Laboratory of Galenic Pharmacy and Biopharmacy, Bordeaux 2 University, France.
Int J Pharm. 2010 Aug 16;395(1-2):198-204.
Artemisinin-based combination therapies, including artesunate (AS) + amodiaquine (AQ), are the currently recommended first-line treatment of uncomplicated falciparum malaria. Fixed-dose co-formulations offer logistic and adherence advantages. This paper reports the initial research phase of the pre-development process of an AS-AQ formulation, further developed by the Drug for Neglected Diseases Initiative (DNDi). Results demonstrate that AS and AQ are not compatible, and AS degradation is related to three main parameters: water content (>1%), elevated temperature (80 degrees C in dry condition) and possibly the 4-aminoquinoline moiety. Furthermore, AS and AQ incompatibility led to AS degradation and pharmaco-technical changes in classical wet granulation tablets. Both active principles are stable as dry powders. These investigations led to further development of various co-formulations, including the bilayer tablet currently on the market.
青蒿素类复方疗法,包括青蒿琥酯(AS)+阿莫地喹(AQ),是目前推荐的治疗无并发症恶性疟的一线疗法。固定剂量的复方制剂具有后勤和依从性方面的优势。本文报告了由药品专利池(DNDi)进一步开发的青蒿琥酯-阿莫地喹复方制剂的预开发过程的初始研究阶段。结果表明,青蒿琥酯和阿莫地喹不相容,青蒿琥酯的降解与三个主要参数有关:含水量(>1%)、高温(干燥条件下 80°C),可能还有 4-氨基喹啉部分。此外,青蒿琥酯和阿莫地喹不相容导致青蒿琥酯降解和经典湿法制粒片剂的药物技术变化。两种活性成分均以干粉形式稳定。这些研究导致了各种复方制剂的进一步开发,包括目前市场上的双层片剂。