Step 1: Understanding log P value. The log P value is a measure of a drug's lipophilicity, representing its distribution between a lipid (oil) phase and an aqueous phase. It determines how easily a drug can permeate lipid membranes, such as the skin.
Step 2: Log P value range for transdermal permeation. For transdermal delivery, the drug must have balanced hydrophilic and lipophilic properties: - A log P value of 1-3 is ideal, ensuring sufficient lipid solubility for permeating the skin's lipid barrier while maintaining water solubility for systemic absorption.
Step 3: Why other options are incorrect.
- (A) Below 1: Too hydrophilic, making it difficult to cross the lipid-rich stratum corneum.
- (C) 5-7: Too lipophilic, leading to accumulation in the skin and poor systemic absorption.
- (D) Above 7: Extremely lipophilic, making it almost impossible to achieve systemic delivery.
A typical skin cream consisting of stearic acid, potassium hydroxide, glycerin, water, preservative and perfume, would be commonly known as:
List I | List II | ||
|---|---|---|---|
| A | \(\Omega^{-1}\) | I | Specific conductance |
| B | \(∧\) | II | Electrical conductance |
| C | k | III | Specific resistance |
| D | \(\rho\) | IV | Equivalent conductance |
List I | List II | ||
|---|---|---|---|
| A | Constant heat (q = 0) | I | Isothermal |
| B | Reversible process at constant temperature (dT = 0) | II | Isometric |
| C | Constant volume (dV = 0) | III | Adiabatic |
| D | Constant pressure (dP = 0) | IV | Isobar |