Department of Quality Control and Analytical Development, General Equipments and Health Products Agency, Assistance Publique - Hôpitaux de Paris, Paris, France.
Department of Quality Control and Analytical Development, General Equipments and Health Products Agency, Assistance Publique - Hôpitaux de Paris, Paris, France.
J Pharm Biomed Anal. 2014 Feb;89:50-5. doi: 10.1016/j.jpba.2013.10.026. Epub 2013 Oct 29.
The FEE cyclic hexapeptide (cFEE) is an investigational new drug added to the insemination medium in order to improve the in vitro fertilization rate. The pharmacological activity of small peptides is highly dependent on the conservation of the amino acid sequence and of the structural conformation of the active site. To enhance the scientific knowledge required for the clinical use of cFEE, a comprehensive determination of its chemical stability in solution was realized in accelerated conditions. Degradation products have been detected and identified by liquid chromatography/Qtrap(®) mass spectrometry. The main degradation products highlighted during the product shelf life were produced by hydrolysis and only certain sites were involved. In most cases, the cyclic conformation was lost and regarding the major degradation pathway, the sequence representing the active site was affected.
FEE 六肽(cFEE)是一种新的研究药物,添加到授精液中,以提高体外受精率。小肽的药理活性高度依赖于氨基酸序列的保守性和活性部位的结构构象。为了增强 cFEE 临床应用所需的科学知识,在加速条件下实现了对其在溶液中的化学稳定性的全面测定。通过液相色谱/Qtrap®质谱法检测和鉴定了降解产物。在产品保质期内,主要降解产物是通过水解产生的,而且只涉及某些部位。在大多数情况下,环状构象丢失,对于主要降解途径,活性部位的序列受到影响。