CN109464407A - 瑞舒伐他汀钙快速释放制剂及其制备方法 - Google Patents
瑞舒伐他汀钙快速释放制剂及其制备方法 Download PDFInfo
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- 235000019359 magnesium stearate Nutrition 0.000 claims abstract description 7
- 239000002245 particle Substances 0.000 claims abstract description 7
- 238000002156 mixing Methods 0.000 claims abstract description 6
- 229920002785 Croscarmellose sodium Polymers 0.000 claims abstract description 5
- DPXJVFZANSGRMM-UHFFFAOYSA-N acetic acid;2,3,4,5,6-pentahydroxyhexanal;sodium Chemical compound [Na].CC(O)=O.OCC(O)C(O)C(O)C(O)C=O DPXJVFZANSGRMM-UHFFFAOYSA-N 0.000 claims abstract description 5
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- 206010013786 Dry skin Diseases 0.000 claims abstract description 4
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- 239000007864 aqueous solution Substances 0.000 claims abstract description 4
- 238000001035 drying Methods 0.000 claims abstract description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 4
- FUFJGUQYACFECW-UHFFFAOYSA-L calcium hydrogenphosphate Chemical compound [Ca+2].OP([O-])([O-])=O FUFJGUQYACFECW-UHFFFAOYSA-L 0.000 claims abstract 3
- 235000019700 dicalcium phosphate Nutrition 0.000 claims abstract 3
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 claims description 8
- 230000015572 biosynthetic process Effects 0.000 claims description 6
- 229940088417 precipitated calcium carbonate Drugs 0.000 claims description 6
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- 238000005469 granulation Methods 0.000 abstract description 3
- 230000003179 granulation Effects 0.000 abstract description 3
- 210000002784 stomach Anatomy 0.000 abstract description 3
- 230000009286 beneficial effect Effects 0.000 abstract 1
- 239000003795 chemical substances by application Substances 0.000 description 5
- 239000003814 drug Substances 0.000 description 3
- 229940079593 drug Drugs 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N phosphoric acid Substances OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- -1 phosphoric acid hydrogen Chemical class 0.000 description 2
- 208000032928 Dyslipidaemia Diseases 0.000 description 1
- 208000035150 Hypercholesterolemia Diseases 0.000 description 1
- 208000000563 Hyperlipoproteinemia Type II Diseases 0.000 description 1
- 102100024640 Low-density lipoprotein receptor Human genes 0.000 description 1
- 206010045261 Type IIa hyperlipidaemia Diseases 0.000 description 1
- 238000009098 adjuvant therapy Methods 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
