Hlo Friends my name is NITESH VISHWKARMA I am student of B.PHARMACY second year (Shree Rawatpura Sarkar Institute of Pharmacy Aari Jhansi Uttar pradesh)

Tuesday 28 January 2020

NATURE AND SOURCE OF DRUG


NATURE AND SOURCE OF DRUG

Hello dear students, welcome to this blog today,  I am going to talk about drugs they are nature and sources and the before discussing the topic in detail let's first know its objectives

*Number one how are drugs defined
*Number two what is the nature of drugs
*Number third what are the main sources from which drugs

 The definition of drug- A drug may be defined as a natural or synthetic substance which when taken into a living body affects its functioning or structure and is used in the diagnosis, mitigation, treatment, or prevention of a disease.

 A drug may also be habbit-forming stimulant or narcotic substance like  alcohol, cannabis, nicotine or a  derivative of poppy. which produces a  state of arousal contentment or eforea.  continued or excessive use of such  substances causes addiction or  dependence. the former refers to legal  drugs and the latter as illegal drugs.  The term drug refers mainly to chemical  or plant derived substances that affect  psychological, behavioral or physical  functions and lead to varying degrees of  dependence or addiction.

Let's discuss  now  the nature of these drugs based on  the nature of their chemical groups drugs can be classed into various groups alkaloids,  glycosides  philomon oyd, and proanthocyanidins, tannins,terpenoids resins and lignans,
                         

Alkaloids

The alkaloids are heterocyclic nitrogen containing compounds usually with potent activity and bitter taste they are of limited distribution in the plant kingdom. the various groups of alkaloids like-
*tropane alkaloids
*pyrrolizidine alkaloids and
* methyl xanthine alkaloids  - have diverse killed nickel properties which are mentioned below….     

 * Tropane alkaloids

* Tropane alkaloids - have anticholinergic activity they are also used medically to reduce smooth muscles palms hypersecretion and paint.       
        
* Pyrrolizidine Alkaloids - inhibit pain cancer cells and bacteria they also help in stimulation of bone marrow leukocytes as well as myocardial contractility.   
                
*Methylxanthines*
 methylxanthines bind to adenosine receptor and elicit neurological effects in man and animals which may be regarded stimulating at low to moderate intake.   
                        
 *Rodents -high intakes of methylxanthines show reduced sperm production and testicular atrophy.             
             

  *Glycosides*

 Glycosides these compounds consist of various categories of secondary metabolites bound to a mono or oligosaccharide or to uronic acid. the saccharide or uronic acid part is called the glycol and the non saccharide part the Aglycon .

The main groups of glycosides are  *cardiac glycosides  *cyanogenic glycosides Glucocynolates , saponins and anthraquinone  glycosides.

 Now the clinical  properties of these glycosides include

They inhibit sodium, potassium,  ATP  pumps and cell membranes. these pumps are  critical for the functioning of the  cardiac cells therefore these compounds  result in increased contractility and  reduced heart rate.

Cyanogenic glycosides  interfere with the iodine utilization  and result in hypothyroidism  some saponins induce photosensitisation  and jaundice.  anthraquinone glycosides helped in  induction of water and electrolytes  creation as well as peristalsis and colon. now flavonoids and proanthocyanidins  flavonoids consist of a central  three-ring structure and  proanthocyanidins are oligomers of  flavonoids and the clinical properties  include they act as general into  oxidants several structures reduce  inflammation or carcinogenicity.

 Tannins
there are two distinct types of  tannins

Condenser tannins - which are  large polymers of flavonoids and  hydrolyzable tannins which are polymers  composed of a monosaccharide core most  of Angelico's with several catechin  derivatives attacked.the clinical  properties include they are used as  astringent in cases of diarrhea skin  bleeding's and transit eights.

Terpenoids - the terpenoids are  synthesized where the five carbon  building block isoprene activity. and the clinical properties include their  antonio plastic antibacterial and  antiviral they are also important in  gastrointestinal stimulation.

Resins - the resins are complex lipid  soluble mixtures usually both non  volatile and volatile compounds. the non  volatile fraction may consist of dye tap  annoyed and write-up annoyed compounds  and more range circa terpenoids  to dominate in the volatile fraction. and  the clinical properties of these resins  are most resins are inter microbial and  wound healing but their actions depend  on the composition of the chemical  mixture resins are generally safe but  contact allergy may occur.

Lignans -  the lignans are composed of two phenyl  propane I'd units to form an 18 carbon  skeleton with various functional groups  can  they are gently lipophilic and have  structural functions within the plant  cell membranes lignin cophytoestrogen  ik and antonio plastic effects.

Discuss The Sources Of Drugs

 Drugs can be  obtained from natural sources like  plants animals microbes etc. Or can be  prepared synthetically.

