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Scientific Program
8th World Congress on Toxicology and Pharmacology, will be organized around the theme “Communing Toxicology & Pharmacology Investigations for Human Health”
Toxicology Congress 2017 is comprised of 17 tracks and 95 sessions designed to offer comprehensive sessions that address current issues in Toxicology Congress 2017.
Submit your abstract to any of the mentioned tracks. All related abstracts are accepted.
Register now for the conference by choosing an appropriate package suitable to you.
Risk assessment includes the characterization of the uncertainties inherent in the process of inferring risk. Toxicology data helps to determine the risk of exposure to certain chemicals. The practices of risk assessment are used to assess the related health risks to provide a scientific basis for regulatory standards development and risk management decision making for human health protection. The presence of chemicals in our environment is a subject of intense interest owing to the many potential adverse health effects to humans following exposure to these chemicals.
- Track 1-1Safety evaluation, risk and hazard assessment
- Track 1-2Chemical research in toxicology
- Track 1-3Regulatory toxicology
- Track 1-4Computational toxicology
- Track 1-5Toxicokinetics and Toxicodynamics
Analytical toxicology is the detection, identification, and measurement of foreign compounds in biological and other specimens. Analytical methods are available for a wide range of compounds like chemicals, pesticides, drugs and natural toxins. Analytical toxicology is used in the diagnosis, management, prognosis, and prevention of poisoning. Analytical toxicology laboratories may be involved in activities such as the assessment of exposure following chemical incidents, forensic analyses, therapeutic drug monitoring and monitoring for drugs of abuse. They may also be involved in research like determining the pharmacokinetic and toxicokinetic properties. Liquid chromatography-mass spectrometry and Gas chromatography-mass spectrometry are generally used today in analytical toxicology.
- Track 2-1Animal testing methods
- Track 2-2Alternative testing methods
- Track 2-3Drug discovery, development and evaluation
- Track 2-4In vitro toxicity testing
- Track 2-5Pre-clinical toxicity testing
Genotoxicity describes the property of chemical agents that damages the genetic information within a cell causing mutations, which may lead to cancer. Genotoxic chemicals exert their adverse effect through interaction with genetic material (DNA) of cells. To assay for genotoxic molecules, researchers assay for DNA damage in cells exposed to the toxic substrates. Techniques like Ames Assay, in vitro and in vivo Toxicology Tests, and Comet Assay have been developed to determine the chemicals' potential to cause DNA damage that may lead to cancer. Genotoxicity tests are designed to detect drugs which can cause genetic damage directly or indirectly by various mechanisms of action. Compounds identified as genotoxic in these tests have the ability to be human carcinogens and ultimately may induce cancer and/or heritable defects. In drug development process, genotoxicity testing of new chemical entities is an integral part and is a regulatory requirement prior to the approval of new drugs. Late stage failures can reduced by identifying genotoxicity at an early stage in drug discovery rather than during regulatory assessment.
- Track 3-1Genotoxic drugs
- Track 3-2Genotoxicity testing
- Track 3-3In vitro and in vivo testing
- Track 3-4Pharmacogenetics & pharmacogenomics
- Track 3-5Gentotoxicity and mutagenicity
- Track 3-6Nanotoxicology
Forensic toxicology uses toxicology and other disciplines such as analytical chemistry, clinical chemistry and pharmacology to aid medical or legal investigation of drug use, poisoning and death. It deals with the investigation of toxic substances, poisonous products and environmental chemicals. The primary concern of forensic toxicology is to obtain and interpret the results. Toxicological analysis can be done to various kinds of samples. Forensic toxicology involves not only determining the presence of toxic substance in the post-mortem body, but how the body’s natural processes affect the substance, including chemical change and dilution. Forensic toxicologists perform scientific tests on tissue samples and bodily fluids to identify any chemicals or drugs present in the body. The choice of method for testing is highly depends on the material on which the testing is performed and what kind of substance one expects to find. Analytical method used in forensic toxicology should be carefully tested by performing a validation of the method to ensure indisputable results at all times.
