Nanomedicine for uterine leiomyoma therapy

被引:0
|
作者
Ali, Hazem [1 ,2 ]
Kilic, Gokhan [1 ]
Vincent, Kathleen [1 ,3 ]
Motamedi, Massoud [3 ]
Rytting, Erik [1 ,3 ,4 ]
机构
[1] Univ Texas Med Branch, Dept Obstet & Gynecol, Galveston, TX 77555 USA
[2] Univ Calif San Diego, Moores Canc Ctr, La Jolla, CA 92093 USA
[3] Univ Texas Med Branch, Ctr Biomed Engn, Galveston, TX 77555 USA
[4] Univ Texas Med Branch, Dept Pharmacol & Toxicol, Galveston, TX 77555 USA
基金
美国国家科学基金会;
关键词
D O I
10.4155/TDE.12.144
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Background: The purpose of this work was to engineer polymeric nanoparticles to encapsulate and deliver 2-methoxyestradiol, a potential antitumor drug for treatment of uterine leiomyoma (fibroids), the most common hormone-dependent pathology affecting women of reproductive age. Methods/Results: Encapsulation efficiency and drug release from the nanoparticles were monitored by HPLC. Cell morphology and in vitro cytotoxicity experiments were carried out in a human leiomyoma cell line. The nanoparticles displayed high encapsulation efficiency (>86%), which was verified by differential scanning calorimetry and x-ray diffraction. Excellent long-term stability of the nanoparticles and gradual drug release without burst were also observed. Cellular uptake of fluorescent nanoparticles was confirmed by confocal imaging. The drug-loaded poly(lactic acid) and poly(lactic-coglycolic acid) nanoparticles induced cytotoxicity in human leiomyoma cells to a significantly greater extent than the free drug at 0.35 mu M. Conclusion: This novel approach represents a potential fertility-preserving alternative to hysterectomy.
引用
收藏
页码:161 / 175
页数:15
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