First we'll  discuss national sources of drugs nature  has been a source of medicinal agents  for thousands of years and continues to  be an abundant source of novel chemo  types and pharmaco force with only 5 to  15 percent of the approximately 2 lakh  50 thousand species of hair plant  systematically investigated and the  potential of marine environment barely  tapped these areas will remain a rich  source of novel bioactive compounds. it's  apparent that nature can provide the  novel chemical scaffolds for elaboration  by chemical and biochemical approach  thus leading to agents that have been  optimized on the basis of their  pharmacological activities.

First we will  discuss the plants as the sources of  drugs plants have formed the basis for  traditional medicine systems which have  been used for thousands of years in  countries such as China and India. these  plant based systems continue to play an  essential role in healthcare and it has  been estimated by the World Health  Organization that approximately 80% of  the world's inhabitants rely mainly on  traditional medicines for their primary  health care. examples of important plant  compounds developed for the benefit of  human health are if a dream first  isolated from ephedra Sinica  is the basis for the synthesis of the  nth asthma agents salbutamol and  salmeterol .

 Tubocurarine - it's the muscle relaxant isolated from  coder Dendron and curare species and  used by indigenous groups in the Amazon  as the basis for the arrow poison cure.

 Vlasting and Vincristine - isolated from catharanthus roseus has  anti-cancerous properties peppered  somniferum has given rise to four  important medicines. the plant is very  old painkiller and a sedative the four  important and collides found in opium  that are used as medicines today are  morphine, codeine, noscapin and pepaverine.

 Strychnine -  it's isolated  from the plant Stychnos nux- vomica  this compound is used as a muscle  relaxant in connection with operations  for killing animals and due to its  bitter taste, it enhances the gastric  juice production leading to a better  appetite.

 Queenie -  malaria is one of the most fatal  diseases worldwide an old well-known  remedy for treatment of malaria is the  queenie isolated from the bark of  trees in Cinchona species.

 Artemisinin -  Artemisia annua is an old Chinese and  malaria remedy called  Quinhao. this was shown to be an  effective remedy both as prophylaxis and  in the treatment of malaria,

Podophylllotoxin - it's a resin  compound isolated from the roots of  Podophyllum peltatum Podophylllotoxin was also the lead compound giving rise  to the development of the medical drugs  teniposide and etoposide today used  again as several types of cancers.

The Microbes As The Source  of Drugs

The exchange and discovery of  penicillin from the filamentous fungus  penisilin notatum by filiming in 1929  and the observation of the broad  therapeutic use of this agent in the  1940s assured in a new era in medicine  the so-called Golden Age of antibiotics.  this discovery promoted the intensive  investigation of nature as a source of  novel bioactive agents and  microorganisms hell proved to be a  prolific source of structurally diverse  bio active metabolites which have  yielded some of the most important  products of the pharmaceutical industry.  and these include antibacterial agents  such as pencillines from pencilum species cephalosporins from syphilis  poram Cryptosporidium tetracycline from  the actinomycintells the  immunosuppressive agents like the  cyclosporine and rapamycin from  streptomyces species the  cholesterol-lowering agents such as  Mavis tannin and  lovastatin from pencilum species and  into hermeneutics and into parasitic  drugs such as ever make tents from  streptomyces species .

Cyclosporin A - isolated from the micro fungus Tolypocladium inflatum  has immunosuppressive properties this  product revolutionized the survival  period for people needing  transplantation of organs and has given  a large number of people an elongated  life.  

The Marine Sources of Drugs

The world's oceans covering more than 70  percent of the Earth's surface represent  an enormous resource for the discovery  of potential chemotherapy agents. the  first notable discovery of biologically  active compounds from marine sources was  the isolation of the C -nucleosides,  spongouridine and spongothymidine  from the caribbean sponge  cryptotheka crypta in the 1950s. these  compounds were found to possess  antiviral activity  the see here Dolabella auricularia from  the Indian Ocean is the source of more  than 15 cytotoxic cyclic and linear  peptides called the Dolastatins.

 The  extremely potent Venom's of predatory  cone snails have yielded complex  mixtures of small peptides which have  provided models for the senses of novel  pain killers. the other sources of drugs  include teprotide  isolated from the  venom of the pit viper bothrops jaracaca  is used in the treatment of  cardiovascular diseases.

Epibatidine -  present in the skin of a frog  EpipedobatesTricolour  has been shown  to be 200 times more stronger painkiller  than morphine. this was discovered  because natives used the extract of the  skin as an arrow poison.

