✦ LIBER ✦

Influence of amount of hard fat in suppositories on the in vitro release rate and bioavailability of paracetamol and codeine. I. A comparison of three suppository compositions in vivo

✍ Scribed by Kirsti Gjellan; Christina Graffner; Hans Quiding

Book ID: 113366618
Publisher: Elsevier Science
Year: 1994
Tongue: English
Weight: 871 KB
Volume: 102
Category: Article
ISSN: 0378-5173
DOI: 10.1016/0378-5173(94)90041-8

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Influence of amount of hard fat in suppo

Influence of amount of hard fat in suppositories on the in vitro release rate and bioavailability of paracetamol II. A comparison between three compositions and a rectal solution

✍ Kirsti Gjellan; Christina Graffner 📂 Article 📅 1994 🏛 Elsevier Science 🌐 English ⚖ 828 KB

Influence of fat composition on the melt

Influence of fat composition on the melting behaviour and on the in vitro release of indomethacin suppositories

✍ Christian De Muynck; Jean Paul Remon 📂 Article 📅 1992 🏛 Elsevier Science 🌐 English ⚖ 919 KB

Influence of physicochemical interaction

Influence of physicochemical interactions on the properties of suppositories V. The in vitro release of ketoprofen and metronidazole from various fatty suppository bases and correlations with in vivo plasma levels

✍ Grant, D.J.W.; Liversidge, G.G.; Bell, J. 📂 Article 📅 1983 🏛 Elsevier Science 🌐 English ⚖ 894 KB

Influence of a high fat breakfast on the

Influence of a high fat breakfast on the bioavailability of theophylline controlled-release formulations: An in vitro demonstration of an in vivo observation

✍ P. K. Maturu; V. K. Prasad; W. N. Worsley; G. K. Shiu; J. P. Skelly 📂 Article 📅 1986 🏛 John Wiley and Sons 🌐 English ⚖ 212 KB 👁 1 views

Comparative bioavailability of josamycin

Comparative bioavailability of josamycin, a macrolide antibiotic, from a tablet and solution and the influence of dissolution on in vivo release

✍ M. Skinner; I. Kanfer 📂 Article 📅 1998 🏛 John Wiley and Sons 🌐 English ⚖ 192 KB 👁 2 views

The bioavailability of josamycin from a tablet formulation (2 × Josacine ® 500 mg tablets) was investigated and compared with the bioavailability of a solution (containing 1 g drug and buffered at pH 4.0) following administration to six healthy human volunteers. Bioavailability profiles for the solu