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Effects of polysorbate 80 on the absorption and distribution of oral methotrexate (MTX) in mice

  • Original Articles
  • Polysorbate 80 Methotrexate
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Summary

This study is part of a programme of work aimed at improving the bioavailability of oral methotrexate (MTX). In preliminary experiments no significant effect of non-ionic surfactant polysorbate 80 (Tween 80) on absorption of 0.5 mg MTX · kg-1 in NMRI mice was observed except when the drug was given together with 6% polysorbate 80 in solution. Absorption from a higher dose of 3 mg MTX · kg-1 was increased when the drug was administered with 2% or 6% polysorbate 80. Plasma MTX measurements confirmed the significantly higher levels of MTX with 6% polysorbate 80 PO. In subsequent experiments, when Porton mice were used and 4 mg MTX · kg-1 was administered PO, higher plasma and brain levels of MTX were measured in animals given the drug with 6% polysorbate 80, suggesting the enhancement of MTX uptake by this non-ionic surfactant. Although the amount of MTX in the liver and kidney of mice given MTX with polysorbate 80 were not significantly different from the amounts in mice given MTX alone, the lower observed levels suggested that polysorbate 80 perhaps facilitates the elimination of the drug from these organs. The amount of plasma MTX in mice measured 1 h after oral administration of various MTX doses in the presence of 6% polysorbate 80 were significantly higher than the levels in mice given the drug without surfactant, but the significantly higher amounts of MTX in the brain were only observed following the doses of 2 and 6 mg MTX · kg-1.

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References

  1. Andren L, Theander G (1961) Emptying effect on the gall bladder of Tween 80 and some related compounds. Gastroenterology 40:636

    Google Scholar 

  2. Bischoff KB, Dedrick RL, Zaharko DS (1970) Preliminary model for Methotrexate pharmacokinetics. J Pharm Sci 59:149

    Google Scholar 

  3. Bleyer WA (1978) The clinical pharmacology of Methotrexate: New application of an old drug. Cancer 41:36

    Google Scholar 

  4. Calman KC, Lawrence JR, McVie JG, Sneader WE, Steele WH, Stuart JFB (1979) Methotrexate kinetics: Effect of subdividing an oral dose. Br J Clin Pharmacol 7:423

    Google Scholar 

  5. Christophidis N, Vajda FJE, Lucas I, Moon WJ, Louis WJ (1979) Comparison of intravenous and oral high-dose Methotrexate in treatment of solid tumours. Br Med J I:298

    Google Scholar 

  6. Elworthy PH, Florence AT, MacFarlance CB (1968) Solubilisation by surface active agents. Chapman & Hall, London

    Google Scholar 

  7. Florence AT (1981) Surfactant interactions with biomembranes and drug absorption. Pure Appl Chem 53:2057

    Google Scholar 

  8. Florence AT (1982) Solubilisation of drugs by surfactants. In: Yalkowsky S (ed) Technique of solubilisation of drugs. Marcel Dekker, New York

    Google Scholar 

  9. Guth PS, Spirtes MA (1964) The phenothiazines tranquillisers: Biochemical and Biophysical actions. Int Rev Neurobiol 7:231

    Google Scholar 

  10. Harrison SD, Cusic AM, McAfee SM (1981) Tween 80 increases plasma Adriamycin concentrations in mice by an apparent reduction of plasma volume. Eur J Cancer 17:387

    Google Scholar 

  11. Henderson EB, Adamson RH, Denham C, Oliverio VT (1965) The metabolic fate of triated Methotrexate. I. Absorption, excretion and distribution in mice, rats, dogs and monkeys. Cancer Res 25:1008

    Google Scholar 

  12. Hikal AH (1981) Effect of polysorbate 80 on the apparent partition coefficient of drugs on their intestinal absorption in the rat. II. Phenobarbital. International Journal of Pharmaceutics 7:205

    Google Scholar 

  13. Krasowska H (1980) Effect on micellar solubilisation on the gastro-intestinal absorption of indomethacin in the rat. International Journal of Pharmaceutics 7:137

    Google Scholar 

  14. Martindale (1977) The Extra Pharmacopaeia. 27th edn. Pharmaceutical Press, London

    Google Scholar 

  15. Ritschel WA (1969) Sorption promotors in biopharmaceutics. Angewandte Chemie (Int. Edit. in English). 8:699

    Google Scholar 

  16. Steele WH, Stuart JFB, Lawrence JR, McNiel CA, Sneader WE, Whiting B, Calman KC, McVie JG (1979) Enhancement of MTX absorption by subdvision of dose. Cancer Chemother Pharmacol 3:235

    Google Scholar 

  17. Strum WB (1977) A pH-dependent, carrier-mediated transport system for the folate analog, Amithopterin, in rat jejunum. J Pharmacol Exp Ther 203:640

    Google Scholar 

  18. Stuart JFB, Calman KC, Walters J, Paxton J, Whiting B, Lawrence JR, Steele WH, McVie JG (1979) Bioavailability of Methotrexate: Implication for clinical use. Cancer Chemother Pharmacol 3:239

    Google Scholar 

  19. Trounce JR (1979) Dosage and pharmacokinetics of cytotoxic drugs. (Editorial) Br J Clin Pharmacol 8:205

    Google Scholar 

  20. Walter KA, Dugard PH, Florence AT (1981) Non-ionic surfactants and gastric mucusal transport of paraquat. J Pharm Pharmacol 33:207

    Google Scholar 

  21. Wan SH, Huffman DH, Azarnoff DL, Stephens R, Hoogstraten B (1974) Effect of route administration and effusion on Methotrexate pharmacokinetics. Cancer Res 38:3487

    Google Scholar 

  22. Watanabe S, Nakao E, Cho K, Nishioka B, Fujita Y, Takahashi T, Majima B (1978) Basic experiment on oral administration of 5-Fluorourasil emulsion as adjuvant chemotherapy to surgical treatment for gastric cancer. Jpn J Surg 8:41

    Google Scholar 

  23. Watson E, Cohen JL, Chan KK (1978) High-pressure liquid chromatographic determination of Methotrexate and its major metabolite, 7-hydroxymethotrexate in human plasma. Cancer Treat Rep 62:381

    Google Scholar 

  24. West GW, Weichselbaum R, Little JB (1980) Limited penetration of Methotrexate into human osteosarcoma spheroids as a proposed model for solid tumour resistence to adjuvant chemotherapy. Cancer Res 40:3665

    Google Scholar 

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Azmin, M.N., Stuart, J.F.B., Calman, K.C. et al. Effects of polysorbate 80 on the absorption and distribution of oral methotrexate (MTX) in mice. Cancer Chemother. Pharmacol. 9, 161–164 (1982). https://doi.org/10.1007/BF00257745

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  • DOI: https://doi.org/10.1007/BF00257745

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