- Track 4-1Forensic samples for toxicology testing
- Track 4-2Forensic toxicology applications
- Track 4-3Challenges in forensic toxicology
- Track 4-4Forensic toxicology today
- Track 4-5Post-mortem Forensic Toxicology
Food safety is a discipline which describes preparation, handling and storage of food in ways that avoid foodborne illness. This involves a number of routines that should be followed to avoid potentially severe health hazards. Food safety include the origins of food including the practices relating to food labelling, food additives, pesticide residues and food hygiene as well as policies on biotechnology and food. Environmental toxicology is a field of science concerned with the study of the harmful effects of various physical, chemical and biological agents on living organisms. Harmful effects of biological and chemical agents can include toxicants from pesticides, pollutants, fertilizers and insecticides all of which can impact an organism and its community through shifts in species diversity and abundance.
- Track 5-1Food safety and food allergies
- Track 5-2Risk assessment of chemicals in food
- Track 5-3Environmental and occupational health
- Track 5-4Particle and fibre toxicology
- Track 5-5Industrial and metallic toxicology
- Track 5-6Plant toxicology
- Track 5-7Aquatic Toxicology
Application of methodology and principles of toxicology to prevent adverse health effects from drug candidates. To evaluate the safety of potential drug candidates in the drug development process is the primary objective of toxicology studies. This can be accomplished by using relevant animal models and validated procedures. The ultimate goal is to translate the animal model responses into an understanding of the risk for human subjects. To this end, the toxicologist must be aware of the international guidelines for safety evaluation, as well as traditional and nontraditional toxicology models. The typical toxicology profile consists of safety pharmacology, acute and subchronic toxicology, chronic toxicology, absorption, distribution, metabolism, and excretion studies, genetic toxicology, reproductive and developmental toxicology and an evaluation of carcinogenic potential.
- Track 6-1Toxicology in vitro
- Track 6-2Innovations in applied toxicology and toxicological sciences
- Track 6-3Emerging in-vitro models for the toxicity studies
- Track 6-4Developmental and reproductive toxicology
- Track 6-5Application of toxicology in drug development
Toxicology is the study of adverse effects of chemical, biological and physical agents in biological systems that establish the extent of damage in living organisms. It includes observing symptoms, mechanisms, detection and treatments of toxic substances, in relation to the poisoning of humans. It is the qualitative and quantitative study of the adverse effects of chemicals and other materials on living organisms. The dose of the substance is an important factor in toxicology, as it has a relationship with the effects on the individual. Factors that influence toxicity include the dose, the route of exposure, shape and structure of the chemical, the species, individual human factors and environment.
- Track 7-1Clinical toxicology
- Track 7-2General toxicity
- Track 7-3Neurotoxicology and teratology
- Track 7-4Systems toxicology
- Track 7-5Organ toxicity
- Track 7-6Comprehensive toxicology
- Track 7-7Drug and chemical toxicology
- Track 7-8Pediatric toxicology
- Track 7-9Geriatric toxicology
- Track 7-10Predictive toxicology
Pharmacology is the scientific study of drug action on biological systems. It is the study of the interactions between a living organism and drugs. If substances have medicinal properties, they are considered pharmaceuticals. Pharmacological studies range from the effects of chemical agents upon subcellular mechanisms, to those that deal with the potential hazards of pesticides and herbicides, to those that focus on the treatment of major diseases by drug therapy. It involves examining the interactions between chemical substances and living systems, with a view to determining the properties of drugs and drug actions, including the drug molecules and drug receptors interactions and how these interactions elicit an effect.
- Track 8-1Clinical pharmacology
- Track 8-2Biochemical pharmacology
- Track 8-3Neuropharmacology
- Track 8-4Psychopharmacology
- Track 8-5Respiratory pharmacology
- Track 8-6Pediatric pharmacology
- Track 8-7Geriatric pharmacology
Applied pharmacology is the study of how drugs affect body. Drugs can be used to both maintain a healthy lifestyle and treat or cure disease. Pharmacology deals with the basis, therapeutics uses of drugs, physiological action and properties of action. Applied pharmacology helps to measure the data obtained from the clinical studies and can correlate it with the clinical processes. It also provides explanation for different drugs having connected with the pharmacological action. It gives clarifications about drug interactions and the action of various drugs on the many organs in the body when they are in diseased state with side effects contradictions. Applied pharmacology makes it possible not only to explain to the doctor the action of drugs in the human body, but also in evaluating the efficacy of drugs in a particular disease condition.
