Tamoxifen Delivery to Breast Cancer Cells (MCF-7) Via Hydroxyapatite Microspheres

Binnaz Kirbiyik, B. Mazmancı, Şeyma Gülnaz Yarlılar, Naz Ugur, K. Ocakoğlu
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Abstract

Drug delivery systems have been used in cancer treatment to increase drug effectiveness. The hydroxyapatite (HAP) based materials used in this area can provide drug transport to the target site without its deterioration. In this study, porous hollow hydroxyapatite microspheres (PHHMs) were produced by using the hydrothermal method. Tamoxifen (TAM) used in the treatment of breast cancer has been covalently attached to the produced microspheres. The obtained microsphere structures (tamoxifen-loaded hydroxyapatite, TAM/H) were successfully characterized by ATR-FTIR, FE-SEM, XRD, and DLS methods. The breast cancer cell line MCF-7 was used to examine the effect of the hybrid structure. The cytotoxic and genotoxic effects of TAM/H was compared with the TAM groups on MCF-7. Our results have showed that, the decrease in cell viability at 24 and 36 hours were still continued at 48 hours only in TAM/H groups. In addition, TAM/H was found to show a genotoxic affect by the increment in genetic damage index (GDI) and damaged cell percentage (DCP%). As a result, use of hydroxyapatite was suitable for the transport of TAM and that covalent binding was suitable for drug particle interaction with hybrid structure and thus controlled drug release occurred.
他莫昔芬通过羟基磷灰石微球递送至乳腺癌细胞(MCF-7)
药物输送系统已用于癌症治疗,以提高药物的有效性。该领域使用的羟基磷灰石(HAP)基材料可以提供药物运输到目标部位而不会变质。采用水热法制备多孔空心羟基磷灰石微球(PHHMs)。用于治疗乳腺癌的他莫昔芬(TAM)已被共价地附着在生产的微球上。通过ATR-FTIR、FE-SEM、XRD和DLS等方法对制备的负载他莫昔芬的羟基磷灰石(TAM/H)进行了表征。以乳腺癌细胞系MCF-7为研究对象,考察了杂交结构的影响。比较TAM/H对MCF-7的细胞毒和基因毒作用。我们的研究结果表明,TAM/H组在24和36小时的细胞活力下降仍然持续到48小时。此外,TAM/H通过增加遗传损伤指数(GDI)和损伤细胞百分比(DCP%)发现其具有遗传毒性作用。因此,羟基磷灰石适合于TAM的转运,共价结合适合于药物颗粒与杂化结构的相互作用,从而实现药物的可控释放。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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