Friday 26 January 2018

series 3:TOXICOLOGY Question and Answer bank by Dr Pawan K (PK) Gupta




TOXICOLOGY Question and Answer bank

General Toxicology: Continued, FROM SERIES 2





Q. What are the sub-disciplines of toxicology?

Biochemical toxicology
Reproductive toxicology
Development toxicology
Teratology
Genetic toxicology
Clinical toxicology
Forensic toxicology
Analytical toxicology
Nutritional toxicology
Veterinary toxicology
Environmental toxicology
Occupational(Industrial) toxicology
Regulatory toxicology
Mechanistic toxicology
Aquatic toxicology
Ecotoxicology
Food toxicology
Formal toxicology
Descriptive toxicology
Q. Define occupational (Industrial) toxicology
Occupational (Industrial) toxicology is concerned with health effects from exposure to chemicals in the workplace.  It deals with the clinical study of workers of industries and environment around him.
Q. Define regulatory toxicology:
It deals with administrative functions concerned with the development and interpretation of mandatory toxicology testing programs and controlling the use, distribution and availability of chemicals used commercially and therapeutically. For example, Food and Drug Administration (FDA) regulates drugs, cosmetics and food additives. Regulatory toxicology gathers and evaluates existing toxicological information to establish concentration-based standards of “safe” exposure. The standard is the level of a chemical that a person can be exposed to without any harmful health effects.
Q. Define food toxicology
It deals with natural contaminants, food and feed additives, and toxic and chemo-protective effects of compounds in food.
Explanation: Food Toxicology is involved in delivering a safe and edible supply of food to the consumer. During processing, a number of substances may be added to food to make it look, taste, or smell better. Fats, oils, sugars, starches and other substances may be added to change the texture and taste of food.
All of these additives are studied to determine if and at what amount, they may produce adverse effects. A second area of interest includes food allergies. Almost 30% of the American people have some food allergy. For example, many people have trouble digesting milk, and are lactose intolerant. In addition, toxic substances such as pesticides may be applied to a food crop in the field, while lead, arsenic, and cadmium are naturally present in soil and water, and may be absorbed by plants. Toxicologists must determine the acceptable daily intake level for those substances.
Q. Define formal toxicology
It deals with the formal toxicological studies which are pre-requisite for release of a new drugs/chemical e.g. calculation of LD50   and minimum toxic dose.
Q. Define descriptive toxicology
Descriptive Toxicology is concerned with gathering toxicological information from animal experimentation. These types of experiments are used to establish how much of a chemical would cause illness or death. The United States Environmental Protection Agency (EPA), the Occupational Safety and Health Administration (OSHA), and the Food and Drug Administration (FDA), use information from these studies to set regulatory exposure limits.
Q. Define mechanistic toxicology
Mechanistic Toxicology makes observations on how toxic substances cause their effects. The effects of exposure can depend on a number of factors, including the size of the molecule, the specific tissue type or cellular components affected, whether the substance is easily dissolved in water or fatty tissues, all of which are important when trying to determine the way a toxic substance causes harm, and whether effects seen in animals can be expected in humans.
Q. Define nutritional toxicology
Nutritional Toxicology is the study of toxicological aspects of food/feed stuffs and nutritional products/habits.
Q. Define toxicodynamics
It deals with the study of biochemical and physiological effects of toxicant and their mechanism of action.
Q. Define toxicokinetics
It deals with the study of absorption, distribution, metabolism and excretion of toxicants in the body.
Q. Define toxicovigilance
It deals with process of identification, investigation, and evaluation of various toxic effects in the community with a view of taking measures to reduce or control exposures involving the substances that produce these effects.
Q. Define toxinology
It deals with assessing the toxicity of substances of plant and animal origin and those produced by pathogenic bacteria/organism.
Q. Define toxicoepidemiology
It refers to the study of quantitative analysis of the toxicity incidences in organisms, factors affecting toxicity, species involved and the use of such knowledge in planning of prevention and control strategies.
Toxic or toxicity is relative terms commonly used in comparing one chemical with another.
Q. Define toxicity
It is a state of being poisonous or capacity to cause injury in living organisms.
Q. Define toxicosis
It is the condition or disease state that results from exposure to a toxicant. The term toxicosis is often used interchangeable with the term of poisoning or intoxication.
Q. Define toxic effects
These are undesirable effects produced by a toxicant/drug which are detrimental to either survival or normal functioning of the individual.
Q. Define side effects
These are undesirable effects which result from the normal pharmacological actions of drugs. These results may not be detrimental or harmful to the individual.
Q. Define selective toxicity
It is the toxicity produced by a chemical to one kind of living matter without harming another form of life even though the two exist in intimate contact.
Q. Define plant toxins?
Different portions of a plant may contain different concentrations of chemicals. Some chemicals made by plants can be lethal. For example, taxon, used in chemotherapy to kill cancer cells, is produced by a species of the yew plant.
Q. Define animal toxins?
Animal toxins can result from venomous or poisonous animal releases. Venomous animals are usually defined as those that are capable of producing a poison in a highly developed gland or group of cells, and can deliver that toxin through biting or stinging. Poisonous animals are generally regarded as those whose tissues, either in part or in their whole, are toxic. For example, venomous animals, such as snakes, spiders, etc., and poisonous animals, such as puffer fish, or oysters, which may be toxic to some individuals when contaminated with vibrio vulnificus.


