protien binding of drugs

18

Upload: malla-reddy-college-of-pharmacy

Post on 21-Jun-2015

237 views

Category:

Documents


6 download

TRANSCRIPT

Page 1: Protien binding of drugs
Page 2: Protien binding of drugs

Bound Drug is Pharmacodynamicaly inert. Binding: Half life of drug. Bonding : Hydrogen bond, Hydrophilic bond,

ionic bond, Vander Walls bond. Irreversible bonding : Covalent bonding :

responsible for the Carcinogenicity or Tissue toxicity.

2

Page 3: Protien binding of drugs

3

Page 4: Protien binding of drugs
Page 5: Protien binding of drugs

5

I) Plasma Protein Binding of I) Plasma Protein Binding of drug:drug:

Reversible Order : Albumin > α1 AG > Lipoproteins >

Globulins. Involves binding to : 1. Human serum Albumin.2. α1 Acid Glycoprotein,

3. Lipoproteins,4. Globulins

Page 6: Protien binding of drugs

6

Primary site: Secondary site: Bond: Hydrophobic bond.

Page 7: Protien binding of drugs

Binding by: Hydrophobic Bond. Non-competative. Mol wt : 2-3 lacks Dalton. Binded drug dissolves in Lipid core.Lipid core. Lipid Core composed of :Inside: Triglycerides, cholesterol esters,Outside: Appoprotein. E.g :Acidic: Diclofenac.Neutral: Cyclosporine ABasic: Chlorpromazine.

7

Page 8: Protien binding of drugs

8

Binding by: Hydrophobic bonds. E.g. : Basic Drugs: Imipramine, Amytriptyline,

Lidocaine.

4. Binding to Globulin4. Binding to Globulin

Page 9: Protien binding of drugs

9

40 % of Blood comprises of blood cells Majority is RBCs: 500 times more diameter as

Albumin. RBC Components that binds to drug:

Page 10: Protien binding of drugs

10

Importance : 1. Apparent Vd. 2. Localization of drug at

specific site :so biological half life.

Factors affecting : Lipophilicity, structural feature of drug, Perfusion rate, pH difference.

Binding Order : Liver > Kidney > Lungs > Muscle.

Page 11: Protien binding of drugs

11

Page 12: Protien binding of drugs

A)Drug Related:A)Drug Related:1.Physicochemical Characteristics:1.Physicochemical Characteristics: Lipophilicity α binding. Eg: Cloxacillin and ampicilin Anionic/Acidic binds : HSA Eg: Sulfonamides Cationic/Basic binds : AAG Eg: imipramine

2. Concentration of Drug:2. Concentration of Drug:3.Drug protein/tissue affinity3.Drug protein/tissue affinity:: Digoxine Affinity

to cardiac muscle, Lidocaine to AAG not for HAS. Iophenoxic acid-2.5 years

B)Protein/Tissue Related:B)Protein/Tissue Related:1.Physicochemical Characteristics : 1.Physicochemical Characteristics : Lipophilicity α binding.

2. Concentration 2. Concentration Binding with albumin because of higher Binding with albumin because of higher concentrationconcentration

12

Page 13: Protien binding of drugs

Alb. Has more. Tamoxifen & Dicumarol binds to 10 & 20 sites of alb. Indomethacine binds to 3 site. AAG- one binding site (lidocaine)

C) Drug Interaction:C) Drug Interaction: 1.Competition between Drugs for 1.Competition between Drugs for

binding site.binding site.

D1: Displaced Drug. D2: Displacer Drug.E.g. Adm. Of Phenylbutazone to Warfarine therapy

patient, result in Hemorrhagic reaction.

13

D1+P

D2D2+P

Page 14: Protien binding of drugs

FFA competes with HSA. Free FFA level increased during conditions : Physiological C. (Fasting) Pathological C. (Diabetes, M.I) Pharmacological (Heparin & Caffeine adm.). Acidic Drug displaces : Bilurubine from Alb. & results

in Kernictarus.

3.Allosteric Changes In Protein Molecule:3.Allosteric Changes In Protein Molecule: By drug or its Metabolite. Allosteric Modulators: are agents responsible. E.g. Aspirins acetylating of Lysine of Alb. So

modifying capacity of NSAIDS binding.

14

Page 15: Protien binding of drugs

1.Age:1.Age:

Neonates: Neonates: Low Alb. content: more free drug. Young Infants: Young Infants: High dose of Digoxine due to large

renal clearance. Elderly: Elderly: Low Alb. : so more free drug.

2.Intersubject Variability: 2.Intersubject Variability: Due to Genetic & Environmental Factors.

3. Disease State:3. Disease State:

15

Page 16: Protien binding of drugs

At distribution Equilibrium : Conc. of drug in body is determined By: Vol. of Tissue in which drug is present.

Different tissue have diff. conc. So Vd cannot have a true physiologic meaning.

(Amount of drug in body) α ( Conc. Of drug in plasma)

X α CX = Vd. C

Def: Hypothetical Vol. of body fluid into which drug is dissolved or distributed.

It is Apparent Vd : Because : All parts of body equilibrated with drug do not have equal conc.

16

Page 17: Protien binding of drugs

Real Vd : has direct physiological meaning,Is related to body water.

17

Body fluid Volume (lit.)

% of Body wt.

% of TWB

1.Vascular fluid (plasma)

6(3)

9(4.5)

15(7.5)

2.Extracellular fluid (excl plasma)

12 14 28

3.Intracellular fluid (excl blood cells)

24 34 57

Total Body Total Body 42 60 100

Page 18: Protien binding of drugs

Physiological fluid compartment

Markers used Approximate vol.

1.Plasma Evans Blue, Indocyanine Green, I-131 alb.

3

2.Erythrocytes Cr-51 2

3.Extracellular fluids Non metabolizable saccharides like Raffinose, Inuline, Mannitol, & Radio isotopes of selected ions: Na+, Cl-, Br-, So4

2-.

15

Total body water D2O, HTO, Antipyrine

42

18