KR20060095500A - 이바브라딘 히드로클로라이드의 βd-결정질 형태, 이의제조 방법 및 이를 함유하는 약제학적 조성물 - Google Patents
이바브라딘 히드로클로라이드의 βd-결정질 형태, 이의제조 방법 및 이를 함유하는 약제학적 조성물 Download PDFInfo
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- KR20060095500A KR20060095500A KR1020060018721A KR20060018721A KR20060095500A KR 20060095500 A KR20060095500 A KR 20060095500A KR 1020060018721 A KR1020060018721 A KR 1020060018721A KR 20060018721 A KR20060018721 A KR 20060018721A KR 20060095500 A KR20060095500 A KR 20060095500A
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- Prior art keywords
- ivabradine hydrochloride
- crystalline form
- expressed
- coefficient
- line
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- HLUKNZUABFFNQS-ZMBIFBSDSA-N ivabradine hydrochloride Chemical compound Cl.C1CC2=CC(OC)=C(OC)C=C2CC(=O)N1CCCN(C)C[C@H]1CC2=C1C=C(OC)C(OC)=C2 HLUKNZUABFFNQS-ZMBIFBSDSA-N 0.000 title claims abstract description 20
- 229960000504 ivabradine hydrochloride Drugs 0.000 title claims abstract description 19
- 238000000034 method Methods 0.000 title claims description 9
- 239000008194 pharmaceutical composition Substances 0.000 title claims description 6
- 238000002360 preparation method Methods 0.000 title claims description 4
- 238000000634 powder X-ray diffraction Methods 0.000 claims abstract description 7
- 239000003814 drug Substances 0.000 claims abstract 2
- 239000013078 crystal Substances 0.000 claims description 7
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims description 7
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 6
- 208000035475 disorder Diseases 0.000 claims description 6
- 230000033764 rhythmic process Effects 0.000 claims description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 6
- 239000000203 mixture Substances 0.000 claims description 5
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 claims description 4
- 238000002425 crystallisation Methods 0.000 claims description 4
- 230000008025 crystallization Effects 0.000 claims description 4
- 206010002383 Angina Pectoris Diseases 0.000 claims description 3
- 206010019280 Heart failures Diseases 0.000 claims description 3
- 206010047281 Ventricular arrhythmia Diseases 0.000 claims description 3
- 230000000059 bradycardiac effect Effects 0.000 claims description 3
- 238000004519 manufacturing process Methods 0.000 claims description 3
- 208000010125 myocardial infarction Diseases 0.000 claims description 3
- 208000031225 myocardial ischemia Diseases 0.000 claims description 3
- 230000002265 prevention Effects 0.000 claims description 3
- 239000004480 active ingredient Substances 0.000 claims description 2
- 238000001816 cooling Methods 0.000 claims description 2
- 238000004090 dissolution Methods 0.000 claims description 2
- 231100000252 nontoxic Toxicity 0.000 claims description 2
- 230000003000 nontoxic effect Effects 0.000 claims description 2
- 239000003795 chemical substances by application Substances 0.000 claims 1
- 230000008961 swelling Effects 0.000 claims 1
- 150000001875 compounds Chemical class 0.000 description 4
- 150000003839 salts Chemical class 0.000 description 4
- 239000002253 acid Substances 0.000 description 3
- 150000007513 acids Chemical class 0.000 description 3
- 238000005259 measurement Methods 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- 150000003840 hydrochlorides Chemical class 0.000 description 2
- HQKMJHAJHXVSDF-UHFFFAOYSA-L magnesium stearate Chemical compound [Mg+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O HQKMJHAJHXVSDF-UHFFFAOYSA-L 0.000 description 2
