, clinicians and advanced students. With the A-Z format of over 2,000 entries, around 350 authors provide a complete reference to the area of molecular pharmacology. The book combines the knowledge of classic pharmacology with the more recent approach of the precise analysis of the molecular mechanisms by which drugs exert their effects. Short keyword entries define common acronyms, terms and phrases. In addition, detailed essays provide in-depth information on drugs, cellular processes, molecular targets, techniques, molecular mechanisms, and general principles.
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Illustrated Pocket Dictionary of Chromatography
The Illustrated Pocket Dictionary of Chromatography offers the perfect quick reference to the parameters, systems, and components that support successful chromatographic separations. Concise, practical, and filled with detailed drawings, diagrams, and photographs, this pocket dictionary is designed for easy use in the laboratory. It provides a complete, up-to-date reference on analytical techniques such as gas chromatography, high-performance liquid chromatography, thin layer chromatography, and capillary electrophoresis as well as preparation techniques such as solid phase extraction and microextraction.
Ideal for the working chemist or technician in pharmaceutical, industrial, forensic, government, or other lab settings, the Illustrated Pocket Dictionary of Chromatography is also appropriate as a supplemental reference for analytical chemistry courses and labs. Students and analysts alike will find this compact yet comprehensive resource a valuable companion to their work in chromatography
Encyclopedia of Analytical Chemistry: Applications, Theory, and Instrumentation
The highly acclaimed Encyclopedia of Analytical Chemistry provides a much needed professional level reference work for the 21st Century. Encyclopedia of Analytical Chemistry is the most comprehensive analytical chemistry reference available, covering all aspects from theory and instrumentation through applications and techniques.
The chemistry and techniques are described as performed in the laboratory (environmental, clinical, QC, research, university), in the field or by remote sensing. The level of detail is similar to that of a lab protocol and together with the cited references, will support the analysis of complex inorganic, organic and biological structures by academic and industrial researchers. Encyclopedia of Analytical Chemistry also enables preparation of procedures, protocols and "cookbooks" by managers and staff of laboratories.
Encyclopedia of Analytical Chemistry comprises over 600 articles, arranged alphabetically by topic, in approximately 14000 pages, in 15 volumes.
Features:
* Outstanding authorship and the highest calibre editors
* Excellence of peer-review
* Article Summaries
* Over 6500 illustrations, many in colour
* Extensive cross-referencing to facilitate navigation between articles
* Extensive bibliographies with up-to-date references
Encyclopedia of Analytical Chemistry is the essential cross-disciplinary reference work for all analytical chemists in academia and industry. All fields of chemical research are covered: analytical, organic, physical, polymer, inorganic biomedical, environmental, pharmaceutical, industrial, petroleum, forensics and food science.
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Color Atlas of Pharmacology, 3rd Edition
Updated with the most important new substances and scientific developments, the third edition of The Color Atlas of Pharmacology makes it easier than ever for students, nurses, and practicing physicians to keep up with the latest developments in this constantly changing field. Featuring a user-friendly layout, jargon-free language, and more than 160 spectacular color charts and illustrations, the atlas is divided in to four, color-coded sections:
Part 1 - General pharmacology - includes descriptions of substance formulation, absorption, distribution, elimination, and molecular mechanisms of action Part 2 - Systems pharmacology - with special emphasis on the functional and therapeutic aspects of a wide range of medicinal agents Part 3 - Therapy of selected diseases - such as osteoporosis, acute myocardial infarction, migraine, asthma, tropical diseases, and many more Part 4 - Drug Index - helpfully listed by substance, generic, and brand names
Annual reference provides a comprehensive evidence-based collection of more than 1,000 drug monographs. Each listing includes FDA-approved uses, evidence-based coverage of off-label uses, drug interactions, cautions, toxicity, dosage recommendations, coverage of pharmacology and pharmacokinetics, and more. For pharmacists and other healthcare professionals. Softcover.