The exposure of experimental animals to chemicals can be divided into four categories: acute toxicity and repeated exposure (sub-acute, sub-chronic, and chronic).
Q. Define acute toxicity
Acute exposure is defined as exposure to a chemical for less than 24 hr. The exposure usually refers to a single administration, repeated exposures may be given within a 24 hr period for some slightly toxic or practically nontoxic chemicals. Acute exposure by inhalation refers to continuous exposure for less than 24 hr, most frequently for 4 hr.
Q. Define repeated exposure
 Repeated exposure is divided into three categories:
sub-acute ii) sub-chronic, and iii) chronic.
Sub-acute exposure to a chemical is for 1 month or less, sub-chronic for 1 to 3 months, and chronic for more than 3 months (usually this refers to studies with at least 1 year of repeated dosing).
Explanation: Acute or repeated exposure can be by any route, but most often they occur by the oral route, with the chemical added directly to the diet. In human exposure situations, the frequency and duration of exposure are usually not as clearly defined as in controlled animal studies. However, almost same terms are used to describe general exposure situations. Thus, workplace or environmental exposures may be described as acute (occurring from a single incident or episode), sub-chronic (occurring repeatedly over several weeks or months), or chronic (occurring repeatedly for many months or years).

1.2 Toxicity in Relation to Time of Development and Duration of Induced Effects            

Q. Define transient or reversible or temporary toxicity
It is the toxicity or harmful effect that remains for short duration of time. e.g., narcosis produced organic solvents.
Q. Define persistent or permanent or irreversible toxicity
It is the toxicity or harmful effects that persists throughout life span of the individual and are of permanent nature, e.g. scarring of skin produced by corrosives.
Q. Define immediate toxicity
It is the toxicity that develops shortly after a single exposure to a toxicant e.g. cyanide poisoning.
Q. Define delayed toxicity
It is the toxicity or harmful effect which has delayed onset of action, e.g. peripheral neuropathy produced by some organophosphorus insecticides and radiation sickness.
Q. Define cumulative toxicity
It is progressive toxicity or harmful effect produced by summation of incremental injury resulting from successive exposures, e.g. liver fibrosis produced by ethanol.
 Accumulative effects:  occurs two ways...
a) accumulation of toxin: exposure to heavy metals (lead, mercury) that have long half-lives result in disease due to metal accumulation.
b) accumulation of effect: low level exposure to organophosphate pesticides depresses acetylcholine esterase to a point where symptoms occur.


