LU86004A1 - ANALGESIC AND ANTI-INFLAMMATORY COMPOSITION FOR THE TREATMENT OF ARTHROSIS - Google Patents
ANALGESIC AND ANTI-INFLAMMATORY COMPOSITION FOR THE TREATMENT OF ARTHROSIS Download PDFInfo
- Publication number
- LU86004A1 LU86004A1 LU86004A LU86004A LU86004A1 LU 86004 A1 LU86004 A1 LU 86004A1 LU 86004 A LU86004 A LU 86004A LU 86004 A LU86004 A LU 86004A LU 86004 A1 LU86004 A1 LU 86004A1
- Authority
- LU
- Luxembourg
- Prior art keywords
- vitamin
- none
- oxytetracycline
- composition according
- hydrochloride
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims description 26
- 201000008482 osteoarthritis Diseases 0.000 title claims description 10
- 230000000202 analgesic effect Effects 0.000 title description 3
- 230000003110 anti-inflammatory effect Effects 0.000 title description 2
- 229940088594 vitamin Drugs 0.000 claims description 21
- 229930003231 vitamin Natural products 0.000 claims description 21
- 235000013343 vitamin Nutrition 0.000 claims description 21
- 239000011782 vitamin Substances 0.000 claims description 21
- 150000003722 vitamin derivatives Chemical class 0.000 claims description 19
- 239000000470 constituent Substances 0.000 claims description 16
- 235000019156 vitamin B Nutrition 0.000 claims description 13
- DFPAKSUCGFBDDF-UHFFFAOYSA-N Nicotinamide Chemical compound NC(=O)C1=CC=CN=C1 DFPAKSUCGFBDDF-UHFFFAOYSA-N 0.000 claims description 12
- AUNGANRZJHBGPY-SCRDCRAPSA-N Riboflavin Chemical compound OC[C@@H](O)[C@@H](O)[C@@H](O)CN1C=2C=C(C)C(C)=CC=2N=C2C1=NC(=O)NC2=O AUNGANRZJHBGPY-SCRDCRAPSA-N 0.000 claims description 12
- IWVCMVBTMGNXQD-UHFFFAOYSA-N terramycin dehydrate Natural products C1=CC=C2C(O)(C)C3C(O)C4C(N(C)C)C(O)=C(C(N)=O)C(=O)C4(O)C(O)=C3C(=O)C2=C1O IWVCMVBTMGNXQD-UHFFFAOYSA-N 0.000 claims description 12
- 239000011720 vitamin B Substances 0.000 claims description 12
- 239000004100 Oxytetracycline Substances 0.000 claims description 11
- 229960000625 oxytetracycline Drugs 0.000 claims description 11
- IWVCMVBTMGNXQD-PXOLEDIWSA-N oxytetracycline Chemical compound C1=CC=C2[C@](O)(C)[C@H]3[C@H](O)[C@H]4[C@H](N(C)C)C(O)=C(C(N)=O)C(=O)[C@@]4(O)C(O)=C3C(=O)C2=C1O IWVCMVBTMGNXQD-PXOLEDIWSA-N 0.000 claims description 11
- 235000019366 oxytetracycline Nutrition 0.000 claims description 11
- YBJHBAHKTGYVGT-ZKWXMUAHSA-N (+)-Biotin Chemical compound N1C(=O)N[C@@H]2[C@H](CCCCC(=O)O)SC[C@@H]21 YBJHBAHKTGYVGT-ZKWXMUAHSA-N 0.000 claims description 10
- 229930003270 Vitamin B Natural products 0.000 claims description 9
- AUNGANRZJHBGPY-UHFFFAOYSA-N D-Lyxoflavin Natural products OCC(O)C(O)C(O)CN1C=2C=C(C)C(C)=CC=2N=C2C1=NC(=O)NC2=O AUNGANRZJHBGPY-UHFFFAOYSA-N 0.000 claims description 8
- 229960002477 riboflavin Drugs 0.000 claims description 8
- MECHNRXZTMCUDQ-UHFFFAOYSA-N Vitamin D2 Natural products C1CCC2(C)C(C(C)C=CC(C)C(C)C)CCC2C1=CC=C1CC(O)CCC1=C MECHNRXZTMCUDQ-UHFFFAOYSA-N 0.000 claims description 7
- 229960002061 ergocalciferol Drugs 0.000 claims description 7
- 235000001892 vitamin D2 Nutrition 0.000 claims description 7
- 239000011653 vitamin D2 Substances 0.000 claims description 7
- MECHNRXZTMCUDQ-RKHKHRCZSA-N vitamin D2 Chemical compound C1(/[C@@H]2CC[C@@H]([C@]2(CCC1)C)[C@H](C)/C=C/[C@H](C)C(C)C)=C\C=C1\C[C@@H](O)CCC1=C MECHNRXZTMCUDQ-RKHKHRCZSA-N 0.000 claims description 7
- 229960004368 oxytetracycline hydrochloride Drugs 0.000 claims description 6
- JZRWCGZRTZMZEH-UHFFFAOYSA-N thiamine Chemical compound CC1=C(CCO)SC=[N+]1CC1=CN=C(C)N=C1N JZRWCGZRTZMZEH-UHFFFAOYSA-N 0.000 claims description 6
- MWKJTNBSKNUMFN-UHFFFAOYSA-N trifluoromethyltrimethylsilane Chemical compound C[Si](C)(C)C(F)(F)F MWKJTNBSKNUMFN-UHFFFAOYSA-N 0.000 claims description 6
- SNPLKNRPJHDVJA-ZETCQYMHSA-N D-panthenol Chemical compound OCC(C)(C)[C@@H](O)C(=O)NCCCO SNPLKNRPJHDVJA-ZETCQYMHSA-N 0.000 claims description 5
- 239000003242 anti bacterial agent Substances 0.000 claims description 5
- 230000003115 biocidal effect Effects 0.000 claims description 5
- 229960002685 biotin Drugs 0.000 claims description 5
- 235000020958 biotin Nutrition 0.000 claims description 5
- 239000011616 biotin Substances 0.000 claims description 5
- 235000020374 simple syrup Nutrition 0.000 claims description 5
- 235000019157 thiamine Nutrition 0.000 claims description 5
