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.
Match the following:
(P) Schedule H
(Q) Schedule G
(R) Schedule P
(S) Schedule F2
Descriptions:
(I) Life period of drugs
(II) Drugs used under RMP
(III) List of Prescription Drugs
(IV) Standards for surgical dressing
Choose the correct match of laxative and its Mechanism of Action (MOA):