Q. Define cheminformatics?
Cheminformatics (also known as chemoinformatics, chemioinformatics and chemical informatics): Cheminformatics is the use of computer and informational techniques applied to a range of problems in the field of chemistry. These in silico techniques are used in, for example, pharmaceutical companies in the process of drug discovery.
Q. Define end point study record?
Endpoint study record or IUCLID (International Uniform Chemical Information Data base) format of the technical dossier is used to report study summaries and robust study summaries of the information derived for the specific endpoint according to the REACH Regulation.
Q. Define end point of study design?
Endpoint: an observable or measurable inherent property/data point of a chemical substance. For example, a physical-chemical property like vapor pressure or degradability or a biological effect that a given substance has on human health or the environment, e.g. carcinogenicity, irritation, aquatic toxicity.
Q. Define in vitro test?
In vitro test: literally stands for “in glass” or “in tube”, refers to the test taking place outside of the body of an organism, usually involving isolated organs, tissues, cells, or biochemical systems. 
Q. Define in vivo test?
In vivo test: a test conducted within a living organism.
Q. Define in silico test?
In silico: In silico (a phrase coined as an analogy to the familiar phrases in vivo and in vitro), is an expression used to denote “performed on computer or via computer simulation.” Means scientific experiments or research conducted or produced by means of computer modeling or computer simulation.
Q. Define IUCLID flag?
IUCLID flag:  an option used in the IUCLID software to indicate submitted data type (e.g. experimental data) or their use for regulatory purposes (e.g. confidentiality). 
Q. Define prediction model?
Prediction model is a theoretical formula, algorithm or program used to convert the experimental results obtained by using a test method into a prediction of the toxic property/effect of the chemical substance.
Q. Define QSARs and SARs?
QSARs and SARs: theoretical models that can be used to predict in a quantitative or qualitative manner the physic-chemical biological (e.g. (eco)toxicological) and environmental fate properties of compounds from knowledge of their chemical structure. A SAR is a qualitative relationship that relates a (sub) structure to the presence or absence of a property or activity of interest. A QSAR is a mathematical model relating one or more quantitative parameters, which are derived from the chemical structure, to a quantitative measure of a property or activity. 
Q. Define test or assay, validation test and validation.
Test (or assay): an experimental system set up to obtain information on the intrinsic properties or adverse effects of a chemical substance. 
Validated test:   a test for which its performance characteristics, advantages, and limitations has been adequately determined for a specific purpose. 
Validation: the process by which the reliability and relevance of a test method are evaluated for the purpose of supporting a specific use. 
Q. Define vertebrate animal?
Animals that belongs to subphylum Vertebrata, chordates with backbones and spinal columns is known as Vertebrate animal. 
Q. Define accidental poisoning
Accidental poisoning may occur when human beings or animals take toxicant accidentally or is added unintentionally in food or through in its feed, fodder or drinking water. Such toxicants come from either natural sources or manmade sources. The natural sources include ingestion of toxic plants, biting or stinging by poisonous reptiles, ingestion of food contaminated with toxins, contaminated water with minerals, etc. Man made sources include therapeutic agents, household products and agrochemicals, etc.
Q. Define malicious poisoning
It is the unlawful or criminal killing of human beings or animals by administering certain toxic/poisonous agents. Incidence of such poisonings is more prevalent in human beings and less in animals.


Toxic agents are classified in number of ways depending on the interests and needs of the classifier. There is no single classification applicable for the entire spectrum of toxic agents and hence combinations of classification systems based on several factors may provide the best rating system. Classification of poisons may take into account both the chemical and biological properties of the agent, however, exposure characteristics are also useful in toxicology.
Q. Classify toxic agents
In toxicology, compounds are classified various ways, by one or more of the following classes: 