- 239000011721 thiamine Substances 0.000 claims description 5
- FPIPGXGPPPQFEQ-UHFFFAOYSA-N 13-cis retinol Natural products OCC=C(C)C=CC=C(C)C=CC1=C(C)CCCC1(C)C FPIPGXGPPPQFEQ-UHFFFAOYSA-N 0.000 claims description 4
- 239000011703 D-panthenol Substances 0.000 claims description 4
- 235000004866 D-panthenol Nutrition 0.000 claims description 4
- FPIPGXGPPPQFEQ-BOOMUCAASA-N Vitamin A Natural products OC/C=C(/C)\C=C\C=C(\C)/C=C/C1=C(C)CCCC1(C)C FPIPGXGPPPQFEQ-BOOMUCAASA-N 0.000 claims description 4
- 229930003471 Vitamin B2 Natural products 0.000 claims description 4
- FPIPGXGPPPQFEQ-OVSJKPMPSA-N all-trans-retinol Chemical compound OC\C=C(/C)\C=C\C=C(/C)\C=C\C1=C(C)CCCC1(C)C FPIPGXGPPPQFEQ-OVSJKPMPSA-N 0.000 claims description 4
- FAPWYRCQGJNNSJ-UBKPKTQASA-L calcium D-pantothenic acid Chemical compound [Ca+2].OCC(C)(C)[C@@H](O)C(=O)NCCC([O-])=O.OCC(C)(C)[C@@H](O)C(=O)NCCC([O-])=O FAPWYRCQGJNNSJ-UBKPKTQASA-L 0.000 claims description 4
- 229960002079 calcium pantothenate Drugs 0.000 claims description 4
- RMRCNWBMXRMIRW-BYFNXCQMSA-M cyanocobalamin Chemical compound N#C[Co+]N([C@]1([H])[C@H](CC(N)=O)[C@]\2(CCC(=O)NC[C@H](C)OP(O)(=O)OC3[C@H]([C@H](O[C@@H]3CO)N3C4=CC(C)=C(C)C=C4N=C3)O)C)C/2=C(C)\C([C@H](C/2(C)C)CCC(N)=O)=N\C\2=C\C([C@H]([C@@]/2(CC(N)=O)C)CCC(N)=O)=N\C\2=C(C)/C2=N[C@]1(C)[C@@](C)(CC(N)=O)[C@@H]2CCC(N)=O RMRCNWBMXRMIRW-BYFNXCQMSA-M 0.000 claims description 4
- 229960003949 dexpanthenol Drugs 0.000 claims description 4
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 claims description 4
- 239000000395 magnesium oxide Substances 0.000 claims description 4
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 claims description 4
- 229960003966 nicotinamide Drugs 0.000 claims description 4
- 235000005152 nicotinamide Nutrition 0.000 claims description 4
- 239000011570 nicotinamide Substances 0.000 claims description 4
- LXNHXLLTXMVWPM-UHFFFAOYSA-N pyridoxine Chemical compound CC1=NC=C(CO)C(CO)=C1O LXNHXLLTXMVWPM-UHFFFAOYSA-N 0.000 claims description 4
- 235000019192 riboflavin Nutrition 0.000 claims description 4
- 239000002151 riboflavin Substances 0.000 claims description 4
- 230000002195 synergetic effect Effects 0.000 claims description 4
- 235000019155 vitamin A Nutrition 0.000 claims description 4
- 239000011719 vitamin A Substances 0.000 claims description 4
- 235000019164 vitamin B2 Nutrition 0.000 claims description 4
- 239000011716 vitamin B2 Substances 0.000 claims description 4
- 235000019160 vitamin B3 Nutrition 0.000 claims description 4
- 239000011708 vitamin B3 Substances 0.000 claims description 4
- 229940045997 vitamin a Drugs 0.000 claims description 4
- 206010061218 Inflammation Diseases 0.000 claims description 3
- 230000004054 inflammatory process Effects 0.000 claims description 3
- 210000003127 knee Anatomy 0.000 claims description 3
- 230000005499 meniscus Effects 0.000 claims description 3
- 229960000344 thiamine hydrochloride Drugs 0.000 claims description 3
- 235000019190 thiamine hydrochloride Nutrition 0.000 claims description 3
- 239000011747 thiamine hydrochloride Substances 0.000 claims description 3
- DPJRMOMPQZCRJU-UHFFFAOYSA-M thiamine hydrochloride Chemical compound Cl.[Cl-].CC1=C(CCO)SC=[N+]1CC1=CN=C(C)N=C1N DPJRMOMPQZCRJU-UHFFFAOYSA-M 0.000 claims description 3
- 208000008035 Back Pain Diseases 0.000 claims description 2
- 239000004322 Butylated hydroxytoluene Substances 0.000 claims description 2
- NLZUEZXRPGMBCV-UHFFFAOYSA-N Butylhydroxytoluene Chemical compound CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 NLZUEZXRPGMBCV-UHFFFAOYSA-N 0.000 claims description 2
- 208000003618 Intervertebral Disc Displacement Diseases 0.000 claims description 2
- 208000008930 Low Back Pain Diseases 0.000 claims description 2
- 208000008765 Sciatica Diseases 0.000 claims description 2
- 208000010040 Sprains and Strains Diseases 0.000 claims description 2
- 229940095259 butylated hydroxytoluene Drugs 0.000 claims description 2
- 235000010354 butylated hydroxytoluene Nutrition 0.000 claims description 2
- 229960002104 cyanocobalamin Drugs 0.000 claims description 2
- 235000000639 cyanocobalamin Nutrition 0.000 claims description 2
- 239000011666 cyanocobalamin Substances 0.000 claims description 2
- 210000003205 muscle Anatomy 0.000 claims description 2
