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Books > Medicine > Other branches of medicine > Pharmacology
This book covers the current research on the plant-based tropane alkaloids (TA) and TA-bearing plants. The first part includes an overview of "tropane alkaloids in context to diversity, biosynthesis and significance. The second part covers aspects of in-vitro and allied interventions in these alkaloids. TAs belong to one of the world's oldest phytomedicines with their valuable ethno-pharmacological applications. The book compiles scientific ideas, perspectives and challenges in this area. Further, the book attempts to investigate the loopholes in existing methodologies, challenges and possible solutions through well thought-out scientific discussions from various eminent research groups. This book is of high interest to students and researchers in biotechnology, plant biology and pharmacology. As the TAs are of high commercial medicinal value, this book is also a relevant collection of articles for industry experts.
"Pharmacogenomics: Challenges and Opportunities in Therapeutic
Implementation" includes discussions and viewpoints from the
academic, regulatory, pharmaceutical, clinical, socio-ethical and
economic perspectives. Each chapter presents an overview of the
potential or opportunity within the areas discussed and also
outlines foreseeable challenges and limitations in moving
pharmacogenomics into drug development and direct therapeutic
applications. This edited book contains review questions for a more
in-depth analysis of the implications of pharmacogenomics and
discussion points to generate ideas on best to move the field
forward. Clinical pearls and case studies are used to illustrate
real-life experiences and both successful and unsuccessful
applications. Tables, figures, and annotations are included
throughout the book to facilitate understanding and further
reference. A companion website offers an elaboration on key points and discussion questions and provides patient case scenarios that illustrate how pharmacogenomics may be applied to a clinical setting
Zacarias Leon's thesis describes the development and validation of analytical methods to estimate the processes set in motion by percutaneous absorption of UV filters in sunscreen cosmetic products. Leon describes these methods in both in vitro and non-invasive in vivo methodologies. Currently dermatologists recommend the use of sunscreen products not only under conditions of extreme exposure to the sun but also in daily situations. However the chemical compounds in these products contain may lead to undesired processes and cause induced toxicity, estrogenic effects and endocrine activity. Leon establishes methods to investigate these effects and provides valuable information on the undesired side effects associated with the use of UV filters found in sunscreen products. The work in this thesis has led to a number of publications in renowned analytical chemistry journals.
This authoritative volume provides a holistic picture of antibody-drug conjugates (ADCs). Fourteen comprehensive chapters are divided into six sections including an introduction to ADCs, the ADC construct, development issues, landscape, IP and pharmacoeconomics, case studies, and the future of the field. The book examines everything from the selection of the antibody, the drug, and the linker to a discussion of developmental issues such as formulations, bio-analysis, pharmacokinetic-pharmacodynamic relationships, and toxicological and regulatory challenges. It also explores pharmacoecomonics and intellectual properties, including recently issued patents and the cost analysis of drug therapy. Case studies are presented for the three ADCs that have received FDA approval: gemtuzumab ozogamicin (Mylotarg (R)), Brentuximab vedotin (Adcetris (R)), and ado-trastuzumab emtansine (Kadcyla (R)), as well as an ADC in late-stage clinical trials, glembatumumab vedotin (CDX-011). Finally, the volume presents a perspective by the editors on the future directions of ADC development and clinical applications. Antibody-Drug Conjugates is a practical and systematic resource for scientists, professors, and students interested in expanding their knowledge of cutting-edge research in this exciting field.