- 230000000144 pharmacologic effect Effects 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- 239000003826 tablet Substances 0.000 description 2
- 230000001225 therapeutic effect Effects 0.000 description 2
- 229920002261 Corn starch Polymers 0.000 description 1
- FBPFZTCFMRRESA-KVTDHHQDSA-N D-Mannitol Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-KVTDHHQDSA-N 0.000 description 1
- 229930195725 Mannitol Natural products 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000008119 colloidal silica Substances 0.000 description 1
- 239000008120 corn starch Substances 0.000 description 1
- 239000006071 cream Substances 0.000 description 1
- 230000018044 dehydration Effects 0.000 description 1
- 238000006297 dehydration reaction Methods 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 201000010099 disease Diseases 0.000 description 1
- 239000008298 dragée Substances 0.000 description 1
- 230000035622 drinking Effects 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000000499 gel Substances 0.000 description 1
- 239000007903 gelatin capsule Substances 0.000 description 1
- 238000003306 harvesting Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 238000001990 intravenous administration Methods 0.000 description 1
- 229960003825 ivabradine Drugs 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 239000007937 lozenge Substances 0.000 description 1
- 235000019359 magnesium stearate Nutrition 0.000 description 1
- 239000000594 mannitol Substances 0.000 description 1
- 235000010355 mannitol Nutrition 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000002674 ointment Substances 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000000546 pharmaceutical excipient Substances 0.000 description 1
- 239000008213 purified water Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000004611 spectroscopical analysis Methods 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000006190 sub-lingual tablet Substances 0.000 description 1
- 238000007920 subcutaneous administration Methods 0.000 description 1
- 239000000829 suppository Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D223/00—Heterocyclic compounds containing seven-membered rings having one nitrogen atom as the only ring hetero atom
- C07D223/14—Heterocyclic compounds containing seven-membered rings having one nitrogen atom as the only ring hetero atom condensed with carbocyclic rings or ring systems
- C07D223/16—Benzazepines; Hydrogenated benzazepines
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- 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
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/55—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
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- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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- A61P9/00—Drugs for disorders of the cardiovascular system
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- A61P9/04—Inotropic agents, i.e. stimulants of cardiac contraction; Drugs for heart failure
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- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/06—Antiarrhythmics
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- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
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- C10G45/00—Refining of hydrocarbon oils using hydrogen or hydrogen-generating compounds
- C10G45/32—Selective hydrogenation of the diolefin or acetylene compounds
