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Books > Medicine > Other branches of medicine > Pharmacology > General
Translational Medicine in CNS Drug Development, Volume 29, is the
first book of its kind to offer a comprehensive overview of the
latest developments in translational medicine and biomarker
techniques. With extensive coverage on all aspects of biomarkers
and personalized medicine, and numerous chapters devoted to the
best strategies for developing drugs that target specific
disorders, this book presents an essential reference for
researchers in neuroscience and pharmacology who need the most
up-to-date techniques for the successful development of drugs to
treat central nervous system disorders. Despite increases in the
number of individuals suffering from CNS-related disorders, the
development and approval of drugs for their treatment have been
hampered by inefficiencies in advancing compounds from preclinical
discovery to the clinic. However, in the past decades,
game-changing strides have been made in our understanding of the
pathophysiology of CNS disorders and the relationship of drug
exposure in plasma and CNS to pharmacodynamic measures in both
animals and humans.
The Core Model: A Collaborative Paradigm for the Pharmaceutical
Industry and Global Health Care develops the innovative core model,
an organizational research and design paradigm and economic theory
that proposes a collaborative approach to resolving global health
issues and improving the productivity of drug development. The
model proposes that scientific collaboration does not occur in an
unstructured manner, but actually takes place within a highly
structured order where knowledge is transferred, integrated and
finally translated into commercial products. An understanding of
this model will help solve the global pharmaceutical industrys
productivity problems and address important global health care and
economic issues. This book is useful to researchers, advanced
students, regulators, and management in pharmaceutical industries,
as well as healthcare professionals, those working in health
economics, and those interested in scientific innovation processes.
This book sheds light on the major functions of microbial
communities in aquaculture ecosystems, showing that by recycling
nutrients, degrading organic matter and preventing disease
outbreaks, a variety of microbes are truly beneficial to a wide
range of aquaculture industries. It discusses how deteriorating
environmental quality enables some microbial strains to trigger
disease, describes the development of highly sustainable tools to
improve water quality, and identifies crucial factors that endanger
microbial homeostasis in aquaculture ecosystems. The book also
covers post-antibiotic approaches for preventing and treating
opportunistic microbial infections based on harnessing
environmental and fish-associated microbial communities.
Furthermore, it explores how manipulating and engineering these
complex microbial communities using bio-agents such as probiotics,
phages, natural nutritional additives, or with fine-tuned
biofilters will open the door for new ways to develop a more
sustainable and cost-effective aquaculture industry. Including an
accessible presentation of modern high-throughput sequencing
technology to identify host-microbial interactions in aquaculture
ecosystems, this book is a valuable resource for scientists,
aquaculture and fishery experts, sustainability enthusiasts and
scholars in the areas of biology and marine agriculture.
This book offers an in indictment of the nation's drug enforcement
approach focusing on the short-sighted policies that often deny
patients suffering from chronic pain the medications they need.
Pain Control and Drug Policy: A Time for Change focuses on
America's national crisis in pain management caused by the widening
divergence between the enormous contributions of opioids
("narcotics") to pain management in the clinical setting and the
mistaken belief that they are dangerous, highly addictive drugs.
After dissecting the strategy and tactics of the War on Drugs from
medical, historical, legal, socioeconomic, and geopolitical
perspectives, Guy Faguet MD indicts the 40-year-long War on Drugs
for having failed to stem the supply of illicit drugs in America
despite expenditures of half a trillion dollars, despite violating
the basic human right to pain relief of tens of millions of
American chronic pain sufferers, and despite fomenting organized
crime, government corruption, racial injustice, and social
disruption in both the United States and the producer countries. He
concludes with a clarion call for the abandonment of the War on
Drugs, disbanding the Drug Enforcement Administration, and
encouraging Congress to repeal the Controlled Substances Act. As a
clinical and research oncologist responsible for the chronic pain
management of thousands of cancer patients over the course of his
30-year career, Dr. Faguet knows that the most effective and safest
way to manage most cases of chronic pain is with opioids. All
modern pain-management textbooks advocate "titration to effect" in
cases where opioids help: that is, gradually increasing the dosage
until either the pain is acceptably controlled or the side effects
begin to outweigh the pain-relief benefits. Yet the vast majority
of doctors don't practice what the medical textbooks teach and
instead prescribe opioids very reluctantly and conservatively. As a
result, only half of all chronic pain sufferers-and fewer than half
of all cancer patients-get adequate pain relief from their doctors.
