医学信息
醫學信息
의학신식
MEDICAL INFORMATION
2015年
3期
21-22
,共2页
石蕊%杨慧%肖芳芳%苏林飞%赵可新%胡建平
石蕊%楊慧%肖芳芳%囌林飛%趙可新%鬍建平
석예%양혜%초방방%소림비%조가신%호건평
配伍禁忌%合理用药%注射用盐酸氨溴索%注射用更昔洛韦钠%pH值
配伍禁忌%閤理用藥%註射用鹽痠氨溴索%註射用更昔洛韋鈉%pH值
배오금기%합리용약%주사용염산안추색%주사용경석락위납%pH치
Compatible%Rational drug use%Ambroxol hydrochloride injection%Ganciclovir sodium injection%pH value
目的:考察注射用盐酸氨溴索、更昔洛韦钠与8种溶媒配伍稳定性,并将二者配伍观察溶液稳定性,为临床合理用药提供参考。方法观察2种药物在0.9%氯化钠、5%葡萄糖、10%葡萄糖、复方氯化钠、葡萄糖氯化钠、木糖醇氯化钠、小儿电解质补给注射液和灭菌注射用水8种溶媒中以临床常用浓度溶解后0、0.5、1、2、4、6、8 h的pH值,观察2种溶液等体积混合和盐酸氨溴索以入壶给药加入到更昔洛韦钠的溶液中颜色、透明度的变化。结果8种溶媒和盐酸氨溴索溶液在8 h内pH值的RSD均在0~2.30%,更昔洛韦钠溶液的pH值的RSD在0~1.2%。2种药物等体积混合后均可见白色颗粒物。盐酸氨溴索入壶给药后立即产生白色沉淀。三组溶液在0~8 h的平均pH值分别进行检验,≤0.05,无显著性差异。结论三组溶液pH值在8 h内稳定,2种药物在8种溶媒中溶解后两两混合存在配伍禁忌,临床应用应注意。
目的:攷察註射用鹽痠氨溴索、更昔洛韋鈉與8種溶媒配伍穩定性,併將二者配伍觀察溶液穩定性,為臨床閤理用藥提供參攷。方法觀察2種藥物在0.9%氯化鈉、5%葡萄糖、10%葡萄糖、複方氯化鈉、葡萄糖氯化鈉、木糖醇氯化鈉、小兒電解質補給註射液和滅菌註射用水8種溶媒中以臨床常用濃度溶解後0、0.5、1、2、4、6、8 h的pH值,觀察2種溶液等體積混閤和鹽痠氨溴索以入壺給藥加入到更昔洛韋鈉的溶液中顏色、透明度的變化。結果8種溶媒和鹽痠氨溴索溶液在8 h內pH值的RSD均在0~2.30%,更昔洛韋鈉溶液的pH值的RSD在0~1.2%。2種藥物等體積混閤後均可見白色顆粒物。鹽痠氨溴索入壺給藥後立即產生白色沉澱。三組溶液在0~8 h的平均pH值分彆進行檢驗,≤0.05,無顯著性差異。結論三組溶液pH值在8 h內穩定,2種藥物在8種溶媒中溶解後兩兩混閤存在配伍禁忌,臨床應用應註意。
목적:고찰주사용염산안추색、경석락위납여8충용매배오은정성,병장이자배오관찰용액은정성,위림상합리용약제공삼고。방법관찰2충약물재0.9%록화납、5%포도당、10%포도당、복방록화납、포도당록화납、목당순록화납、소인전해질보급주사액화멸균주사용수8충용매중이림상상용농도용해후0、0.5、1、2、4、6、8 h적pH치,관찰2충용액등체적혼합화염산안추색이입호급약가입도경석락위납적용액중안색、투명도적변화。결과8충용매화염산안추색용액재8 h내pH치적RSD균재0~2.30%,경석락위납용액적pH치적RSD재0~1.2%。2충약물등체적혼합후균가견백색과립물。염산안추색입호급약후립즉산생백색침정。삼조용액재0~8 h적평균pH치분별진행검험,≤0.05,무현저성차이。결론삼조용액pH치재8 h내은정,2충약물재8충용매중용해후량량혼합존재배오금기,림상응용응주의。
Objective To investigated the compatible stability of Ambroxol hydrochloride injection and Ganciclovir sodium injection in 8 solutions and to improve the rational use in the clinic. Methods The pH value of the compatible stability of the 2 injections in 8 solutions were determined within 0-8 h, respectively. The changes of color and transparency were observed after the 2 injections were mixed equal y at room temperature. Results The range of the relative standard deviation (RSD) of the pH value of the 8 solutions and the Ambroxol hydrochloride were between 0~2.3%in 8 h, respectively. The ganciclovir sodium was 0~1.2%. The white precipitate was observed when the ambroxol hydrochloride injection was mixed with ganciclovir sodium injection by the way of going into pot. The P value of the t test for the 3 groups were al less than 0.05. Conclusion The pH value of the 3 groups were al stable in 8 h. Ambroxol hydrochloride injection was shown to be incompatible with ganciclovir sodium injection in the 8 solutions.