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Peptides from A to Z: A Concise Encyclopedia
This mini-encyclopedia contains more than 1,500 alphabetical entries from the entire field of peptide science in one handy volume, as well as the technical terms, acronyms and concepts used in peptide chemistry. It also features the complete sequence of more than 800 peptides, numerous illustrations and numerous cross-references.
Areas covered include:
- biological peptides and small proteins
- peptide hormones
- pharmaceutical peptides
- peptide antibiotics
- peptide inhibitors
- peptide reagents
- peptide tags
- structural classes
- synthesis and purification
- analytical methods
- proteomics and peptidomics.
Condensed yet accessible, only essential information is displayed, extensively linked via references to the recent scientific literature for further study.
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Elsevier's Dictionary of Vitamins and Pharmacochemistry
v
The dictionary will contain terms covering the following fields and subfields: Vitamin Technology: Vitamin biochemistry / Physiology; Origin of vitamins: natural, synthetic; Fat-soluble vitamins; Water-soluble vitamins; Vitamins as antioxidants; Vitamin deficiencies / Hypervitaminosis - Enzymes/Proteins: Biotechnology as applied biological science aimed at industrial exploitation - Hormones: Biochemistry; Physiology - Pharmaceutical Chemistry / Pharmaceutical Technology / Pharmaceutical Processes: Conception of the active principles; Structural analysis; Antibiotics and their way of action; Biochemistry; The Drug / The Medicament: Definition, origin, way of action; Biochemistry - Medical Aspects in the languages English, German, French and Portuguese..
*An important resource for pharmacologists, pharmaceutists and medical doctors
*Includes definitions in several prominent languages (English, German, French, Portuguese)
*Covers subfields of Vitamin Technology, Enzymes/Proteins, Hormones, Pharmaceutical Chemistry, Pharmaceutical Technology, Pharmaceutical Processes, and more.
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(Download tips: When u click in download it goes to megaupload where you can see a picture code you type it in the box and click download then you wait for few seconds a free download button will appear near to premium download. Click there in free download.)
This is the sixth edition of Medicines: The Comprehensive Guide – the most popular and best-selling dictionary-style reference source-book for the range of medicines, along with possible side-effects, that is available in the UK today. Previous editions of this book have sold almost two million copies. The text has been extensively revised – to take account of the many new drugs, both generic and proprietary, as well as entire new drug groups, that have been developed and marketed since publication of the fifth edition in 2000. Changes in details of those medicines that remain on the market are also included. Requests from the public have led to the inclusion in this edition of expanded warnings about possible interactions between drugs with other medicines – especially those that can be obtained without a prescription –herbal remedies and nutritional supplements. There is also an expanded glossary of medical terms, which hopefully readers will find useful in understanding some of the more technical terms.
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Dictionary of Pharmacoepidemiology
Written by an internationally renowned authority in the field, this is the most complete dictionary devoted specifically to the terms currently used in pharmacoepidemiology. The use of
clear and consistent terminology in science has never been more important, and this dictionary, which has been translated from the third edition of a French original, has been reworked to include suggestions made by pharmacoepidemiologists currently using existing versions. It contains revised definitions for nearly all established terms in addition to comprehensive descriptions of new terms and is well illustrated with practical examples. This outstandingly high-quality dictionary will be essential for all those whose work is within or touches upon this field: regulatory authorities, pharmaceutical physicians, lawyers, pharmacists, researchers, evaluators and students.
Dictionary of Medical Acronyms & Abbreviations (5th Edition)
This best-selling portable resource provides authoritative definitions for all of the medical acronyms and abbreviations you can expect to encounter in medicine today. The new, 5th Edition features 10,000 completely new entries reflecting the most recent developments in health careincluding new clinical trials, new technologies, and new advances. Highlights include the latest virus nomenclature, computer technology, medical informatics, and molecular biology, along with more from the ever-expanding list of organizations and associations.
