Uran Steinar, Landmark Kristin, Normann Per Trygve, Hals Petter-Arnt, Toft Kim Gunnar, Skotland Tore
Research and Development, GE Healthcare Bio-Sciences, Nycoveien 2, N-0401 Oslo, Norway.
J Pharm Biomed Anal. 2005 Sep 15;39(3-4):746-51. doi: 10.1016/j.jpba.2005.04.038.
Sonazoid is a new contrast agent for ultrasound imaging comprising an aqueous suspension of lipid-stabilised perfluorobutane (PFB) gas microbubbles. A respiration-metabolism chamber system was developed to collect exhaled air following intravenous administration of Sonazoid to rats. Analysis of PFB in the exhaled rat air was performed using a modified version of an earlier published method for blood samples, i.e. an automatic headspace gas chromatographic mass spectrometric (GC-MS) method using electron impact ionisation. The calibration standards were PFB diluted in air (2.5-1800 pg/ml). Perfluoropentane (PFP) was used as an internal standard and the MS detector was set to single ion monitoring of the base fragment ions of PFB (m/z 69 and 119) and PFP (m/z 69). The calibration curve, made by plotting the peak area ratios of PFB (m/z 69) to PFP (m/z 69) against the theoretical concentration of PFB, was fitted to a linear equation with weighting 1/y2 and found to be reproducible. The lower limit of quantification (LLOQ) was 2.5 pg PFB/ml. The between-day variation of the method was below 2.6% relative standard deviation (R.S.D.) and the within-day variation of the method was below 6.4% R.S.D. The accuracy of the method was evaluated and showed a relative error less than 5.2%. PFB was found to be stable for 14 days when stored in Tedlar sample bags at room temperature. An even lower detection limit may be obtained by using the more time-consuming process of solid-phase micro extraction; thus, by concentrating PFB on carboxen-PDMS fibres an LLOQ of 0.5 pg PFB/ml was obtained. When five rats were given an i.v. bolus injection of Sonazoid at a dose of 8 microl microbubbles/kg a mean recovery of 96% (range, 81-110%) was found during 24 h; more than 50% was exhaled during the first 30 min after injection.
声诺维是一种用于超声成像的新型造影剂,由脂质稳定的全氟丁烷(PFB)气体微泡的水悬浮液组成。开发了一种呼吸代谢室系统,用于在给大鼠静脉注射声诺维后收集呼出的空气。采用先前发表的针对血液样本方法的改良版,即使用电子轰击电离的自动顶空气相色谱 - 质谱(GC - MS)法,对大鼠呼出气体中的PFB进行分析。校准标准品是在空气中稀释的PFB(2.5 - 1800 pg/ml)。全氟戊烷(PFP)用作内标,质谱检测器设置为对PFB(m/z 69和119)和PFP(m/z 69)的基峰离子进行单离子监测。通过绘制PFB(m/z 69)与PFP(m/z 69)的峰面积比相对于PFB的理论浓度作图得到校准曲线,将其拟合为加权1/y²的线性方程,发现具有可重复性。定量下限(LLOQ)为2.5 pg PFB/ml。该方法的日间变异低于2.6%相对标准偏差(R.S.D.),日内变异低于6.4% R.S.D。对该方法的准确性进行评估,结果显示相对误差小于5.2%。发现PFB在室温下储存在泰德拉样品袋中时可稳定保存14天。通过使用更耗时的固相微萃取过程可能获得更低的检测限;因此,通过将PFB浓缩在碳分子筛 - 聚二甲基硅氧烷纤维上,获得了0.5 pg PFB/ml的LLOQ。当以8微升微泡/千克的剂量给5只大鼠静脉推注声诺维时,发现在24小时内平均回收率为96%(范围为81 - 110%);超过50%在注射后的前30分钟内呼出。