Functionalized SBA-15: engineering, detailed study on release and kinetics of alendronate as well as its anti-tumour properties towards osteosarcoma

Anjali Patel and Shivangi Mehta
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Abstract

The present work deals with designing a biocompatible controlled drug delivery system (DDS) based on 12-tungstophosphoric acid (TPA)-functionalized SBA-15 for anti-osteoporotic drug alendronate sodium (ALD) and its characterization using different physicochemical techniques such as TGA, FT-IR spectroscopy, XRD, N2 adsorption measurements, HRTEM, and SEM. The designed DDS, ALD/TPA/SBA-15, was assessed for its drug delivery potential by carrying out in vitro drug release in simulated body fluid (pH 7.4, 37 °C) under stirring conditions as well as for the dissolution study. Release kinetics and mechanisms using zero order, first order, and Higuchi model were also carried out. Further, the release profile of the designed DDS was compared with the available marketed formulation (Osteofos), and ALD/TPA/SBA-15 shows a more controlled release. To explore the direct anti-tumour potency of ALD on osteosarcoma cells, an MTT assay was carried out at different concentrations, and the results show concentration-dependent inhibition of osteosarcoma cell proliferation.

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功能化 SBA-15:工程设计、阿仑膦酸钠释放和动力学详细研究及其对骨肉瘤的抗肿瘤特性
本研究以 12-钨磷酸(TPA)功能化的 SBA-15 为基础,为抗骨质疏松药物阿仑膦酸钠(ALD)设计了一种生物相容性可控给药系统(DDS),并采用不同的理化技术对其进行了表征,如 TGA、傅立叶变换红外光谱、XRD、N2 吸附测量、HRTEM 和 SEM。通过在搅拌条件下在模拟体液(pH 值为 7.4,温度为 37 °C)中进行体外药物释放以及溶解研究,评估了所设计的 DDS(ALD/TPA/SBA-15)的给药潜力。此外,还利用零阶、一阶和樋口模型进行了释放动力学和机制研究。此外,还将所设计的 DDS 的释放曲线与市售制剂(Osteofos)进行了比较,结果表明 ALD/TPA/SBA-15 的释放更可控。为了探索 ALD 对骨肉瘤细胞的直接抗肿瘤作用,研究人员进行了不同浓度的 MTT 试验,结果表明 ALD 对骨肉瘤细胞增殖的抑制作用与浓度有关。
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