Small-volume oral transmucosal dosage forms
Small-volume oral transmucosal dosage forms or NanoTabs® comprising a predetermined amount of a pharmaceutically active drug are provided. Exemplary applications include use of the NanoTabs® to administer a drug for the treatment of acute, post-operative or breakthrough pain.
1. A method of treating pain in a subject, comprising administering a single dose of sufentanil to the oral mucosa of a subject, wherein the single dose is provided as a small volume solid tablet, and said solid tablet comprises:
from about 0.25 micrograms (mcg) to 200 micrograms sufentanil, wherein;
a) said solid tablet is bioadhesive and adheres to the oral mucosa of said subject,
b) said solid tablet is a substantially homogeneous composition and has a volume of less than 30 microliters (mei); and
c) after administration of said solid tablet to said subject, said solid tablet provides a minimal saliva response and minimal swallowing of sufentanil; at least 55% of drug delivery of sufentanil occurs via the oral transmucosal route; said solid tablet provides a dose-normalized C max of about 2.72+/−0.84 pg/mL per mcg dosed.
2. The method according to claim 1 , wherein complete erosion of said solid tablet is evident by visual examination in about 30 seconds up to about 15 minutes following administration.
3. The method according to claim 1 , wherein the erosion time of said solid tablet is about 10 minutes.
4. The method according to claim 1 , wherein said solid tablet has a volume of less than 10 mcl.
5. The method according to claim 1 , wherein said oral transmucosal administration is sublingual administration.
6. The method according to claim 1 , wherein said oral transmucosal administration is buccal administration.
7. The method according to claim 1 , comprising from about 2.5 micrograms to 100 micrograms of sufentanil.
8. The method according to claim 7 , wherein said solid tablet comprises a dose of sufentanil selected from the group consisting of 5 micrograms, 10 mcg, 15 mcg, 20 mcg, 30 mcg, 40 mcg, 50 mcg, 60 mcg, 70 mcg, 80 mcg and 100 mcg.
9. The method according to claim 1 , wherein a single oral transmucosal administration of said solid tablet to a subject results in a sufentanil bioavailability of greater than 65%.
10. The method according to claim 1 , wherein a single oral transmucosal administration of said solid tablet to a subject results in a sufentanil bioavailability of greater than 75%.
11. The method according to claim 1 , wherein a single oral transmucosal administration of said solid tablet to a subject results in a sufentanil bioavailability of greater than 85%.
12. The method according to claim 1 , wherein at least 60% of the total amount of sufentanil in said solid tablet is absorbed via the oral transmucosal route.
13. The method according to claim 1 , wherein said solid tablet is administered using a drug delivery device.
14. The method according to claim 1 , wherein when solid tablet is subjected to an in vitro dissolution test in a Type II USP dissolution apparatus, at least 75% of the total amount of sufentanil in said solid tablet is released within 10 minutes.
15. The method according to claim 1 , wherein sufentanil is provided as sufentanil citrate.
16. The method according to claim 1 , wherein after administration of said tablet to said subject, said solid tablet provides a T max range of from about 19.8 minutes to about 60 minutes.
17. The method according to claim 1 , wherein after administration of said tablet to said subject, said solid tablet provides a T max with a coefficient of variation of less than 40%.