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Novel pH- and Temperature-Responsive Blend Hydrogel Microspheres of Sodium Alginate and PNIPAAm-g-GG for Controlled Release of Isoniazid

机译:海藻酸钠和PNIPAAm-g-GG的新型pH响应和温度响应混合水凝胶微球用于异烟肼的控释

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摘要

This paper reports the preparation and characterization of novel pH- and thermo-responsive blend hydrogel microspheres of sodium alginate (NaAlg) and poly(N-isopropylacrylamide)(PNIPAAm)-grafted-guar gum (GG) i.e., PNIPAAm-g-GG by emulsion cross-linking method using glutaraldehyde (GA) as a cross-linker. Isoniazid (INZ) was chosen as the model antituberculosis drug to achieve encapsulation up to 62%. INZ has a plasma half-life of 1.5 h, whose release was extended up to 12 h. Fourier transform infrared spectroscopy was used to confirm the grafting reaction and chemical stability of INZ during the encapsulation. Differential scanning calorimetry was used to investigate the drug’s physical state, while powder X-ray diffraction confirmed the molecular level dispersion of INZ in the matrix. Scanning electron microscopy confirmed varying surface morphologies of the drug-loaded microspheres. Temperature- and pH-responsive nature of the blend hydrogel microspheres were investigated by equilibrium swelling, and in vitro release experiments were performed in pH 1.2 and pH 7.4 buffer media at 37°C as well as at 25°C. Kinetics of INZ release was analyzed by Ritger–Peppas empirical equation to compute the diffusional exponent parameter (n), whose value ranged between 0.27 and 0.58, indicating the release of INZ follows a diffusion swelling controlled release mechanism.
机译:本文报道了通过海藻酸钠(NaAlg)和聚(N-异丙基丙烯酰胺)(PNIPAAm)接枝瓜尔胶(GG)即PNIPAAm-g-GG制备的新型pH响应和热响应混合水凝胶微球的制备和表征。戊二醛(GA)作为交联剂的乳液交联方法。选择异烟肼(INZ)作为抗结核药物的模型,以实现高达62%的包封率。 INZ的血浆半衰期为1.5小时,释放时间延长至12小时。傅里叶变换红外光谱用于确认封装过程中INZ的接枝反应和化学稳定性。差示扫描量热法用于研究药物的物理状态,而粉末X射线衍射证实INZ在基质中的分子水平分散。扫描电子显微镜证实载药微球的表面形态变化。通过平衡溶胀研究了共混水凝胶微球的温度和pH响应特性,并在37°C和25°C的pH 1.2和pH 7.4缓冲液中进行了体外释放实验。用Ritger-Peppas经验公式分析了INZ的释放动力学,以计算扩散指数参数(n),其值在0.27至0.58之间,表明INZ的释放遵循扩散溶胀控制释放机制。

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