Question:

Core tablet coated with cellulose acetate phthalate has been administered to a patient. Where do you expect the drug to be released:

Updated On: Jul 14, 2026
  • Liver
  • Intestine
  • Oral cavity
  • Stomach
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The Correct Option is B

Approach Solution - 1

The correct option is (B): Intestine.
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Approach Solution -2

Cellulose acetate phthalate (CAP) is a classic enteric coating polymer used on tablets that should not release their drug in the stomach. The question is testing whether the reader knows how a pH-dependent coating decides where a tablet breaks open. Let's look at each site listed as an option.

  1. Liver: No oral coating, enteric or otherwise, is designed to release a drug directly in the liver. Drug reaches the liver only after absorption from the gut, through the portal blood supply, so this is not a release site a coating can target.
  2. Intestine: CAP contains free carboxylic acid (phthalate) groups that stay un-ionized and insoluble at the low pH of the stomach, so the coating stays intact there. Once the tablet moves into the small intestine, where the pH rises above about 5 to 6, these acid groups ionize, the polymer becomes soluble, and the coating dissolves away to expose the core. This is exactly the release pattern CAP is chosen for.
  3. Oral cavity: A tablet swallowed whole passes through the mouth in seconds, far too briefly and at the wrong pH for any coating, enteric or not, to dissolve there.
  4. Stomach: This is the one place CAP is specifically designed to resist. Gastric pH is typically between 1 and 3, well below the pH at which CAP's carboxyl groups ionize, so the film stays closed and protects the core from gastric fluid.

Because CAP is acid-insoluble and only dissolves once the pH climbs in the small intestine, the tablet core is released there rather than in the stomach.

The correct answer is Intestine.

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