Use e.g, pesticides (atrazine), solvents (benzene), food additives (nutrasweet), metals, war gases,  
Effects e.g. carcinogen (benzo-a-pyrene), mutagen (methylnitrosamine), hepatotoxicant (CHCl3) …….
Physical state such as oxidant (ozone), gas (CO2), dust (Fe2O3), liquid (H2O) .........
Chemistry such as:  aromatic amine(aniline), halogenated hydrocarbon (methylene chloride) and so on.
Sources of toxicants e.g. plant or animal or natural and so on.
Mechanism of action:  cholinesterase inhibitor (malathion), methemoglobin producer (nitrite).... ….
Q. Classification based on sources of toxicants
i) plant toxins,
ii) animal toxicants,
iii) mineral toxicants,
iv) synthetic toxicants
v) physical or mechanical agents
Q. Classification based on physical state of toxicants
i) gaseous toxicants
ii) liquid toxicants
iii) solid toxicants
iv) dust toxicants,
Q. Classification based on target organ or system
i) neurotoxicants
ii) hepatotoxicants
iii) nephrotoxicants
iv) pulmotoxicants
v) hematotoxicants
vi) dermatotoxicants
vii) development and reproductive toxicants
Q. Classification based chemical nature/structure of toxicants
i) metals
ii) non-metals
iii) acids and alkalis
iv) organic toxicants (carbon compounds other than oxides of carbon, the carbonates, and metallic carbides and cyanides),
Q. Classification based on analytical behavior of toxicants
i) volatile toxicants
ii) extractive toxicants
iii) metals and metalloids
Q. Classification based on type of toxicity
i) acute
b) subacute
c) chronic
Q. Classification based on toxic effects
i) carcinogens
ii) mutagens
iii) teratogens
iv) clastogens
Q. Classification based on their uses
i) insecticides
ii) fungicides
iii) herbicides
iv) rodenticides
v) food additives, etc
Q. Classification based on symptoms produced
i) corrosive poisons
ii) irritant poisons
iii) systemic poisons
iv) miscellaneous poisons
In addition, there are other types of classifications that are based up on the environmental and public health considerations and so on.


Q. Describe briefly the term “Toxicity rating”.
A system of “toxicity rating” has been evolved for common poisons. The higher the toxicity rating for a particular substance (over a range of 1-6), the greater is the potency. The toxicity rating based on toxic potential of substances (super toxic, extremely toxic, very toxic, moderately toxic, slightly toxic and practically non-toxic.

FURTHER READING

Gupta PK (2018) Illustrative Toxicology with Question bank. 1st Edition. Elsevier, USA

Gupta PK (2016) Fundamentals of Toxicology: Essential concepts and applications. 1st Edition. ISBN-9780128054260, pp 438, BSP/Elsevier, USA

The Merck Veterinary Manual (2016). Chapter “Herbicide Poisoning” by PK GUPTA 11th edition, Merck & Co. Inc Whitehouse Station, NJ, USA  2969-99

The Merck Veterinary Manual (2016). Chapter “Pentachlorophenol Poisoning” by PK GUPTA 11th edition, Merck & Co. Inc Whitehouse Station, NJ, USA  pp 3052-53

Gupta PK (2016) Essential Concepts in Toxicology. Published by PharmaMed Press (A unit of BSP Books Pvt. Ltd), Hyderabad, India pp 362.

Gupta PK (2010) Modern Toxicology, Basis of organ and reproduction toxicity. Vol 1. Published by Pharma  Med Press (A unit of BSP Books Pvt. Ltd). Hyderabad, India pp 1-460.

Gupta PK (2010) Modern Toxicology, Adverse effects of xenobiotics. Vol 2, Published by PharmaMed Press (A unit of BSP Books Pvt. Ltd). Hyderabad, India pp 1-460.


Gupta PK (2010) Modern Toxicology, Immuno and clinicsal toxicology Vol 3. Published by PharmaMed Press (A unit of BSP Books Pvt. Ltd). Hyderabad, India pp 1-340.

Tuesday 16 January 2018

Series 2: TOXICOLOGY Question and Answer bank-TOXICOLOGY by Prof (Dr) Pawan K (PK) Gupta

TOXICOLOGY Question and Answer bank  
(series 2)
                                                                                                             In continuation of  series 1st 
Q. What is REACH regulation?
REACH regulation is concerned with registration, evaluation, authorization and restriction of chemicals in European Union (EU). It entered into force on 1st June 2007. It streamlines and improves the former legislative framework on chemicals of the EU.

