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Books > Medicine > Nursing & ancillary services > Pharmacy / dispensing
An established textbook that provides you with full coverage of the
physicochemical principles essential to the modern pharmacist and
pharmaceutical scientist. This sixth edition has a broad chemical
and physicochemical base and covers every aspect of drug properties
from the design of dosage forms to their delivery by all routes to
sites of action in the body. Now with more clinical examples, new
questions and extra case studies.
Honey typically has a complex chemical and biochemical composition
that invariably includes complex sugars, specific proteins, amino
acids, phenols, vitamins, and rare minerals. It is reported to be
beneficial in the treatment of various diseases, such as those
affecting the respiratory, cardiovascular, gastrointestinal, and
nervous systems, as well as diabetes mellitus and certain types of
cancers; however, there is limited literature describing the use of
honey in modern medicine. This book provides evidence-based
information on the pharmaceutical potential of honey along with its
therapeutic applications and precise mechanisms of action. It
discusses in detail the phytochemistry and pharmacological
properties of honey, highlighting the economic and culturally
significant medicinal uses of honey and comprehensively reviewing
the scientific research on the traditional uses, chemical
composition, scientific validation, and general pharmacognostical
characteristics. Given its scope, it is a valuable tool for
researchers and scientists interested in drug discovery and the
chemistry and pharmacology of honey.
Quick 2-sided reference card with pre-calculated epinephrine and
volume expander doses for babies weighing 0.5 kg-5 kg and pictoral
guide for preparation of epinephrine. Size: 8.5 x 11
This textbook builds on the success of the earlier edition,
offering alternative strategies for discovering new antibiotics. It
discusses how the various types of antibiotics and related drugs
work to cure infections. Then it delves into the very serious
matter of how bacteria are becoming resistant to these antibiotics.
It also covers the global action plan on antimicrobial resistance
from the World Health Organization and discusses several Antibiotic
Stewardship Programs adopted by agencies at local levels.
Appropriate for a one-semester course at either the graduate or
advanced undergraduate level, the book is self-contained and
written in accessible language. It includes all necessary
background biochemistry material and a discussion of the latest
developments in the field of antibiotics. Original research works
are frequently cited and experimental procedures and interpretation
of results are emphasized.
This book focuses on the multi-omics big-data integration, the
data-mining techniques and the cutting-edge omics researches in
principles and applications for a deep understanding of Traditional
Chinese Medicine (TCM) and diseases from the following aspects: (1)
Basics about multi-omics data and analytical methods for TCM and
diseases. (2) The needs of omics studies in TCM researches, and the
basic background of omics research in TCM and disease. (3) Better
understanding of the multi-omics big-data integration techniques.
(4) Better understanding of the multi-omics big-data mining
techniques, as well as with different applications, for most
insights from these omics data for TCM and disease researches. (5)
TCM preparation quality control for checking both prescribed and
unexpected ingredients including biological and chemical
ingredients. (6) TCM preparation source tracking. (7) TCM
preparation network pharmacology analysis. (8) TCM analysis data
resources, web services, and visualizations. (9) TCM geoherbalism
examination and authentic TCM identification. Traditional Chinese
Medicine has been in existence for several thousands of years, and
only in recent tens of years have we realized that the researches
on TCM could be profoundly boosted by the omics technologies.
Devised as a book on TCM and disease researches in the omics age,
this book has put the focus on data integration and data mining
methods for multi-omics researches, which will be explained in
detail and with supportive examples the "What", "Why" and "How" of
omics on TCM related researches. It is an attempt to bridge the gap
between TCM related multi-omics big data, and the data-mining
techniques, for best practice of contemporary bioinformatics and
in-depth insights on the TCM related questions.
This book is focused on marine based biomedical carriers for
delivery of therapeutics. Marine biomaterials and bio-based
carriers show wide applications in pharmaceutical as well as
biomedical fields for delivery of small and large molecules.