- 235000008160 pyridoxine Nutrition 0.000 claims description 2
- 239000011677 pyridoxine Substances 0.000 claims description 2
- 229940011671 vitamin b6 Drugs 0.000 claims description 2
- 206010070817 Bone decalcification Diseases 0.000 claims 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims 1
- 229960003495 thiamine Drugs 0.000 claims 1
- 229940046001 vitamin b complex Drugs 0.000 claims 1
- 235000020357 syrup Nutrition 0.000 description 5
- 239000006188 syrup Substances 0.000 description 5
- 239000002552 dosage form Substances 0.000 description 4
- 239000003814 drug Substances 0.000 description 4
- 230000003902 lesion Effects 0.000 description 4
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 3
- 229940079593 drug Drugs 0.000 description 3
- 239000000546 pharmaceutical excipient Substances 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- GHOKWGTUZJEAQD-ZETCQYMHSA-N (D)-(+)-Pantothenic acid Chemical compound OCC(C)(C)[C@@H](O)C(=O)NCCC(O)=O GHOKWGTUZJEAQD-ZETCQYMHSA-N 0.000 description 2
- 241000894006 Bacteria Species 0.000 description 2
- -1 Oxytetracycline compound Chemical class 0.000 description 2
- 208000002193 Pain Diseases 0.000 description 2
- JGSARLDLIJGVTE-MBNYWOFBSA-N Penicillin G Chemical compound N([C@H]1[C@H]2SC([C@@H](N2C1=O)C(O)=O)(C)C)C(=O)CC1=CC=CC=C1 JGSARLDLIJGVTE-MBNYWOFBSA-N 0.000 description 2
- 241000589516 Pseudomonas Species 0.000 description 2
- 241000607142 Salmonella Species 0.000 description 2
- 229940088710 antibiotic agent Drugs 0.000 description 2
- 210000000988 bone and bone Anatomy 0.000 description 2
- 239000003246 corticosteroid Substances 0.000 description 2
- 230000001079 digestive effect Effects 0.000 description 2
- 239000003085 diluting agent Substances 0.000 description 2
- 201000010099 disease Diseases 0.000 description 2
- 201000004595 synovitis Diseases 0.000 description 2
- 230000001988 toxicity Effects 0.000 description 2
- 231100000419 toxicity Toxicity 0.000 description 2
- 241000186361 Actinobacteria <class> Species 0.000 description 1
- 208000006820 Arthralgia Diseases 0.000 description 1
- 241000193830 Bacillus <bacterium> Species 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- GHOKWGTUZJEAQD-UHFFFAOYSA-N Chick antidermatitis factor Natural products OCC(C)(C)C(O)C(=O)NCCC(O)=O GHOKWGTUZJEAQD-UHFFFAOYSA-N 0.000 description 1
- 108010078777 Colistin Proteins 0.000 description 1
- 208000035473 Communicable disease Diseases 0.000 description 1
- 206010063045 Effusion Diseases 0.000 description 1
- 208000037147 Hypercalcaemia Diseases 0.000 description 1
- 206010033971 Paratyphoid fever Diseases 0.000 description 1
- 241000187419 Streptomyces rimosus Species 0.000 description 1
- 206010042674 Swelling Diseases 0.000 description 1
- 229930003316 Vitamin D Natural products 0.000 description 1
- QYSXJUFSXHHAJI-XFEUOLMDSA-N Vitamin D3 Natural products C1(/[C@@H]2CC[C@@H]([C@]2(CCC1)C)[C@H](C)CCCC(C)C)=C/C=C1\C[C@@H](O)CCC1=C QYSXJUFSXHHAJI-XFEUOLMDSA-N 0.000 description 1
- KIPLYOUQVMMOHB-MXWBXKMOSA-L [Ca++].CN(C)[C@H]1[C@@H]2[C@@H](O)[C@H]3C(=C([O-])[C@]2(O)C(=O)C(C(N)=O)=C1O)C(=O)c1c(O)cccc1[C@@]3(C)O.CN(C)[C@H]1[C@@H]2[C@@H](O)[C@H]3C(=C([O-])[C@]2(O)C(=O)C(C(N)=O)=C1O)C(=O)c1c(O)cccc1[C@@]3(C)O Chemical compound [Ca++].CN(C)[C@H]1[C@@H]2[C@@H](O)[C@H]3C(=C([O-])[C@]2(O)C(=O)C(C(N)=O)=C1O)C(=O)c1c(O)cccc1[C@@]3(C)O.CN(C)[C@H]1[C@@H]2[C@@H](O)[C@H]3C(=C([O-])[C@]2(O)C(=O)C(C(N)=O)=C1O)C(=O)c1c(O)cccc1[C@@]3(C)O KIPLYOUQVMMOHB-MXWBXKMOSA-L 0.000 description 1
- USDJGQLNFPZEON-UHFFFAOYSA-N [[4,6-bis(hydroxymethylamino)-1,3,5-triazin-2-yl]amino]methanol Chemical compound OCNC1=NC(NCO)=NC(NCO)=N1 USDJGQLNFPZEON-UHFFFAOYSA-N 0.000 description 1
- 208000005298 acute pain Diseases 0.000 description 1
- 230000000844 anti-bacterial effect Effects 0.000 description 1
- 229940124599 anti-inflammatory drug Drugs 0.000 description 1
- 206010003246 arthritis Diseases 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 208000037976 chronic inflammation Diseases 0.000 description 1
- 230000006020 chronic inflammation Effects 0.000 description 1
- 229960001127 colistin sulfate Drugs 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 229960001334 corticosteroids Drugs 0.000 description 1