Q. Describe briefly the term “Toxicity rating”.
A system of “toxicity rating” has been evolved for common poisons. The higher the toxicity rating for a particular substance (over a range of 1-6), the greater is the potency. The toxicity rating based on toxic potential of substances. For example, super toxic, extremely toxic, very toxic, moderately toxic, slightly toxic and practically non-toxic.
Q. What do you mean by super toxic
Less than 5 mg/kg
Q. What do you mean by extremely toxic
5-50  mg/kg
Q. What do you mean by very toxic
51-500 mg/kg
Q. What do you mean by moderately toxic
501 mg/kg to 5 g/kg
Q. What do you mean by slightly toxic
5.1 g/kg to 15 g/kg
Q. What do you mean by practically non-toxic
More than 15 g/kg
Q. What is acute toxicosis
refers to effects during the first 24hr period
Q. What is subchronic toxicosis
effects produced by repeated exposure (<3months)
Q. What is chronic toxicosis
effects produced by prolonged exposure (>3months)
Q. What is LD?
lethal dose
Q. What is LD (LO)?
 lethal dose low; lowest dose that produced deaths
Q. What is LD (50)?
median lethal dose - calculated dose that is projected as being likely to cause death in half (50%) of the exposed animals of the species/strain/age/sex exposed.
Q. What is LC?
lethal concentration = lethal concentration of a toxicant in feed, water, soil or other 'matrix' to which the animals are exposed
Q. What is an addition/additive effect?
 When the combined effect of two compounds given together is equal in magnitude to sum of the effects of each compound given alone, the interaction is called addition and the effect produced is called additive effect.In this case no specific interactions occur.
  1 + 1 = 2

Q. What is synergism/synergistic effect?
The combined effect of the administration of two compounds may be greater than the sum of the two effects; this is called synergism.  The synergist piperonyl butoxide is added to some insecticides to greatly increase their toxicity to insects. 

Q. What is potentiation/potentiative effect?
When one compound having no effect of its own increases the effect of another compound the interaction is called potentiation and the effect produced is called potentiative effect. For example, a dose of a compound A is toxic to animals in vivo. Another chemical B is not toxic when given at doses several orders of magnitude higher but when the two are given together the toxic response is greater than that of the given dose of A alone. This means the compound B has a potentiative effect on compound A. This is known as potentiation.
For example:  1+ 1 = more than two
Q. What is the difference between synergism and potentiation?
The difference between the two concepts is that synergism is the interaction of two or more substances, while potentiation is about a singular substance and how it may act when in a synergy relationship.

Q. What is the difference between toxicity and toxicosis?
Toxicity is the relative potency of a toxicant - usually compared on a mg/kg basis. Toxicosis is a pathologic condition that results from exposure to a toxicant.

Q. What is the difference between dose and dosage?
Dose is the total amount of toxicant received by the animal and animal dosage is the amount of toxicant per unit of animal weight.

Q. What is the difference between quantal response and graded response?
A quantal response (population response) is a binary response, the effect happens or it does not happen i.e. all or none response. A graded response (individual response) is where the toxic effects become more severe as the dose increases.

Q. What is the difference between LD50 and therapeutic ratio?
LD50 is the dose likely to cause death in 50% of a given species/age/sex group under specified conditions. The therapeutic ratio is the ratio of LD50 to ED50 (units are %).

Q. What are the timeframes associated with acute, sub-chronic and chronic exposures?
Within 24 hrs:             acute toxicity
Within 30 days or less:            sub-acute toxicity.
within 1 to 3 months:               sub-chronic toxicity.
More than 3 months:               chronic

Q. Compare the different routes of toxicant exposure and their toxicant concentration.
IV has the highest concentration, followed by inhalation, then oral and dermal, which have similar concentrations.

Q. Name five toxicity factors associated with the toxicant.
1. Solubility
2. Polarity
3. Vehicle
4. Formulation effects
5. Chemical interactions

Q. Name eight factors associated with the environment that affect toxicity
1. season
2. temperature
3. light factors
4. housing
5. constructions
6. heating systems
7. air circulation
8. bedding

Q. What type of biotransformation happens in Phase I?
oxidation
reduction
hydrolysis

Q. What type of biotransformation happens in Phase II?
Conjugation with endogenous molecules

Q. Name five things that influence biotransformation?
1. Parenchymal organ disease
 2. Toxicant localization in tissues with little PI/PII activity
3. Age and metabolic activity 
4. Species-specific variation and individual variation
5. Gender and hormone differences

Toxicokinetics

Q. Describe First Order elimination Kinetics? How is this different to zero order kinetics?
https://lifeinthefastlane.com/first-order-and-zero-order-kinetics-pharmacology-bscc/

First order: First order reactions are the most common. These reactions occur when a constant proportion of the drug/toxicant is eliminated per unit time. Rate of elimination is proportional to the amount of drug/toxicant in the body. The higher the concentration, the greater the amount of drug/toxicant eliminated per unit time. For every half-life that passes the drug/toxicant concentration is halved (t1/2=0.693). For example, a drug/toxicant concentration of 100 and a half-life of one hour will reduce to 50 in the first hour, 25 in the second hour and 12.5 in the 3rd hour and so on. Most drugs/toxicant are eliminated this way. Elimination mechanisms are NOT saturable. 10 half-lives will virtually eliminate all the drug/ toxicant from the body.


