If a buccal/sublingual tablet is pulverized, how does the CT curve change?

Study for the Pharmaceutics Xenobiotics Across Bio Membrane Test. Prepare with flashcards and multiple-choice questions, each providing hints and explanations. Get ready for your pharmacy exam!

Multiple Choice

If a buccal/sublingual tablet is pulverized, how does the CT curve change?

Explanation:
Pulmonary? No — focus on how buccal/sublingual dosing works. For these routes, dissolution into saliva is often the rate-limiting step before the drug can cross the mucosa and enter the bloodstream. When you pulverize a tablet, you dramatically increase surface area, so it dissolves much faster. That makes absorption happen sooner, shifting the concentration–time curve to earlier times (a leftward shift in Tmax). However, the total amount of drug that can be absorbed from the same dose through the mucosa doesn’t necessarily change, so the peak concentration (Cmax) stays about the same. In short, faster dissolution speeds up onset without increasing the maximum level reached.

Pulmonary? No — focus on how buccal/sublingual dosing works. For these routes, dissolution into saliva is often the rate-limiting step before the drug can cross the mucosa and enter the bloodstream. When you pulverize a tablet, you dramatically increase surface area, so it dissolves much faster. That makes absorption happen sooner, shifting the concentration–time curve to earlier times (a leftward shift in Tmax). However, the total amount of drug that can be absorbed from the same dose through the mucosa doesn’t necessarily change, so the peak concentration (Cmax) stays about the same. In short, faster dissolution speeds up onset without increasing the maximum level reached.

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