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本文引用的文献

1
Microbubbles coated with disaturated lipids and DSPE-PEG2000: phase behavior, collapse transitions, and permeability.包覆有二饱和脂质和DSPE-PEG2000的微泡:相行为、塌陷转变及渗透性
Langmuir. 2009 Apr 9;25(6):3705-12. doi: 10.1021/la803774q.
2
Microbubble destruction during intravenous administration: a preliminary study.静脉给药过程中的微泡破坏:一项初步研究。
Ultrasound Med Biol. 2009 Mar;35(3):515-22. doi: 10.1016/j.ultrasmedbio.2008.07.008. Epub 2008 Dec 24.
3
Modeling of nonlinear viscous stress in encapsulating shells of lipid-coated contrast agent microbubbles.脂质包被的造影剂微泡包膜中非线性粘性应力的建模。
Ultrasonics. 2009 Feb;49(2):269-75. doi: 10.1016/j.ultras.2008.09.007. Epub 2008 Sep 30.
4
Microbubble size isolation by differential centrifugation.通过差速离心法分离微泡大小
J Colloid Interface Sci. 2009 Jan 15;329(2):316-24. doi: 10.1016/j.jcis.2008.09.066. Epub 2008 Oct 1.
5
Response of contrast agents to ultrasound.造影剂对超声的反应。
Adv Drug Deliv Rev. 2008 Jun 30;60(10):1117-36. doi: 10.1016/j.addr.2008.03.011. Epub 2008 Apr 9.
6
Do bubble characteristics affect recanalization in stroke patients treated with microbubble-enhanced sonothrombolysis?气泡特性是否会影响接受微泡增强超声溶栓治疗的中风患者的再通情况?
Ultrasound Med Biol. 2008 Oct;34(10):1573-7. doi: 10.1016/j.ultrasmedbio.2008.02.011. Epub 2008 May 1.
7
Needle size and injection rate impact microbubble contrast agent population.针头尺寸和注射速率会影响微泡造影剂的数量。
Ultrasound Med Biol. 2008 Jul;34(7):1182-5. doi: 10.1016/j.ultrasmedbio.2007.12.018. Epub 2008 Mar 4.
8
Detection of coronary artery disease with a continuous infusion of definity ultrasound contrast during adenosine stress real time perfusion echocardiography.在腺苷负荷实时灌注超声心动图检查期间持续输注Definity超声造影剂检测冠状动脉疾病
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9
Molecular ultrasound imaging using microbubble contrast agents.使用微泡造影剂的分子超声成像。
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Enhancement of vascular permeability with low-frequency contrast-enhanced ultrasound in the chorioallantoic membrane model.在绒毛尿囊膜模型中,低频超声造影增强血管通透性。
Radiology. 2007 Apr;243(1):112-21. doi: 10.1148/radiol.2431060167.

连续输注过程中脂质包裹微泡群体的变化及保持一致性的方法。

Changes in lipid-encapsulated microbubble population during continuous infusion and methods to maintain consistency.

作者信息

Kaya Mehmet, Gregory Thomas S, Dayton Paul A

机构信息

Joint Department of Biomedical Engineering, University of North Carolina and North Carolina State University, Chapel Hill, NC 27599, USA.

出版信息

Ultrasound Med Biol. 2009 Oct;35(10):1748-55. doi: 10.1016/j.ultrasmedbio.2009.04.023. Epub 2009 Jul 26.

DOI:10.1016/j.ultrasmedbio.2009.04.023
PMID:19632760
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2752484/
Abstract

Stabilized microbubbles are used as ultrasound contrast agents. These micron-sized gas capsules are injected into the bloodstream to provide contrast enhancement during ultrasound imaging. Some contrast imaging strategies, such as destruction-reperfusion, require a continuous injection of microbubbles over several minutes. Most quantitative imaging strategies rely on the ability to administer a consistent dose of contrast agent. Because of the buoyancy of these gas-filled agents, their spatial distribution within a syringe changes over time. The population of microbubbles that is pumped from a horizontal syringe outlet differs from initial population as the microbubbles float to the syringe top. In this manuscript, we study the changes in the population of a contrast agent that is pumped from a syringe caused by microbubble flotation. Results are presented in terms of change in concentration and change in mean diameter, as a function of time, suspension medium and syringe diameter. Data illustrate that the distribution of contrast agents injected from a syringe changes in both concentration and mean diameter over several minutes without mixing. We discuss the application of a mixing system and viscosity agents to keep the contrast solution more evenly distributed in a syringe. These results are significant for researchers using microbubble contrast agents in continuous-infusion applications where it is important to maintain consistent contrast agent delivery rate, or in situations where the injection syringe cannot be mixed immediately before administration.

摘要

稳定的微泡用作超声造影剂。这些微米级的气体胶囊被注入血流中,以便在超声成像期间提供造影增强。一些造影成像策略,如破坏-再灌注,需要在几分钟内持续注入微泡。大多数定量成像策略依赖于能够给予一致剂量的造影剂。由于这些充气剂的浮力,它们在注射器内的空间分布会随时间变化。当微泡漂浮到注射器顶部时,从水平注射器出口泵出的微泡群体与初始群体不同。在本手稿中,我们研究了由微泡漂浮导致的从注射器泵出的造影剂群体的变化。结果以浓度变化和平均直径变化的形式呈现,作为时间、悬浮介质和注射器直径的函数。数据表明,在不混合的情况下,从注射器注入的造影剂分布在几分钟内会在浓度和平均直径方面发生变化。我们讨论了混合系统和粘性剂的应用,以使造影剂溶液在注射器中更均匀地分布。这些结果对于在连续输注应用中使用微泡造影剂的研究人员具有重要意义,在这些应用中,保持一致的造影剂输送速率很重要,或者在注射前不能立即混合注射器的情况下也是如此。