- 230000003412 degenerative effect Effects 0.000 description 1
- 208000035475 disorder Diseases 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 208000010227 enterocolitis Diseases 0.000 description 1
- 230000000148 hypercalcaemia Effects 0.000 description 1
- 208000030915 hypercalcemia disease Diseases 0.000 description 1
- 208000015181 infectious disease Diseases 0.000 description 1
- 230000002458 infectious effect Effects 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 208000014674 injury Diseases 0.000 description 1
- 230000000968 intestinal effect Effects 0.000 description 1
- 230000002427 irreversible effect Effects 0.000 description 1
- 210000003734 kidney Anatomy 0.000 description 1
- 210000000629 knee joint Anatomy 0.000 description 1
- 230000004807 localization Effects 0.000 description 1
- 238000002483 medication Methods 0.000 description 1
- 230000004060 metabolic process Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- ZESIAEVDVPWEKB-ORCFLVBFSA-N n-[(2s)-4-amino-1-[[(2s,3r)-1-[[(2s)-4-amino-1-oxo-1-[[(3s,6s,9s,12s,15r,18s,21s)-6,9,18-tris(2-aminoethyl)-3-[(1r)-1-hydroxyethyl]-12,15-bis(2-methylpropyl)-2,5,8,11,14,17,20-heptaoxo-1,4,7,10,13,16,19-heptazacyclotricos-21-yl]amino]butan-2-yl]amino]-3-h Chemical compound OS(O)(=O)=O.OS(O)(=O)=O.CC(C)CCCCC(=O)N[C@@H](CCN)C(=O)N[C@H]([C@@H](C)O)CN[C@@H](CCN)C(=O)N[C@H]1CCNC(=O)[C@H]([C@@H](C)O)NC(=O)[C@H](CCN)NC(=O)[C@H](CCN)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](CC(C)C)NC(=O)[C@H](CCN)NC1=O.CCC(C)CCCCC(=O)N[C@@H](CCN)C(=O)N[C@H]([C@@H](C)O)CN[C@@H](CCN)C(=O)N[C@H]1CCNC(=O)[C@H]([C@@H](C)O)NC(=O)[C@H](CCN)NC(=O)[C@H](CCN)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](CC(C)C)NC(=O)[C@H](CCN)NC1=O ZESIAEVDVPWEKB-ORCFLVBFSA-N 0.000 description 1
- 230000000926 neurological effect Effects 0.000 description 1
- 229940055726 pantothenic acid Drugs 0.000 description 1
- 239000011713 pantothenic acid Substances 0.000 description 1
- 235000019161 pantothenic acid Nutrition 0.000 description 1
- 229940056360 penicillin g Drugs 0.000 description 1
- 244000144977 poultry Species 0.000 description 1
- 230000035755 proliferation Effects 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- 208000024891 symptom Diseases 0.000 description 1
- 239000011885 synergistic combination Substances 0.000 description 1
- 229940063650 terramycin Drugs 0.000 description 1
- 238000002560 therapeutic procedure Methods 0.000 description 1
- 230000008733 trauma Effects 0.000 description 1
- 235000019166 vitamin D Nutrition 0.000 description 1
- 239000011710 vitamin D Substances 0.000 description 1
- 150000003710 vitamin D derivatives Chemical class 0.000 description 1
- 229940046008 vitamin d Drugs 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/65—Tetracyclines
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Description
3ι < ' » «*3ι <'»« *
La présente invention est relative à une composition antibiotique éventuellement injectable, constituée d'un mélange synergique d'un composé d'Oxytetracycline et d'un autre constituant.The present invention relates to an optionally injectable antibiotic composition, consisting of a synergistic mixture of an Oxytetracycline compound and another constituent.
Elle est destinée, en médecine humaine et éventuellement vétérinaire, à guérir l'arthrose et toutes les lésions dégénératives des articulations, ainsi que les synovites et particulièrement les inflammations d1 ménisque du genou.It is intended, in human and possibly veterinary medicine, to cure osteoarthritis and all degenerative lesions of the joints, as well as synovitis and particularly inflammations of the meniscus of the knee.
Les lésions arthrosiques sont des inflammations chroniques des articulations dues à une prolifération des tissus osseux sous-jacents.Arthrosis lesions are chronic inflammations of the joints due to a proliferation of underlying bone tissue.
Les localisations les plus fréquentes des lésions arthrosiques sont les articulations intervertébrales, coxo-fémorales, les genoux et certaines articulations de la main et du pied.The most frequent localizations of arthritis lesions are the intervertebral, coxo-femoral joints, knees and certain joints of the hand and foot.