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Tuesday, January 27, 2009
Good Manufacturing Practice ( GMP )
Good Design Practices for GMP Pharmaceutical Facilities
A convenient single-source reference for anyone involved in the planning, construction, validation, and maintenance of modern pharmaceutical facilities, this guide assists project managers as they develop, diagram, and implement pharmaceutical production facility projects-demonstrating how advances in technology and external regulation can impact the production and efficacy of a pharmaceutical facility and the products it produces.
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Good Pharmaceutical Manufacturing Practice: Rationale and Compliance
With over twenty different official regulatory statements worldwide on Good Manufacturing Practice (GMP) for pharmaceutical, drug, or medicinal products, two stand out as being the most influential and most frequently referenced. Bridging the gap between U.S. regulations and European Good Manufacturing Practice guidelines, Good Pharmaceutical Manufacturing Practice: Rationale and Compliance gleans the most important substance from the U.S. Current Good Manufacturing Practice, parts 210 and 211 (US cGMPs, 2002) and the European Guide to Good Manufacturing Practice for Medicinal Products for Human and Veterinary Use (EU GMP guide, 2002). The author uses his 40+ years of experience in technical management, production, quality assurance, and distribution within the pharmaceutical industry, offering a hands-on guide to better understand and implement optimal pharmaceutical practices. This book also compares the principle requirements of GMP, and explores the reasoning behind these requirements and ways to comply with them. Relevant topics include personnel, documentation, premises and equipment, production, quality control, self-inspection, recalls, and more. This is an essential guidebook for those who wish to expand their pharmaceutical business in any international capacity.
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FDA Regulatory Affairs: A Guide for Prescription Drugs, Medical Devices, and Biologics
This book covers the regulatory process for getting pharmaceuticals, biologics, and medical devices approved. It examines the pertinent aspects of the Federal Food, Drug and Cosmetic Act as it applies to human drug and device development, research, manufacturing, and marketing. Topics include: the drug approval process, Current Good Manufacturing Practices, Good Clinical Practices, Quality System Compliance and the corresponding documentation requirements, and FDA inspection processes and enforcement options. Although many references exist on this subject, this one is written in a general prose style that makes it useful to both students and professionals.
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Cyclic Gmp: Synthesis, Metabolism, and Function
This volume is dedicated to the topic of cyclic GMP. Chapters include discussions on the guanylyl cyclase and phosphodiesterase isoenzyme families for cyclic GMP synthesis and hydrolysis, cyclic GMP-dependent protein kinases, and various hormones and ligands that regulate cyclic GMP formation and/or metabolism. Several chapters also deal with some of the effects of cyclic GMP on other second messengers such as calcium ion transport and smooth muscle relaxation. Some clinical studies with cyclic GMP and atrial natriuretic peptide are also discussed. The last chapter raises many important questions in the field that remain to be addressed.
Key Features
* Isoforms of guanylyl cyclase and phosphodiesterase isoenzyme families for cyclic GMP synthesis and hydrolysis
* Cyclic GMP-dependent protein kinase
* Hormones and ligands that regulate GMP formation and/or metabolism
* Effects of cyclic GMP on other second messengers and some functions such as smooth muscle relaxation and ion transport
* Clinical studies with cyclic GMP and atrial natriuretic peptide
* Important questions and experiments for the future.
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Pharmaceutical Master Validation Plan: The Ultimate Guide to FDA, GMP, and GLP Compliance
The Master Validation Plan provides a roadmap to management for on-time start-up of facility operations, and validation of existing facilities, in compliance with GMP requirements. The lack of a comprehensive Master Validation Plan and well-documented validation procedures is the main reason that new drug, medical device, medical equipment, and related product applications are rejected by the FDA. In fact, only about 2% of the applications submitted by foreign pharmaceutical companies are approved each year. This thorough guide provides the needed solutions and guidance for both foreign and U.S. companies to achieve FDA compliance and authorization to market their products in the United States. Pharmaceutical Master Validation Plan: The Ultimate Guide to FDA, GMP, and GLP Compliance will allow you to more easily achieve satisfactory inspections, new medical product approval, minimize non-conformance, reduce rework and rejected lots, and avoid recall lots by developing and managing a Master Validation Plan. The accompanying CD allows users to input the template plan into their computers and tailor it to incorporate additional regulatory requirements specific to individual companies worldwide and print the required documents. Together, the book and CD contain everything required to develop and execute a successful Master Validation Plan based on FDA guidelines for the pharmaceutical industry, and allows the templates to be extended to diagnostic products, medical device, medical equipment, and biotech industry products.
