Pharmacy Gyan

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)

Wednesday 15 April 2020

Colloidal dispersion part-2 Physical pharmaceutics-2



2.KINETIC PROPERTY

a)Brownian Movement-: The colloidal in dispersion are always in a state of random motion.

*This random motion can be abserved under ultra microsocpe.

*It was first observed by Robert Brown.

*The velocity of the partiles increase with the decrease in particle size.

b) Diffusion-: Particle diffusion from a region of higher concentrations to lower concentration until the system is uniform.

*The rate of diffusion is experessed by FICKED'S FIRST LAW –
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C) Sedimentation-:  the colloidal dispersion, the brownian movement tend to disterb sedimentation.

*There force stronger force must be applied for sedimentation.

*Ultra centrifuge is used for studying sedimentation.

d) Viscosity-: Viscosity is an expression of resistance to flow under applied street (pressure).

*The more viscous a liquid, the grater the applied force to make it flow.

*Viscosity study provide shape of particle in solution.

3. Electrical property 

When an electric is applied to a colloidal dispersion, the particle carrieing charge move toword opposite charge electrode.

The negative charged particle (such as kaoline and sulphur) move towards anode.

The positive charged particle ( such as metal hydroxide and ferric hydroxide) move toword cathode.

The rate of particle movement is observed by ultra microscope.

The rate of movement is a function of charge on the particle and related to zeta potential.
Zeta potential can be calculate by



Where ---:
S  =  Zeta potential in volt
V  = Velocity of movement of colloidal particle
E  =  Applied potential
n  = Viscosity of the medium
e  = Dielectric constant

     EFFECT OF ELECTROLYTES


Consider a solid surface carrying a negative charge and is in contact with Aqous solution containg both positive and negative ion.

The positively charged solid surface will influence distribution of ions.

The thermal mostion also influence distribution of charges.

The resulting effect will be formation of electric double layers.

Ex- AgVo3 +Na I ------------- Ag I + Na Vo3

The surface of AgI contains more I ions than Ag+ ion.

Aqours solution contain large amount of Na+ ion and No3 and tracks of H+ and oH-.

AgI surface is negative charge due to I ions.
It attract positive ions( Na+)  towards it surface.

The thermal motion cavses equal distribution of ion.

Na+ concentration is high over I ion  surface and from compact as stern layer.

An other layer of Na3- ion forms called as gally chaman layer.

Thus combination of 2 layer opposite charge are called os electrical double layer.

Protective Action

Large concentration of hydrophilic colloids increase the stability of hydrophilic colloids towards precipitation by electrolyte.

The hydrophilic colloids adsorb on the surface of hydrophobic colloids and from a protective layer.

This layer prevent them from precipitation on addition of electrolyte.

The phenomenon is constant as protection or protection action.



Most stable ion not reach the colloidal particle no coagulation.

When bismuth sub nitrate is suspended in Tragaenth dispersion.

These phenomena involve coagulation of gum by bismuth ion.

The flocculated gum aggregation with the bismuth ion to from gel or hard cake.

If phosphate citrate or tartrate aded.

The protect from coagulation influence of bismuth ion.

PEPTIZATION

It is a process of converting ppt of large size to colloidal size by means of electrolyte is k/as peptization.

Some ionic material get adserbed on the surface of finally divided solid and convert it into colloidal dispersion.

COACERVATION (phase separation) 

When oppositly charged hydro colloids are mixed a colloid rich layer separate out. This process is k/as coacertation.

The phenomena in which a micro molecule dispersion on mixing separation into two layer is called as coacervation.

Ex. Creative is positively charged below pH 4.7 .
Acacia is negative change at this pH.

When they 2 are mixed together, two layer are formed.

The upper layer of low viscosity have poor concentration of colloidal material.

The lower layer hae thighs viscosity contain high concentration material.




Sunday 29 March 2020

Conformational analysis of cyclohexane

        CONFORMATIONAL ANALYSIS

Different spatial arrangements of atom in a molecule which are readily interconvertable by rotation of single bond are configuration.
Configuration represent confirmer which are readily inter convertible to they are not be separated.
Conformational analysis of cycloalkanes


The study of existence of configuration in molecule and their physical and chemical property is k/as CONFIRMATION ANALYSIS.

The structure of confirmers is of 2 types

1.STAGGERD -: When tarsinal angle b/w 2 atom molecule is 60°.

