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功能化的稀土掺杂纳米粒子用于乳腺癌的荧光和 CT 成像纳米诊断。

Functionalized rare earth-doped nanoparticles for breast cancer nanodiagnostic using fluorescence and CT imaging.

机构信息

Biomedical Innovation Department, Centro de Investigación Científica y de Educación Superior de Ensenada (CICESE), Carretera Ensenada-Tijuana No. 3918, Zona Playitas, C.P. 22860, Ensenada, B.C., Mexico.

Posgrado en Física de Materiales, Centro de Investigación Científica y de Educación Superior de Ensenada (CICESE), Carretera Ensenada-Tijuana No. 3918, Zona Playitas, C.P. 22860, Ensenada, B.C., Mexico.

出版信息

J Nanobiotechnology. 2018 Mar 22;16(1):26. doi: 10.1186/s12951-018-0359-9.


DOI:10.1186/s12951-018-0359-9
PMID:29566719
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5863469/
Abstract

BACKGROUND: Breast cancer is the second leading cause of cancer death among women and represents 14% of death in women around the world. The standard diagnosis method for breast tumor is mammography, which is often related with false-negative results leading to therapeutic delays and contributing indirectly to the development of metastasis. Therefore, the development of new tools that can detect breast cancer is an urgent need to reduce mortality in women. Here, we have developed GdO:Eu nanoparticles functionalized with folic acid (FA), for breast cancer detection. RESULTS: GdO:Eu nanoparticles were synthesized by sucrose assisted combustion synthesis and functionalized with FA using EDC-NHS coupling. The FA-conjugated GdO:Eu nanoparticles exhibit strong red emission at 613 nm with a quantum yield of ~ 35%. In vitro cytotoxicity studies demonstrated that the nanoparticles had a negligible cytotoxic effect on normal 293T and T-47D breast cancer cells. Cellular uptake analysis showed significantly higher internalization of FA-conjugated RE nanoparticles into T-47D cells (Folr ) compared to MDA-MB-231 breast cancer cells (Folr ). In vivo confocal and CT imaging studies indicated that FA-conjugated GdO:Eu nanoparticles accumulated more efficiently in T-47D tumor xenograft compared to the MDA-MB-231 tumor. Moreover, we found that FA-conjugated GdO:Eu nanoparticles were well tolerated at high doses (300 mg/kg) in CD1 mice after an intravenous injection. Thus, FA-conjugated GdO:Eu nanoparticles have great potential to detect breast cancer. CONCLUSIONS: Our findings provide significant evidence that could permit the future clinical application of FA-conjugated GdO:Eu nanoparticles alone or in combination with the current detection methods to increase its sensitivity and precision.

摘要

背景:乳腺癌是女性癌症死亡的第二大主要原因,约占全球女性死亡人数的 14%。乳房肿瘤的标准诊断方法是乳房 X 光摄影术,但它常与假阴性结果相关,导致治疗延误,并间接地促进转移的发展。因此,开发新的工具来检测乳腺癌是降低女性死亡率的迫切需要。在这里,我们开发了叶酸(FA)功能化的 GdO:Eu 纳米粒子,用于乳腺癌检测。

结果:通过蔗糖辅助燃烧合成合成了 GdO:Eu 纳米粒子,并使用 EDC-NHS 偶联将 FA 功能化。FA 缀合的 GdO:Eu 纳米粒子在 613nm 处表现出强的红色发射,量子产率约为 35%。体外细胞毒性研究表明,纳米粒子对正常 293T 和 T-47D 乳腺癌细胞几乎没有细胞毒性作用。细胞摄取分析表明,FA 缀合的 RE 纳米粒子在 T-47D 细胞(Folr )中的内化明显高于 MDA-MB-231 乳腺癌细胞(Folr )。体内共聚焦和 CT 成像研究表明,与 MDA-MB-231 肿瘤相比,FA 缀合的 GdO:Eu 纳米粒子在 T-47D 肿瘤异种移植中更有效地积累。此外,我们发现 FA 缀合的 GdO:Eu 纳米粒子在 CD1 小鼠中以高剂量(300mg/kg)静脉注射后具有良好的耐受性。因此,FA 缀合的 GdO:Eu 纳米粒子具有很大的潜力用于检测乳腺癌。

结论:我们的研究结果提供了重要的证据,这可能允许未来临床应用 FA 缀合的 GdO:Eu 纳米粒子单独或与当前的检测方法结合使用,以提高其敏感性和精度。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e88/5863469/b978f961b40d/12951_2018_359_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e88/5863469/aca112d5071c/12951_2018_359_Sch1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e88/5863469/40c9c6f92b43/12951_2018_359_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e88/5863469/bbbb1eaac090/12951_2018_359_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e88/5863469/86151e7f1bf5/12951_2018_359_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e88/5863469/201874eb6e22/12951_2018_359_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e88/5863469/a829f52358ab/12951_2018_359_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e88/5863469/c03e10eceaee/12951_2018_359_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e88/5863469/d05cc5fb0c6f/12951_2018_359_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e88/5863469/b978f961b40d/12951_2018_359_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e88/5863469/aca112d5071c/12951_2018_359_Sch1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e88/5863469/40c9c6f92b43/12951_2018_359_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e88/5863469/bbbb1eaac090/12951_2018_359_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e88/5863469/86151e7f1bf5/12951_2018_359_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e88/5863469/201874eb6e22/12951_2018_359_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e88/5863469/a829f52358ab/12951_2018_359_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e88/5863469/c03e10eceaee/12951_2018_359_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e88/5863469/d05cc5fb0c6f/12951_2018_359_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e88/5863469/b978f961b40d/12951_2018_359_Fig8_HTML.jpg

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