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CN1115979A - 维生素d类似物的新晶形 - Google Patents

维生素d类似物的新晶形 Download PDF

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CN1115979A
CN1115979A CN94190868A CN94190817A CN1115979A CN 1115979 A CN1115979 A CN 1115979A CN 94190868 A CN94190868 A CN 94190868A CN 94190817 A CN94190817 A CN 94190817A CN 1115979 A CN1115979 A CN 1115979A
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calcipotriol
hydrate
crystalline form
vitamin
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CN1040746C (zh
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E·T·汉森
N·S·拉特楚·安德森
L·H·灵博格
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    • C07C401/00—Irradiation products of cholesterol or its derivatives; Vitamin D derivatives, 9,10-seco cyclopenta[a]phenanthrene or analogues obtained by chemical preparation without irradiation
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00—Drugs for dermatological disorders
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00—Drugs for dermatological disorders
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    • A—HUMAN NECESSITIES
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    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C5/00—Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms
    • C07C5/32—Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms by dehydrogenation with formation of free hydrogen
    • C07C5/321—Catalytic processes
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    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C5/00—Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms
    • C07C5/32—Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms by dehydrogenation with formation of free hydrogen
    • C07C5/327—Formation of non-aromatic carbon-to-carbon double bonds only
    • C07C5/333—Catalytic processes
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C5/00—Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms
    • C07C5/32—Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms by dehydrogenation with formation of free hydrogen
    • C07C5/327—Formation of non-aromatic carbon-to-carbon double bonds only
    • C07C5/333—Catalytic processes
    • C07C5/3335—Catalytic processes with metals
    • C07C5/3337—Catalytic processes with metals of the platinum group
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
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    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
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    • B01J2219/0277—Metal based
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    • C07—ORGANIC CHEMISTRY
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    • C07C2523/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00
    • C07C2523/38—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00 of noble metals
    • C07C2523/40—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00 of noble metals of the platinum group metals
    • C07C2523/42—Platinum

