Zhou Li-Xue, Ding Hong, Jia Cai-Xia, Li Yan, Wei Qing
Department of Gynecology and Obstetrics, The Second Affiliated Hospital, Sun Yat-sen University, Guangzhou, Guangdong, 510120, P R China.
Ai Zheng. 2008 Jul;27(7):692-7.
BACKGROUND & OBJECTIVE: At present, the investigation of microbubble contrast agents is a hot spot. Although these contrast agents can increase the ultrasound detection rate of tumor vessels, they lack tissue specificity. This study was to evaluate the impact of instantaneous uniformity of SonoVue microbubbles on binding characteristics, including the adhesion rate and stability, of a new contrast agent targeted to choriocarcinoma cells (JARs) in vitro, in order to establish a foundation to explore targeted ultrasound imaging for localization of tumor cell antigens and increase the early diagnostic rate for tumors.
The objects were divided into three groups: the uneven microbubble group (n=10), the uniform microbubble group (n=10) and the tiny microbubble group (n=10). The rosette formation rate was counted. JARs were calculated by flow cytometry (FCM). The shape of the rosette was recorded. The targeted contrast agent was prepared by mixing SonoVue microbubbles of different uniformity with rabbit anti-human chorionic gonadotrophin (HCG) antibody. The binding rates of the contrast agent to JARs before and after PBS rinse were analyzed.
The binding rate was significantlylower in the uneven microbubble group (60.4+/-1.5)% than in the uniform microbubble group (84.3+/-5.5)% and the tiny microbubble group (90.6+/-6.8)% (P<0.05). The binding rates of different microbubbles to JARs before and after PBS rinse were different. The uniform microbubbles were the most stable ones, with the binding rate of (84.3+/-5.5)% and (82.4+/-3.7)% before and after PBS rinse (P>0.05). The binding rates of the targeted microbubbles labeled with fluorescence to JARs were 72.9%, 81.03% and 88.5% in the uneven microbubble group, the uniform microbubble group and the tiny microbubble group, respectively (P<0.05).
The binding capacity of the targeted SonoVue microbubbles to JARs is related to instantaneous uniformity of the microbubble, which is determined by the shaking method before preparation. Improving instantaneous uniformity of SonoVue microbubbles may increase the binding rate and stability of targeted microbubbles to JARs, thus to improve the image of JARs.
目前,微泡造影剂的研究是一个热点。尽管这些造影剂能提高肿瘤血管的超声检测率,但它们缺乏组织特异性。本研究旨在评估声诺维微泡的瞬间均匀性对一种靶向绒毛膜癌细胞(JARs)的新型造影剂体外结合特性(包括黏附率和稳定性)的影响,为探索肿瘤细胞抗原定位的靶向超声成像及提高肿瘤早期诊断率奠定基础。
将实验对象分为三组:微泡不均匀组(n = 10)、微泡均匀组(n = 10)和微泡微小组(n = 10)。计数玫瑰花环形成率。采用流式细胞术(FCM)检测JARs。记录玫瑰花环的形态。将不同均匀性的声诺维微泡与兔抗人绒毛膜促性腺激素(HCG)抗体混合制备靶向造影剂。分析造影剂在PBS冲洗前后与JARs的结合率。
微泡不均匀组的结合率(60.4±1.5)%显著低于微泡均匀组(84.3±5.5)%和微泡微小组(90.6±6.8)%(P<0.05)。不同微泡在PBS冲洗前后与JARs的结合率不同。微泡均匀组最稳定,PBS冲洗前后结合率分别为(84.3±5.5)%和(82.4±3.7)%(P>0.05)。微泡不均匀组、微泡均匀组和微泡微小组中荧光标记的靶向微泡与JARs的结合率分别为72.9%、81.03%和88.5%(P<0.05)。
靶向声诺维微泡与JARs的结合能力与微泡的瞬间均匀性有关,而微泡的瞬间均匀性由制备前的振荡方法决定。提高声诺维微泡的瞬间均匀性可能会增加靶向微泡与JARs的结合率和稳定性,从而改善JARs的成像效果。