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Bisphosphonates and Tetracycline: Experimental Models for Their Evaluation in Calcium-Related Disorders

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Abstract

Purpose. This work was aimed at synthesizing novel bisphosphonates (BPs) and examining them in comparison to clinically used BPs such as pamidronate and alendronate, and to tetracycline, in order to evaluate their potential as anticalcification and antiresorption agents. The correlation between the various models was examined in order to establish facile experimental models for pre-screening of potential compounds.

Methods. Nitrogen-containing heterocyclic, novel BPs such as 2-(3-methylimidazolio) ethylidene-l,l-bisphosphonic acid betaine (VS-5b), 2-(2-dimethylamino-4-pyrazinio)ethylidene-1,1 -bisphosphonic acid betaine (VS-6b), and 2-(2-α-pyridylethylthio) ethylidene-1,1-bisphosphonic acid (ISA-225), were synthesized and evaluated in comparison to clinically used BPs, in various experimental models of resorption and calcification.

Results. The physicochemical properties of the novel compounds are slightly different than the BPs in clinical use: the pKa values are lower, the affinity for hydroxyapatite is lower and the solubilities of the calcium salts are higher. The anticalcification potencies of the novel compounds were high and ranked as follows: alendronate = pamidronate > VS-6b = VS-5b = ISA-225 > tetracycline. The in vivo antiresorption activity of VS-5b and VS-6b in comparison to that of the clinically employed, pamidronate, was shown to be similar and higher, respectively.

Conclusions. The anticalcification activity of the novel compounds as well as that of tetracycline was lower than that of alendronate. The antiresorption activity of VS-6b was similar to that of pamidronate. A good correlation between the different models was found, enabling the facile screening of novel compounds. The activities of tetracycline and EDTA highlight the distinct behavior of BPs as "crystal poison”. In addition, tetracycline was found to be a potent anticalcification agent in the ectopic calcification model.

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REFERENCES

  1. O. L. M. Bijvoet, H. A. Fleisch, R. E. Canfield, and R. G. G. Russell. Bisphosphonates on bones, Elsevier Science B.V., Amsterdam, 1995.

    Google Scholar 

  2. H. Fleisch. Bisphosphonates: A new class of drugs in diseases of bone and calcium metabolism. In K. W. Brunner, H. Fleisch, and H.-J. Senn (eds.), Bisphosphonates and tumor osteolysis, Springer-Verlag, Berlin Heidelberg, 1989, pp. 1–29.

    Google Scholar 

  3. J. M. Van Gelder, E. Breuer, A. Ornoy, A. Schlossman, N. Patlas, and G. Golomb. Anticalcification and antiresorption effects of bisacylphosphonates. Bone 16:511–520 (1995).

    Google Scholar 

  4. J. M. Van Gelder and G. Golomb. The evaluation of bisphosphonates as potential drugs for the treatment of calcium-related disorders. In A. Ornoy (eds.), Animal models of human related calcium metabolic disorders, CRC, Boca Raton, 1995, pp. 181–205.

    Google Scholar 

  5. U. A. Liberman, et al. Effect of oral alendronate on bone mineral density and incidence of fractures in postmenopausal osteoporosis. N. Eng. J. Med. 333:1437–1443 (1995).

    Google Scholar 

  6. H. A. Fleisch. Bisphosphonates: Preclinical aspects and use in osteoporosis. Annals Medicine 29(1):55–62. (1997).

    Google Scholar 

  7. W. Jeal, L. B. Barradell, and D. McTavish. Alendronate: A review of its pharmacological properties and therapeutic efficacy in postmenopausal osteoporosis. Drugs 53(3):415–434. (1997).

    Google Scholar 

  8. H. Fleisch. Bisphosphonates: Mechanism of action and clinical use. In G. R. Mundy, and T. J. Martin (eds.), Physiology and pharmacology of bone, Springer-Verlag, Heidelberg, 1993.

    Google Scholar 

  9. M. Sahni, H. L. Guenther, H. Fleisch, P. Collin, and T. J. Martin. Biphosphonates act on rat bone resorption through the mediation of osteoblasts. J. Clin. Invest. 91:2004–2011 (1993).

    Google Scholar 

  10. G. A. Rodan and R. Balena. Bisphosphonates in the treatment of metabolic bone diseases. Ann. Med. 25:373–378 (1993).

    Google Scholar 

  11. G. Golomb, A. Schlossman, H. Saadeh, M. Levi, J. M. Van Gelder, and E. Breuer. Bisacylphosphonates inhibit hydroxyapatite formation and dissolution in vitro and dystrophic calcification in vivo. Pharm. Res. 9:143–148 (1992).

