![CONT…
i.e., for weak acids:
pH=pka+log[IDC/UDC]
%drug ionized=[10pH-pka/1+10pH-pka]*100
For weak bases:
pH=pka+log[UDC/IDC]
%drug ionized=[10pH-pka/1+10pH-pka]*100
o When the concentration of ionized drug becomes equal, the
second term of the equation becomes zero (since log1=0) and
thus pH=pka. The pka is the characteristic of the drug.](https://image.slidesharecdn.com/phpartitionhypothesis-180421162313/85/P-h-partition-hypothesis-9-320.jpg)
P h partition hypothesis
- 1. pH PARTITION HYPOTHESIS Presented by Zahid Husain M.Pharm (Pharmaceutics) Faculty of Pharmacy, Integral University, Lucknow
- 2. INTRODUCTION DRUG ABSORPTION: It is defined as the process of movement of unchanged drug from the site of administration to systemic circulation. FACTORS INFLUENCING GI ABSORPTION OF A DRUG FROM ITS DOSAGE FORM: They are classified into two types, 1. Pharmaceutics factors 2. Patient related factors
- 3. PHYCOCHEMICAL PROPERTIES OF DRUG SUBSTANCES 1. Drug solubility and dissolution rate 2. Particle size and effective surface area 3. Polymorphism and amorphism 4. Pseudo polymorphism 5. Salt form of the drug 6. Lipophilicity of the drug 7. pKa of the drugand pH 8. Drug stability
- 4. pH PARTITION THEORY The theory states that for drug compounds of molecular weight greater than 100, which are primarily transported across the biomembrane by passive diffusion. o The process of absorption is governed by: 1. The dissociation constant (pKa) of the drug. 2. The lipid solubility of the unionized drug (a function of drug Ko/w). 3. The pH at the absorption site.
- 5. CONT… • Brodie proposed the partition theory to explain the influence of GI pH and drug pKa on the extent of drug transfer or drug absorption. • pH partition theory of drug absorption is based on the GIT is a simple lipid barrier to the transport of drugs and chemicals. • Accordingly the unionized form of an acid or basic drug, if sufficient lipid soluble, is absorbed but the ionized formis not. • The larger the fraction of drug is in the unionized form at a specific absorption site, the faster is the absorption.
- 6. DIAGRAM SHOWING THE TRANSFER OF DRUG ACROSS THE MEMBRANE
- 7. DRUG pKa AND GI pH • The fraction of drug in solution that exist in the unionized form is a function of both dissociation constant of the drug and the pH of the solution. • The dissociation constant is often expressed for both acids and bases as pKa (the basic logarithm of the acidic dissociation constant). • It is customary to express the dissociation constants of both acidic and basic drugs by pKa values. • The lower the pKa of an acidic drug, the stronger the acid i.e., greater the proportion of ionized form at a particular pH. The higher the pKa of a basic drug, the stronger the base.
- 8. CONT… • Thus from the knowledge of pKa of the drug and pH at the absorption site (or biological fluid), the relative amount of ionized and unionized drug in solution at a particular pH and the percent of drug in solution at this pH can be determined by Henderson-Hasselbach equation, for an acid: pka-pH=log(fu/fi) for a base: pka-pH=log(fi/fu)
- 9. CONT… i.e., for weak acids: pH=pka+log[IDC/UDC] %drug ionized=[10pH-pka/1+10pH-pka]*100 For weak bases: pH=pka+log[UDC/IDC] %drug ionized=[10pH-pka/1+10pH-pka]*100 o When the concentration of ionized drug becomes equal, the second term of the equation becomes zero (since log1=0) and thus pH=pka. The pka is the characteristic of the drug.
- 10. CONT… • A barrier that separates the aqueous solutions of different pH such as GIT and plasma then the theoretical ratio R of drug concentration on either side of the membrane can be given by the equation, For weak acids: Ra=CGIT/CPlasma=1+10pHGIT-pka/1+10pH plasma-pka For weak bases: R=CGIT/Cplasma=1+10pka-pHGIT/1+10pka-pH plasma
- 11. pH Range In GIT • The pH range in GIT from 1-8 that of the stomach is from 1-3 and of the intestine (from duodenum to colon) 5-8, then certain generalization regarding ionization and absorption of drugs can be made, as predicted from pH partition hypothesis.
- 12. LIPOPHILICITY AND DRUG ABSORPTION • The GI cell membrane are essentially lipoidal. Highly lipid soluble drugs are generally absorbed while decidedly lipid insoluble drugs are in general poorly absorbed. • The lipid solubility of a drug is determined from its oil/water partition coefficient (Ko/w) value.
- 13. DEVIATIONS FROM pH-PARTITION THEORY • The pH-partition theory provides a basic frame work for understanding drug absorption, but it is an over simplification of a more complex process. • Theory indicates that the relationship between pH and permeation or absorption rate is described by an S- shaped curve corresponding to the dissociation curve of the drug. • For a simple acid or base, the inflection point of the pH absorption curve should occur at a pH equal to the pka of the drug. This is rarely observed experimentally.
- 14. Cont… • In general pH absorption curves are less step then expected and are shifted to higher pH values for acids and to lower pH values for bases. • The factors that may contribute to the deviations are, 1. Absorption of the ionized form of the drug. 2. Presence of an aqueous unstirred duffusion layer adjacent to the cell membrane. 3. Difference between luminal pH and pH at the surface of the cell membrane.
- 15. CONCLUSION • The pH-partition principle has been tested in large number of IV and IV studies, and it has been found to be only partly applicable in real biologic systems. In many cases, the ionized and unionized forms of a drug partitions are appreciably transported across lipophilic membrane. But the extension of pH- partition theory to incorporate the effects of the unstirred layer and microclimate pH provides a far more satisfactory rationalization of the experimental data.
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