Zero order: Zero order is a saturated process proceeding at maximum amount the body can handle per unit time. Reaction rate is independent of amount of drug/toxicant in the body. Kinetics may change to first order after process is no longer saturated. In this case a constant amount of drug/toxicant is eliminated per unit time. For example, 10mg of a drug may be eliminated per hour, this rate of elimination is constant and is independent of the total drug/toxicant concentration in the plasma. These reactions (zero order kinetics) are rare. Elimination mechanisms are saturable. Examples of zero order elimination include ethanol, phenytoin and salicylates (at high doses).

                                                                                                                       To be cont’d

FURTHER READING

Gupta PK (2018) Illustrative Toxicology with Question bank. 1st Edition. Elsevier, USA

Gupta PK (2016) Fundamentals of Toxicology: Essential concepts and applications. 1st Edition. ISBN-9780128054260, pp 438, BSP/Elsevier, USA

The Merck Veterinary Manual (2016). Chapter “Herbicide Poisoning” by PK GUPTA 11th edition, Merck & Co. Inc Whitehouse Station, NJ, USA  2969-99

The Merck Veterinary Manual (2016). Chapter “Pentachlorophenol Poisoning” by PK GUPTA 11th edition, Merck & Co. Inc Whitehouse Station, NJ, USA  pp 3052-53

Gupta PK (2016) Essential Concepts in Toxicology. Published by PharmaMed Press (A unit of BSP Books Pvt. Ltd), Hyderabad, India pp 362.

Gupta PK (2010) Modern Toxicology, Basis of organ and reproduction toxicity. Vol 1. Published by Pharma  Med Press (A unit of BSP Books Pvt. Ltd). Hyderabad, India pp 1-460.

Gupta PK (2010) Modern Toxicology, Adverse effects of xenobiotics. Vol 2, Published by PharmaMed Press (A unit of BSP Books Pvt. Ltd). Hyderabad, India pp 1-460.

Gupta PK (2010) Modern Toxicology, Immuno and clinicsal toxicology Vol 3. Published by PharmaMed Press (A unit of BSP Books Pvt. Ltd). Hyderabad, India pp 1-340.

Series 1: General Toxicology: TOXICOLOGY Question and Answer bank- by Prof (Dr) Pawan K (PK) Gupta

General Toxicology: TOXICOLOGY Question and Answer bank


INTRODUCTION

TOXICOLOGY Question and Answer bank is aimed to make the study of toxicology simple and understandable through illustrations, images, custom made drawings, self-explanatory tables, and questions and answers collated from standard and authoritative textbooks, and widely scanned. The author’s own experience in different branches of toxicology including environmental and veterinary toxicology has been abstracted in these series of articles. This is first articles of series. The article has been written in a manner to stimulate interest on various facets of the subject and make it more exciting. It is general experience that theoretical description does not attract as much attention and interest as the illustrations and images. At the same time the information learnt through questions and their satisfactory replies make the topics easier to grasp them.
The book provides comprehensive quick reference for various examinations. However, it should be noted that this series serve only as a supplement and not as a replacement for any textbook and class room learning.
The series is expected to cover several topics such as general toxicology, principles of toxicology, risk assessment, disposition, mechanism of toxicity, toxic effects of various xenobiotics, poisonings of poisonous and venomous organisms, plant toxins, poisonous and food poisonings, radiation hazards and, abuse of drugs. The following series will also the adverse effects on environment and ecosystem exposed to various toxicants and poisonings as relevant to domestic and other animals.
Each article will be in the format of questions and answers, multiple choice questions, true and false statements or correct/ incorrect statements, fill in blanks, and matching the statements that will be useful for students, teachers and practicing in medical sciences, toxicology, pharmacology, medicine, pharmacy, environmental toxicology and in veterinary sciences.