Compact Regs Parts 210 and 211: CFR 21 Parts 210 and 211 Pharmaceutical and Bulk Chemical GMPs
Sterile Product Facility Design and Project Management, Second Edition
Examines harmonization of the US Federal Food, Drug, and Cosmetic Act with international regulations as they apply to human drug and device development, research, manufacturing, and marketing. The Second Edition focuses on the new drug approval process, cGMPs, GCPs, quality system compliance, and corresponding documentation requirements. Written in a jargon-free style, it draws information from a wide range of resources. It demystifies the inner workings of the FDA and facilitates an understanding of how it operates with respect to compliance and product approval.
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A Practical Guide to Quality Management in Clinical Trial Research
Setting up a GXP environment where none existed previously is a very daunting task. Getting staff to write down what they do for every task is a correspondingly difficult and time-consuming exercise. Examining how to maintain quality control in clinical trial research, A Practical Guide to Quality Management in Clinical Trial Research provides a cornerstone of knowledge for establishing a quality system that complies with the relevant regulations. There are many books available that cover how to interpret regulations. Going a step or two further, this book provides practical advice that is useful on a daily basis. The book contains information for various standards including GLPs, GCPs, and GMPs. It gives detailed explanations of how to prepare, update, and maintain SOPs and includes advice on training and development of personnel. Drawing directly on his years of experience, the author delineates a from-the-trenches methodology that creates a value-added quality management system from a business perspective. He provides a solid foundation as well as tips and techniques for establishing a quality system that will comply with all the relevant regulations. The author's integrated approach and anecdotal style turns technically accurate information into easy reading. The book arms you with tools and concepts that you can use to go beyond regulatory compliance and move into the realm of business quality improvement.
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Quality (Pharmaceutical Engineering Series), Volume 2
The Pharmaceutical Engineering Series is a comprehensive reference for the pharmaceutical professional covering all aspects from quality, documentation and validation through manufacturing processes to facility design and management. In 'Quality', Dr Kate McCormick provides the reader with comprehensive coverage of this vital subject, including the quality life cycle, management and cost of quality, GMP, auditing and inspections. This book with the others in the series will become a unique source of reference and educational material for the readership.
Case studies and examples make the book of direct practical relevance to the professional in the pharmaceutical industry
Find the answers you are looking for quickly and easily with clear indexing and referencing
Reference to international standards and practice mean this book will be useful wherever you are working.
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Pharmaceutical Pre-Approval Inspections: A Guide to Regulatory Success, Second Edition
This Second Edition is an essential guide to preparing for FDA pre-approval inspections—taking into account current trends in FDA expectations and inspection activities, such as the GMPs of the 21st Century, quality systems-based approach to inspections, risk-based inspections, quality by design, process analytical technology, design space, etc. The goal of this book is to help organizations gain rapid regulatory approval.
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Guide to Microbiological Control in Pharmaceuticals and Medical Devices, Second Edition
Microbiological matters continue to exercise considerable influence on product quality. In both the pharmaceutical and medical device industries, products of greater sophistication, along with evolving regulatory requirements, are elevating the challenges related to maintaining microbiological integrity.
