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Last Updated: April 27, 2024

Claims for Patent: 8,598,152


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Summary for Patent: 8,598,152
Title:Co-crystals of tramadol and coxibs
Abstract: The present invention relates to co-crystals of tramadol and co-crystal formers selected from NSAIDs/coxibs, processes for preparation of the same and their uses in pharmaceutical formulations for the treatment of pain.
Inventor(s): Plata Salaman; Carlos Ramon (Esplugues de Llobregat, ES), Tesson; Nicolas (L'Hospitalet de Llobregat, ES)
Assignee: Laboratorios Del Dr. Esteve, S.A. (Barcelona, ES)
Application Number:13/395,021
Patent Claims: 1. A co-crystal comprising (rac)-tramadol.cndot.HCl and celecoxib in a molecular ratio of 1:1, characterized in that it shows a Powder X-Ray Diffraction pattern with peaks [2.theta.] at 7.1, 9.3, 10.2, 10.7, 13.6, 13.9, 14.1, 15.5, 16.1, 16.2, 16.8, 17.5, 18.0, 19.0, 19.5, 19.9, 20.5, 21.2, 21.3, 21.4, 21.8, 22.1, 22.6, 22.7, 23.6, 24.1, 24.4, 25.2, 26.1, 26.6, 26.8, 27.4, 27.9, 28.1, 29.1, 29.9, 30.1, 31.1, 31.3, 31.7, 32.5, 32.8, 34.4, 35.0, 35.8, 36.2 and 37.2[.degree.], with the 2.theta. values being obtained using copper radiation (Cu.sub.K.alpha.1 1.54060 .ANG.).

2. The co-crystal of claim 1 further characterized in that it shows a Fourier Transform Infra Red pattern with absorption bands at 3481.6 (m), 3133.5 (m), 2923.0 (m), 2667.7 (m), 1596.0 (m), 1472.4 (m), 1458.0 (m), 1335.1 (m), 1288.7 (m), 1271.8 (m), 1168.7 (s), 1237.3 (m), 1168.7 (s), 1122.6 (s), 1100.9 (m), 1042.2 (m), 976.8 (m), 844.6 (m), 820.1 (m), 786.5 (m) 625.9 (m) cm.sup.-1.

3. The co-crystal of claim 1 further characterized in that it has an orthorhombic unit cell with the following dimensions: a=11.0323(7) .ANG. b=18.1095(12) .ANG. c=17.3206(12) .ANG..

4. The co-crystal of claim 1 further characterized in that the endothermic sharp peak corresponding to the melting point has an onset at 164.degree. C.

5. Pharmaceutical composition characterized in that it comprises a therapeutically effective amount of the co-crystal according to claim 1 in a physiologically acceptable medium.

6. Pharmaceutical composition characterized in that it comprises a therapeutically effective amount of the co-crystal according to claim 2 in a physiologically acceptable medium.

7. Pharmaceutical composition characterized in that it comprises a therapeutically effective amount of the co-crystal according to claim 3 in a physiologically acceptable medium.

8. Pharmaceutical composition characterized in that it comprises a therapeutically effective amount of the co-crystal according to claim 4 in a physiologically acceptable medium.

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