Planta Med 2012; 78(3): 260-268
DOI: 10.1055/s-0031-1280367
Pharmacokinetic Investigations
Original Papers
© Georg Thieme Verlag KG Stuttgart · New York

In Vitro Permeation of Mesembrine Alkaloids from Sceletium tortuosum across Porcine Buccal, Sublingual, and Intestinal Mucosa

Emmanuel A. Shikanga1 , Josias H. Hamman2 , 3 , Weiyang Chen2 , Sandra Combrinck1 , Nigel Gericke4 , Alvaro M. Viljoen2
  • 1Department of Chemistry, Tshwane University of Technology, Pretoria, South Africa
  • 2Department of Pharmaceutical Sciences, Tshwane University of Technology, Pretoria, South Africa
  • 3Unit for Drug Research and Development, North-West University, Potchefstroom, South Africa
  • 4Medical & Scientific Affairs, HG & H Pharmaceuticals (Pty) Ltd., Bryanston, South Africa
Further Information

Publication History

received June 30, 2011 revised October 17, 2011

accepted October 25, 2011

Publication Date:
21 November 2011 (online)

Abstract

Sceletium tortuosum is an indigenous South African plant that has traditionally been used for its mood-enhancing properties. Recently, products containing S. tortuosum have become increasingly popular and are commonly administered as tablets, capsules, teas, decoctions, or tinctures, while traditionally the dried plant material has been masticated. This study evaluated the in vitro permeability of the four major S. tortuosum alkaloids (i.e., mesembrine, mesembrenone, mesembrenol, and mesembranol) across porcine intestinal, sublingual, and buccal tissues in their pure form and in the form of three different crude plant extracts, namely water, methanol, and an acid-base alkaloid-enriched extract. The permeability of mesembrine across intestinal tissue was higher than that of the highly permeable reference compound caffeine (which served as a positive control for membrane permeability) both in its pure form, as well as in the form of crude extracts. The intestinal permeability of mesembranol was similar to that of caffeine, while those of mesembrenol and mesembrenone were lower than that of caffeine, but much higher than that of the poorly permeable reference compound atenolol (which served as a negative control for membrane permeability). In general, the permeabilities of the alkaloids were lower across the sublingual and the buccal tissues than across the intestinal tissue. However, comparing the transport of the alkaloids with that of the reference compounds, there are indications that transport across the membranes of the oral cavity may contribute considerably to the overall bioavailability of the alkaloids, depending on pre-systemic metabolism, when the plant material is chewed and kept in the mouth for prolonged periods. The results from this study confirmed the ability of the alkaloids of S. tortuosum in purified or crude extract form to permeate across intestinal, buccal, and sublingual mucosal tissues.