Le symptôme essentiel est la douleur. Celle-ci est calmée par le repos mais exacerbée par les mouvements. Au stade initial, l'arthrose entraîne une limitation des * mouvements et des craquements à la mobilisation. Elle fait ainsi apparaître des joints douloureux à la pression.The main symptom is pain. It is calmed by rest but exacerbated by movement. At the initial stage, osteoarthritis leads to a limitation of * movements and crunches to mobilization. It thus shows painful joints when pressed.
; A un stade avancé, on remarque des gonflements et même des déformations irréversibles des articulations.; At an advanced stage, we notice swellings and even irreversible deformations of the joints.
î 2 fî 2 f
Le traitement médical de l'arthrose envisage principalement l’administration de médications antalgiques et la prescription de médicaments anti-inflammatoires.The medical treatment of osteoarthritis mainly involves the administration of analgesic medications and the prescription of anti-inflammatory drugs.
Entre autres, les corticoïdes sont sans conteste efficaces et calment immédiatement l’accès aigu des ' douleurs, mais ils présentent aussi de graves inconvé nients. Ils entraînent en effet des risque infectieux çpi reident pa^Æbis nécessaire une association d’antibiotiques et des risques digestifs, rénaux et neurologiques, du fait de leur grande toxicité.Among others, corticosteroids are undoubtedly effective and immediately relieve acute pain, but they also have serious drawbacks. In fact, they involve infectious risks çpi reident pa ^ Æbis necessary a combination of antibiotics and digestive, renal and neurological risks, because of their great toxicity.
La présente invention vise à traiter l’arthrose sans présenter les inconvénients de la corticothérapie. Elle est relative à une composition médicamenteuse, permet un traitement de fond, précoce et prolongé de l’arthrose et prévient toute récidive.The present invention aims to treat osteoarthritis without having the drawbacks of corticosteroid therapy. It relates to a medicinal composition, allows a basic, early and prolonged treatment of osteoarthritis and prevents any recurrence.
Cette composition médicamenteuse peut être administrée selon sa forme galénique, par voie orale ou parentérale. Elle concerne un mélange synergique d’un antibiotique du type oxytétracycline et d’un autre constituant, essentiellement caractérisé en ce que cet autre constituant est un complexe vitaminique A-D.This drug composition can be administered in its dosage form, orally or parenterally. It relates to a synergistic mixture of an antibiotic of the oxytetracycline type and of another constituent, essentially characterized in that this other constituent is a vitamin A-D complex.
Suivant une particularité de l’invention, l’oxy-tétracycline et le complexe vitamine A-D sont mélangés dans un rapport pondéral de 0,3 à 3..According to a feature of the invention, the oxytetracycline and the vitamin A-D complex are mixed in a weight ratio of 0.3 to 3.
L’activité de la composition susdite est avanta- , geusement renforcée par la présence d'un complexe de vitamines B, contenant en particulier de la vitamine ’'antinévritique*’, de la vitamine ’’antidermatosique'’ et de la vitamine PP (ou B^) ’’antipellagreuse’’.The activity of the aforementioned composition is advantageously reinforced by the presence of a complex of B vitamins, containing in particular vitamin '' antineuritis * ', vitamin' 'antidermatosique' 'and vitamin PP ( or B ^) '' antipellagreuse ''.
i 3 D’autres particularités et détails de l’invention apparaîtront au cours de la description détaillée donnée ci-dessus, d’une forme gallénique particulière de l’invention.i 3 Other features and details of the invention will become apparent from the detailed description given above, of a particular dosage form of the invention.
i si L'oxytétracycline est un composé antibiotique que l'on isole des substances élaborées par les actinomycètes et en particulier du Streptomyces rimosus. Elle a été décrite pour la première fois dans le brevet américain N° 2 516 080 (Pfizer). Elle est principalement utilisée comme anti-bactérien contre certaines maladies infectieuses. Elle est administrée en particulier pour combattre les bactéries du groupe des Salmonella et des Pseudomonas.i if Oxytetracycline is an antibiotic compound which is isolated from substances produced by actinomycetes and in particular from Streptomyces rimosus. It was first described in US Patent No. 2,516,080 (Pfizer). It is mainly used as an anti-bacterial against certain infectious diseases. It is administered in particular to combat bacteria from the group of Salmonella and Pseudomonas.
L'adjonction d'autres antibiotiques, de Pénicilline G et de sulfate de colistine suivant le brevet belge N® 505 709 et la demande de brevet luxembourgeois Ne 84 786 élargit de façon remarquable les spectres d’applicabilité de l’oxytétracycline pour combattre le bacille de Koch et les bactéries du groupe des Salmonella et des Pseudomonas, responsables de maladies dangereuses pour l’homme et la volaille. Notons pour l’homme, la fièvre paratyphoïde et l’entérocolite salmonellique. L’oxytétracycline est caractérisée par un spectre extrêmement large et une toxicité réduite.The addition of other antibiotics, of Penicillin G and of colistin sulfate according to Belgian patent N® 505 709 and the Luxembourg patent application Ne 84 786 remarkably broadens the spectra of applicability of oxytetracycline to fight bacillus de Koch and bacteria from the Salmonella and Pseudomonas group, responsible for diseases dangerous to humans and poultry. Note for humans, paratyphoid fever and salmonellous enterocolitis. Oxytetracycline is characterized by an extremely broad spectrum and reduced toxicity.
La présente invention élargit le champ d’application de l’oxytétracycline et étend celui-ci au traitement j _ précoce et néanmoins radical de maladies et traumatismes des articulations.The present invention widens the field of application of oxytetracycline and extends it to the early and nevertheless radical treatment of diseases and traumas of the joints.
