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作 者:杨春[1] 张玲[2] 尹燕[1] 陈超[1] 徐凯[1] 郑骏年
机构地区:[1]徐州医学院附属医院影像科,江苏221002 [2]徐州医学院药学院 [3]江苏省肿瘤生物治疗研究所
出 处:《中华实验外科杂志》2013年第6期1123-1125,共3页Chinese Journal of Experimental Surgery
基 金:江苏省自然科学基金资助项目(BK2010178);江苏省高校自然科学基金资助项目(10KJB320025);徐州市科技项目(XFllC062);徐州医学院肿瘤生物治疗重点实验室资助项目(C0803)
摘 要:目的探讨葡萄糖受体靶向的钆喷酸葡胺(Gd—DTPA)脂质体对裸鼠肾癌移植瘤的靶向性。方法制备聚乙二醇(PEG)修饰的Gd.DTPA脂质体(PEG—Gd.DTPA)及N-棕榈酸葡萄糖胺(NPG)、PEG修饰的Gd—DTPA脂质体(NPG—PEG.Gd—DTPA)。将21只肾癌移植瘤的裸鼠分为3组(n=7),分别经腹腔注射Gd—DTPA、PEG.Gd.DTPA及NPG—PEG.Gd.DTPA后0.5、1.5、2.5、3.5h行磁共振成像(MRI)扫描,计算相对增强值。结果Gd—DTPA组强化峰值出现在0.5h,相对增强值为1.83±0.25;PEG—Gd—DTPA及NPG—PEG—Gd.DTPA组强化峰值均出现在2.5h,相对增强值分别为2.33±0.30、2.87±0.40。3组移植瘤1.5、2.5、3.5h扫描时间点相对增强值比较,差异有统计学意义(P〈0.01),且NPG—PEG—Gd—DTPA组相对增强值最高。结论NPG、PEG修饰Gd—DTPA脂质体能与葡萄糖受体结合,实现MRI靶向成像。Objective To prepare long cycle of gadopentetate dimeglumine (Gd-DTPA) liposome and glucose receptor-targeted long cycle of Gd-DTPA liposome and to study the targeting to the renal ceil car- cinoma. Methods Long cycle of Gd-DTPA liposome and glucose receptor-targeted long cycle of Gd-DTPA li- posome were prepared. Twenty-one male nude mice were divided into 3 groups (7 nude mice in each group) , and T1WI scanning was done at 0. 5, 1.5, 2. 5 and 3.5 h after intraperitoneal injection of Gd-DTPA, long cycle of Gd-DTPA liposome and glucose receptor-targeted long cycle of Gd-DTPA liposome, separately. After the magnetic resonance (MR) scanning, signal intensity was measured and the relative enhanced value (REV) was calculated. Results In vivo MR imaging, the injection of Gd-DTPA resulted in a maximum tumor REV of 1.83±0. 25 at 0. 5 h. The injection of PEG-modified Gd-DTPA liposome and NPG-PEG-modi- fled Gd-DTPA liposome resulted in a maximum tumor REV of 2. 33±0. 30 and 2. 87±0. 40 at 2. 5 h, respectively. There was significant difference in REV among three groups at 1.5, 2. 5, and 3.5 h after injfection (P 〈 0. 01 ), and the REV of NPG-PEG-modified Gd-DTPA liposome group was the highest. Conclusion Glucose-receptor-targeted long-circulating Gd-DTPA liposome could be combined to tumor cells via glucose receptor and significantly targeted to tumor cells with rich glucose receptors for MR imaging.
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