- Track 9-1Molecular and cellular pharmacology
- Track 9-2Nanomedicine in pharmacology
- Track 9-3Pharmacological testing
- Track 9-4Behavioral pharmacology
- Track 9-5Clinical application of systems pharmacology models
Environmental pharmacology is a new and emerging specialty of pharmacology. It involves the study of gene-environment interaction, toxin-environment interaction and drug- environment interaction. Environmental pharmacology entails the study of environmental science, medicine, ecology, genetics and chemistry. The impact of pharmaceuticals on the ecosystem has significance public health implications. The demand for more pharmaceuticals relative to world’s population growth may place the public at risk though the destruction of species. The entry of chemicals and drugs into the aquatic ecosystem is of a serious concern and empirical evidences are making these concerns more compelling.
- Track 10-1Drug-environment interaction
- Track 10-2Toxin-environment interaction
- Track 10-3Environmental damage
- Track 10-4Gene-environment interaction
Pharmacological tests are used to evaluate if a substance or plant extract is biologically active. There are many pharmacological tests and each test demonstrates various aspects that are important for the understanding of the mechanisms behind illnesses, their causes and cures. Pharmacologic stress testing is a diagnostic procedure which is established after exercise testing, in which cardiovascular stress induced by pharmacologic agents is demonstrated in patients who cannot exercise or in patients with decreased functional capacity. Pharmacologic stress testing is used in combination with imaging modalities such as radionuclide imaging and echocardiography.
- Track 11-1In vitro and In vivo models
- Track 11-2Randomized controlled clinical trials
- Track 11-3Pharmacokinetics
- Track 11-4Pharmacologic stress testing
- Track 11-5Drug reaction testing
Medication development is a vital concern to medicine and also has strong economic implications. To protect the consumer and prevent abuse of drugs, many governments regulate the manufacture, sale and administration of medication. The reactivity and the metabolic stability of a library of compounds have to be assessed for toxicological studies and drug metabolism. Many methods are proposed for quantitative predictions in drug metabolism. The pharmaceutical market been increasingly more affected through laws and regulations but has shown continuous growth as the diagnosis and understanding of diseases and condition has evolved and improved.
- Track 12-1Pharmacodynamics and pharmacokinetics
- Track 12-2Ethical and legal issues
- Track 12-3Drug screening and discovery
- Track 12-4Drug-drug interactions
- Track 12-5Pharmacovigilance
- Track 13-1Heart diseases and failure
- Track 13-2Cardiovascular pharmacotherapies, cardiac procedures and surgeries
- Track 13-3Risk factors for cardiovascular diseases
- Track 13-4Interventional cardiology
- Track 13-5Nuclear cardiology and echocardiography
- Track 13-6Cerebrovascular heart diseases
- Track 13-7Diseases associated with cardiovascular diseases
- Track 13-8Heart diseases in different rationale
- Track 14-1Clinical trials in Cardiology
- Track 14-2Cardiovascular and biological tissue regeneration and tissue engineering
- Track 14-3Cardiotoxicity
- Track 14-4Emerging epidemic of cardiovascular disease in developing countries
- Track 14-5Cardiovascular drugs market analysis
- Track 15-1Toxicologic pathology
- Track 15-2In Vitro and In Vivo mechanisms
- Track 15-3Xenobiotic Risk Characterization
- Track 16-1Drugs of abuse
- Track 16-2Unintentional and intentional overdoses
- Track 16-3Evaluation of chemically induced diseases
- Track 16-4Pre-Clinical toxicology studies
- Track 17-1In vitro toxicity testing
- Track 17-2Toxicity testing in preclinical development
- Track 17-3Toxicity evaluation
- Track 17-4Toxicological screening methods
- Track 17-5Experimental toxicology
- Track 17-6Human toxicology