海峡药学
海峽藥學
해협약학
Strait Pharmaceutical Journal
2015年
9期
12-15
,共4页
曹春来%马瑞%张家行%张伟%蒋振东%肖拥军
曹春來%馬瑞%張傢行%張偉%蔣振東%肖擁軍
조춘래%마서%장가행%장위%장진동%초옹군
门冬胰岛素%结晶方法%回收率
門鼕胰島素%結晶方法%迴收率
문동이도소%결정방법%회수솔
Insulin aspart%Crystallization method%Recovery rate
目的:本文旨在初步研究出一种稳定的门冬胰岛素结晶制备的方法,优化生产工艺,降低生产成本,减少原料药生产过程中的损失,提高门冬胰岛素的稳定性,为制剂提供优质的原料药产品。方法在室温下经过有机酸对比,有机溶剂以及其他胰岛素结晶所必须添加的物质的选择,再经过一系列对比实验优化,并通过显微镜图片分析,要求晶型稳定均一性好,晶体形状规则;超高效液相色谱仪(HPLC)检测,各项指标符合药典标准,继而找到一种稳定且结晶收率高的方案。结果研究发现有机酸宜选用0.5M ~1.5M 的甘氨酸,同时采用体积分数12%~18%的乙腈、体积分数为0.2%~0.3%的苯酚、0.2~0.3M氯化钠溶液以及含2.0~5.0g· L -1重组门冬胰岛素,在初始pH为6.0~6.5的条件下加入醋酸锌组成的结晶液,经放大验证得到单斜针状晶体,形状规则均一,结晶收率可达99%以上。结论通过以上实验表明,门冬胰岛素原料药的结晶方法符合生产要求,结晶收率良好,易于工业化生产,可为制剂提供优质的原料药。
目的:本文旨在初步研究齣一種穩定的門鼕胰島素結晶製備的方法,優化生產工藝,降低生產成本,減少原料藥生產過程中的損失,提高門鼕胰島素的穩定性,為製劑提供優質的原料藥產品。方法在室溫下經過有機痠對比,有機溶劑以及其他胰島素結晶所必鬚添加的物質的選擇,再經過一繫列對比實驗優化,併通過顯微鏡圖片分析,要求晶型穩定均一性好,晶體形狀規則;超高效液相色譜儀(HPLC)檢測,各項指標符閤藥典標準,繼而找到一種穩定且結晶收率高的方案。結果研究髮現有機痠宜選用0.5M ~1.5M 的甘氨痠,同時採用體積分數12%~18%的乙腈、體積分數為0.2%~0.3%的苯酚、0.2~0.3M氯化鈉溶液以及含2.0~5.0g· L -1重組門鼕胰島素,在初始pH為6.0~6.5的條件下加入醋痠鋅組成的結晶液,經放大驗證得到單斜針狀晶體,形狀規則均一,結晶收率可達99%以上。結論通過以上實驗錶明,門鼕胰島素原料藥的結晶方法符閤生產要求,結晶收率良好,易于工業化生產,可為製劑提供優質的原料藥。
목적:본문지재초보연구출일충은정적문동이도소결정제비적방법,우화생산공예,강저생산성본,감소원료약생산과정중적손실,제고문동이도소적은정성,위제제제공우질적원료약산품。방법재실온하경과유궤산대비,유궤용제이급기타이도소결정소필수첨가적물질적선택,재경과일계렬대비실험우화,병통과현미경도편분석,요구정형은정균일성호,정체형상규칙;초고효액상색보의(HPLC)검측,각항지표부합약전표준,계이조도일충은정차결정수솔고적방안。결과연구발현유궤산의선용0.5M ~1.5M 적감안산,동시채용체적분수12%~18%적을정、체적분수위0.2%~0.3%적분분、0.2~0.3M록화납용액이급함2.0~5.0g· L -1중조문동이도소,재초시pH위6.0~6.5적조건하가입작산자조성적결정액,경방대험증득도단사침상정체,형상규칙균일,결정수솔가체99%이상。결론통과이상실험표명,문동이도소원료약적결정방법부합생산요구,결정수솔량호,역우공업화생산,가위제제제공우질적원료약。
ABSTRACT:OBJECTIVE To study a kind of preparation method for the stable crystalline insulin aspart optimize production processes.Reduce production costs , reduce the loss of raw material medicine in production process , im-prove the stability of insulin aspart ,and provide high quality raw material medicine for the preparation.METHODS Compared by organic acid at room temperature.Selected the organic solvent and other insulin crystal material ,and then through a series of comparative experiments and optimization ,through the microscope image analysis for stable crystal form,good uniformity,crystal shape;ultra performance liquid chromatography ( HPLC) detection,the indica-tors are in line with the standard of Chinese Pharmacopoeia ,and then find a stable solution that the crystallization is of high yield.RESULTS The study found that organic acid should be selected as the best 0.5M~1.5M of glycine, at the same time ,using acetonitrile volume fraction of the volume fraction of 12%~18%,0.2~0.3%of phenol ,0.2~0.3 M Sodium Chloride Solution 2.0~5.0 g· L-1 containing recombinant insulin aspart ,crystallization solution at the initial pH to 6.0~6.5 under the conditions of adding zinc acetate.After amplification ,verification of monoclinic crystal regular shape ,uniform,the crystallization yield can reach more than 99%.CONCLUSION Through the a-bove experiments show that the method of crystallization ,insulin aspart raw materials meet the requirements of pro-duction,the yield of crystallization is good ,and it is easy for industrialized production ,can provide raw materials for preparation of high quality.