Confocal Raman microspectroscopic study of folate receptor-targeted delivery of 6-mercaptopurine-embedded gold nanoparticles in a single cell

被引:7
|
作者
Park, Jin [3 ]
Jeon, Won Il [1 ,2 ]
Lee, So Yeong [1 ,2 ]
Ock, Kwang-Su [3 ]
Seo, Ji Hye [3 ]
Park, Jinho [3 ]
Ganbold, Erdene-Ochir [3 ]
Cho, Keunchang [4 ]
Song, Nam Woong [5 ,6 ]
Joo, Sang-Woo [3 ]
机构
[1] Seoul Natl Univ, Coll Vet Med, Pharmacol Lab, Seoul 151742, South Korea
[2] Seoul Natl Univ, Res Inst Vet Sci, Seoul 151742, South Korea
[3] Soongsil Univ, Dept Chem, Seoul 156743, South Korea
[4] Logos Biosyst Inc, Anyang 431070, South Korea
[5] Korea Res Inst Stand & Sci Gajeong Ro, Ctr NanoBio Convergence, Taejon 305340, South Korea
[6] Univ Sci & Technol, Dept Nano & Bio Surface Sci, Taejon, South Korea
关键词
gold nanoparticles; folate-receptor target; drug delivery; anticancer effect; confocal Raman microspectroscopy; SURFACE-ENHANCED RAMAN; DRUG-DELIVERY; IN-VITRO; ADSORPTION; SILVER;
D O I
10.1002/jbm.a.33294
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
We investigate the cellular uptake behaviors and efficacy of folate-coated gold nanoparticles (AuNPs) for the targeted drug delivery system in human cancer cells. Folate-conjugated AuNPs embedded with a purine analogue cancer drug of 6-mercaptopurine (6MP) were assembled via a 1-ethyl-3-[3-dimethylaminopropyl] carbodiimide hydrochloride (EDC) coupling reaction between the amino group of 4-aminobenzenethiol (ABT) and the carboxyl group of folic acid. The assembly of folate and 6MP on AuNPs has been examined by absorption spectroscopy, transmission electron microscopy (TEM), and confocal Raman spectroscopy. The internalization of the conjugated AuNPs inside the folate receptor-positive HeLa and KB cells was checked by TEM and dark-field microscopy (DFM) combined with label-free confocal spectroscopy over the depth variable z at a micrometer resolution. DFM live cell imaging of folate-conjugated AuNPs in HeLa cells indicated that the targeted AuNPs appeared to attach on the cell surfaces and enter into the cell with an hour. The cell viability was also compared to estimate the efficacy of folate-conjugated AuNP delivery systems. Folate receptor-targeted AuNP systems appeared to decrease cancer cell viability both in vitro and in vivo more than did the use of the 6MP-coated AuNPs drug without any targeting systems. (C) 2012 Wiley Periodicals, Inc. J Biomed Mater Res Part A:, 2012.
引用
收藏
页码:1221 / 1228
页数:8
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