- C10G45/34—Selective hydrogenation of the diolefin or acetylene compounds characterised by the catalyst used
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Abstract
Description
선 번호 | 각 2 θ(°) | 높이(계수) | 영역(계수 × °) | FWHM(°) | 결정면간 거리(Å) |
1 | 4.0 | 244 | 80 | 0.3346 | 22.139 |
2 | 5.9 | 377 | 56 | 0.1506 | 14.829 |
3 | 6.9 | 94 | 50 | 0.5353 | 12.835 |
4 | 9.2 | 1975 | 293 | 0.1506 | 9.623 |
5 | 11.8 | 136 | 27 | 0.2007 | 7.473 |
6 | 12.5 | 1826 | 241 | 0.1338 | 7.083 |
7 | 13.6 | 1834 | 303 | 0.1673 | 6.491 |
8 | 14.5 | 51 | 20 | 0.4015 | 6.119 |
9 | 16.0 | 1441 | 214 | 0.1506 | 5.525 |
10 | 17.3 | 4472 | 738 | 0.1673 | 5.134 |
11 | 18.4 | 546 | 108 | 0.2007 | 4.808 |
12 | 19.6 | 1025 | 169 | 0.1673 | 4.524 |
13 | 20.0 | 688 | 91 | 0.1338 | 4.448 |
14 | 20.4 | 1027 | 186 | 0.184 | 4.362 |
15 | 21.4 | 102 | 24 | 0.2342 | 4.143 |
16 | 22.3 | 1903 | 283 | 0.1506 | 3.990 |
17 | 22.8 | 674 | 89 | 0.1338 | 3.897 |
18 | 23.0 | 623 | 62 | 0.1004 | 3.866 |
19 | 24.4 | 845 | 56 | 0.0669 | 3.647 |
20 | 25.0 | 3749 | 557 | 0.1506 | 3.554 |
21 | 25.5 | 512 | 84 | 0.1673 | 3.497 |
22 | 26.6 | 289 | 76 | 0.2676 | 3.346 |
23 | 28.3 | 275 | 91 | 0.3346 | 3.151 |
24 | 29.1 | 126 | 21 | 0.1673 | 3.066 |
선 번호 | 각 2 θ(°) | 높이(계수) | 영역(계수 × °) | FWHM(°) | 결정면간 거리(Å) |
1 | 4.0 | 244 | 80 | 0.3346 | 22.139 |
2 | 5.9 | 377 | 56 | 0.1506 | 14.829 |
3 | 6.9 | 94 | 50 | 0.5353 | 12.835 |
4 | 9.2 | 1975 | 293 | 0.1506 | 9.623 |
5 | 11.8 | 136 | 27 | 0.2007 | 7.473 |
6 | 12.5 | 1826 | 241 | 0.1338 | 7.083 |
7 | 13.6 | 1834 | 303 | 0.1673 | 6.491 |
8 | 14.5 | 51 | 20 | 0.4015 | 6.119 |
9 | 16.0 | 1441 | 214 | 0.1506 | 5.525 |
10 | 17.3 | 4472 | 738 | 0.1673 | 5.134 |
11 | 18.4 | 546 | 108 | 0.2007 | 4.808 |
12 | 19.6 | 1025 | 169 | 0.1673 | 4.524 |
13 | 20.0 | 688 | 91 | 0.1338 | 4.448 |
14 | 20.4 | 1027 | 186 | 0.184 | 4.362 |
15 | 21.4 | 102 | 24 | 0.2342 | 4.143 |
16 | 22.3 | 1903 | 283 | 0.1506 | 3.990 |
17 | 22.8 | 674 | 89 | 0.1338 | 3.897 |
18 | 23.0 | 623 | 62 | 0.1004 | 3.866 |
19 | 24.4 | 845 | 56 | 0.0669 | 3.647 |
20 | 25.0 | 3749 | 557 | 0.1506 | 3.554 |
21 | 25.5 | 512 | 84 | 0.1673 | 3.497 |
22 | 26.6 | 289 | 76 | 0.2676 | 3.346 |
23 | 28.3 | 275 | 91 | 0.3346 | 3.151 |
24 | 29.1 | 126 | 21 | 0.1673 | 3.066 |
Claims (6)
- 패널리티컬 엑스퍼트 프로(PANalytical X'Pert Pro) 회절분석기와 엑스셀러레이터(X'Celerator) 검출기를 사용하여 측정되고, 선 위치(브래그 각(Bragg's angle) 2 θ, °로 표시됨), 선 높이(계수로 표시됨), 선 영역(계수 × °로 표시됨), 반높이에서의 선 폭("FWHM", °로 표시됨) 및 결정면간 거리 d(Å으로 표시됨)로 표현된 하기의 분말 X-선 회절(powder X-ray diffraction) 도표를 특징으로 하는, 하기 화학식(Ⅰ)의 이바브라딘 히드로클로라이드의 βd-결정질 형태:
선 번호 각 2 θ(°) 높이(계수) 영역(계수 × °) FWHM(°) 결정면간 거리(Å) 1 4.0 244 80 0.3346 22.139 2 5.9 377 56 0.1506 14.829 3 6.9 94 50 0.5353 12.835 4 9.2 1975 293 0.1506 9.623 5 11.8 136 27 0.2007 7.473 6 12.5 1826 241 0.1338 7.083 7 13.6 1834 303 0.1673 6.491 8 14.5 51 20 0.4015 6.119 9 16.0 1441 214 0.1506 5.525 10 17.3 4472 738 0.1673 5.134 11 18.4 546 108 0.2007 4.808 12 19.6 1025 169 0.1673 4.524 13 20.0 688 91 0.1338 4.448 14 20.4 1027 186 0.184 4.362 15 21.4 102 24 0.2342 4.143 16 22.3 1903 283 0.1506 3.990 17 22.8 674 89 0.1338 3.897 18 23.0 623 62 0.1004 3.866 19 24.4 845 56 0.0669 3.647 20 25.0 3749 557 0.1506 3.554 21 25.5 512 84 0.1673 3.497 22 26.6 289 76 0.2676 3.346 23 28.3 275 91 0.3346 3.151 24 29.1 126 21 0.1673 3.066 - 이바브라딘 히드로클로라이드 및 물의 혼합물, 또는 이바브라딘 히드로클로라이드, 이소프로판올 및 물의 혼합물을 용해가 완결될 때까지 가열한 후, 결정화가 완결될 때까지 점진적으로 냉각시키고, 형성된 결정을 수거한 후, 탈수시킴을 특징으로 하는, 이바브라딘 히드로클로라이드의 βd-결정질 형태를 제조하는 방법.
- 제 2 항에 있어서, 이바브라딘 히드로클로라이드 용액이 냉각 단계 동안 시딩(seeding)됨을 특징으로 하는 방법.
