CN104510730A - 小体积双氯芬酸钠利多卡因冻干粉针及其制备方法和生产装置 - Google Patents

小体积双氯芬酸钠利多卡因冻干粉针及其制备方法和生产装置 Download PDF

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CN104510730A
CN104510730A CN201310461339.7A CN201310461339A CN104510730A CN 104510730 A CN104510730 A CN 104510730A CN 201310461339 A CN201310461339 A CN 201310461339A CN 104510730 A CN104510730 A CN 104510730A
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diclofenac sodium
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苗得足
张光明
白先杰
司吉晖
张国明
宋忠国
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Reyoung Pharmaceutical Co Ltd
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Abstract

本发明属于冻干粉针及其制备配制方法和设备领域,特别涉及双氯芬酸钠利多卡因冻干粉针及其制备方法和设备领域。所述的小体积双氯芬酸钠利多卡因冻干粉针装在7ml棕色管制西林瓶中,其水痕位置以下体积为2.0ml,其生产装置依次由保温管道连接的保温配药罐、第二格兰富泵、泵棒过滤器、第二除菌滤芯、无菌保温液储罐、第一格兰富泵、第一除菌滤芯、灌装机和冻干机组成。

Description

小体积双氯芬酸钠利多卡因冻干粉针及其制备方法和生产装置
技术领域
本发明属于冻干粉针及其制备配制方法和设备领域,特别涉及双氯芬酸钠利多卡因冻干粉针及其制备方法和设备领域。
背景技术
目前市售的(规格:双氯芬酸钠75mg、利多卡因20mg)双氯芬酸钠利多卡因冻干粉针使用10ml棕色管制西林瓶灌装,从而存在内包装容器体积大,造成每批生产的产品产量低的缺点,由于双氯芬酸钠利多卡因本身的水溶性不好,因而在制备过程中需要用大量的溶剂才可溶解,以便制成双氯芬酸钠利多卡因冻干粉针。原先的配制工艺没有使用超声波助溶,在浓配时溶剂的用量加大,而且加入水量也较大(为主药的100倍水)导致双氯芬酸钠利多卡因析出,从而增大了灌装量致使产品的溶解性不理想、产量降低、冻干含水多能耗增大、包装和运输成本增加。
发明内容
本发明的目的是提供一种小体积双氯芬酸钠利多卡因冻干粉针、制备方法及其生产装置。
本发明所述的一种小体积双氯芬酸钠利多卡因冻干粉针装在7ml棕色管制西林瓶中,其水痕位置以下体积为2.0ml。
本发明所述小体积双氯芬酸钠利多卡因冻干粉针的制备方法,包括以下步骤:
(1)在20℃~25℃将盐酸利多卡因、甘露醇和亚硫酸钠加入水中溶解,得浓配液A;
(2)聚乙二醇4000溶于丙二醇后加双氯芬酸钠,超声波超声30分钟使药物溶解,得B液;
(3)将B液缓慢倒入浓配液A中,调节pH控制在7.5-8.5,搅拌均匀;加入活性炭,搅拌吸附20~40min,用钛棒脱碳过滤,精滤;
(4)20℃~25℃将步骤(3)得到的溶液加水制成稀配液,保温,灌装于7ml棕色管制西林瓶中,冻干,压塞、轧盖即得。
浓配液A中各组分的质量分数为:盐酸利多卡因2%~4%;甘露醇10%~15%;亚硫酸钠0.15%~1%和水82%~86%。
聚乙二醇4000、丙二醇和双氯芬酸钠的质量比为12~18∶4~6∶1。
本发明所述的小体积双氯芬酸钠利多卡因冻干粉针的生产装置,依次由保温管道连接的保温配药罐、第二格兰富泵、泵棒过滤器、第二除菌滤芯、无菌保温液储罐、第一格兰富泵、第一除菌滤芯、灌装机和冻干机组成。
与现有技术相比,本发明具有以下有益效果:
提高了产品质量、有效地增加了产量降低了能耗,减小了包装体积,从而降低了包装、运输成本;降低了灌装量仅为2.0ml,大大降低了冻干蒸发能耗,进一步降低了成本。
附图说明
图1是本发明生产线结构示意图。
图中:1、保温配液罐;2、钛棒过滤器;3、无菌液储罐;4、冻干机;5、灌装机;6、第一格兰富泵;7、第一除菌滤芯;8、第二除菌滤芯;9、第二格兰富泵;10、保温管道。
具体实施方式
以下结合实施例对本发明做进一步描述。
实施例1
针对双氯芬酸钠利多卡因在水中溶解度的性质,筛选不同用量的溶剂、亚硫酸钠、聚乙二醇4000、丙二醇、甘露醇、注射用水和不超声进行对比,结果见表1,并考察溶剂用量改变后、超声对双氯芬酸钠利多卡因和辅料混合溶液稳定性的影响,结果见表2。
表1在不同量的溶剂下溶解24.65g盐酸利多卡因和双氯芬酸钠75g,制成1000支,超声和不超声的那个最好。
表2充分溶解后,相同溶剂不同用量下对主药双氯芬酸钠利多卡因稳定性的影响(含量、有关物质)
从上表可以看出,双氯芬酸钠利多卡因在相同溶剂不同用量的溶剂中溶解通过试验考察超声的2#处方稳定性最好,所以我们选择此处方为最终处方双氯芬酸钠75g盐酸利多卡因24.65g、聚乙二醇-4000730g、丙二醇155g、亚硫酸钠1g、甘露醇75g注射用水800ml。
加入70%处方量注射用水,冷却至20℃,取处方量的盐酸利多卡因、甘露醇和亚硫酸钠,加入容器内开启搅拌溶解,在23±3℃充分搅拌使溶解,得浓配液A;另取一容器称取处方量的聚乙二醇4000、丙二醇,搅拌使聚乙二醇4000熔融后加双氯芬酸钠,超声波超声30分钟使药物溶解(为B液)。将B液缓慢倒入A液中,调节pH控制在8±1,搅拌均匀;称取0.1%(W/V)的活性炭加入,搅拌吸附30min,用钛棒脱碳过滤,精滤,将剩余配制量的注射用水,水温23±3℃)加入配液罐中,通过钛棒过滤后精滤,并与精滤后的浓配液混合制成稀配液,保温23±3℃,灌装于7ml棕色管制西林瓶中,冻干,压塞、轧盖即得。
降制品温度均将至-40℃,制品-40℃维持2小时,将冷凝筒温度降至-45℃后,设定载冷剂温度为-10℃,维持30小时。再升介质25℃,制品到20℃维持2小时,最后干燥后打开箱体的气源开关输入无菌空气,按《冻干机标准操作规程》压塞。
采用此方法制得的小体积双氯芬酸钠利多卡因冻干粉针产品装在7ml棕色管制西林瓶中,达到水痕位置以下体积为2.0ml。

