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采用正相高效液相色谱-蒸发光散射检测法对超声造影剂中的磷脂酰丝氨酸、磷脂酸和游离脂肪酸进行定量分析。

Quantification of phosphatidylserine, phosphatidic acid and free fatty acids in an ultrasound contrast agent by normal-phase high-performance liquid chromatography with evaporative light scattering detection.

作者信息

Hvattum Erlend, Uran Steinar, Sandbaek Anne Gunvor, Karlsson Anders A, Skotland Tore

机构信息

GE Healthcare Medical Diagnostics, Nycoveien 2, N-0401 Oslo, Norway.

出版信息

J Pharm Biomed Anal. 2006 Oct 11;42(4):506-12. doi: 10.1016/j.jpba.2006.04.027. Epub 2006 Jun 9.

Abstract

Sonazoid is a new contrast agent for ultrasound imaging. The product is an aqueous suspension of perfluorobutane microbubbles coated with phospholipids obtained from hydrogenated egg phosphatidylserine (H-EPS). A normal-phase high-performance liquid chromatographic (HPLC) method with evaporative light scattering detection was developed for quantification of free fatty acids, phosphatidylserine and phosphatidic acid in H-EPS and Sonazoid. Separation of the lipids was carried out on an HPLC diol column and a gradient of chloroform and methanol with 0.2% formic acid titrated to pH 7.5 with ammonia. The calibration standards contained stearic acid, distearoyl-phosphatidic acid (DSPA) and distearoyl-phosphatidylserine (DSPS) in the concentration range of 0.016-1.0mg/ml (0.4-25microg injected). The method was validated with a limit of quantification of the three lipids set to 0.4microg (approximately 20-60microM). The best fit of the three calibration curves were obtained when the logarithmic transformed theoretical lipid concentration was plotted against the logarithmic transformed area under the peak and fitted to a second order polynomial equation. Stearic acid, DSPA and DSPS were analysed with an intermediate precision ranging from 4.4% to 5.3% R.S.D. and they were extracted from an aqueous suspension with a recovery ranging from 103.3% to 113.3%. The sum of total phospholipid concentration determined in H-EPS ranged from 96.4% to 103.2% of the theoretical values. The lipids in the ultrasound product were quantitated with a repeatability ranging from 6.2% to 11.7% R.S.D.

摘要

声诺维是一种用于超声成像的新型造影剂。该产品是由氢化鸡蛋磷脂酰丝氨酸(H-EPS)包覆的全氟丁烷微泡的水悬浮液。开发了一种采用蒸发光散射检测的正相高效液相色谱(HPLC)方法,用于定量H-EPS和声诺维中的游离脂肪酸、磷脂酰丝氨酸和磷脂酸。脂质的分离在HPLC二醇柱上进行,采用氯仿和甲醇的梯度洗脱,其中含有0.2%的甲酸,用氨滴定至pH 7.5。校准标准品包含硬脂酸、二硬脂酰磷脂酸(DSPA)和二硬脂酰磷脂酰丝氨酸(DSPS),浓度范围为0.016 - 1.0mg/ml(进样量为0.4 - 25μg)。该方法经过验证,三种脂质的定量限设定为0.4μg(约20 - 60μM)。当将对数转换后的理论脂质浓度与对数转换后的峰面积绘制在一起,并拟合到二阶多项式方程时,获得了三条校准曲线的最佳拟合。硬脂酸、DSPA和DSPS的分析中间精密度为相对标准偏差(R.S.D.)4.4%至5.3%,它们从水悬浮液中的提取回收率为103.3%至113.3%。H-EPS中测定的总磷脂浓度总和为理论值的96.4%至103.2%。超声产品中的脂质定量重复性为R.S.D. 6.2%至11.7%。

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