Hernot Sophie, Klibanov Alexander L
Cardiovascular Division, Department of Medicine, University of Virginia School of Medicine, P.O. Box 800158, RM1026, Hospital Drive, Cobb Hall, Charlottesville, VA 22908-0158, USA.
Adv Drug Deliv Rev. 2008 Jun 30;60(10):1153-66. doi: 10.1016/j.addr.2008.03.005. Epub 2008 Apr 3.
Ultrasound contrast agents, in the form of gas-filled microbubbles, are becoming popular in perfusion monitoring; they are employed as molecular imaging agents. Microbubbles are manufactured from biocompatible materials, they can be injected intravenously, and some are approved for clinical use. Microbubbles can be destroyed by ultrasound irradiation. This destruction phenomenon can be applied to targeted drug delivery and enhancement of drug action. The ultrasonic field can be focused at the target tissues and organs; thus, selectivity of the treatment can be improved, reducing undesirable side effects. Microbubbles enhance ultrasound energy deposition in the tissues and serve as cavitation nuclei, increasing intracellular drug delivery. DNA delivery and successful tissue transfection are observed in the areas of the body where ultrasound is applied after intravascular administration of microbubbles and plasmid DNA. Accelerated blood clot dissolution in the areas of insonation by cooperative action of thrombolytic agents and microbubbles is demonstrated in several clinical trials.
超声造影剂呈充气微泡形式,在灌注监测中越来越受欢迎;它们被用作分子成像剂。微泡由生物相容性材料制成,可以静脉注射,有些已获批准用于临床。微泡可被超声照射破坏。这种破坏现象可应用于靶向给药和增强药物作用。超声场可聚焦于目标组织和器官;因此,可以提高治疗的选择性,减少不良副作用。微泡增强超声能量在组织中的沉积,并作为空化核,增加细胞内药物递送。在血管内给予微泡和质粒DNA后,在超声作用的身体部位观察到DNA递送和成功的组织转染。几项临床试验证明,溶栓剂和微泡协同作用可加速超声照射区域的血栓溶解。