Updated to reflect technological and regulatory changes, the Guide to Microbiological Control in Pharmaceuticals and Medical Devices, Second Edition covers thoseprincipal aspects of microbiology that arerelevant to the preformulation, formulation, manufacturing, and license application stages involved with the production of pharmaceuticals and medical devices. In recognition of the diverse disciplines involved in pharmaceutical and medical device production, this work provides a brief introduction to microbiology geared towards the nonmicrobiologist. Covering good manufacturing practice in the control of contamination, the text explores quality control, the preservation of formulations, and principles of sterilization, including microbiological-specific considerations for biotechnological products and other medical devices. It also provides additional materials on package integrity and contamination risks in clean rooms. The editors have produced a companion text, the Handbook of Microbiological Quality Control in Pharmaceuticals and Medical Devices (see reverse), which when paired with the Guide offers a complete theoretical and practical treatment of microbiological control. This book provides a comprehensive distillation of information concerning methodology and regulations that would otherwise remain scattered throughout the literature. It allows scientists from many fields to address potential problems in advance and implement suitable strategies at the earliest stages of development.
Establishing A CGMP Laboratory Audit System: A Practical Guide
The first systematic, hands-on auditing guide for today's pharmaceutical laboratories
In today's litigious environment, pharmaceutical laboratories are subject to ever stricter operational guidelines as mandated by the FDA, and must be able to establish and demonstrate sustainable operational practices that ensure compliance with the current good manufacturing practice (CGMP) regulations. David Bliesner's Establishing a CGMP Laboratory Audit System: A Practical Guide is designed to provide laboratory supervisors and personnel with a step-by-step, hands-on audit system that they can rely on to ensure their facility remains compliant with all current and future requirements. Focusing on a "team approach," the author uses detailed flowcharts, checklists, and descriptions of the auditing process to help readers develop a new audit system or upgrade their current system in order to:
* Improve current compliance
* Demonstrate sustainable compliance
* Produce data for federal inspections
* Avoid regulatory action
This book provides an ideal resource for new and future laboratory personnel, and an excellent means for keeping existing industry practitioners up to date on the nuances of operating a consistently compliant pharmaceutical laboratory.
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Method Validation in Pharmaceutical Analysis: A Guide to Best Practice
Adopting a practical approach, the authors provide a detailed interpretation of the existing regulations (GMP, ICH), while also discussing the appropriate calculations, parameters and tests. The book thus allows readers to validate the analysis of pharmaceutical compounds while complying with both the regulations as well as the industry demands for robustness and cost effectiveness.
Following an introduction to the basic parameters and tests in pharmaceutical validation, including specificity, linearity, range, precision, accuracy, detection and quantitation limits, the text focuses on a life-cycle approach to validation and the integration of validation into the whole analytical quality assurance system. The whole is rounded off with a look at future trends
With its first-hand knowledge of the industry as well as regulating bodies, this is an invaluable reference for analytical chemists, the pharmaceutical industry, pharmaceutists, QA officers, and public authorities.
Pharmaceutical Manufacturing Handbook: Regulations and Quality
Everything you need to ensure full compliance and superior quality control
With its coverage of Food and Drug Administration regulations, international regulations, good manufacturing practices, and process analytical technology, this handbook offers complete coverage of the regulations and quality control issues that govern pharmaceutical manufacturing. In addition, the book discusses quality assurance and validation, drug stability, and contamination control, all key aspects of pharmaceutical manufacturing that are heavily influenced by regulatory guidelines.
The team of expert authors, all familiar with the many issues involved in compliance and quality control, offer you advice based on their own firsthand experience in all phases of pharmaceutical manufacturing. The editor, who has more than thirty years' experience working with pharmaceutical and biotechnology companies, carefully reviewed all the chapters to ensure that each one is thorough, accurate, and clear.
* Among the key topics covered are:
* Enforcement of current good manufacturing practices
* Inspections by health regulatory agencies
* Creating and managing a quality management system
* Personnel training within pharmaceutical manufacturing
* Microbiology of non-sterile pharmaceutical manufacturing
Pharmaceutical manufacturing validation principles
Following the handbook's carefully developed guidelines and advice helps you ensure your company's full compliance and avoid potential costly pitfalls. This publication should be readily accessible to all scientists, engineers, and managers involved in pharmaceutical manufacturing.
