In Vivo Anticancer Activity of Methotrexate-loaded Layered Double Hydroxide Nanoparticles

被引:26
|
作者
Choi, Soo-Jin [1 ]
Oh, Jae-Min [2 ]
Chung, Hae-Eun [1 ]
Hong, Seung-Hee [3 ]
Kim, In-Hoo [4 ]
Choy, Jin-Ho [5 ,6 ]
机构
[1] Seoul Womens Univ, Dept Food Sci & Technol, Seoul 139774, South Korea
[2] Yonsei Univ, Coll Sci & Technol, Dept Chem & Med Chem, Wonju 220710, Gangwondo, South Korea
[3] Hanbuk Univ, Dept Nutr & Food Sci, Gyeonggi Do 483120, South Korea
[4] Natl Canc Ctr, Res Inst, Gyeonggi Do 410769, South Korea
[5] Ewha Womans Univ, Ctr Intelligent Nanobio Mat, Dept Bioinspired Sci, Seoul 120750, South Korea
[6] Ewha Womans Univ, Dept Chem & Nano Sci, Ewha Global Top Program 5 2011, Seoul 120750, South Korea
基金
新加坡国家研究基金会;
关键词
layered double hydroxide; methotrexate; anti-tumor activity; pharmacokinetics; toxicity; CELLULAR UPTAKE; UPTAKE MECHANISM; DRUG; DELIVERY; LDH; NANOHYBRID; EFFICACY;
D O I
10.2174/138161281941131219123718
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
A methotrexate (MTX)-loaded layered double hydroxide (LDH) nanoparticle system was synthesized by intercalating MTX into the interlayer spaces of LDH. In vivo pharmacokinetic study demonstrated that the MTX-LDH hybrid had similar kinetic behaviors as free MTX, showing a rapid decline in the plasma MTX level, with characteristics of a biexponential function. However, the hybrid system remarkably suppressed tumor growth in human osteosarcoma-bearing mice compared to an equivalent amount of free MTX. Using MTX-LDH nanoparticles, a significantly high amount of MTX was delivered to target tumor tissue, whereas a low level was found in normal tissues. Moreover, LDH nanocarriers did not accumulate in any specific tissue nor cause acute toxicity up to the applied dose for the hybrid system. These results suggest that the MTX-LDH nanohybrid system has great potential as an anti-cancer drug with enhanced in vivo anti-tumor activity and bioavailability in target tumor tissue along with reduced side effects.
引用
收藏
页码:7196 / 7202
页数:7
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