WHO will be benefitted

The author believes that these series would be:
Ø          A good alternative to be used for various courses and an excellent contribution for the students who needs a study aid for toxicology but wants more than a textbook as they need a self-testing regime.
Ø                The teachers of toxicology who needs inspiration when composing questions for their students.
         The established toxicologists who wants to test their own knowledge of understanding

the subject matter.
Ø  Will be useful at universities and colleges, in industry for in-house training courses in toxicology which I know exist in some pharmaceutical and chemical companies
Ø  Required for studying for the toxicology Boards and for preparation of different examinations.

Thus, the main strength of the series will reflect the breadth and multi-disciplinary nature of toxicology with illustrative approach to the subject that is needed to improve engagement with and understanding of the subject having a very wide audience.

Toxicology is a rapidly evolving field. Suggestions and comments are welcome to help the author improve the contents of the series. Please also suggest or send comments at drpkg_brly@yahoo.co.in or drpkg1943@gmail.com

GENERAL TOXICOLOGY

Q. What is toxicology?
Toxicology is the study of the adverse effects of chemicals or physical agents on living organisms. The word  ‘toxicology’ is derived from the Greek word ‘toxicon’ which means ‘poison’ and logos means to study. It also includes study of special effects of toxicants developmental toxicity, teratogenicity, carcinogenicity, mutagenesis, immune-toxicity, neurotoxicity, endocrine disruption, etc.
Q. Who is the father of rational medicine?
Hippocrates (460-375 BC) is regarded as the “Father of Rational Medicine”. He created the Hippocratic oath. He believed that disease came naturally and not from superstitions and GOD. He advocated hot oil as an antidote in poisoning and induced vomiting to prevent absorption of the poisons.
Q. What do you know about Paracelsus?
Hohenheim-Paracelsus (1493–1541) a first century Roman physician, who promoted a focus on the toxicon, the toxic agent, as a chemical entity. He recognized the dose-response concept and in one of his writings stated, “All substances are poisons, there is none which is not a poison. The right dose differentiates a poison and a remedy”. 
Q. Who is Friedrich Serturner? What is his contribution?
Friedrich Serturner (1783-1841), German pharmacist who isolated the specific narcotic substance from opium and named as morphine after Morpheus, the Roman God of sleep.
Q. Who is a Father of Toxicology?
M J B (Mattie Josesph Benaventura) Orfila (1787-1853), a Spanish physician is a considered as “Father of Toxicology”.
Q. Describe main contributions of M J B Orfila (1787-1853).
He established toxicology as a discipline distinct from others and defined toxicology as the study of poisons. He advocated the practice of autopsy followed by chemical analysis of viscera to prove that poisoning has taken place. His “treatise” Traite des Poisons published in 1814 laid the foundations of forensic toxicology.
Q.   Who is father of experimental pharmacology? Describe in brief his contributions.
Francois Magendie (1783-1855) is known as the “Father of Experimental Pharmacology”, a pioneer French physiologist and toxicologist studied the mechanism of action of emetine, morphine, quinine, strychnine and other alkaloids.
Q. Who was Claude Bernard?
Claude Bernard (1813-1878) was a French physiologist who is considered the "Father" of Modern Experimental Physiology. Claude Bernard's first important works were carried out on the physiology of digestion, particularly the rôle of the pancreas exocrine gland, the gastric juices and of the intestines. In addition to this, Bernard also made other important contributions to the neurosciences.
Q. Who was Louis Lewin (1854-1929)?
Louis Lewin (1854-1929) was a German scientist who took up the task of classifying drugs and plants in accordance with their psychological effects. He also published many articles and books dealing with toxicology of methyl alcohol, ethyl alcohol, chloroform, opium, and some other chemicals. His important publications are “toxicologist’s view of world history” and “A textbook of toxicology”.
Q. Who discovered the insecticidal properties of DDT? What is his major contribution?
Paul Hermann Muller in 1939 discovered they of insecticidal properties of dichlorodiphenyltrichloroethane (DDT) .He was awarded Nobel Prize in 1948 “for his discovery of the high efficiency of DDT as a contact poison against several arthropods”.
Q. Who is “Father of Nerve Agents”?
Gerhard Schrader (1903-1990) was a German chemist who accidentally