4 ! L’invention est basée sur la découverte que l’oxy- tétracycline ou Terramycine présente une efficacité étonnante contre l’arthrose lorsqu’elle est administrée η en même temps qu’un complexe vitaminé A-D2* D'excellents résultats sont obtenus lorsque les composants sont mélan- s gés dans un rapport pondéral variant de 0,3 à 5.4! The invention is based on the discovery that oxytetracycline or Terramycin exhibits astonishing efficacy against osteoarthritis when it is administered η at the same time as a vitamin complex A-D2 * Excellent results are obtained when the components are mixed in a weight ratio varying from 0.3 to 5.
< j Les vitamines A-D^ sont destinées principalement à fixer le calcium.<j Vitamins A-D ^ are mainly intended to fix calcium.
Cette synergie de 1’oxytétracycline et d'un complexe vitaminé A-D2 est renforcée par la présence de quantité d'un complexe B destiné à pallier les troubles digestifs éventuels.This synergy of oxytetracycline and a vitamin A-D2 complex is reinforced by the presence of a quantity of a B complex intended to alleviate possible digestive disorders.
Les vitamines du complexe B comprenant les vitamines B,j, Bg, PP, Bg, B^2» l'acide pantothénique et la biotine entrent dans la composition des différents systèmes fer-mentaires qui régularisent le métabolisme général et permet de rétablir rapidement la fonction normale de la flore intestinale après une perturbation.The B complex vitamins including vitamins B, j, Bg, PP, Bg, B ^ 2 "pantothenic acid and biotin are part of the composition of different fermental systems that regulate the general metabolism and can quickly restore the normal function of the intestinal flora after a disturbance.
On remarque donc que les indications médicales premières de chacun des constituants décrites ci-dessus, j pris séparément, sont totalement différentes de celles ; de leur mélange.It should therefore be noted that the primary medical indications for each of the constituents described above, taken separately, are completely different from those; of their mixture.
La composition synergique suivant l’invention trouve son application préférée dans le traitement de I l'arthrose. Elle permet de guérir les lésions dégéné- ! ratives des articulations. Ses effets antalgiques et anti-inflammatoires sont immédiats. Elle permet de traiter efficacement les synovites, les épanchements de synovie et les autres inflammations du ménisque du genou, t 5 fréquents chez les footballeurs professionnels.The synergistic composition according to the invention finds its preferred application in the treatment of osteoarthritis. It heals degenerate lesions! ratives of the joints. Its analgesic and anti-inflammatory effects are immediate. It makes it possible to effectively treat synovitis, synovial effusions and other inflammations of the meniscus of the knee, t 5 common in professional footballers.
Elle procure des résultats spectaculaires dans " le traitement <hs sciatiques, rhumatismes, décalcifi cations des os, hernies discales, lombagos, entorses et déchirures musculaires.It provides spectacular results in the treatment of sciatica, rheumatism, decalcification of bones, herniated discs, lumbago, sprains and muscle tears.
L’exemple suivant de composition est destiné à illustrer le caractère nouveau et inventif de la composition médicamenteuse. Ni la composition précise, ni la forme galénique ne doit être considérée comme une limitation. L’analyse suivante détermine les quantités de chacun des constituants présents dans une cuillerée à café, c’est-à-dire 5 ml de la composition suivant l'invention.The following example of composition is intended to illustrate the new and inventive nature of the drug composition. Neither the precise composition nor the dosage form should be considered a limitation. The following analysis determines the amounts of each of the constituents present in a teaspoon, that is to say 5 ml of the composition according to the invention.
Constituants Quantité par 5 ml 1/ Chlorhydrate d’oxytétracycline 50-150 mg (calculée sur base d’oxytétra-cycline-base) 2/ Vitamine A. (Ergocalciférol) 50.000-150.000 Ü.I.Constituents Quantity per 5 ml 1 / Oxytetracycline hydrochloride 50-150 mg (calculated on the basis of oxytetra-cyclin-base) 2 / Vitamin A. (Ergocalciferol) 50,000-150,000 Ü.I.
3/ Vitamine D2 (Hydroxytoluène butyle) 50.000-150.000 U.I.3 / Vitamin D2 (Butylated hydroxytoluene) 50,000-150,000 IU
4/ Vitamine (chlorhydrate de 1,5-3 mg thiamine ou Aneurine) 5/ Vitamine B2 (Riboflavine) 400-650 pg 6/ Vitamine (Pyridoxine) 200-450 pg 7/ Vitamine B^ (Cyanocaboiamine) néant 8/ Vitamine PP (Nicotinamide) 3-10 mg 9/ Vitamine B^ (Pantothénate de calcium) néant 10/ Dexpanthénol 40-80 pg 11/ Biotine néant 12/ Oxyde de magnésium 100-300 pg 13/ Sirop de sucre ad 5 mi .4 / Vitamin (1.5-3 mg thiamine hydrochloride or Aneurine) 5 / Vitamin B2 (Riboflavin) 400-650 pg 6 / Vitamin (Pyridoxine) 200-450 pg 7 / Vitamin B ^ (Cyanocaboiamine) none 8 / Vitamin PP (Nicotinamide) 3-10 mg 9 / Vitamin B ^ (Calcium pantothenate) none 10 / Dexpanthenol 40-80 pg 11 / Biotin none 12 / Magnesium oxide 100-300 pg 13 / Sugar syrup ad 5 mi.