Good Manufacturing Practices and Inspection (Quality Assurance of Pharmaceuticals)
Quality assurance of pharmaceutical products is a continuing concern of WHO. Despite efforts made around the world to ensure a supply of quality and effective medicines, substandard, spurious and counterfeit products still compromise health care delivery in many countries. To respond to the global need for adequate quality assurance of pharmaceuticals, WHO's Expert Committee on Specifications for Pharmaceutical Preparations has over the years made numerous recommendations to establish standards and guidelines and to promote the effective functioning of national regulatory and control systems and the implementation of internationally agreed standards by trained personnel. Many of the relevant documents endorsed by the Committee are reproduced in this volume, providing guidance covering all aspects of good manufacturing practices (GMP). Important texts on inspection are also included. Most of the material has been published separately in the Expert Committee's reports. This compendium brings it together to make it more accessible and of greater practical value to those working in faculties of pharmacy, in medicines regulation and control, and in the pharmaceutical industry
Monday, January 26, 2009
Liposome
Liposomes are artificial microscopic vesicles consisting of an aqueous core enclosed in one or more phospholipid layers, used to deliver drugs.
E - Books Related To Liposomal Drug Delivery
Its absolutely free Ebooks for you peoples
Edited by: Andrew S. Janoff
This up-to-date reference covers the basics of liposomology, offering insights from over 30 scientists involved in its growth and considering the direction of future developments. Describes the liposome patent portfolio developed over the last 30 years! Outlining the procedures that bring liposome pharmaceuticals from laboratory to clinic, Liposomes · discusses the design of clinical trials · analyzes morphological diversity and functionality in gene delivery · highlights antitumor activities of lipids acting as second messengers · suggests how antibodies to cholesterol can be used therapeutically · explores applications of liposomes with high captured volumes · details the clinical detection of antilipid antibodies · addresses the lyophilization of liposomes · and more! With over 1400 references, tables, drawings, and photographs, Liposomes is suitable for industrial, clinical, and research pharmacists; pharmacologists; research and development scientists in the pharmaceutical, food, cosmetic, veterinary, agricultural, and chemical industries; biochemists; industrial, medicinal, organic, and pharmaceutical chemists; biophysicists; biotechnologists; microbiologists; molecular and cell biologists; and graduate students in these disciplines.
2. Liposome Technology, Volume I:
Liposome Preparation and Related Techniques, 3rd Edition
Edited by : Gregory Gregoriadis
Liposome Technology, Volume I: Liposome Preparation and Related Techniques, Third Edition, is a thoroughly updated and expanded new edition of a classic text in the field. Including step-by-step technical details, Volume I illustrates numerous methods for liposome preparation and auxiliary techniques necessary for the stabilization and characterization of liposomes. This source also offers critical discussions of the methodologies of each technology described so that readers can examine the benefits and limitations and compare it to other approaches.
3. Liposome Technology, Volume II:
Entrapment of Drugs and Other Materials
Edited by : Gregory Gregoriadis
Liposome Technology, Volume II: Entrapment of Drugs and Other Materials into Liposomes, Third Edition is a comprehensively updated and expanded new edition of a classic text in the field. Including step-by-step technical details, Volume II describes procedures for the incorporation of drugs and other materials into liposomes for a variety therapeutics, chosen because of their relevance to current trends in liposome applications or because they represent groups of active pharmaceutical ingredients with similar physical and chemical properties. This source also offers critical discussions of the methodologies of each technology described so that readers can examine the benefits and limitations and compare it to other approaches.
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Liposome Technology, Volume III:
Interactions of Liposomes with the Biological
Milieu, Third Edition
Liposome Technology, Volume III: Interactions of Liposomes with the Biological Milieu, Third Edition, is a comprehensively updated and expanded new edition of a classic text in the field. Including step-by-step technical details, Volume III describes technologies for yielding liposomes that can function in a targeted fashion, and highlights methods for studying the interaction of liposomes within the biological environment to be applied in the detection, therapy, or prevention of disease. This source also offers critical discussions of the methodologies of each technology described so that readers can examine the benefits and limitations and compare it to other approaches.
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Wednesday, July 9, 2008
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