Discuss Synthetic Sources of Drugs

Synthetic drugs are synthetic compounds  of naturally occurring chemicals for  example synthetic marijana  and bath salts. the short term toxicity  of these drugs has been shown to be  problematic for individuals and could  have lifelong impacts also however as  these drugs have only recently in  filtered society not much is known about  the long term effects and further  research is needed based on their  chemical makeup synthetic drugs are  commonly divided into two categories, first we will discuss cannabinoids pop  indeed known as k2 or spice cannabinoids  are chemically formulated versions of  synthetic marijana  that consist of lab manufactured  tetrahydrocannabinol users report  greater anxiety, discomfort, nausea,  confusion,  perinea, desired for the feeling to end. these  synthetic chemicals negatively affect  short-term memory, emotional stability,  motivation, learning, reasoning ability  and stamina.

Cathinones

Often known  as bath salts, Catalans  contain chemical compounds that mimic  the effects of cocaine. this is a  powerful drug that causes severe side  effects.
Bbath salts are sold as  crystalline powder with names such as  ivory wave, blow, red Daoe, vanilla sky, aura, zeus 2,  zoom, bliss, blue silk, white lightening,  ocean, charge,  white dove and others.
The symptoms of bath  salt use are severe paranoia, seizures,  violent behavior, decreased need for  sleep, hallucinations, lack of appetite,  chest pain, and self-mutilation.
 Users  frequently described the highest  horrible and report seeing demons,  monsters, foreign soldiers or aliens some  have symptoms for two to three days some  require long-term psychiatric care  because their symptoms do not improve.

Long-term health problems that result  from the use of bath salts are kidney  failure, long-term mental illness,  increased risk of suicide,  self-mutilation, liver failure and death.

Discuss The Roots of Drug  Administration

 A drug will produce its  section only when it enters the body  tissue or cells that is site of action.
  so the entrance through which a drug is  delivered is called the  of drug administration there are various  ways of administering a drug or a  chemical to a site in a patient or  animal from where the chemical is  absorbed into the blood and these  include systemic route and local Road.

The systemic route - Drug administration in systemic route  the drug reads to the systemic  circulation that's the blood.

This  systemic route is further classified as  internal route and parenteral route an  internal route the drug is placed in the  gastrointestinal tract and it absorbs to  the blood the drug can be administered  into gastrointestinal tract through oral  route, sublingual route or rectal route.

Oral route- the drug is placed in the  mouth and swallowed and absorption takes  place along the whole length of the  gastrointestinal tract, but drug  administration through oral route is  sometimes inefficient because only part  of the drug may be absorbed and  destruction of drug occurs by gastric  acid and digestive juices.

The most  important concept associated with oral  route of drug administration is the  first pass effect.

The first pass effect  is the term used for the hepatic  metabolism of a pharmacological agent  when it is absorbed from the gut and  delivered to the liver via the portal  circulation.
The greater the first pass  effect the less the agent will reach the  systemic circulation when the agent is  administered orally.

Sublingual route or Buccal root -  in this route of drug  administration the drug is placed under  the tongue and absorption occurs in the  mouth.

So rapid absorption occurs and the  drug is quite stable because the drug  does not go to the stomach so it is not  destroyed  the enzymes and acids present in the  stomach.

Rectal root - in this form a drug is  mixed with the waxy substance that  dissolves or liquefies after it is  inserted into the director because the  rectums wall is thin and it's rich blood  supply the drug is readily absorbed.

 It's  prescribed for people who cannot take a  drug orally because they have no she  cannot swallow or have restrictions on  eating as is required after many  surgical operations.

Parenteral route  of drug administration in this route of  administration the drug does not pass  through the gastrointestinal tract,  it  directly reaches to the blood. the drug  can be administered with the help of  injections which can be intravascular,  intramuscular or subcutaneous or without  injections.

Which include inhalations  injections can begin - unconscious  patients and it has quick action but  there is greater risk of adverse effects  because high concentration is attained  rapidly and pain occurs at the site of  injection.

Drug administration without  injections is pain-free and rapid onset  of action occurs due to rapid access to  circulation.

Llocal or topical  route of drug administration in this  route the drug is applied on the skin  and mucous membrane for the local action.

  It's All About This Topic Hope You  Understood Well
                                     Thank You

Friday 24 January 2020

HISTORY AND LANDMARKS&SCOPE OF PHARMACOLOGY


HISTORY AND LANDMARKS 

1)  OSWALD  SCHMIEDEBERG (1838-1921) =  Oswald  is A  founder of morden pharmacology.  In 1872 Schmiedeberg set up an organization of pharmacology in Strasbourg, France (Germany around then) which turned into a world renowned hub for understudies who were enthusiasm for pharmacological issues.

Discovery= 
*Estimation of – chloroform in blood. 
*Study of chlorohydrate. 