- 하나 이상의 약제학적으로 허용되는 비활성의 무독성 담체와 함께, 활성 성 분으로서 제 1 항에 따른 이바브라딘 히드로클로라이드의 βd-결정질 형태를 포함하는 약제학적 조성물.
- 서맥제(bradycardics)로 사용되는 약제의 제조에 있어서, 제 1 항에 따른 이바브라딘 히드로클로라이드의 βd-결정질 형태의 용도.
- 심근 허혈, 예를들어 협심증, 심근경색증 및 연합 리듬 장애(associated rhythm disturbance)의 다양한 임상적 상태, 및 리듬 장애, 특히 심실위 리듬 장애를 수반하는 다양한 병상, 및 심부전의 치료 또는 예방에 사용되는 약제의 제조에 있어서, 제 1 항에 따른 이바브라딘 히드로클로라이드의 βd-결정질 형태의 용도.
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FR0501987A FR2882554B1 (fr) | 2005-02-28 | 2005-02-28 | Forme critalline beta d du chlorhydrate de l'ivabradine, son procede de preparation, et les compositions pharmaceutiques qui la contiennent |
FR05.01987 | 2005-02-28 |
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FR2882555B1 (fr) * | 2005-02-28 | 2007-05-04 | Servier Lab | Forme cristalline gamma du chlorhydrate de l'ivabradine, son procede de preparation, et les compositions pharmaceutiques qui la contiennent |
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PL2902384T3 (pl) | 2010-02-12 | 2018-04-30 | Krka, D.D., Novo Mesto | Postać chlorowodorku iwabradyny |
HUP1000245A2 (en) | 2010-05-07 | 2011-11-28 | Richter Gedeon Nyrt | Industrial process for the production ivabradin salts |
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CZ305096B6 (cs) | 2013-10-02 | 2015-04-29 | Zentiva, K.S. | Pevná forma Ivabradin hydrochloridu a (S)-mandlové kyseliny a její farmaceutická kompozice |
ES2672472T3 (es) | 2013-12-12 | 2018-06-14 | Synthon Bv | Composición farmacéutica que comprende ivabradina amorfa |
EP2774606B1 (en) | 2014-02-14 | 2019-01-30 | Synthon B.V. | Pharmaceutical composition comprising ivabradine hydrochloride polymorph IV |
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DE3418270A1 (de) * | 1984-05-17 | 1985-11-21 | Dr. Karl Thomae Gmbh, 7950 Biberach | Neue aminotetralinderivate, diese verbindungen enthaltende arzneimittel und verfahren zu ihrer herstellung |
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FR2868777B1 (fr) * | 2004-04-13 | 2006-05-26 | Servier Lab | Nouveau procede de synthese de l'ivabradine et de ses sels d'addition a un acide pharmaceutiquement acceptable |
FR2882555B1 (fr) * | 2005-02-28 | 2007-05-04 | Servier Lab | Forme cristalline gamma du chlorhydrate de l'ivabradine, son procede de preparation, et les compositions pharmaceutiques qui la contiennent |
FR2882556B1 (fr) * | 2005-02-28 | 2007-05-04 | Servier Lab | Forme cristalline gamma d du chlorhydrate de l'ivabradine, son procede de preparation, et les compositions pharmaceutiques qui la contiennent |
FR2882553B1 (fr) * | 2005-02-28 | 2007-05-04 | Servier Lab | Forme cristalline beta du chlorhydrate de l'ivabradine, son procede de preparation, et les compositions pharmaceutiques qui la contiennent |
FR2882554B1 (fr) * | 2005-02-28 | 2007-05-04 | Servier Lab | Forme critalline beta d du chlorhydrate de l'ivabradine, son procede de preparation, et les compositions pharmaceutiques qui la contiennent |
FR2891827B1 (fr) * | 2005-10-11 | 2007-12-28 | Servier Lab | Forme cristalline deltad du chlorhydrate de l'ivabradine, son procede de preparation, et les compositions pharmaceutiques qui la contiennent |
FR2891826B1 (fr) * | 2005-10-11 | 2007-12-28 | Servier Lab | Forme cristalline 6 du chlorhydrate de l'ivabradine, son procede de preparation et les compositions pharmaceutiques qui la contiennent |
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