6 EXEMPLE 16 EXAMPLE 1
Une forme préférée d*exécution présente une composition répondant à la formule suivante, contenant par 5 ml, les constituants suivants:A preferred embodiment has a composition corresponding to the following formula, containing per 5 ml, the following constituents:
Constituants Par cuillerée à & _ café de 5 ml 1/ Chlorhydrate d’oxytétracycline 70 mg (calculée sur base d’oxytétra-cycline-base) 2/ Vitamine A (Ergocalciférol) 115.000 U.I.Constituents Per teaspoonful of 5 ml 1 / Oxytetracycline hydrochloride 70 mg (calculated on the basis of oxytetra-cyclin-base) 2 / Vitamin A (Ergocalciferol) 115,000 IU.
3/ Vitamine D^ (Hydroxytoluène-butyle) 115.000 U.I.3 / Vitamin D ^ (Hydroxytoluene-butyl) 115,000 IU
4/ Vitamine B. 2,2 mg (chlorhydrate de thiamine ou Aneurine) 5/ Vitamine B2 (Riboflavine) 530 pg 6/ Vitamine B^ (Piridoxine) 300 pg 7/ Vitamine B^ (Cyanocobalamine) néant 8/ Vitamine PP (Nicotinamide) 6 mg 9/ Vitamine (Pantothénate de calcium) néant 10/ Dexpanthénol 60 pg 11/ Biotine néant 12/ Oxyde de magnésium 175 Pg 13/ Sirop de sucre ad 5 ml EXEMPLE 24 / Vitamin B. 2.2 mg (thiamine hydrochloride or Aneurine) 5 / Vitamin B2 (Riboflavin) 530 pg 6 / Vitamin B ^ (Piridoxine) 300 pg 7 / Vitamin B ^ (Cyanocobalamin) none 8 / Vitamin PP (Nicotinamide ) 6 mg 9 / Vitamin (Calcium pantothenate) none 10 / Dexpanthenol 60 pg 11 / Biotin none 12 / Magnesium oxide 175 Pg 13 / Sugar syrup ad 5 ml EXAMPLE 2
Une autre formule possible d’exécution présente une composition répondant à la formule suivante, contenant par 5 ml les constituants suivants donnés en milligrammes: 7 *►Another possible execution formula has a composition corresponding to the following formula, containing per 5 ml the following constituents given in milligrams: 7 * ►
Constituants Par cuillerée de 5 roiConstituents Per spoonful of 5 king
Chlorhydrate d'oxytétracycline 70 mgOxytetracycline hydrochloride 70 mg
Vit. k 50.000 U.I.Lives. k 50,000 U.I.
Vit. D2 50.000 U.I.Lives. D2 50,000 U.I.
Vit. B.j 1,425 mgLives. B.j 1.425 mg
Vit. B2 0,225 mgLives. B2 0.225 mg
Vit. B6 0,225 mg D-Pantothénol 0,225 mgLives. B6 0.225 mg D-Pantothenol 0.225 mg
Vit. PP 3 mgLives. PP 3 mg
Excipient* 3 mgExcipient * 3 mg
Le mélange de l'exemple 1 est réalisé en mélangeant entre eux 100 ml d’une solution injectable d'oxytétra-cycline à 10 %, contenant par exemple 92,6 mg de chlorhydrate d'oxytétracycline par ml de solution, 150 mg d'un complexe vitaminique A-D, commercialisé par exemple par Pfizer pour usage vétérinaire. On ajoute ensuite 100 ml de sirop de complexes vitaminiques B, car exemple de BBCOZYM^ Roche (sirop) et/ou de BECOVITAI*(sirop, produit par Cilag N.U./S.A. et environ 200 ml d'un sirop de sucre, de manière à obtenir 650 ml de composition médicamenteuse sous forme d'un sirop.The mixture of Example 1 is produced by mixing together 100 ml of a 10% solution of injectable oxytetra-cyclin, containing for example 92.6 mg of oxytetracycline hydrochloride per ml of solution, 150 mg of an AD vitamin complex, marketed for example by Pfizer for veterinary use. Then add 100 ml of syrup of vitamin B complexes, as an example of BBCOZYM ^ Roche (syrup) and / or BECOVITAI * (syrup, produced by Cilag NU / SA and approximately 200 ml of a sugar syrup, so as to obtain 650 ml of medicinal composition in the form of a syrup.
La préparation sous forme de sirop aux dosages indiqués ci-dessus est administrée par voie buccale à raison de trois cuillerées à café pendant 3 jours. Le traitemait est poursuivi par la prise d'une cuillerée i à café pendant quelques jours.The preparation in syrup form at the dosages indicated above is administered orally at the rate of three teaspoons for 3 days. The treatment is continued by taking a teaspoon i for a few days.
Les contre-indications sont déterminées par les hypercalcémies qui peuvent entraîner un blocage de reins.Contraindications are determined by hypercalcemia which can lead to kidney blockage.
La composition doit être prise sous contrôle médical.The composition must be taken under medical supervision.
AAT
i 8 * * * ï- , « Il convient de noter qu’en variante, chacun des constituants peut être ajouté sous forme injectable, en particulier le complexe vitaminé BECOZYM^Roche et/ou BECOVITAN forte, de manière à obtenir une solution huileuse injectable. Cette forme galénique favorise l’assimilation de la vitamine et de la biotine.i 8 * * * ï-, "It should be noted that, as a variant, each of the constituents can be added in injectable form, in particular the vitamin complex BECOZYM ^ Roche and / or BECOVITAN forte, so as to obtain an oily solution for injection. . This dosage form promotes the assimilation of vitamin and biotin.
D’autres modifications peuvent être apportées à la forme de réalisation de l’invention. Il est évident que l’homme de métier peut apporter de nombreuses variantes dans le choix, notamment des excipients, supports ou diluants. En principe donc, l’invention couvre toutes les combinaisons synergiques de l'invention avec les supports, diluants et excipients utilisés habituellement en pharmacologie. .Other modifications may be made to the embodiment of the invention. It is obvious that the skilled person can bring many variations in the choice, in particular excipients, supports or diluents. In principle therefore, the invention covers all the synergistic combinations of the invention with the carriers, diluents and excipients usually used in pharmacology. .
