Nanohybrid based on layered zinc hydroxide with salicylic acid drug: Investigation of the structure and controlled release properties

H. Nabipour, Yuan Hu
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引用次数: 3

Abstract

Recently, nanoparticles have attracted much attention owing to their potential in biomedical applications, such as drug delivery systems, sustained release and controlled release. Various nanocarriers have been employed to ameliorate the efficacy and cytotoxicity of drugs, reducing their side effects through changing their pharmacokinetic properties. A simple and well-known model of pharmaceutical carriers is the layered zinc hydroxide (LZH) compound. In the present research, salicylic acid (Sal)-loaded LZH was synthesized using the ion-exchange method. The resulted nanohybrid (Sal-LZH) was characterized using the PXRD, FT-IR spectroscopy, STA analysis, BET, and SEM. Sal anions were intercalated into the interlayer gallery space of LZH, leading to different drug releases at pH 4.8 and 7.4. It was found that, the release of Sal anions from the synthetic nanohybrid occurred in a controlled manner, and the resulting material is suitable for use as a controlled-release formulation for various kinds of anti-inflammatory agent.
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水杨酸类药物层状氢氧化锌纳米杂化物的结构与控释性能研究
近年来,纳米颗粒因其在药物传递系统、缓释和控释等生物医学领域的潜在应用而备受关注。各种纳米载体已被用于改善药物的功效和细胞毒性,通过改变药物的药代动力学特性来减少药物的副作用。层状氢氧化锌(LZH)化合物是一种简单而著名的药物载体模型。本研究采用离子交换法合成了水杨酸负载LZH。采用PXRD、FT-IR、STA分析、BET和SEM对所制得的纳米杂化物(Sal-LZH)进行表征。在pH为4.8和7.4时,盐阴离子嵌入到LZH的层间通道空间,导致不同的药物释放。结果表明,所合成的纳米杂化物中盐离子的释放是可控的,所制备的材料适合作为各种抗炎药的控释制剂。
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