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肺癌靶向性纳米磁共振造影剂实验研究 被引量:1

Lung Neoplasm Targeted Nanotechnology MR Contrast Medium:Experimental Study of Mice Model
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摘要 目的:探索磁共振靶向纳米造影剂在早期肺癌诊断方面的应用。方法:采用1.5TMR对直径为2~4mm的鼠肺癌模型做三种不同靶点纳米造影剂成像效果研究。结果:①靶点为血管内皮细胞生长因子受体(VEGFR)-1的纳米造影剂Pal-F56-Lip-Gd可以使肿瘤信号于15min迅速升高88%,1h为90%,2h为25%,3h为10%;②靶点为整合素αvβ3的Pal-RGD10-Lip-Gd可以使肿瘤信号于15min升高100%,1h达到160%,2h为120%,3h为70%;③靶点为VEGFR-2的Pal-K237-Lip-Gd可以使肿瘤信号于15min迅速升高91%,1h达到142%,2h为111%,3h为30%。结论:磁共振靶向纳米造影剂在肺癌早期诊断中具有潜在的应用前景,可以特异性地发现微小肿瘤结节。 Purpose: To study the value of lung neoplasm targeted nanotechnology MR contrast medium on early lung cancer. Methods: Three kinds of targeted MR contrast were used to image human lung adenocarcinoma implanted in nude mice with 1.5T MR, all the nodes were ranged from 2 to 4mm in size. Results: With palmitic acid - F56 - liposome Gd - DTPA - BMA(Pal - F56 - Lip - Gd) which targeted vascular endothelial growth factor receotor(VEGFR) - 1 , the signal of tumor was enhanced 88% in fifteen minutes,90% in one hour,25% in two hours and 10% in three hours. With Pal - RGD10- Lip - Gd which targted αvβ3, the signal of tumor was enhanced 100% in fifteen minutes, 160% in one hour, 120% in two hours and 70% in three hours. With Pal - K237 - Lip - Gd which targeted VEGFR - 2, the signal of tumor was enhanced 91% in fifteen minutes, 142% in one hour, 111% in two hours and 30% in three hours. Conclusion: Lung neoplasm targeted nanotechnology MR contrast can be used to diagnosis small tumors.
出处 《中国医学计算机成像杂志》 CSCD 北大核心 2009年第4期377-379,共3页 Chinese Computed Medical Imaging
基金 上海市纳米专项基金资助项目(编号0752nm018)~~
关键词 磁共振 靶向 纳米 造影剂 肺癌 Magnetic resonance imaging Target Nanotechnology Contrast Lung cancer
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  • 1徐清华,粟波,赵印敏,唐亮,周彩存.^(131)Ⅰ标记血管靶向分子在肿瘤显像中的应用[J].肿瘤防治研究,2007,34(11):860-863. 被引量:5
  • 2Lei H, An P, Song S, et al. A novel peptide isolated from a phage display library inhibits tumor growth and metastasis by blocking the binding of vascular endotheligal growth factor to is kinase domain receptor. J Biol Chem, 2002,277:43137- 43142.
  • 3Mulder W J, Strijkers G J, Habets JW, et al. MR molecular imaging and fluorescences microscopy for identification of activated tumou endothelium using a bimodal lipidic nanoparticle. Faseb, 2005, 19: 2008- 2010.
  • 4Peter H, Miriam B, Tina V, et al. Npvel RGD lipopeptides for the targeting of liposomes to integrin - expressing endothelial and melanoma cells. Protein Engineering Design and Selection, 2004, 17: 433- 441.

二级参考文献9

  • 1Folkman J. Angiogenesis in cancer, vascular, rheumatoid and other disease[J]. Nat Med, 1995,1 (1) : 27-31.
  • 2Folkman J. Addressing tumor blood vessels[J]. Nature Biotechnol, 1997,15(6) :510.
  • 3Luttun A, Autiero M, Tjwa M, et al. Genetic dissection of tumor angiogenesis: Are PIGF and VEGFR-1 novel anti-cancer targets? [J]. Biochem Biophys Acta,2004,1654( 1 ) : 79-74.
  • 4Boyer SJ. Small molecule inhibitors of KDR(VEGFR-2) kinase: an overview of structive activity relationships[J]. Curr Top Med Chem, 2002,2 (9) : 973-1000.
  • 5Holig P, Bach M, Volkel T, et al. Novel RGD lipopeptides for the targeting of liposomes to integrin-expressing endothelial and melanoma cells[J]. Protein Engineering, Desing & Selection,2004,17(5) :433-441.
  • 6An P, Lei H, Zhang J, et al. Suppression of tumor growth and metastasis by a VEGFR-1 antagonizing peptide identified from a phage display library[J]. Int J Cancer, 2004, 111 (2) : 165- 173.
  • 7Hetian L, Ping A, Shumei S,et al. A novel peptide isolated from a phage display library inhibits tumor growth and metastasis by blocking the binding of vascular endothelial growth factor to its kinase domain receptor[J]. J Biol Chem, 2002, 277(45) : 43137-43142.
  • 8Jain RK. The next frontier of molecular medicine: delivery of therapeutics[J]. Nat Med, 1998 ,4(6) :655-657.
  • 9Dutour A, Rigaud M. Tumor endothelial cells are targets for selective therapies: in vitro and in vivo models to evaluate antiangiogenic strategies[J]. Anticancer Res, 2(105,25(6B) :3799- 3807.

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