References

  • 1 Smith M T, Crouch N R, Gericke N, Hirst M. Psychoactive constituents of the genus Sceletium N.E.Br. and other Mesembryanthemaceae: a review.  J Ethnopharmacol. 1996;  50 119-130
  • 2 Gomes N G M, Campos M G, Orfao J M C, Riberio C A F. Plants with neurobiological activity as potential targets for drug discovery.  Prog Neuropsychopharmacol Biol Psychiatry. 2009;  33 1372-1389
  • 3 Gericke N, Van Wyk B-E. Pharmaceutical compositions containing mesembrine and related compounds. US Patent PCT/GB97/01493 1997
  • 4 Gericke N. Clinical application of selected South African medicinal plants.  Aust J Med Herb. 2002;  13 3-17
  • 5 Gericke N, Viljoen A M. Sceletium – a review update.  J Ethnopharmacol. 2008;  119 653-663
  • 6 Patnala S, Kanfer I. Investigation of the phytochemical content of Sceletium tortuosum following preparation of “Kougoed” by fermentation.  J Ethnopharmacol. 2009;  121 86-91
  • 7 Gericke N, Harvey A, Viljoen A, Hofmeyr D. Sceletium extract and uses thereof. International Patent Application Number PCT/IB2010/051133 2010
  • 8 Harvey A, Gericke N, Viljoen A. Use of pharmaceutical compositions containing mesembrenone. International Patent Application Number PCT/IB2010/051132 2010
  • 9 O'Donnell J M, Zhang H T. Antidepressant effects of inhibitors of cAMP phosphodiesterase (PDE4).  Trends Pharmacol Sci. 2004;  25 158-163
  • 10 Rutten K, Prickaerts J, Blokland A. Rolipram reverses scopolamine-induced and time-dependent memory deficits in object recognition by different mechanisms of action.  Neurobiol Learn Mem. 2006;  85 132-138
  • 11 Cashman J R, Voelker T, Johnson R, Janowsky A. Stereoselective inhibition of serotonin re-uptake and phosphodiesterase by dual inhibitors as potential agents for depression.  Bioorg Med Chem. 2000;  17 337-343
  • 12 Watt J M, Breyer-Brandwijk M G. The medicinal and poisonous plants of southern and eastern Africa. 2nd edition. London: Livingstone; 1962: 12
  • 13 Lubbe A, Khati A, Yuliana N D, Jinap S, Verpoorte R. Cannabinoid CB1 receptor binding and acetylcholinesterase inhibitory activity of Sceletium tortuosum L.  Int Food Res J. 2010;  17 349-355
  • 14 Van Wyk B-E, Gericke N. People's plants. Pretoria: Briza publications; 2003: 172
  • 15 Sceletium – Kougoed – A natural mood elevator. Available at http://www.Sceletium.org Accessed Jan 20, 2011
  • 16 Fearn A R, Hirst B H. Predicting oral drug absorption and hepatobiliary clearance: human intestinal and hepatic in vitro cell models.  Environ Toxicol Pharmacol. 2006;  21 168-178
  • 17 He X, Sugawara M, Kobayashi M, Takekum Y, Miyakazi K. An in vitro system for prediction of oral absorption of relatively water-soluble drugs and ester prodrugs.  Int J Pharm. 2003;  263 35-44
  • 18 Van Eyk A D, van der Bijl P. Comparative permeability of various chemical markers through human vaginal and buccal mucosa as well as porcine buccal and mouth floor mucosa.  Arch Oral Biol. 2004;  49 387-392
  • 19 Shojaei A H. Buccal mucosa as a route for systematic drug delivery.  J Pharm Sci. 1998;  1 15-30
  • 20 Obradovic T, Hidalango I J. In vitro models for investigations of buccal drug permeation and metabolism. In: Ehrhardt C, Kim K-J, editors Drug absorption studies: In situ, in vitro and in silico models. New York: Springer; 2008: 167-181
  • 21 Shikanga E A, Viljoen A, Combrinck S, Marston A. Isolation of Sceletium alkaloids by high-speed countercurrent chromatography.  Phytochem Lett. 2011;  4 190-193
  • 22 Hamman J H. Oral drug delivery: Biopharmaceutical principles, evaluation and optimization. 2nd edition. Pretoria: Tshwane University of Technology; 2007: 21
  • 23 Miller J N, Miller J C. Statistics and chemometrics for analytical chemistry, 4th edition. New York: Prentice Hall; 2000: 65
  • 24 Artursson P. Epithelial transport of drugs in cell culture. I: A model for studying the passive diffusion of drugs over intestinal absorptive (Caco-2) cells.  J Pharm Sci. 1990;  79 476-482
  • 25 Jeffs P W, Hawks R L, Farrier D S. Structures of the mesembranols and the absolute configuration of mesembrine and related alkaloids.  J Am Chem Soc. 1970;  91 3831-3839

Prof. Alvaro M. Viljoen (PhD)

Department of Pharmaceutical Sciences
Tshwane University of Technology

Private Bag X680

Pretoria 0001

South Africa

Phone: +27 12 3 82 63 60

Fax: +27 12 3 82 62 43

Email: viljoenam@tut.ac.za