2.ECLIPSED -: Group of front and rear carbon overlap.
Conformational analysis of cycloalkanes
Confirmational analysis


         Conformational analysis in ethane

*In the structure of ethane 3 hydrogen is bonded with both carbon
*In the special arrangements with bond is rotated 60° then total six types of structure is obtained in which three is staggered from and three is eclipsed from.
Conformational analysis in ethane


        Conformational analysis in butane

*In the structure of n-butane hydrogen and 1 methyl group is present on both carbon.
*During conformational analysis after reaction of 60° in each time total 6 structure is formed in which full staggered is 1,fully eclipsed 1 , partial staggered 2 and portial eclipsed 2.
Conformational analysis in butane

                 
                Energetic in n-butane

* In the confirmational analysis total 6 structure are form in which 3 is staggered from and other 3is edipsed.
* In staggered from no steric hindrance occurs so they are stable and their energy is low.
* But in the case of eclipsed from bilky group are comes closer and dur to steric hindrance their stability is reduce and potential energy is increase.
Energetic in n-butane


Conformational analysis in cyclohexane 

Cyclohexane is a cyclic compound which show confirmational analysis by rotation or straining of bonds Mohr and Sachse in 1890-91 gives the idea of confirmational analysis in cyclohexane.
*After angel stain cyclohexane show 2 form of structure.
Conformational analysis in cyclohexane


*The chair form is rigid and where it is trans form into boat form same angulr deformation is Nesserey.
*The energy barrier in this process is about 9-11 kd/mole.
*This value is large enough for each confirmation to retain its identity.
*The chair and boat form are triangle stain but because of difference in staining strain and border a position state the 2 form are different in energy content.
Conformational analysis in cyclohexane

   
                   Energy in cyclohexane

*When chair form structure of cyclohexane is convert into boat form then they change into total five structure-
1. Chair
2. Half chair
3. Twisted boat
4. Half boat
5. Boat
*They energy of chair from is highest becoz this is similar to the eclipsed form.
*The energy of boat form is very less is about to 1.5 kcl.
Energy in cyclohexane


Stereo isomerism in biphenyl compound ( Atrop isomerism) 

*Those single bonded compound in which 2 cyclic group are bulky group present,  they also show restricted rotation, that way these compound biphenyl also show stereo isomerism.
* Stereo isomerism in biphenyl compound is also k/as atrop isomerism.
* The term atrop isomerism consist of 3 words.
A + Trop + isomerism
A means NON
TROP means TERM
*It means those isomerism which can not tern into another axis.
     
              Atrop isomerism in biphenyl


Atrop isomerism in biphenyl

*There are basically 2 condition for spoeing atrop isomerism.
1. There should be any functional group or atom at the ortho position.
2. The group or atom should not be simiiat position 1 and 2,and 3 and 4.
*Diphenyl compound can be diverded into 2 equal half so they can be symmetrical if there is no any group at ortho position.

*But when different atom or group is attached with ortho position then will be asymmetrical and show atrop isomerism.

Stereospecific and steroselective reaction

*Those chemical reaction after which a stereo compound is form which is either may be destroyed or levo then this is called stereospecific reaction.
*In this type of reaction both dextro and levo compound can be synthesized in different proportion.

Stereospecific and steroselective reaction


             Stereo selective reaction

These chemical reaction after which only one dextro or one levo compound is form and which is 100% selective they are called Stereo selective reaction.

Friday 27 March 2020

GEOMETRICAL ISOMERISM

               Geometrical isomerism 

The isomerism which due to restricted or forzen rotation about a bond in a molecular is k/as Geometrical isomerism.

GEOMETRICAL ISOMERISM
Pharmacygyan by NITESH VISHWKARMA

The rotation either about a double bond or about single bond or in a cyclic compound can be seen.

Geometrical isomerism is exhibited by variety of compound lile
--- Compound Containing a double bond
(C=C) (C=N) (N=N)
GEOMETRICAL ISOMERISM


Compound containing cyclic structure homocyclic Or hetrocylic.


Compound having restricted rotation about a single bond. Due to steric hindrance in biphenyl compound.


CONDITION FOR GEOMETRICAL ISOMERISM
A compound will show geometrical if it fulfill following three conditions.

1- There should be atleast one double bond            b/w and carboy, carbon and nitrogen.
2- There should be restricted rotation in                  double bond.
3- There should be at lest one similar group             b/w both double bond carbon.

NOMENCLATURE OF GEOMETRICAL ISOMERISM

GEOMETRICAL ISOMERISM can be nomenclature by 3 method -:

1. Cis- trans nomenclature
2. E and Z nomenclature
3. Syn and Anti nomenclature

1. CIS TRANS NOMENCLATURE

*There should be atleast one double bond b/w C=C, C=N.
*There should be restricted rotation in double bond.
*Tere should be atleast one similar group b/w both double bond carbon.
*If the similar atom are group is present on the same axis an both carbon then it is called CIS ISOMER and if they are present on opposite axis then they are TRANS ISOMER.


2. E and Z NOMENCLATURE

*There should be atleast one double bond b/w carbon and C, C and N or N and N.
*Four atoms or group which are held with both carbon should be different.
*There should be restricted in rotation.  E and Z is the derived from two Jarmon words -:

Z – ZUSSAMAN – CIS (SOME SIDE)
E – ENTEGGEN – TRANS (OPPOSITE SIDE)

EXAMPLE –
PICTURE📷📷📷📷📷📷

3. SYN – ANTI NOMENCLATURE

*This kind of isomerism is shown by those compound which have atleast one  C=N OR N=N.