HISTORY AND LANDMARKS&SCOPE OF PHARMACOLOGY
HISTORY OF PHARMACOLOGY


2) JOHN J. ABEL ( 1857-1938) =  Established the primary chair of pharmacology within the U.S.A. (U. Michigan, 1891) after training in Germany. Able visited Johns Hopkins in 1893, and trained many U.S. pharmacologists. "The Father of american Pharmacology".

Discovery= 
* Isolation of Histamine from pituitary gland. 
* Preparation of pure crystalline insulin. 

3) ALFERED JOSEPH (1885-1941) = General mechanism of drug action. 

4) HENRY DOLE (1875-1968) =

Discovery= 
* Isolate the neurotransmitters – Acetylcholine (1914). 
* Identify histamine in animal tissue. 
* Role of histamine in allergy and hyposensitivity. 
* Alfa blocker reduces blood pressure. 

5) POUL EHRLICH (FATHER OF CHEMOTHERPHY) = Use arsenicals for – syphilis, work on tumors 

6) ALEXENDER FLEMING (1929) = discovered Penicillin

7) JAMES BLACK = Discovery of Beta blocker. 

8) RAMNATH CHOPRA (FATHER OF INDIAN PHARMACOLOGY) = Systematic study of Indian medicinal plant.

9) DOMAGK(1937) =Prontesil sulphonamide

10) PASTEURE (1877) = Phenomenon of antibiosis.

11) WAKSMAN (1944) = Actinomycetes 

12) J.N. Langley (1852-1925 and Sir Henry Dale (1875-1968) = pioneered pharmacology in England, taking a physiological approach.

13) Rudolph Buchheim (1820-1879) = In 1847 Bucheim set up the main research facility gave to trial pharmacology in the storm cellar of his home in Dorpat which is known as the support of exploratory pharmacology.

14) Francois Magendie (1783-1855) = A French physiologist set out the decree "Actualities and certainties alone are the premise of science." Experimental methods with creatures are the proving grounds for assurance of medication activity.





SCOPE OF PHARMACOLOGY


1)  To study of disease/disorder (pathophysiology)

2) Study of pharmacodynamics

3) Study of pharmacokinetics (properties  A. D. M. E.)

HISTORY AND LANDMARKS&SCOPE OF PHARMACOLOGY
SCOPE OF PHARMACOLOGY


4) Clinical pharmacology & Therapecutics  ( use – contraindication , posology, bioablevility )

5) Toxicology – Toxic substance , antidate , treatment

6) Forensic science

7) Pharmacovigilance –Allergic response , Heptotoxicity, Teretrgenicity, etc

8)  Pre-clinical trials

9)  Pharmacogenonics

10) Clinicals trials

11) P. DRUG – personal drug

12) New drug development






Friday 17 January 2020

Introduction of pharmacology unit-I (BP404T)


                      Introduction of pharmacology unit-I (BP404T)   

Basic introduction of pharmacology : The word Pharmacology is derived from Greek words pharmakon =drug, logos =science. 


 Introduction of pharmacology unit-I (BP404T)


Definition:  Pharmacology could also be a topic of bioscience which deals with the study of drugs or medicine that interact with the living system through chemical processes, specially by binding to regulatory molecules and activating or inhibiting body processprocess is know as pharmacology.


Pharmacodynamics:  is that the study of the actions of medicine on track organs. 

Pharmacotherapeutics:  Pharmacotherapeutics is that the life science concerned with the utilization of medicine within the treatment of disease.

Toxicology:  is the study of harmful rather than therapeutic effects.

Pharmacy:  nvolves manufacture, preparation, and dispensing of drugs. 

Pharmacoepidemiology:  investigates the effects of drugs on populations. 

Pharmacoeconomics:  examines the cost-effectiveness of drug treatments. 

Pharmacogenetics and pharmacogenomics:  is study the influence of genetic variation on pharmacodynamic and pharmacokinetic properties of drugs.

Medical Pharmacology: Branch of Pharmacology deals with the utilization of medicine in physical body for Diagnosis, Prevention, Suppression and Treatment of the Diseases.

Clinical Pharmacology: is the study of characteristics, effects, properties, reactions and uses of drugs.

DRUG: Drug is any substance or product that is used to modify used intended is be to or physiological systems or pathological states for the benefit of the recipient .

Pharmacokinetics : is the thing that the body does to the medication."

 1.Absorption 
 2.Distribution 
 3.Metabolized 
 4.Excreted 

ABSORPTION: Absorption is development of the medication from its site of organization into the course.

DISTRIBUTION: A medication has accessed the circulation system, it gets appropriated to different tissues that initially had no medication, fixation inclination being inside the heading of plasma to tissues."

METABOLISM(BIOTRANSFORMATION):  Biotransformation means chemical alteration of the drug in the body.