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- 238000000354 decomposition reaction Methods 0.000 description 1
- 235000001916 dieting Nutrition 0.000 description 1
- 230000037228 dieting effect Effects 0.000 description 1
- 201000001386 familial hypercholesterolemia Diseases 0.000 description 1
- 210000004211 gastric acid Anatomy 0.000 description 1
- 239000002471 hydroxymethylglutaryl coenzyme A reductase inhibitor Substances 0.000 description 1
- 238000012856 packing Methods 0.000 description 1
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Abstract
本发明涉及瑞舒伐他汀钙快速释放制剂的制备方法,步骤为:S1,先将舒伐他汀钙与微晶纤维素101,再与交联羧甲纤维素钠、磷酸氢钙混合,形成混合物,再将含有10%的低取代羟丙纤维素水溶液作为粘合剂倒入步骤S1中的混合物中,形成软材;S2,将软材用30目筛的制粒,保持50~55℃干燥,水分控制在3%~4%;S3,将步骤S2中的干燥颗粒与硬脂酸镁混合均匀后压片制成片芯;S4,将包衣粉和水配制成10%~13%的包衣液,对步骤S3中的片芯进行包衣。还公开了瑞舒伐他汀钙快速释放制剂。本发明达到的有益效果是:提高胃中溶出速度及生物利用度。
Description
技术领域
本发明涉及生物医学领域,特别是瑞舒伐他汀钙快速释放制剂及其制备方法。
背景技术
瑞舒伐他汀钙是一种选择性HMG-CoA还原酶抑制剂,适用于原发性高胆固醇血症(Ⅱa型,包括杂合子家族性高胆固醇血症)或混合性脂血障碍(Ⅱb型)患者在节食或锻炼疗法不理想时的辅助治疗。
但是瑞舒伐他汀钙为难溶性药物,传统的释放剂制备时是将硬脂酸镁和活性成分(瑞舒伐他汀钙)进行混合,虽然硬脂酸镁在胃酸的作用下也会分解,但是其分解速度影响溶出速度。
发明内容
本发明的目的在于克服现有技术的缺点,提供提高服口感、提高胃中溶出速度的瑞舒伐他汀钙快速释放制剂及其制备方法。
本发明的目的通过以下技术方案来实现:瑞舒伐他汀钙快速释放制剂,按重量份算,包括:
所述的微晶纤维素101选用喷雾干燥的形成品;
所述的轻质碳酸钙,选用D90为10~30μm;
所述的舒伐他汀钙,选用D90为35~55μm。
瑞舒伐他汀钙快速释放制剂的制备方法,步骤为:
S1,初步混合,先将舒伐他汀钙与微晶纤维素101,再与交联羧甲纤维素钠、磷酸氢钙混合,形成混合物,再将含有10%的低取代羟丙纤维素水溶液作为粘合剂倒入步骤S1中的混合物中,制成软材;
S2,将软材制作成30目筛的制粒,保持在50~55℃干燥,干燥颗粒水分控制在3%~4%;
S3,将步骤S2中的干燥颗粒与硬脂酸镁混合均匀压片;
S4,将包衣粉和水配制成10%~13%的包衣液,利用该包衣液对步骤S3压成的片进行包衣。
所述的包衣粉选用卡乐康Y-1-7000包衣粉。
本发明具有以下优点:本方案中:微晶纤维素101选用喷雾干燥的形成品、选用轻质碳酸钙且要求D90为10~30μm、舒伐他汀钙要求选用D90为35~55μm;能有效提高胃中溶出速度及生物利用度。
具体实施方式
下面对本发明做进一步的描述,但本发明的保护范围不局限于以下所述。
瑞舒伐他汀钙快速释放制剂的制备方法,步骤为:
步骤为:
S1,初步混合,先将舒伐他汀钙与微晶纤维素101,再与交联羧甲纤维素钠、磷酸氢钙混合,形成混合物,再将含有10%的低取代羟丙纤维素水溶液作为粘合剂倒入步骤S1中的混合物中,形成软材;
S2,将软材制作成30目筛的制粒,保持在50~55℃干燥,干燥颗粒水分控制在3%~4%;
S3,将硬脂酸镁加入S2干燥颗粒中,混合均匀后戊制成片;
S4,将包衣粉和水配制成10%~13%的包衣液,利用该包衣液对步骤S3片芯进行包衣。
本方案中,所述的包衣粉选用卡乐康Y-1-7000包衣粉。
【实施例一】瑞舒伐他汀钙快速释放制剂法
按重量份算,包括:
进一步地,所述的微晶纤维素101选用喷雾干燥的形成品。
本实施例中,轻质碳酸钙,选用D90为10μm;舒伐他汀钙,选用D90为35μm。
【实施例二】瑞舒伐他汀钙快速释放制剂
按重量份算,包括:
进一步地,所述的微晶纤维素101选用喷雾干燥的形成品。
本实施例中,轻质碳酸钙,选用D90为20μm;舒伐他汀钙,选用D90为45μm。
【实施例三】瑞舒伐他汀钙快速释放制剂
按重量份算,包括:
进一步地,所述的微晶纤维素101选用喷雾干燥的形成品;
本实施例中,轻质碳酸钙,选用D90为30μm;舒伐他汀钙,选用D90为55μm。
将实施例一、实施例二和实施例三中的试验释放制剂,与原研阿斯利康制药有限公司分装(国药准字J20120006,批号:X159178)的对比释放剂,进行溶出实验对比。分别选取5min、10min、20min、30min、45min、60min七个时间点进行测量,测量计算平均溶出度如表一所示。
从表一中可以看出:实施例一、实施例二和实施例三三个试验释放制剂,在5min~45min的溶解初期,其溶解速度明显比对比释放剂溶解块;从45min开始,溶出度逐步被赶上,到60min,基本完全溶出后,两者的溶出度基本接近。说明被释放剂的释放速度是优于原研阿斯利康制药有限公司分装(国药准字J20120006,批号:X159178)的对比释放剂的,且后期溶出度也基本接近,本方案不仅合格且比释放速度快。
