Dash Alekha K, Sawhney Angeli
Department of Pharmacy Sciences, School of Pharmacy and Allied Health Professions, Creighton University, 2500 California Plaza, Omaha, NE 68178, USA.
J Pharm Biomed Anal. 2002 Jul 31;29(5):939-45. doi: 10.1016/s0731-7085(02)00167-x.
The objective of this study was to develop a simple and sensitive LC method for the determination of creatine and creatinine in various creatine supplement formulations. The chromatographic system comprised of a LC-600 pump, SCL-6B system controller, and SPD-6AV detector (Shimadzu, Japan). The mobile phase consisted of 0.045 M ammonium sulfate in water. The chromatographic separation was achieved at ambient temperature on a Betabasic C-18 column (250 x 4.6 mm, Keystone Sci.). The flow rate was maintained at 0.75 ml/min and effluents are monitored at 205 nm. 4-(2-Aminoethyl)benzene sulfonamide was used as an internal standard (IS). This method required less than 7 min of chromatographic time. The standard curves were linear over the concentration range of 1-100 microg/ml for creatine and 2-100 microg/ml for creatinine, respectively. The relative standard deviations (RSD) for the within-day and day-to-day precision for creatine were within 1.0-4.6 and 2.2-4.7%, respectively. The RSD for the accuracy of creatine assay was in the range of 2.4-4.7%. The RSD values for the within-day precision, day-to-day precision and accuracy for creatinine validation were 1.7-4.4, 2.3-5.4 and 2.4-4.8%, respectively. This method was used to determine: (i) the creatine concentration in various marketed products; (ii) saturated solubility of various creatine salts; and (iii) stability of creatine in aqueous solution. In conclusion, a simple and sensitive LC method with UV detection was developed for the simultaneous determination of creatine and creatinine in formulations. Di-creatine citrate salt showed a higher aqueous solubility (at 25 degrees C) as compared to creatine and creatine monohydrate. Some of the over-the-counter (OTC) products tested contained a very low level of creatine in contrast to their label claim. Substantial conversion of creatine into creatinine was noticed in liquid formulation.
本研究的目的是开发一种简单且灵敏的液相色谱法,用于测定各种肌酸补充剂配方中的肌酸和肌酐。色谱系统由一台LC - 600泵、SCL - 6B系统控制器和SPD - 6AV检测器(日本岛津公司)组成。流动相由水中的0.045 M硫酸铵组成。在室温下,于Betabasic C - 18柱(250×4.6 mm,Keystone Sci.)上实现色谱分离。流速保持在0.75 ml/min,在205 nm处监测流出物。4 - (2 - 氨乙基)苯磺酰胺用作内标(IS)。该方法所需的色谱时间少于7分钟。肌酸的标准曲线在1 - 100μg/ml浓度范围内呈线性,肌酐的标准曲线在2 - 100μg/ml浓度范围内呈线性。肌酸日内精密度和日间精密度的相对标准偏差(RSD)分别在1.0 - 4.6%和2.2 - 4.7%范围内。肌酸测定准确度的RSD在2.4 - 4.7%范围内。肌酐验证的日内精密度、日间精密度和准确度的RSD值分别为1.7 - 4.4%、2.3 - 5.4%和2.4 - 4.8%。该方法用于测定:(i)各种市售产品中的肌酸浓度;(ii)各种肌酸盐的饱和溶解度;(iii)肌酸在水溶液中的稳定性。总之,开发了一种采用紫外检测的简单且灵敏的液相色谱法,用于同时测定配方中的肌酸和肌酐。与肌酸和一水肌酸相比,柠檬酸二肌酸盐在25℃时表现出更高的水溶性。与标签声明相比,一些测试的非处方(OTC)产品中肌酸含量极低。在液体制剂中注意到肌酸大量转化为肌酐。