    Google Scholar 

  12. G. Golomb, A. Schlossman, Y. Eitan, H. Saadeh, J. M. Van Gelder, and E. Breuer. In vitro and in vivo anticalcification effects of novel bishydroxyiminophosphonates. J. Pharm. Sci. 81:1004–1007 (1992).

    Google Scholar 

  13. E. Van Beek, M. Hoekstra, M. Van de Ruit, C. W. G. M. Lowik, and S. E. Papapoulos. Structural requirements for bisphosphonate actions in vitro. J. Bone Miner. Res. 9:1875–1882 (1994).

    Google Scholar 

  14. M. J. Rogers, D. J. Watts, R. G. G. Russell, X. Ji, X. Xiong, G. M. Blackburn, A. V. Bayless, and F. H. Ebetino. Inhibitory effects of bisphosphonates on growth of amoebae of the cellular slime mold dictyostelium discoideum. J. Bone Miner. Res. 9:1029–1039 (1994).

    Google Scholar 

  15. A. D. Geddes, S. M. D'Souza, F. H. Ebetino, and K. J. Ibbotson. Bisphosphonates: Structure-activity relationships and therapeutic implications. In J. N. M. Heersche, and J. A. Kanis (eds.), Bone and Mineral Research, Elsevier, Amsterdam, 1994, pp. 265–306.

    Google Scholar 

  16. W. K. Sietsema, F. H. Ebetino, A. M. Salvagno, and J. A. Bevan. Antiresorptive dose-response relationships across three generations of bisphosphonates. Drugs Exptl. Clin. Res. XV:389–396 (1989).

    Google Scholar 

  17. J. R. Green, K. Muller, and K. A. Jaeggi. Preclinical pharmacology of CGP 42'446, a new, potent, heterocyclic bisphosphonate compound. J. Bone Miner. Res. 9:745–751 (1994).

    Google Scholar 

  18. I. S. Alferiev, I. L. Kotlyarevski, N. V. Mikhalin, and V. M. Novikova. Reactions of vinylidenebisphosphonic acid with nucleophiles. Comm. 1. Addition of aliphatic amines. Bull. Nat. Acad. USSR Ser. Chem. 2802–2806 (1983).

  19. J. H. Lin, I.-W. Chen, and F. A. Deluna. On the absorption of alendronate in rats. J. Pharm. Sci. 83:1741–1746 (1994).

    Google Scholar 

  20. J. H. Lin. Bisphosphonates: a review of their pharmacokinetic properties. Bone 18: 75–85 (1996).

    Google Scholar 

  21. G. R. Kieczkowski, R. B. Jobson, D. G. Melillo, D. F. Reinhold, V. J. Grenda, and I. Shinkai. Preparation of (4-Amino-1-Hydroxybutylidene) bisphosphonic acid sodium salt, MK-217 (alendronate sodium). An improved procedure for the preparation of 1-hydroxy-1,1-bisphosphonic acids. J. Org. Chem. 60:8310–8312 (1995).

    Google Scholar 

  22. G. Golomb and D. Wagner. Development of a new in vitro model for studying implantable polyurethane calcification. Biomaterials 12:397–405 (1991).

    Google Scholar 

  23. J. Turnquist, A. Ornoy, D. Eini, and Z. Schwartz. The effects of 1α(OH)2D3 and 24, 25(OH)2D3 on long bones of glucocorticoid treated mice. Acta Anat. 145:61–67 (1992).

    Google Scholar 

  24. G. Golomb, Y. Eitan, and A. Hoffman. Measurement of serum [3H] tetracycline kinetics andd indices of kidney function facilitate study of the activity and toxic effects of bisphosphonates in bone resorption. Pharm. Res. 9:1018–1023 (1992).

    Google Scholar 

  25. D.D. Perrin. Dissociation constants of organic bases in aqueous solution, Butterworths, London, 1965.

    Google Scholar 

  26. M. Sato and W. Grasser. Effects of bisphosphonates on isolated rat osteoclasts as examined by reflected light microscopy. J. Bone Miner. Res. 5:31–40 (1991).

    Google Scholar 

  27. D. E. Hughes, M. Mian, D. F. Guilland-Cumming, and R. G. G. Russell. The cellular mechanism of action of bisphosphonates. Drugs Exptl. Clin. Res. XVII:109–114 (1991).

