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泡腾肌酸制剂制备的溶液中肌酸稳定性的评估。

Evaluation of the stability of creatine in solution prepared from effervescent creatine formulations.

作者信息

Ganguly Sudipta, Jayappa Sheela, Dash Alekha K

机构信息

Department of Pharmacy Sciences, School of Pharmacy and Health Professions, Creighton University, Omaha, NE 68178, USA.

出版信息

AAPS PharmSciTech. 2003;4(2):E25. doi: 10.1208/pt040225.

Abstract

The objectives of this study were to determine the cause of the crystallization in a large volume creatine supplement solution made from effervescent powders containing di-creatine citrate, and to characterize these crystals using thermal analyses and x-ray diffractometry. Creatine effervescent powders were dissolved in deionized water (pH 6.2) and stored both at room temperature (RT) (25 degrees C) and refrigerated condition (4 degrees C) over a period of 45 days. Creatine concentration was determined using high-performance liquid chromatography (HPLC). Intrinsic dissolution and saturated solubility of creatine, creatine monohydrate, and di-creatine citrate in water were determined and compared. Crystal growth was detected only in the refrigerated samples on the seventh day of storage. Differential Scanning Calorimetry (DSC) and x-ray diffraction (XRD) studies revealed that the crystals formed were of creatine monohydrate. Ninety percent creatine degradation was observed within 45 days for RT samples. However, at refrigerated condition this degradation was 80% within the same time period. The pH of the RT samples also increased from 3.6 to 4.5 during storage. No such increase was observed in the case of refrigerated samples. The intrinsic dissolution rate constants of the compounds decreased in the following order: di-creatine citrate > creatine > creatine monohydrate. In conclusion, di-creatine citrate used in effervescent formulation dissociates to creatine in aqueous solution and eventually crystallizes out as creatine monohydrate. Significant decrease in solubility and effect of pH contribute to this crystallization process.

摘要

本研究的目的是确定由含二柠檬酸肌酸的泡腾粉制成的大容量肌酸补充剂溶液中结晶的原因,并使用热分析和X射线衍射法对这些晶体进行表征。将肌酸泡腾粉溶解于去离子水(pH 6.2)中,在室温(25℃)和冷藏条件(4℃)下储存45天。使用高效液相色谱法(HPLC)测定肌酸浓度。测定并比较了肌酸、一水肌酸和二柠檬酸肌酸在水中的固有溶解速率和饱和溶解度。仅在储存第7天的冷藏样品中检测到晶体生长。差示扫描量热法(DSC)和X射线衍射(XRD)研究表明,形成的晶体是一水肌酸。室温样品在45天内观察到90%的肌酸降解。然而,在冷藏条件下,同一时间段内这种降解为80%。室温样品的pH在储存期间也从3.6增加到4.5。冷藏样品未观察到这种增加。这些化合物的固有溶解速率常数按以下顺序降低:二柠檬酸肌酸>肌酸>一水肌酸。总之,泡腾制剂中使用的二柠檬酸肌酸在水溶液中解离为肌酸,最终结晶为一水肌酸。溶解度的显著降低和pH的影响促成了这一结晶过程。

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