The last 10 years have seen a seismic shift in therapeutic product development and testing. In both the pharmaceutical (both small and large molecule) and medical device sectors, the vast majority of testing and evaluation of products is not performed within innovator companies, but rather has been outsourced to a growing universe of commercial organizations. The authors both have more than 30 years experience in this field, and both have worked within innovator companies, for CROs, and as consultants in the field. "Contract Research and Development Organizations: Their Role in Global Product Development" has been crafted by these authors to provide a how to guide for all aspects of working with CROs in selecting, working with and ensuring the best possible desirable outcome of having the R&D function, or substantial parts of it, outsourced. It uses as the exemplary case nonclinical safety assessment, biocompatibility and efficacy testing which are to be performed to select the best possible candidate compound, device or formulation and then moving the resulting regulated therapeutic medical product into and through the development process and to marketing approval. But also covered are the contract synthesis of drug substances and corresponding manufacture of biologics and manufacture of products, formulation development, clinical evaluation, regulatory and document preparation support, and use of consultants. Included in the volume are an exhaustive listing of those CROs in the (drug and device) safety evaluation sector and their contact information and capabilities, and extensive similar listing for the other types of contract service providers. Also included are guidances on how to monitor ongoing work at contract facilities and audit check lists for GLP, GMP and GCP facilities. These listings are international in scope, and a specific chapter addresses working with some of the newer international CROs. "
Recent findings have implied a distinct therapeutic potential for drugs targeting Transient Receptor Potential (TRP) channels in a wide variety of diseases, many with no existing satisfactory treatment options. Thus, the TRP superfamily of ion channels has attracted a great deal of well-deserved attention. TRP Channels in Drug Discovery provides a thorough collection of the most up-to-date reviews and protocols on the subject, coming from top experts in the field. Volume II presents a practical methodologies involving models for disorders of the cardiovascular system, the brain, skin, the metabolic system, as well as colitis, cancer, thermosensation, and musculoskeletal disorders. Written for the Methods in Pharmacology and Toxicology(t) series, this work includes the kind of detailed description and key implementation advice that ensures successful results in the lab. Comprehensive and cutting-edge, TRP Channels in Drug Discovery serves as an ideal reference for graduate students in academic laboratories as well as for pharmaceutical scientists developing new drugs and clinicians interested in novel drugs in the pipeline.
Obesity is an epidemic with enormous health, economic and social
burdens. Current drugs for obesity treatment are far from ideal in
terms of efficacy and side effects. Reviews in this volume of
Progress in Molecular Biology and Translational Science summarize
current status in studies of a number of G protein-coupled
receptors that were shown to be promising targets for obesity
treatments. Some of these receptors also cause monogenic obesity in
humans. Chapters are written by leading experts.
This book provides a comprehensive look at renal cell carcinoma, exploring its biology as well as current and future molecular targets for renal cancer carcinoma.
Edited by Kenneth A. Jacobson and Michael F. Jarvis 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.
Updated every five years, the series represents the optimal compromise between currency and a sufficient body of material for cohesive and comprehensive treatment in a monograph. Provides a quick yet thorough overview of the synthetic routines that have been used to access specific classes of therapeutic agents. Materials are organized by chemical class, and syntheses are taken back to available starting materials. Discusses disease state, rational for method of drug therapy, biological activities of each compound and preparation. Coverage also includes those generic pharmaceutical compounds not accorded clinical status. A glossary defines biological terms.
This jargon-free guide is suitable for all trainee and registered health professionals who require knowledge and understanding of drugs used in the treatment of mental health conditions for prescribing or administering purposes. A life-saving book that you can carry anywhere you go! Introductory material provides a background on psychotropic drugs, the etiology of mental illness, some of the commonly used drugs in practice and brief notes on common non-pharmacological interventional options. It also examines the pathophysiology of mental illness and clinical decision making. The central chapters provide comprehensive coverage of all the major medications used in the most common mental health disorders, detailing key drugs and including side effects, average doses, contra-indications and precautions, and clinical management interventions. Case studies, multiple choice questions and summary tasks in each chapter enable readers to clearly relate theory to practice and thoroughly review their learning. The second edition of this best-selling text has been completely revised to include: updated information and refreshed case studies throughout; more activities for self-study and interactive learning, including multiple choice questions; an emphasis on new ways of working within mental health settings, such as non-restrictive practice; a completely new chapter on alcohol and substance misuse.
This series was founded in 1959, and its focus has shifted from medicinal chemistry to a much wider scope. It now encompasses all fields concerned with the development of therapeutic drugs and the elucidation of their mechanisms of action, reflecting the increasingly complex nature of modern drugs research. Invited authors write reviews on the following fields: biology, chemistry, biochemistry, physiology, immunology, pharmacy, toxicology, pharmacology, and clinical aspects. The books are linked by indexes in each volume, forming an almost encyclopaedic work.