» ' St ] i»'St] i
JJ
Claims (6)
Priority Applications (6)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| LU86004A LU86004A1 (en) | 1985-07-15 | 1985-07-15 | ANALGESIC AND ANTI-INFLAMMATORY COMPOSITION FOR THE TREATMENT OF ARTHROSIS |
| EP86870092A EP0214947A1 (en) | 1985-07-15 | 1986-06-24 | Antalgic and anti-inflammatory composition for the treatment of arthrosis |
| ZA864740A ZA864740B (en) | 1985-07-15 | 1986-06-25 | Antalgic and antiinflammatory composition for healing arthritis |
| IL79272A IL79272A0 (en) | 1985-07-15 | 1986-06-27 | Oxytetracycline type antibiotic composition |
| CA000513736A CA1279013C (en) | 1985-07-15 | 1986-07-14 | Antibiotic composition for the treatment of arthritis |
| PT82982A PT82982B (en) | 1985-07-15 | 1986-07-14 | PRODUCTION PROCESS OF AN SYNERGIC ANTIBIOTIC COMPOSITION OF AN OXYETRACYCIN COMPOUND |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| LU86004A LU86004A1 (en) | 1985-07-15 | 1985-07-15 | ANALGESIC AND ANTI-INFLAMMATORY COMPOSITION FOR THE TREATMENT OF ARTHROSIS |
| LU86004 | 1985-07-15 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| LU86004A1 true LU86004A1 (en) | 1987-02-04 |
Family
ID=19730511
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| LU86004A LU86004A1 (en) | 1985-07-15 | 1985-07-15 | ANALGESIC AND ANTI-INFLAMMATORY COMPOSITION FOR THE TREATMENT OF ARTHROSIS |
Country Status (5)
| Country | Link |
|---|---|
| EP (1) | EP0214947A1 (en) |
| CA (1) | CA1279013C (en) |
| LU (1) | LU86004A1 (en) |
| PT (1) | PT82982B (en) |
| ZA (1) | ZA864740B (en) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8906966B2 (en) | 2006-07-13 | 2014-12-09 | Paul Sherwood | Medicaments containing panthenol |
| WO2009010707A1 (en) * | 2007-07-13 | 2009-01-22 | Prototype Bioforum Limited | Injectable pharmaceutical compositions containing panthenol |
-
1985
- 1985-07-15 LU LU86004A patent/LU86004A1/en unknown
-
1986
- 1986-06-24 EP EP86870092A patent/EP0214947A1/en not_active Withdrawn
- 1986-06-25 ZA ZA864740A patent/ZA864740B/en unknown
- 1986-07-14 PT PT82982A patent/PT82982B/en not_active IP Right Cessation
- 1986-07-14 CA CA000513736A patent/CA1279013C/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| CA1279013C (en) | 1991-01-15 |
| PT82982B (en) | 1988-07-01 |
| EP0214947A1 (en) | 1987-03-18 |
| PT82982A (en) | 1986-08-01 |
| ZA864740B (en) | 1987-02-25 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US5929066A (en) | Chromium/biotin treatment of Type II diabetes | |
| US4351831A (en) | Process and composition for treating disorders by administering isoxsurpine and choline | |
| US4588589A (en) | Antidiarrheal compositions and use thereof | |
| US6605605B2 (en) | Estrogenic substances combined with cruciferous indole compounds | |
| CA2297834C (en) | Chromium/biotin treatment of type ii diabetes | |
| US4743596A (en) | Anti-arthritic preparation | |
| KR20110112279A (en) | Medicines and Treatment | |
| KR20020050249A (en) | Method for administering a phosphodiesterase 4 inhibitor | |
| US4346084A (en) | Process and composition for treating disorders by administering lithium and choline | |
| US4591503A (en) | Composition for improved absorption of 2A cations and gold comprising yeast or Lactobacillus | |
| LU86004A1 (en) | ANALGESIC AND ANTI-INFLAMMATORY COMPOSITION FOR THE TREATMENT OF ARTHROSIS | |
| US9545419B1 (en) | Method and compositions for treating chronic inflammatory disorders | |
| US20110117070A1 (en) | Compositions and methods for treating headache | |
| EP0190851A1 (en) | Improved antiinflammatory composition | |
| GB2248392A (en) | Composition to combat alcoholism | |
| US4122188A (en) | Treatment of hyperlipoproteinemia with a dichloroacetate salt | |
| CN1917868A (en) | Composition, comprising l-serine, l-isoleucine, folic acid and trace elements, for treating psoriasis | |
| US4663345A (en) | Etodolac for treatment of gout | |
| EP1121124A1 (en) | Pharmaceutical combination of ibuprofen-lysine and domperidone for treating migraine | |
| RU2063753C1 (en) | Method for treating extrapyramidal syndrome in the cases of acute poisoning with haloperidol | |
| BURNETT et al. | Report on the use of cycloserine and isoniazid in twenty-seven cases of pulmonary tuberculosis in psychotic patients | |
| US20070053930A1 (en) | Combination therapy for treatment of high cholesterol | |
| JPH07233062A (en) | Composition for treating skin pruritus of patient requiring artificial dialysis and composition for treating hyperparathyroidism | |
| CN113543649A (en) | Compositions and methods for treating constipation and other gastrointestinal disorders | |
| MIN | PRESCRIBE |