Biomaterial-based composites, scaffolds or matrix systems are
promising systems for controlled and prolonged release of drug in
target site and control the premature release of drugs or bioactive
compounds. This book discusses the targeted delivery of drugs and
therapeutic applications. It also describes the use of marine
biopolymers in cancer therapy. Different chapters describe the
tissue engineering techniques to develop these carriers. The marine
biomaterial-based systems are widely used for tissue engineering,
and biomedical imaging. This book is meant for industry experts,
students and researchers in the area of pharmaceutical sciences,
biomedical engineering and material science and pharmacology.
A must-have companion for medical students and junior doctors for
almost four decades, Lecture Notes: Clinical Pharmacology and
Therapeutics provides concise yet thorough coverage of the
principles of clinical pharmacology, the major characteristics of
therapeutics, and the practical aspects of prescribing drugs to
alleviate symptoms and to treat disease. Whether you are preparing
for examinations or prescribing to patients, the tenth edition
offers readers current and authoritative insight into the essential
practical and clinical knowledge. Logically organised chapters
allow for rapid location of key information, while examples of
commonly encountered scenarios illustrate how and when to use drugs
in clinical situations. Throughout the text, practice questions,
prescribing guidelines, and self-assessment tests clarify and
reinforce the principles that inform appropriate clinical
decision-making. Presents an up-to-date review of drug use across
all major clinical disciplines Offers a timely overview of clinical
drug trials and development Provides new clinical scenarios to
relate chapter content to real-life application Contains
colour-coded "Key Points" and "Prescribing Points" to highlight
important information Includes chapter introductions and summaries,
and numerous figures, tables, and colour illustrations Lecture
Notes Clinical Pharmacology and Therapeutics, Tenth Edition, is an
essential resource for medical students, junior doctors, and other
prescribers looking for an up-to-date reference on pharmacological
principles, prescribing, and therapeutics.
Essentials of Industrial Pharmacy is an attempt to comprehensively
present, in a single book, various pharmaceutical processes and
equipment that are frequently used for production of pharmaceutical
dosage forms, along with quality control tests of these dosage
forms. Pictorial/graphical illustrations provide easier
understanding of complex pharmaceutical concepts, manufacturing
processes of pharmaceutical dosage forms. Since it is imperative
for pharmacy students to have a clear understanding of the basic
concepts used in development of drugs into suitable and stable
dosage forms. This book offers a wealth of information regarding
basic aspects of pharmaceutical processes and dosage forms, in a
single book, for undergraduate pharmacy students or science
students (with no pharmacy background) intended to work in the
pharmaceutical Industry.
Until the 1990s, it was generally accepted that medicines were
first developed for adults and their use in children was
investigated later, if at all. One of the main tasks of hospital
pharmacies was the manufacturing of child-appropriate formulations
in a more or less makeshift way. The first change came in 1997 with
U.S. legislation that rewarded manufacturers to do voluntary
pediatric research. Ten years later, the European Union passed
legislation that required manufacturers to discuss all pediatric
aspects, including formulations, with the regulatory authorities as
a condition of starting the registration procedure. In consequence,
manufacturers must now cover all age groups, including the youngest
ones. So far, pediatric formulations were more a focus for academic
researchers. Through the changed regulatory environment, there is
now a sudden high commercial demand for age-appropriate
formulations. This book begins by highlighting the anatomical,
physiological and developmental differences between adults and
children of different ages. It goes on to review the existing
technologies and attempts to draw a roadmap to better, innovative
formulations, in particular for oral administration. The
regulatory, clinical, ethical and pharmaceutical framework is also
addressed.