    Google Scholar 

  28. S. J. Sunberg, F. H. Ebetino, C. T. Mosher, and C. F. Root. Designing drugs for stronger bones. Chemtech 21:304–309 (1991).

    Google Scholar 

  29. D.J. Rowe and L. A. Etre. Uptake of a fluorinated bisphosphonate by cultured bones. Bone 9:297–301 (1988).

    Google Scholar 

  30. T. Fonong, D. J. Burton, and D. J. Pietrzyk. Determination of formation constants of calcium complexes of difluoromethylene-diphosphonic acid and related diphosphonates. Anal. Chem. 55:1089–1094 (1983).

    Google Scholar 

  31. F. H. Ebetino and L. A. Jamieson. The design and synthesis of bone-active phosphinic acid analogues: I. The pyridylaminomethane phosphonoalkylphosphinates. Phosphorus Sulfur Silicon 51:23–26 (1990).

    Google Scholar 

  32. Remington. The science and practice of pharmacy, Mack Publishing Company, Pennsylvania, 1995.

    Google Scholar 

  33. M. L. Lamson, J. M. Fox, and W. I. Higuchi. Calcium and 1-hydroxyethylidene-1,1-bisphosphonic acid: Polynuclear complex formation in the physiological range of pH. Int. J. Pharm. 21:143–154 (1984).

    Google Scholar 

  34. D. Hirsch, F. J. Schoen, and R. J. Levy. Effects of metallic ions and diphosphonates on inhibition of pericardial bioprosthetic tissue calcification and associated alkaline phosphatase activity. Biomaterials 14:371–377 (1993).

    Google Scholar 

  35. M. D. Francis and R. R. Martodam. Chemical, biochemical, and medicinal properties of the diphosphonates. In R. L. Hilderbrand (eds.), The role of phosphonates in living systems, CRC Press, Boca Raton, 1983, pp. 55–96.

    Google Scholar 

  36. R. Schenk, W. A. Merz, R. Muhlbauer, R. G. G. Russell, and H. Fleisch. Effect of ethane-1-hydroxy-1,1-diphosphonate (EHDP) and dichloromethylene diphosphonate (CIMDP) on the calcification and resorption of cartilage and bone in the tibial epiphysis and methaphysis of rats. Calcif. Tiss. Res. 11:196–214 (1973).

    Google Scholar 

  37. P. H. Reitsma, O. L. M. Bijvoet, H. Verlinden-Ooms, and L. J. A. van der Wee-Pals. Kinetic studies of bone and mineral metabolism during treatment with (3-amino-1-hydroxypropylidene)-1,1-bisphosphonate (APD) in rats. Calcif. Tiss. Int. 32:145–157 (1980).

    Google Scholar 

  38. B. Adamson, S. Gallacher, J. Byars, S. Ralston, I. Boyle, and B. Boyce. Mineralization defects with pamidronate therapy for Paget's disease. Lancet 342:1459–1460 (1993).

    Google Scholar 

  39. S. Q. Cohlan and T. Tiamsic. Growth inhibition of prematures receiving tetracycline. Am. J. Dis. Child. 105:65–73 (1963).

    Google Scholar 

  40. S. Williams, A. Wakisaka, Q. Q. Zeng, J. Barnes, G. Martin, W. J. Wechter, and C. T. Liang. Minocycline prevents the decrease in bone mineral density and trabecular bone in ovariectomized aged rats. Bone 19:637–644 (1996).

    Google Scholar 

  41. X. Q. Li, C. A. Donovan, and L. Klein. A pharmacokinetic model in the rat and rabbit of the direct measurement of mature bone resorption in vivo with [3H] tetracycline. J. Pharm. Sci. 78:823–828 (1989).

    Google Scholar 

  42. M. I. Kabachnik, T. Y. Medreved', N. M. Dyaglova, Y. M. Policarpov, B. K. Scherbakov, and F. I. Bel'skii. Synthesis and acid-base and complexing properties of amino-substituted α-hydroxyalkyli-denediphosphonic acids. Bull. Nat. Acad. USSR Ser. Chem. 374–377 (1978).

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Cohen, H., Solomon, V., Alferiev, I.S. et al. Bisphosphonates and Tetracycline: Experimental Models for Their Evaluation in Calcium-Related Disorders. Pharm Res 15, 606–613 (1998). https://doi.org/10.1023/A:1011990129437

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