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Phospholipid Stabilised Emulsions for Parenteral Nutrition and Drug Delivery

  • Chapter
Phospholipids

Abstract

Emulsions have been used in medical practice from the very earliest times. They comprise the dispersion of one immiscible liquid in another, and consequently can take different physical forms.7 For example, the dispersion of an oil in water provides the oil-in-water (o/w) emulsion system whereas the converse is the water-in-oil system (w/o). The physical nature of the system often dictates its route of administration into the body. Water-in-oil emulsions are normally given topically to the skin or the eye, or used as controlled release injectables (intramuscular or subcutaneous). Oil-in-water emulsions are those that can be given orally or by injection into the bloodstream. More complicated types of emulsion also exist, where a prototype system is reemulsified to give a so-called multiple emulsion system. Some of these, in the form of water-oil-water (w/o/w) systems, have been used as vaccine carriers.10 While these multiple emulsions may have advantage in terms of controlled release, they are difficult to stabilise and therefore have found limited use in medical and pharmaceutical practice. One further class of emulsions is known as microemulsions. These are thermodynamically stable solubilized systems and are rarely employed in pharmaceutical practice.14 As far as the author is aware, they have not been used as injectable systems. Unfortunately, within the pharmaceutical world, there is presently confusion over the term “microemulsion”. Emulsions can be produced that have a small particle size, for example less than 500 nm average diameter. If needed, such systems can be referred to as “fine” emulsions but they should not be termed “microemulsions”. This confusion seems to have arisen from the promotional activities of certain manufacturers of homogenisation equipment.

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References

  1. Burnham, W.R., Hansrani, P.K., Knott, C.E., Cook, J.A. and Davis, S.S., 1983, Stability of a fat emulsion based intravenous feeding mixture, Int. J. Pharm. 13:9.

    Article  Google Scholar 

  2. Buscall, R., Davis, S.S. and Potts, D.C., 1979, The effect of long chain alkanes on the stability of oil-in-water emulsions. The significance of Ostwald ripening, Colloid Polym. Sci. 257:636.

    Article  CAS  Google Scholar 

  3. Carlson, L.A., 1980, Studies on the fat emulsion intralipid. I. Association of Serum Proteins to Intralipid Triglyceride Particles (ITP), Scand. J. Clin. Lab. Invest. 40:139.

    Article  PubMed  CAS  Google Scholar 

  4. Cummings, G.C. and Spence, A.A., 1985, Comparison of propofol in emulsion with althesin for induction of anaesthesia, Br. J. Anaeth. 57:234.

    Article  CAS  Google Scholar 

  5. Dardel, O. von., Mebius, C, Mossberg, T. and Svensson, B., 1983, Fat emulsion as a vehicle for diazepam. A study in 9492 patients, Brit. J. Anaesth. 55:41.

    Article  Google Scholar 

  6. Davis, S.S. and Hansrani, P.K., 1985, The influence of emulsifying agents on the phagocytosis of lipid emulsions, Int. J. Pharm. 23:69.

    Article  CAS  Google Scholar 

  7. Davis, S.S. and Walker, I.M., 1987, Multiple Emulsions as Targetable Delivery Systems, In “Drug and Enzyme Targeting”, R. Green and K.J. Widder, eds. Methods in Enzymology, Vol. 149, p. 51, Academic Press, New York.

    Google Scholar 

  8. Davis, S.S., 1983, The stability of fat emulsions for intravenous administration, In “Advances in Clinical Nutrition”, I.D.A. Johnson, ed. p.213, M.T.P. Press, Lancaster.

    Chapter  Google Scholar 

  9. Davis, S.S., Hadgraft, J. and Palin, K., 1985, Pharmaceutical Emulsions, In “Encyclopedia of Emulsion Technology”, Vol. 2, P. Becher, ed., p.159, Dekker, New York.

    Google Scholar 

  10. Davis, S.S., Ilium, L., West, P. and Galloway, M., 1987, Studies on the fate of fat emulsions following intravenous administration to rabbits and the effect of added electrolyte, Clin. Nutr. 6:13.

    Article  CAS  Google Scholar 

  11. Davis, S.S., Washington, C., Ilium, L., Liversidge, G., Sternson, L. and Kirsh, R., 1987, Ann. N.Y. Acad. Sci. 507:75.

    Article  PubMed  CAS  Google Scholar 

  12. Douglas, S.J. and Davis, S.S., 1986, Particle size analysis of colloidal systems by photon correlation spectroscopy, In “Targeting of drugs with synthetic systems”, G. Gregoriadis, J. Senior and G. Poste, eds. p.265, Plenum Press, New York.

    Chapter  Google Scholar 

  13. Forster, D., Washington, C. and Davis, S.S., 1988, Toxicity of solubilized and colloidal amphotericin B formulations to human erythrocytes, J. Pharm. Pharmac. 40:325.

    Article  CAS  Google Scholar 

  14. Friberg, S.E. and Bothorel, P. (editors), 1987, Microemulsions: Structure and Dynamics, CRC Press, Boca Raton.

    Google Scholar 

  15. Fujita, T., Sumaya, T., and Yokohama, K., 1971, Fluorocarbon emulsion as a candidate for artificial blood. Correlation between particle size of the emulsion and acute toxicity. Europ. Surg. Res. 3:436.