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Abstract

本发明涉及Calcipotriol水合物，一种Calcipotriol的新晶形，具有优越的技术性能和高稳定性。

Description

维生素D类似物的新晶形
本发明涉及一种在结晶悬液制剂的生产中有优越技术特征并具有优越的稳定性能的Calcipotriol水合物—一种Calcipotriol的新晶形。
国际申请NO.PCT/DK86/00081，申请日为1986年7月14日，公开号为WO87/00834，描述了Calcipotriol(INN)(Calcipotriene(US-AN)，(1α，3β，5Z、7E、22E、24S)—24—环丙基—9，10—开环胆甾—5，7—10(19)，22—四烯—1，3，24—三醇)。
Calcipotriol具有优异的生物活性形象，已证明如在局部治疗牛皮癣中非常有用。
由于Calcipotriol在某些溶液中稳定性差，其在某些剂型，特别是霜剂和凝胶中，优选使用结晶悬液。
为了制备适当的结晶悬液制剂，必须能够控制结晶大小，该参数对于得到化合物从制剂中可重复地释放是很重要的。结晶的整体药物在制成最终悬浮液制剂前，一般进行微粒化或进行湿碾磨加工，以减小结晶大小。
对于Calcipotriol，已使用了湿球碾磨加工。当用WO87/00834中描述的无水晶形进行此加工时，已证明在技术上是困难的。这些结晶不易湿润，在碾磨过程中，它们产生稳定的泡沫，这给得到适当的小而均一的颗粒大小带来了困难。
现令人惊异地发现，当使用在此以前未知的Calcipotriol晶形，即Calcipotriol水合物，代替已知的无水晶形时，可以避免这些技术困难。此水合物在技术上优于无水物；它易于湿润，可顺利地进行湿球碾磨加工。
该新产品是Calcipotriol的单水合物，结晶完美、稳定，特别适用于现代治疗中。
稳定性研究表明Calcipotriol水合物令人惊异地稳定，这由40℃的稳定性数据证明。
在此温度下，无水形式的Calcipotriol显示相当程度的分解，在贮存12个月后，发现30％以上的分解。
相反，本发明的化合物—Calcipotriol水合物—在40℃贮存12个月后没有显示分解。
Calcipotriol单水合物可通过将结晶或非结晶Calcipotriol溶解在有机溶剂如乙酸乙酯或丙酮中，然后加入水和任选地加入非极性溶剂如己烷来制备。
Calcipotriol单水合物应形成局部使用的部分药物制剂，如霜剂、软膏、溶液、洗液或凝胶。活性成分的浓度一般将为1—100μg/g。
这些制剂每天可施用一次或多次。
根据本发明制得的制剂包括活性化合物以及药学上可接受的载体和任选的其它治疗成分。载体必须是“可接受的”，意即与制剂的其它成分相容，而不使其接受性变差。
适于局部施用的制剂包括液体或半液体制剂，如搽剂、洗剂、敷剂，水包油或油包水乳剂如霜剂、软膏、糊剂或凝胶；或溶液或悬液。
除了上述提到的成分以外，本发明的制剂还包括一种或多种添加成分，如稀释剂、缓冲液、表面活性剂、增稠剂、润滑剂、防腐剂如羟基苯甲酸甲酯(包括抗氧化剂)、乳化剂等。
在下列非限定性实施例中将进一步说明本发明。
实施例1
将Calcipotriol(2.5g)溶解在50—80℃的乙酸乙酯中，过滤。该溶液用水饱和，自发冷却至室温后，沉淀出了产物。将形成的浆液冷却至0—10℃，过滤。将滤出的产物真空干燥，得到Calcipotriol水合物(2.35g)。
lR光谱(KBr)
该水合物的特征峰分别为1455(m)、1442(m)、1330(W)、1290(m)、1210(m)、1085(m)、907(m)、895(m)和573(W)cm-1。
固态CPMAS(Cross Polarization angle Mugle Spinning)NMR
Calcipotriol水合物的特征共振如下：147.9，146.5，134.8，130.3，129.0，126.5，116.0，109.4，75.5，68.2，67.2，56.9，55.2，47.8，47.5，42.9，42.0，41.3，30.7，28.9，25.6，23.1，22.6，19.5，14.6，6.2和1.9ppm。
示差扫描量热法(DSC)
Perkin Elmer DSC7仪，20℃/分，约2mg样品，该水合物在近117℃失水，在近169.7℃显示熔化峰。
实施例2
将Calcipotriol(22.7g)溶解在甲醇(200—250ml)中，过滤并真空浓缩，将残余物于50—80℃溶解在乙酸乙酯中(200—250ml)，加入水(2ml)。向形成的溶液中加入Calcipotriol水合物晶种，自动冷却至室温，产物沉淀。从滴液漏斗加入己烷(100ml)，冷却形成的浆液至0—10℃，过滤。
滤出的产物用乙酸乙酯和己烷的1∶1混合物(200ml)洗涤，真空干燥，得到Calcipotriol水合物(19.7g)，表明与实施例1中所述产物相同。
实施例3
将Calcipotriol(120mg)溶解在丙酮(2ml)中，加入水(1.5—3ml)。产物自动结晶，将形成的浆液冷却至0—10℃，过滤，将滤出的产物真空干燥，得到Calcipotriol水合物(100mg)，表明其与实施例1中所述产物相同。
实施例4
霜剂50μg/g
Calcipotriol水合物                         50mg
Cetomacrogol 1000                           30g
Cetostearylalcohol                          60g
氯代烯丙基六铵氯化物                       0.5g
丙二醇                                      30g
磷酸氢二钠                                   2g
液体石蜡                                    50g
白软石蜡                                   170g
纯水                                  加至1000g
在75℃将Cetomacrogol 1000。Cetostearylalcohol、液体石蜡和白软石蜡熔化。将丙二醇溶解在75℃水中，将此溶液与脂肪相混合。将此乳液均质化，并冷却至30℃。将Calcipotriol水合物在部分水相中碾磨，使颗粒大小大部分小于10μm，并悬浮在磷酸氢二钠和氯代烯丙基六铵氯化物的水溶液中。将此悬液加到乳液中，将此霜剂填充在管中。实施例5凝胶50μg/g
Calcipotriol水合物                          52.2mg
(相当于50mg无水物)
Carbomer                                        7g
Cetomacrogol 1000                               1g
二氮戊环基脲                                    2g
二氯苄醇                                        1g
乙二胺四乙酸二钠盐                            0.5g
氢氧化钠                                      3.7g
丙二醇                                         30g
纯水                                     加至1000g
将Cetomacrogol、二氮戊环基脲、二氯苄醇、乙二胺四乙酸二钠盐和丙二醇溶解在水中。加入Carbomer，高速均化。搅拌下加入溶解在部分水中的氢氧化钠。在一瓶水中用玻璃珠碾磨Calcipotriol水合物，直到得到小于10μm大小的颗粒。将此Calcipotriol水合物悬液加到凝胶中，混合30分钟。将此凝胶装入可折迭管中。