This issue of Endocrinology Clinics brings the reader up do date on the current standards and important advances in insulin therapy.? The following clinical topics are discussed: types of insulins, including new insulins; goals of therapy; pathophysiology of, and insulin treatment in type1 and type 2 diabetes mellitus; pumps and glucose sensors; alternative insulin delivery; patient and provider insulin resistance; inpatient insulin therapy; insulin therapy in pregnancy; and pediatric insulin therapy.
"Clinical Pharmacology During Pregnancy" is written for clinicians, physicians, midwives, nurses, pharmacists and other medical professionals directly involved in the care of women during pregnancy. This book focuses on the impact of pregnancy on drug disposition and also includes coverage of treatments for diseases of specific body systems as well as essential content on dosing and efficacy. The broad range of this book encompasses analgesics,
antiasthmatics, antidepressants, heart and circulatory drugs,
vitamins and herbal supplements, and more. Topics in chemotherapy
and substance abuse are covered, as are research issues, including
clinical trial design and ethical considerations.
This book will be focused on mitochondria as very promising targets for anti-cancer drugs, yet to be fully exploited. It will contain chapters focused on aspects of basic research as well as on clinical relevance, which will be written by specialists in the field. That the role of mitochondria in human pathologies goes beyond the neoplastic diseases will be documented by a chapter of the role of mitochondria in Friedreich's ataxia.
"Translational Neuroimaging: Tools for CNS Drug Discovery,
Development and Treatment" combines the experience of academic,
clinical and industrial neuroimagers in a unique collaborative
approach to provide an integrated perspective of the use of small
animal and human brain imaging in developing and validating
translational models and biomarkers for the study and treatment of
neuropsychiatric disorders. "Translational Neuroimaging: Tools for
CNS Drug Discovery, Development and Treatment" examines the
translational role of neuroimaging in model development from
preclinical animal models, to human experimental medicine, and
finally to clinical studies. The focus of this book is to identify
and provide common endpoints between species that can serve to
inform both the clinic and the bench with the information needed to
accelerate clinically-effective CNS drug discovery. This book
covers methodical issues in human and animal neuroimaging
translational research as well as detailed applied examples of the
use of neuroimaging in neuropsychiatric disorders and the
development of drugs for their treatment. Offering an accompanying
website with illustrations and text available for further knowledge
and presentations, "Translational Neuroimaging: Tools for CNS Drug
Discovery, Development and Treatment" appeals to non-clinical and
clinical neuroscientists working in and studying neuropsychiatric
disorders and their treatment as well as providing the novice
researcher or researcher outside of his/her expertise the
opportunity to understand the background of translational research
and the use of imaging in this field.
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 informative Annual by critically interpreting it and by
pointing to whatever is misleading.
Lead Compounds from Medicinal Plants for the Treatment of Cancer
is the first volume in the series, Pharmaceutical Leads from
Medicinal Plants. The plant species described in this reference
have been carefully selected based on pharmacological evidence and
represent today s most promising sources of natural products for
the discovery of anti-cancer drugs. Containing references to
primary source material, over a hundred botanical illustrations, a
table of chemical structures and much more, this book is an
essential starting point for cancer researchers and those involved
in anti-cancer drug discovery helping you identify the best novel
lead molecules for further anti-cancer drug development.
This volume covers all aspects of the antibiotic discovery and development process through Phase II/III. The contributors, a group of highly experienced individuals in both academics and industry, include chapters on the need for new antibiotic compounds, strategies for screening for new antibiotics, sources of novel synthetic and natural antibiotics, discovery phases of lead development and optimization, and candidate compound nominations into development. Beyond discovery , the handbook will cover all of the studies to prepare for IND submission: Phase I (safety and dose ranging), progression to Phase II (efficacy), and Phase III (capturing desired initial indications). This book walks the reader through all aspects of the process, which has never been done before in a single reference. With the rise of antibiotic resistance and the increasing view that a crisis may be looming in infectious diseases, there are strong signs of renewed emphasis in antibiotic research. The purpose of the handbook is to offer a detailed overview of all aspects of the problem posed by antibiotic discovery and development.
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