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[KGDS靶向超声造影剂的制备及初步评价]

[Preparation and preliminary evaluation of KGDS-targeted ultrasound contrast agent].

作者信息

Gao Feng, Ding Yanfei, Sheng Xiaoxi, Wang Wei, Liang Qi, Luo Zhuoqiong, Zhou Ping, Li Hui

机构信息

Institute of Cell Transplantation & Gene Therapy, Third Xiangya Hospital, Central South University, Changsha 410013, China.

出版信息

Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2009 Dec;34(12):1255-60.

Abstract

OBJECTIVE

To prepare a thrombus-targeted ultrasonic contrast agent and to investigate its targeted ability to fresh blood clots.

METHODS

We first synthesized FITC-KGDS-Palm compound, and then prepared thrombus-targeted microbubbles using "ultrasound & high speed shearing method". Fluorescence labeling thrombus-specific peptides and KGDS, directed at the activated glycoprotein(GP)IIb/IIIa receptor of platelets were attached to the surface of lipid microbubbles. The concentration and size of TUCA were measured by Malvern Zeta Sizer Nano-ZS590 and Coulter counter. Immunofluorescence was applied to confirm the conjugation. The conjunct ratio was assessed by flow cytometer (FCM).

RESULTS

The KGDS-TUCA was straw yellow turbid liquor, and the concentration was 1.5 x 10(9)/mL, and the average size was 1.5 microm. The targeted microbubbles conjugated with the thrombus-specific peptides showed bright green rings by fluorescence microscope. FCM demonstrated that the wavelength of shell of KGDS-TUCA changed greatly, and the conjunct ratio was 90.04%. In vitro study showed KGDS-TUCA remained stable for 48 h at 4 degree C and target-attached to blood clots and showed good stability.

CONCLUSION

The ultrasound & high speed shearing method to prepare TUCA is easy and in favor of purification. KGDS-TUCA has high specific biological activity. The conjunct ratio and stability of KGDS-TUCA are excellent.

摘要

目的

制备一种血栓靶向超声造影剂,并研究其对新鲜血凝块的靶向能力。

方法

首先合成异硫氰酸荧光素-赖氨酸-甘氨酸-天冬氨酸-棕榈酸(FITC-KGDS-Palm)化合物,然后采用“超声&高速剪切法”制备血栓靶向微泡。将荧光标记的血栓特异性肽和针对血小板活化糖蛋白(GP)IIb/IIIa受体的KGDS连接到脂质微泡表面。用马尔文Zeta粒度分析仪Nano-ZS590和库尔特计数器测量血栓靶向超声造影剂(TUCA)的浓度和大小。采用免疫荧光法确认结合情况。通过流式细胞仪(FCM)评估结合率。

结果

KGDS-TUCA为草黄色浑浊液体,浓度为1.5×10⁹/mL,平均大小为1.5微米。与血栓特异性肽结合的靶向微泡在荧光显微镜下显示亮绿色环。流式细胞仪显示KGDS-TUCA外壳的波长变化很大,结合率为90.04%。体外研究表明,KGDS-TUCA在4℃下可稳定保存48小时,能靶向附着于血凝块,稳定性良好。

结论

采用超声&高速剪切法制备TUCA简便且利于纯化。KGDS-TUCA具有较高的特异性生物活性。其结合率和稳定性良好。

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