Claims (5)

1.一种小体积双氯芬酸钠利多卡因冻干粉针,其特征在于,所述的小体积双氯芬酸钠利多卡因冻干粉针装在7ml棕色管制西林瓶中,其水痕位置以下体积为2.0ml。
2.一种根据权利要求1所述的小体积双氯芬酸钠利多卡因冻干粉针的制备方法,其特征在于,包括以下步骤:
(1)在20℃~25℃将盐酸利多卡因、甘露醇和亚硫酸钠加入水中溶解,得浓配液A;
(2)聚乙二醇4000溶于丙二醇后加双氯芬酸钠,超声波超声30分钟使药物溶解,得B液;
(3)将B液缓慢倒入A液中,调节pH控制在7.5-8.5,搅拌均匀;加入活性炭,搅拌吸附20~40min,用钛棒脱碳过滤,精滤;
(4)20℃~25℃将步骤(3)得到的溶液加水制成稀配液,保温,灌装于7ml棕色管制西林瓶中,冻干,压塞、轧盖即得。
3.根据权利要求2所述的小体积双氯芬酸钠利多卡因冻干粉针的制备方法,其特征在于,步骤(1)中浓配液A中各组分的质量分数为:盐酸利多卡因2%~4%;甘露醇10%~15%;亚硫酸钠0.15%~1%和水82%~86%。
4.根据权利要求2所述的小体积双氯芬酸钠利多卡因冻干粉针的制备方法,其特征在于,聚乙二醇4000、丙二醇和双氯芬酸钠的质量比为12~18∶4~6∶1。
5.一种根据权利要求1所述的小体积双氯芬酸钠利多卡因冻干粉针的生产装置,其特征在于,依次由保温管道连接的保温配药罐、第二格兰富泵、泵棒过滤器、第二除菌滤芯、无菌保温液储罐、第一格兰富泵、第一除菌滤芯、灌装机和冻干机组成。
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Cited By (1)

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CN115682646A (zh) * 2022-11-22 2023-02-03 中玉制药(海口)有限公司 注射用双氯芬酸钠利多卡因冻干设备及其制备方法

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CN102743344A (zh) * 2012-06-25 2012-10-24 瑞阳制药有限公司 小体积炎琥宁冻干粉针及其制备方法、生产装置
CN102743346A (zh) * 2012-06-25 2012-10-24 瑞阳制药有限公司 小体积脂溶性维生素冻干粉针制备方法及其制备装置

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Publication number Priority date Publication date Assignee Title
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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN115682646A (zh) * 2022-11-22 2023-02-03 中玉制药(海口)有限公司 注射用双氯芬酸钠利多卡因冻干设备及其制备方法
CN115682646B (zh) * 2022-11-22 2024-05-14 中玉制药(海口)有限公司 注射用双氯芬酸钠利多卡因冻干设备及其制备方法

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