Chemopreventive efficacy of all-trans-retinoic acid in biodegradable microspheres against epithelial cancers:: Results in a 4-nitroquinoline 1-oxide-induced oral carcinogenesis model

被引:5
作者
Choi, Yongdoo
Kim, Sang Yoon
Park, Kyeongsoon
Yang, Jehoon
Cho, Kyung-Ja
Kwon, Hyun Ja
Byun, Youngro
机构
[1] Seoul Natl Univ, Coll Pharm, Seoul 151742, South Korea
[2] Gwangju Inst Sci & Technol, Ctr Cell & Macromol Therapy, Dept Mat Sci & Engn, Kwangju 500712, South Korea
[3] Univ Ulsan, Coll Med, Asan Med Ctr, Dept Otolaryngol, Seoul 138736, South Korea
[4] Univ Ulsan, Coll Med, Asan Med Ctr, Dept Pathol, Seoul 138736, South Korea
关键词
chemoprevention; oral carcinogenesis; all-trans-retinoic acid; biodegradable microspheres; PDLLA;
D O I
10.1016/j.ijpharm.2006.04.003
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Retinoids are known to suppress carcinogenesis in various epithelial tissues. Among them, all-trans-retinoic acid (atRA) is recognized as one such active retinoid. However, despite the known anticarcinogenic activity of atRA, it exhibits its short plasma half-life during repeated oral administration due to the "acute retinoid resistance" in the liver. This has been the major limitation in clinical applications of atRA. Therefore, in order to render atRA more suitable for clinical uses, sustained delivery of atRA using biodegradable microspheres is suggested in this study. When 50 mg atRA/kg of atRA-loaded microspheres were subcutaneously administered to rats once, the atRA concentration in plasma was maintained around 6.5 ng/ml for 7 weeks, with only minor signs of toxicity. When the chemopreventive efficacy of atRA-loaded microspheres was evaluated using a model of 4-nitroquinoline I-oxide-induced oral carcinogenesis in F344 rats, a single injection of atRA-loaded microspheres significantly suppressed oral carcinogenesis. Additional injections of atRA-loaded microspheres, however, did not indicate further suppression of carcinogenesis. (c) 2006 Elsevier B.V All rights reserved.
引用
收藏
页码:45 / 52
页数:8
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