表一
| 时间点 | 实施例1 | 实施例2 | 实施例3 | 原研阿斯利康 |
| 5min | 64.3% | 67.5% | 63.8% | 60.3% |
| 10min | 86.2% | 87.2% | 85.9% | 81.7% |
| 20min | 90.1% | 91.1% | 89.6% | 87.2% |
| 30min | 92.2% | 93.5% | 91.7% | 88.8% |
| 45min | 94.0% | 95.6% | 94.7% | 94.4% |
| 60min | 96.9% | 98.1% | 96.6% | 97.7% |
Claims (3)
1.瑞舒伐他汀钙快速释放制剂,其特征在于:按重量份算,包括:
舒伐他汀钙 5~20重量份, 交联羧甲纤维素钠 3~9重量份,
磷酸氢钙 40~60重量份, 轻质碳酸钙 20~30重量份,
微晶纤维素101 40~60重量份, 低取代羟丙纤维素 6~10重量份,
硬脂酸镁 1~2重量份, 包衣粉 1~3重量份;
所述的微晶纤维素101选用喷雾干燥的形成品;
所述的轻质碳酸钙,选用D90为10~30μm;
所述的舒伐他汀钙,选用D90为35~55μm。
2.瑞舒伐他汀钙快速释放制剂的制备方法,其特征在于:步骤为:
S1,初步混合,先将舒伐他汀钙与微晶纤维素101,再与交联羧甲纤维素钠、磷酸氢钙混合,形成混合物,再将含有10%的低取代羟丙纤维素水溶液作为粘合剂倒入步骤S1中的混合物中,形成软材;
S2,将软材通过30目筛制粒,保持在50~55℃干燥,干燥颗粒水分控制在3%~4%;
S3,将步骤S2中的干燥颗粒加入硬脂酸镁混合均匀后压制成片芯;
S4,将包衣粉和水配制成10%~13%的包衣液,利用该包衣液对步骤S3制得的片芯进行包衣。
3.根据权利要求2所述的瑞舒伐他汀钙快速释放制剂的制备方法,其特征在于:所述的包衣粉选用卡乐康Y-1-7000包衣粉。
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Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20070202159A1 (en) * | 2006-02-02 | 2007-08-30 | Mathur Rajeev S | Pharmaceutical composition comprising stabilized statin particles |
| CN104398484A (zh) * | 2014-12-04 | 2015-03-11 | 石家庄四药有限公司 | 瑞舒伐他汀钙片及其制备方法 |
| CN104473899A (zh) * | 2014-12-19 | 2015-04-01 | 河南润弘制药股份有限公司 | 一种瑞舒伐他汀钙片剂及其制备方法 |
| WO2017003186A1 (en) * | 2015-06-30 | 2017-01-05 | Hanmi Pharm. Co., Ltd. | Pharmaceutical complex formulation comprising amlodipine, losartan and rosuvastatin |
| CN108785266A (zh) * | 2018-08-13 | 2018-11-13 | 江苏悦兴医药技术有限公司 | 一种瑞舒伐他汀钙片剂及其制备方法 |
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Patent Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20070202159A1 (en) * | 2006-02-02 | 2007-08-30 | Mathur Rajeev S | Pharmaceutical composition comprising stabilized statin particles |
| CN104398484A (zh) * | 2014-12-04 | 2015-03-11 | 石家庄四药有限公司 | 瑞舒伐他汀钙片及其制备方法 |
| CN104473899A (zh) * | 2014-12-19 | 2015-04-01 | 河南润弘制药股份有限公司 | 一种瑞舒伐他汀钙片剂及其制备方法 |
| WO2017003186A1 (en) * | 2015-06-30 | 2017-01-05 | Hanmi Pharm. Co., Ltd. | Pharmaceutical complex formulation comprising amlodipine, losartan and rosuvastatin |
| CN108785266A (zh) * | 2018-08-13 | 2018-11-13 | 江苏悦兴医药技术有限公司 | 一种瑞舒伐他汀钙片剂及其制备方法 |
Non-Patent Citations (1)
| Title |
|---|
| PAVAN RAM KAMBLE1等: ""Application of Liquisolid Technology for Enhancing Solubility and Dissolution of Rosuvastatin"", 《ADVANCED PHARMACEUTICAL BULLETIN》 * |
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Application publication date: 20190315 |