Buchanan Kyle D, Huang Shaoling, Kim Hyunggun, Macdonald Robert C, McPherson David D
Department of Biochemistry, Molecular Biology, and Cell Biology, Northwestern University, 2205 Tech Drive, Hogan Hall 3-100, Evanston, Illinois 60208, USA.
J Pharm Sci. 2008 Jun;97(6):2242-9. doi: 10.1002/jps.21173.
Targetable echogenic liposomes (ELIP) for ultrasound enhancement of atheroma have recently been developed; however, their retention of echogenicity at physiological temperature is less than desirable. The purpose of this study was to improve ELIP stability and increase clinical potential. The approach utilized the original procedures but involved manipulation of the lipid composition by reducing the level of unsaturation of the phospholipids components to minimize the rate of loss of echogenicity. Echogenicity was measured using a 20 MHz intravascular ultrasound (IVUS) catheter and quantified (as mean gray scale values) using computer-assisted videodensitometry. The optimal preparation for retention of echogenicity stability at physiologic temperature was egg phosphatidylcholine/dipalmitoylphosphatidylcholine/dipalmitoylphos-phatidylethanolamine/dipalmitoylphosphatidylglycerol/cholesterol (27:42:8:8:15, molar percent). This preparation retained 51 +/- 3.5% of its echogenicity after 1 h at 37 degrees C, more than 5x that retained by the previously descried preparation. In this composition nearly 2/3 of the phosphosphatidylcholine is fully saturated. Such an increase in saturation is anticipated to stiffen the lipid acyl chains. The air pockets that are responsible for reflection of ultrasound waves can be assumed to be stabilized by a lipid monolayer at the interface between the air and bulk water. The increased rigidity of that monolayer is presumed to be responsible for reducing the loss of air and extending the duration of echogenic activity. The stability of this improved formulation now appears to be more than adequate for clinical applications.
用于超声增强动脉粥样硬化的可靶向回声脂质体(ELIP)最近已被开发出来;然而,它们在生理温度下的回声保持性并不理想。本研究的目的是提高ELIP的稳定性并增加其临床应用潜力。该方法采用了原始程序,但通过降低磷脂成分的不饱和度来操纵脂质组成,以尽量减少回声丧失的速率。使用20MHz血管内超声(IVUS)导管测量回声,并使用计算机辅助视频密度测定法进行量化(以平均灰度值表示)。在生理温度下保持回声稳定性的最佳制剂是卵磷脂酰胆碱/二棕榈酰磷脂酰胆碱/二棕榈酰磷脂酰乙醇胺/二棕榈酰磷脂酰甘油/胆固醇(27:42:8:8:15,摩尔百分比)。该制剂在37℃下1小时后保留了其51±3.5%的回声,是先前描述的制剂保留量的5倍多。在这种组成中,近2/3的磷脂酰胆碱是完全饱和的。预计这种饱和度的增加会使脂质酰链变硬。负责反射超声波的气穴可以假定由空气与大量水之间界面处的脂质单层稳定。假定该单层增加的刚性是减少空气损失并延长回声活性持续时间的原因。这种改进制剂的稳定性现在似乎足以满足临床应用。