Drug – bio-affecting and body treating compositions – Designated organic active ingredient containing – Phosphorus containing other than solely as part of an...
Patent
1994-11-10
1997-05-13
Spivack, Phyllis G.
Drug, bio-affecting and body treating compositions
Designated organic active ingredient containing
Phosphorus containing other than solely as part of an...
A61K 3166
Patent
active
056293003
DESCRIPTION:
BRIEF SUMMARY
This application is a 371 of PCT/EP93/01228 filed Dec. 9,1993.
The invention relates to medicaments which as the sole active compound contain the (-)-enantiomeric metrifonate, their preparation and their use.
O,O-Dimethyl 2,2,2-trichloro-1-hydroxyethyl-phosphonate of the formula ##STR1## also known under the name metrifonate, is an insecticide which has been known for a long time.
Moreover, it is known that metrifonate has anthelmintic properties and can therefore be used for the treatment of disorders (such as, for example, bilharziasis) caused by certain worm types both in veterinary and human medicine.
U.S. Pat. No. 4,950,658 disclosed that both metrifonate itself and the 2,2-dichlorovinyl dimethyl phosphonate of the formula ##STR2## (also known as dichlorfon or DDVP) obtainable by elimination of hydrogen chloride from and rearrangement of metrifonate is suitable for the treatment of senile dementia, in particular of the Alzheimer's disease type, on account of its property of inhibiting cholinesterase.
Metrifonate has an asymmetric carbon atom and can thus exist in two enantiomers. Both when used as an insecticide and when used therapeutically, metrifonate is only employed as a racemate. As is known for many active compounds and here, in particular, for medicament active compounds, one enantiomeric form is frequently more active than the other enantiomeric form, and in individual cases the biological activity is really only to be attributed to one of the enantiomers.
Very little is known hitherto about the enantiomers of metrifonate. Utschik describes the existence of enantiomers of metrifonate in connection with crystal modifications, but without characterizing the enantiomers themselves [H. Utschik Z. Chem. 23 (8), 207 (1983) and Z. Chem. 29 (1), 26 (1989)].
In 1975, the enantiomers were purposely synthesized for the first time and investigated for their biological activity with respect to their cholinesterase-inhibiting properties in comparison to the racemate. The authors found that the enantiomers only differed negligibly from one another [J. Brienne et al., C. R. Hebd. Seances Acad. Sci. Ser. C 280 (5), 291-292 (1975)].
For this reason, until now no advantage was seen in using one of the enantiomers of metrifonate on its own instead of the racemate used hitherto.
Surprisingly, it has now been found that, contrary to the established opinion, according to which it is not an advantage to use a metrifonate enantiomer on its own, the (-)-form of metrifonate has a considerably greater pharmacological potential than was to be suspected.
It has been found that (-)-metrifonate has a considerably higher stability against active compound-degrading (metabolizing) enzymes than the (+)-enantiomer. For example, it was possible to show that, after reaction with human liver microsomes, there was up to 20 times more (-)-metrifonate available than (+)-metrifonate. When using (-)-metrifonate on its own as an active compound, a considerably better cholinesterase inhibition can thus be achieved than when using the racemate or the (+)-enantiomer.
When using (-)-metrifonate instead of the racemate to achieve the same action, it is possible to manage with considerably less active compound, even less than half, and the patients are considerably less stressed, in particular during continuous treatment.
Moreover, it is also advantageous that medicaments which only contain (-)-metrifonate have a smaller volume than the racemate-containing ones, which, for example, has a positive effect on the tablet size.
The metrifonate enantiomers can either be synthesized by the method given in the literature [J. Brienne et al., C. R. Hebd. Seances Acad. Sci. Ser. C 280 (5), 291-292 (1975)]or obtained from the racemate by resolution on a chiral adsorbent.
The invention relates to (-)-metrifonate-containing medicaments, pharmaceutical preparations for oral, parenteral or transdermal administration being understood among these, which besides the active compound (-)-metrifonate contain suitable auxiliaries and excipients. Examples which may b
REFERENCES:
patent: 4950658 (1990-08-01), Becker et al.
Keio Journal of Medicine, vol. 36, No. 4, (1987), E. Giacobini, pp. 381-391.
Drug Development Research, vol. 12, No. 3/4, (1988) R.E. Becker et al., pp. 163-195.
Clinical Pharmacokinetics, vol. 15, No. 2, (1988) G. Edwards et al, pp. 67-93.
Brienne et al., C.R. Hebd. Seances Acad. Sci. (1975), 280 (5), 291-2.
Boberg Michael
Kanhai Wolfgang
Kern Armin
Muschalek Volker
Pleiss Ulrich
Bayer Aktiengesellschaft
Spivack Phyllis G.
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