Author:
Hecq Jean-Daniel,Bihin Benoit,Jamart Jacques,Galanti Laurence
Abstract
AbstractIn hospitals, a major part of the drugs is administered via the intravenous route. When one wants to evaluate or know the stability of a drug in solution, it is necessary to know several physico-chemical parameters. Several reference works are available to help the hospital pharmacist with this research. However, reading these different sources can make you discover conflicting data. It is therefore necessary at this time to obtain the publications with contradictory results and to read them again. Seven criteria have been identified for judging the quality of a publication on physicochemical stability: full description of equipment, methods and analytical conditions of molecules studied; complete description of the procedures used to validate the analytical method; full indication of time testing and measurement bases or control; documentation on the analytical reproducibility; adequate statistical analysis; appropriate conclusions; appropriate references. In conclusion, everything in a compatibility study is important.
Subject
Pharmacology (medical),Pharmacology,Pharmacy
Reference84 articles.
1. Evaluating intravenous compatibility literature;New-York Health-System Pharmacist,2002
2. Website www stabilis org;Vigneron
3. Guidelines for the practical stability studies of anticancer drugs: A european consensus conference;Ann Pharm Fr,2011
4. Practical aspects of the stability testing of formulated drug products;Aust J Hosp Pharm,1995
Cited by
3 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献