Ultrasound contrast agents targeted to malignancies: optimizing cellular attachment

K. Oum, J. Vega, L. Leodore, F. Forsberg, J. Liu, D. Merton, M. Wheatley
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引用次数: 0

Abstract

Hollow poly (lactic acid) (PLA) microcapsules were modified with Arg-Gly-Asp (RGD) peptide to create a targeted contrast agent (CA) that enhances ultrasound imaging. The RGD peptide targets cell-surface receptors (integrins /spl alpha//sub v//spl beta//sub 3/ and /spl alpha//sub v//spl beta//sub 5/) which are overexpressed in cancer and angiogenesis. The influence of RGD surface density and RGD spacer length were evaluated for their contribution to CA attachment to human breast cancer cells. The CA performance was dependent on both the RGD surface density and glycine spacer length and therefore should be considered in the design of a site-targeted CA. The optimized RGD peptide modified microcapsules are ideal candidates for targeted diagnostic imaging and for drug delivery.
针对恶性肿瘤的超声造影剂:优化细胞附着
用Arg-Gly-Asp (RGD)肽修饰中空聚乳酸(PLA)微胶囊,制备一种增强超声成像的靶向造影剂(CA)。RGD肽靶向细胞表面受体(整合素/spl α //sub v//spl β //sub 3/和/spl α //sub v//spl β //sub 5/),这些受体在癌症和血管生成中过度表达。评估了RGD表面密度和RGD间隔长度对CA附着于人乳腺癌细胞的影响。CA的性能取决于RGD表面密度和甘氨酸间隔长度,因此在设计位点靶向CA时应考虑到这一点。优化后的RGD肽修饰微胶囊是靶向诊断成像和药物递送的理想候选者。
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