Pharmacognosy, the science of nature-derived drugs,
pharmaceuticals, and poisons, played a crucial role in the
development of modern medicine, and now has an equally important
place in healthcare all over the world. This wide scope ranges from
traditional medicine systems and herbal and nutritional therapies,
the preparation and use of highly standardised and clinically
tested herbal medicines, to the production of potent drugs used
only in a purified form. Natural sources mainly focus on plants,
fungi and algae, but drug discovery of novel compounds and
structures includes bacteria and even marine animals. Fundamentals
of Pharmacognosy and Phytotherapy is a landmark textbook that
covers this spectrum of medicinal plant use. Written by leading
experts in this field, this book takes the reader through the
history, identification, and quality assurance of plant-based
medicines to their therapeutic properties, safety, and
compatibility and interaction with prescribed drugs. Aimed at
students of all healthcare professions, including pharmacy,
medicine, nursing and complementary therapies, the comprehensively
updated information in this textbook is also relevant to those
companies and organisations concerned with the regulation and
testing of herbal medicines (phytomedicines), other natural health
products, nutraceuticals and dietary supplements. Introduces the
concepts and scope of pharmacognosy Examines the scientific
evidence of plant-based medicines for a range of health conditions
Extended and updated referencing includes recent reviews, WHO and
official documents (open access where available) for quick access
to further scientific literature Antimicrobial natural products: as
antibiotics and antiseptics, and their potential as bacterial
resistance modifiers Anticancer natural products: scope now
includes their role in chemoprevention and associated
anti-inflammatory mechanisms New chapter on pharmacovigilance for
herbal medicines and related products Quality assurance and
pharmacopoeial methods extended, with many new figures and examples
Plant medicines of recent scientific interest (popularity, or
notoriety) added throughout
Written for practitioners in both the drug and biotechnology
industries, this handbook carefully compiles current regulatory
requirements on the validation of new or modified analytical
methods. Shedding light on method validation from a practical
standpoint, it contains practical, up-to-date guidelines for
analytical method validation. It also covers development,
optimization, validation, and transfer of many different types of
methods used in the regulatory environment. Simplifying the overall
process of method development, optimization and validation, the
guidelines in the Handbook apply to both small molecules in the
conventional pharmaceutical industry, as well as the biotech
industry.
This book explains how peptide-based drug design works, what steps
are needed to develop a peptide-based therapeutic, and challenges
in synthesis as well as regulatory issues. It covers the design
concept of peptide therapeutics from fundamental principles using
structural biology and computational approaches. The chapters are
arranged in a linear fashion. A fresh graduate or a scientist who
works on small molecules can use this to follow the design and
development of peptide therapeutics to use as understanding the
basic concepts. Each chapter is written by experts from academia as
well as industry. Rather than covering extensive literature, the
book provides concepts of design, synthesis, delivery, as well as
regulatory affairs and manufacturing of peptides in a systematic
way with examples in each case. The book can be used as a reference
for a pharmaceutical or biomedical scientist or graduate student
who wants to pursue their career in peptide therapeutics. Some
chapters will be written as a combination of basic principles and
protocol so that scientists can adopt these methods to their
research work. The examples provided can be used to perform peptide
formulation considerations for the designed peptides. The book has
nine chapters, and each chapter can be read as an independent unit
on a particular concept.
Pharmacy Practice Research Case Studies provides examples and
details regarding how pharmacy practice research has transformed
over the past decade and how this is impacting overall health. This
book presents several methodologies and techniques used in current
pharmacy practice. According to the United Nations Sustainable
Development Goals, countries around the world are aiming to achieve
Universal Health Coverage. In this context, pharmacists are a vital
part of the healthcare teams and the book portrays the research
methods used in conducting pharmacy practice and medicines use
research. The professional role of pharmacists has evolved
tremendously over the past few decades across the globe and the
pace of change has been interestingly phenomenal in varying
aspects. The book provides a great resource for pharmacists,
pharmaceutical scientists, policymakers, and researchers to
understand the dimensions of practice, education, research, and
policy concerning pharmacy, and it provides the synthesis of the
development so far, pointing to the needs and demands of the
future.
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