Why do physicians radically undertreat pain that is susceptible to
opioid analgesics? They fear that if they prescribe Schedule II
opioids in accordance with the professional standards of pain
management set by such medical bodies as the American Pain Society,
they will be investigated by the DEA, stigmatized, prosecuted as
criminals, stripped of their licenses, and sent to jail. Visit Guy
B. Faguet, MD's website here: www.faguet.net.
Microencapsulations may be found in a number of fields like
medicine, drug delivery, biosensing, agriculture, catalysis,
intelligent microstructures and in many consumer goods. This new
edition of Microencapsulation revises chapters to address the
newest innovations in fields and adds three new chapters on the
uses of microencapsulations in medicine, agriculture, and consumer
products.
The Side Effects of Drugs Annual was first published in 1977. It
has been continually published since then, as a yearly update to
the voluminous encyclopedia Meyler's Side Effects of Drugs. Each
new Annual continues to provide clinicians and medical
investigators with a reliable and critical yearly survey of new
data and trends in the area of Adverse Drug Reactions and
Interactions. An international team of specialists has contributed
to the Annuals by selecting critically from each year's writing all
that is truly new and informative, by critically interpreting it,
and by pointing to whatever is misleading.
*Provides a critical yearly survey of new data and trends
*Includes an essay that describes the modern approach to
classifying adverse drug reactions
*Special reviews in this Annual include, among other topics:
Antipsychotic drugs and now-onset diabetes mellitus, Treating
asthma during pregnancy, and MMR vaccine and autism
The aim of this book is not only to introduce readers with a broad
spectrum of biological actions of the NOP receptor, but also to
feature a detailed look at the N/OFQ-NOP receptor system, medicinal
chemistry, pharmacology, and clinical data of NOP-targeted ligands.
This special volume book - for the first time focusing on the NOP
receptor - is designed to serve as a useful reference, stimulate
more research on the N/OFQ-NOP receptor system, and lead to more
development of NOP-related ligands for several therapeutic
applications.
Edited by Kenneth A. Jacobson and Michael F. Jarvis
The roles of extracellular purines and pyrimidines in cellular
homeostasis and disease etiology have come to be understood
gradually over the past 40 years. However, due to the recent
cloning and expression of receptors for ATP and adenosine, novel
compounds have been developed with unique therapeutic potential for
the treatment of thrombosis, stroke, epilepsy, chronic pain,
immunological disorders, and cancer. As a result, the study of
adenosine- and ATP-mediated responses in cellular regulation is
entering a phase of opportunity and development unmatched since the
days of serotonin receptor research in the 1970s.
The only definitive book on the topic, Purinergic Approaches in
Experimental Therapeutics covers all of the major therapeutic
applications of purinergic receptors and reflects the very latest
developments in this new area of therapeutic research. Twenty-eight
chapters, authored by an international group of contributors who
are the leading authorities in the field, provide details on
molecular pharmacology; medicinal chemistry; and therapeutic
implications, including cardiology, metabolism, immunology,
neurology, and cancer.
Among the topics covered:
* Purinergic Neurotransmission and Neuromodulation: A Historical
Perspective
* Adenosine Receptor Subtypes: New Insights from Cloning and
Functional Studies
* Modulators of Adenosine Uptake, Release, and Inactivation
* Cardiac Electrophysiology of Adenosine: Antiarrhythmic and
Proarrhythmic Actions
* Purinergic Modulation of Gastrointestinal Function
* The Role of Adenosine in Asthma
* ATP in Brain Function
* ATP in the Treatment of Cancer
For researchers in pharmacology, physiology, molecular biology,
and medicinal chemistry, Purinergic Approaches in Experimental
Therapeutics heralds an exciting new era in the understanding of
purinergic neurotransmission and the development of novel
therapeutic modalities.
This volume explores techniques that are currently used to
understand solid target-specific models in computational
toxicology. The chapters are divided into four sections and discuss
topics such as molecular descriptors, QSAR and read-across;
molecular and data modeling techniques to comply with both
scientific and regulatory sides; computational toxicology in drug
discovery; and strategies on how to predict various human-health
toxicology endpoints. Written in the highly successful Methods in
Molecular Biology series format, chapters include introductions to
their respective topics, lists of the methods and software tools
used, step-by-step, readily reproducible computational protocols,
and tips on troubleshooting and avoiding known pitfalls.
Comprehensive and cutting-edge, Computational Toxicology: Methods
and Protocols is a valuable resource for researchers who are
interested in learning more about this expanding field.
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