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Mg-Al layered double hydroxide-methotrexate nanohybrid drug delivery system: Evaluation of efficacy

机译:镁铝层状双氢氧化物-甲氨蝶呤纳米杂化给药系统:疗效评估

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Mg-Al layered double hydroxide nanoparticles were synthesized by one-pot co-precipitation method and anticancerous drug methotrexate was incorporated into it by in-situ ion exchange. The LDH-MTX nanohybrid produced moderately stable suspension in water, as predicted by zeta potential measurement. X-ray diffraction revealed that the basal spacing increased to nearly twice the same for pristine LDH on MTX intercalation. Thermogravimetric analyses confirmed an increase in thermal stability of the intercalated drug in the LDH framework. A striking enhancement in efficacy/sensitivity of MTX on the HCT-116 cells was obtained when intercalated within the LDH layers, as revealed by the attainment of half maximal inhibitory concentration of LDH-MTX nanohybrid by 48 h, whereas, bare MTX required 72 h for the same. The MTX release from MgAl-LDH-MTX hybrids in phosphate buffer saline at pH 7.4 followed a relatively slow, first order kinetics and was complete within 8 days following diffusion and crystal dissolution mechanism.
机译:通过一锅共沉淀法合成了Mg-Al层状双氢氧化物纳米粒子,并通过原位离子交换将抗癌药甲氨蝶呤掺入其中。如通过ζ电势测量所预测的,LDH-MTX纳米杂交体在水中产生中等稳定的悬浮液。 X射线衍射显示,在MTX插入过程中,原始LDH的基础间距增加到几乎两倍。热重分析证实了LDH骨架中插入药物的热稳定性增加。当插入LDH层中时,MTX对HCT-116细胞的功效/敏感性有了显着提高,这是LDH-MTX纳米杂化物的最大抑制浓度达到48 h的一半所显示的,而裸MTX需要72 h对于相同的。在pH 7.4的磷酸盐缓冲盐水中,MgAl-LDH-MTX杂种从MgAl-LDH-MTX杂合物中释放的MTX遵循相对缓慢的一级动力学,并在扩散和晶体溶解机制后8天内完成。

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