Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 1998 Apr-Jun;23(2):87-91.
doi: 10.1007/BF03189320.

Development of midazolam sublingual tablets: in vitro study

Affiliations

Development of midazolam sublingual tablets: in vitro study

P Odou et al. Eur J Drug Metab Pharmacokinet. 1998 Apr-Jun.

Abstract

Midazolam is a benzodiazepine with short elimination half-life, used as induction or continuous agent for general anesthesia. At present, only injectable solution is available from French hospital pharmacies. The aim of the study is the development of 5 mg midazolam sublingual tablets to realize a short general anesthesia without intravenous or intramuscular injection. Incorporation of citric acid in the tablet formulation leads to an increase of dissolution rates of active drug, but a decrease of diffusion through lipid membranes is observed with 10 mg of citric acid when using the Dibbern's Resomat three phases apparatus. One explanation of this result is that midazolam (pKa = 6.1) in presence of 10 mg of citric acid is ionised. The ionised form, more hydrophilic, cannot cross the artificial lipid membrane and therefore the diffusion decreases. On the other hand, the decrease of diffusion's rate, when pH increases, is explained by the precipitation of midazolam at pH higher than 6. A compromise between dissolution and diffusion results leads us to choose the sublingual formulation containing 5 mg of citric acid per tablet.

PubMed Disclaimer

Similar articles

Cited by

References

    1. J Pharmacobiodyn. 1988 Mar;11(3):206-9 - PubMed
    1. Farmaco Prat. 1986 Nov;41(11):363-76 - PubMed
    1. Eur J Clin Pharmacol. 1981 Mar;19(4):271-8 - PubMed
    1. Clin Pharmacokinet. 1984 Sep-Oct;9(5):469-74 - PubMed
    1. J Chromatogr. 1985 Nov 8;344:199-209 - PubMed

LinkOut - more resources