It is of two types

1. SYN – SAME  SIDE – CIS
2. ANTI – OPPOSITE – TRANS

*If the heigher polar group is present on the same side of carbon and nitrogen atom then it is called SYN and if height polar group are present an opposite side then is called ANTI.

*Determination of configuration of geometrical isomerism.

There are a number of method to determine the configuration of geometrical isomerism


1. Physical method
2. Cyclisation method
3. Conversion method 

1.Physical method -: The melting point and intently of absorption of cis isomer are lower than trans.
* The boiling point solubility heat of combution heat of hydrogenation, densiy, reflective index, dipole movement and dissociation constant of cis are greater then trans isomer.
By the comparison of above there physical properties we can determine the configuration of isomers.

2.Cyclisation Method -: Intermolecular reaction are more likely to occurs the closer together are the reaction group in the molecular, cis isomer undergoess the cyclisation reaction bit the trans isomer does not go for cyclisation reaction.

Ex. Malic acid after dehydration gives a cyclic compound maloc anhydride but fumaric acid do not gives dehydrated reaction so molic acid is cis isomer and feumeriv acid is trans isomer.

Picture📷📷📷📷📷

3.Conversion method -: In this method unkown compound is convert compound after chemical reaction conversion method we can configuration of compound.

Ex. If tri chloro erotenic after oxidation gives fumeric acid then it is trans and if it gives malic acid then it is cis isomers.

Picture📷📷📷📷📷

Saturday 21 March 2020

COLLOIDAL DISPERSION PHYSICAL PHARMACEUTICS 2


                                             COLLOIDAL DISPERSION

Dispersion medium – A dispersion system is define as a system during which dispersed particles is distributed uniformly thought-out dispersing phase .

Colloidal dispersion- System during which dispersed particles size range 1nm to 1um is distributed uniformly thought out the dispersing phase are called as colloidal dispersion.

  COLLOIDAL DISPERSION PHYSICAL PHARMACEUTICS 2
Pharmacygyan by Nitesh Vishwkarma

                                              Classification of colloidal dispersion

S.N.
DISPERSION MEDIUM
DISPERSED PHASE
EXAMPLES
1
GAS
LIQUID
FOG
2
GAS
SOLID
SMOKE
3
LIQUID
GAS
FOAM(ARESOAL)
4
LIQUID
SOLID
COLLOIDAL GOLD IN WATER
5
LIQUID
LIQUID
OIL GLOBULES OR WATER GLOBULES
6
SOLID
GAS
SOLID FOAM
7
SOLID
LIQUID
MINIRAL OIL IN WATER
8
SOLID
SOLID
COLLOIDAL GOLD IN GLASS

          Colloidal dispersion are classified into following types

1- Lyophillic colloid
2- Lyophobic colloid
3- Association colloid

Lyophillic colloid :-

* Lyo means solvent.
*Lyophillic colloids are solvent loving colloids.
*Hydrophilic and lipophilic type
* Hydrophilic colloids- includes gelation or acacia which form colloidal dispersion in water.
* Lipophilic colloids- include rubber for Polystyrene whic form colloidal dispersion in organic             solvent. example benzene
*they are thermodynamically stable.
 *viscosity increase with adding dispersed particles .

Lyophobic colloid

 *They are organic and aquas solvent hating colloids.
*When dispersing phase is water they're k/as hydrophobic colloids.
* Colloidal Dispersion of gold or silver in water.
*They are thermodynamically an stable
*Viscosity doesn't increase and adding dispersion phase.

Association collide

*They also are k/as amphilic colloids.
*Few molecules or Ion have both polar and nonpolar Groups.
*There exist separately and Associate at critical micelle and concentration to make micelle of collide size.
*Viscosity increase by adding ampliphile.
Properties of Colloids

                                    Optical properties of colloids are as follows
1. Ultra microscopy
2. Electronic microscopy
3. Light scattering
4. Tyndall effect

Ultra microscopy- 
*When a cell containg colloidal dispersion is viewed through a utltra microscopy against dark background.
*The partical appear as bright spart against dark background.

Electron microscopy- 
*The microscopy is use full in getting picture of a actual particle.
*It helps in studying size, shape, and structure of colloidal particles.

Light scattering –
*When a beam of sunshine is skilled a colloidal dispersion.
*Some light absorbend, some is cattered and remainders is transmuted.
*Absorbed light is liable for calaered nature.
*Scattered light caused the colloidal dispersion to seem Teubidity.

Tyndall effect –
*When a narrow beam of sunshine is skilled a colloidal dispersion.
*The path of sunshine become illuminated.
*This are often abserbed at right angel under ultra microscopy.
*Lyophobic system show I tence tydall effect them lyophollic system.





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