Claims (5)

1.Calcipotriol，(1α，3β，5Z，7E，22E，24S)—24—环丙基—9，10—开环胆甾—5，7，10(19)，22—四烯—1，3，24—三醇，单水合物。
2.含有权利要求1的化合物的药物组合物。
3.权利要求2的药物组合物，其为霜剂。
4.权利要求2的药物组合物，其为凝胶。
5.权利要求2—4中任一项的药物组合物，其中活性成分的含量为1—100μg/g组合物。
CN94190817A 1993-01-15 1994-01-07 维生素d类似物的新晶形 Expired - Lifetime CN1040746C (zh)

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GB9300763.1 1993-01-15
GB939300763A GB9300763D0 (en) 1993-01-15 1993-01-15 Chemical compound
PCT/DK1994/000011 WO1994015912A1 (en) 1993-01-15 1994-01-07 New crystalline form of a vitamin d analogue

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CN1115979A true CN1115979A (zh) 1996-01-31
CN1040746C CN1040746C (zh) 1998-11-18

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EP (1) EP0679154B1 (zh)
JP (1) JP3729847B2 (zh)
KR (1) KR100309751B1 (zh)
CN (1) CN1040746C (zh)
AT (1) ATE159717T1 (zh)
AU (1) AU663249B2 (zh)
CA (1) CA2151730C (zh)
DE (1) DE69406529T2 (zh)
DK (1) DK0679154T3 (zh)
ES (1) ES2111287T3 (zh)
FI (1) FI108638B (zh)
GB (1) GB9300763D0 (zh)
GR (1) GR3025668T3 (zh)
NZ (1) NZ259679A (zh)
RU (1) RU2128646C1 (zh)
WO (1) WO1994015912A1 (zh)

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CN101400649B (zh) * 2006-03-17 2012-07-04 利奥制药有限公司 药物中间体的异构化

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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101001835B (zh) * 2004-09-01 2010-09-08 利奥制药有限公司 烯丙醇的差向异构化
CN101400649B (zh) * 2006-03-17 2012-07-04 利奥制药有限公司 药物中间体的异构化

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FI108638B (fi) 2002-02-28
JPH08505612A (ja) 1996-06-18
CA2151730C (en) 2005-01-04
KR100309751B1 (ko) 2002-11-08
GR3025668T3 (en) 1998-03-31
AU5857394A (en) 1994-08-15
DK0679154T3 (da) 1998-03-30
FI952797A0 (fi) 1995-06-07
KR950704249A (ko) 1995-11-17
GB9300763D0 (en) 1993-03-03
EP0679154B1 (en) 1997-10-29
DE69406529D1 (de) 1997-12-04
RU95116650A (ru) 1997-06-10
RU2128646C1 (ru) 1999-04-10
WO1994015912A1 (en) 1994-07-21
EP0679154A1 (en) 1995-11-02
USRE39706E1 (en) 2007-06-26
ATE159717T1 (de) 1997-11-15
JP3729847B2 (ja) 2005-12-21
ES2111287T3 (es) 1998-03-01
DE69406529T2 (de) 1998-05-28
NZ259679A (en) 1996-11-26
US5763426A (en) 1998-06-09
AU663249B2 (en) 1995-09-28
CN1040746C (zh) 1998-11-18
FI952797A (fi) 1995-06-07
CA2151730A1 (en) 1994-07-21

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