    Article  CAS  Google Scholar 

  16. Glen, J.B. and Hunter, S.C., 1984, Pharmacology of an emulsion formulation of ICI 35868, Brit. J. Anaesth. 56:617.

    Article  PubMed  CAS  Google Scholar 

  17. Ilium, L., Davis, S.S., Muller, R.H., Mak, E. and West, P., 1987, The organ distribution and circulation time of intravenously injected colloidal carriers sterically stabilized with a block copolymer poloxamine 908, Life Sci. 40:367.

    Article  Google Scholar 

  18. Jeppsson, R.I., 1976, Plasma levels of diazepam in the dog and rabbit after two different injection formulations, emulsion and solution, J. Clin. Pharm. 1:181.

    CAS  Google Scholar 

  19. Johnson, I.D.A. (editor), 1983, “Advances in Clinical Nutrition”, MTP Press, Lancaster.

    Google Scholar 

  20. Lenzo, N.P., Martins, I., Mortimer, B.C. and Redgrave, T.G., 1988, Effects of phospholipid composition on the metabolism of triacylglycerol, cholesterol ester and phosphatidylcholine from lipid emulsions injected intravenously in rats, Biochim. Biophys. Acta 960:111.

    Article  PubMed  CAS  Google Scholar 

  21. Ljungberg, S. and Jeppsson, R., 1970, Intravenous administration of lipid soluble drugs, Acta Pharm. Suec. 7:435.

    PubMed  CAS  Google Scholar 

  22. Lopez-Berestein, G., Mehta, R., Hopfer, R.L., Mills, K., Kasi, L., Mehta, K., Fainstein, U., Luna, M., Hersh, E.M. and Juliano, R.L., 1983, Treatment and prophylaxis of disseminated Candida albicans injections in mice with liposome encapsulated amphotericin B, J. Infec. Dis. 147:939.

    Article  CAS  Google Scholar 

  23. Mitsuno, T., Ohyanagi, H. and Naito, R., 1982, Clinical studies of a perfluorochemical whole blood substitute (Fluosol DA) Summary of 186 cases. Ann. Surg. 195:60.

    Article  PubMed  CAS  Google Scholar 

  24. Mizushima, Y., 1985, Lipid microspheres as novel drug carriers, Drugs Expl. Clin. Res. 9:595.

    Google Scholar 

  25. Mizushima, Y., Shoji, Y., Fukushima, M. and Kurozumi, S., 1986, Use of lipid microspheres as a drug carrier for anti-tumour drugs, J. Pharm. Pharmacol. 38:132.

    Article  PubMed  CAS  Google Scholar 

  26. Muller, R.H., Davis, S.S., Illum, L. and Mak, E., 1986, Particle charge and surface hydrophobicity of colloidal drug carriers, In “Targeting of Drugs with Synthetic Systems”, G. Gregoriadis, J. Senior and G. Poste, eds., p.239, Plenum Press, New York.

    Chapter  Google Scholar 

  27. Muller, R.H., Nehne, J., Davis, S.S. and Heinemann, S., 1988, Characterisation of fat emulsions for parenteral nutrition, Acta Pharm. Technol., 34:235.

    Google Scholar 

  28. Repta, A.J., 1981, Formulation of investigational anticancer drugs, In “Topics in Pharmaceutical Sciences”, D.D. Breimer and P. Speiser, eds. p.131, Elsevier, Amsterdam.

    Google Scholar 

  29. Rydhag, L., 1979, The importance of the phase behaviour of phospholipids for emulsion stability, Fette Seif. Anstrich. 81:168.

    Article  CAS  Google Scholar 

  30. Sim, A.K., McCraw, A.P., Cleland, M.E., Aihara, H., Otomo, S. and Hosoda, K., 1986, The effect of prostaglandin El incorporated in lipid microspheres on thrombus formation and disaggregation and its potential to target to the site of vascular lesions, Arzn. Forsch. 36:1206.

    CAS  Google Scholar 

  31. Tarr, B.D., Sambandan, T.G. and Yalkowsky, S.H., 1987, A new parenteral emulsion for the administration of Taxol, Pharm. Res., 4:162.

    Article  PubMed  CAS  Google Scholar 

  32. Washington, C. and Davis, S.S., 1988, Stability evaluation of total parenteral nutrition mixtures, In “Clinical Progress in Nutrition Research”, Sitges-Serra, Sitges-Creus, Schwartz-Riera, eds., p.189, Karger, Basel.

    Google Scholar 

  33. Washington, C. and Davis, S.S., 1988, The production of parenteral feeding emulsions by microfluidizer, Int. J. Pharm. 44:169.

    Article  CAS  Google Scholar 

  34. Wretlind, A., 1976, Current Status of Intralipid and other Fat Emulsions, In “Fat Emulsions in Parenteral Nutrition”, H.C. Meng and D.W. Wilmore, eds., p.109, American Medical Association, Chicago.

    Google Scholar 

  35. Ziak, E., Pristautz, H., Brandt, D., Schaupp, K. and Musil, E., 1984, Vergleichsstudie zwischen drei fetteemulsionen zur parenteralen Ernahrung, Ernahrung 8:617.

    CAS  Google Scholar 

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Davis, S.S. (1990). Phospholipid Stabilised Emulsions for Parenteral Nutrition and Drug Delivery. In: Hanin, I., Pepeu, G. (eds) Phospholipids. Springer, Boston, MA. https://doi.org/10.1007/978-1-4757-1364-0_6

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  • DOI: https://doi.org/10.1007/978-1-4757-1364-0_6

  • Publisher Name: Springer, Boston, MA

  • Print ISBN: 978-1-4757-1366-4

  • Online ISBN: 978-1-4757-1364-0

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