VB
Vikas Bhardwaj
Medical Technologist, AIIMS New Delhi
Updated: Apr 17, 2026
**Core Concept**
The pharmacokinetic properties of a drug, particularly its absorption, are influenced by its physicochemical properties such as pKa, lipophilicity, and charge. In this case, the weak organic acid's pKa of 3.0 is relevant for understanding its ionization state at different pH levels, which affects its absorption.
**Why the Correct Answer is Right**
At a pH of 2.0, the stomach's acidic environment, the antibiotic's pKa of 3.0 means that the majority of the drug will be in its nonionized, uncharged form. This is because the pKa is higher than the pH, causing the equilibrium to shift towards the nonionized form. The nonionized form can easily cross biological membranes, including the intestinal epithelium, and is thus rapidly absorbed from the stomach.
**Why Each Wrong Option is Incorrect**
* **Option B:** Incorrect because the pH is lower than the pKa, which would result in the drug being mostly ionized and not absorbed.
* **Option C:** Incorrect because the pKa of 3.0 is not relevant to the ionization state at a pH of 7.4, which is the pH of the small intestine, not the stomach.
* **Option D:** Incorrect because it does not provide a specific percentage, and even if it did, it would not be based on the correct understanding of the pKa and pH relationship.
**Clinical Pearl / High-Yield Fact**
When dealing with weak acids or bases, remember that the percentage of the drug in the nonionized form (and thus available for absorption) is determined by the Henderson-Hasselbalch equation: pH = pKa + log10([A-]/[HA]). A low pH (acidic environment) and a pKa close to the pH result in a high percentage of the drug in the nonionized form, facilitating rapid absorption.
**Correct Answer: B. 0.01%**