Effects of phosphate salts and ultrasonication on the formation and characteristics of phosphate-chitosan microparticles

Hugo Espinosa-Andrews , Jorge Alejandro Barbosa-Nuñez , Moisés Martínez-Velázquez , Gustavo Adolfo Castillo-Herrera , José Nabor Haro-González
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Abstract

The physicochemical properties of chitosan-microparticles are related to the crosslinking salts. The effects of sodium-pyrophosphate or sodium-tripolyphosphate and ultrasonication on the formation of phosphate-chitosan microparticles were evaluated. Potentiometric titration curves were used to determine the ionization degree of chitosan by employing the Henderson-Hasselbach equation and milliequivalents. Colloidal formation was validated by turbidity and conductivity at different phosphate-chitosan salt ratios. The ultrasonication effect was characterized by visual appearance, zeta potential, particle size, FTIR, SEM, and EDS analyses. Additionally, the impact of particle size on the cytotoxicity and the encapsulation properties of a curcumin microemulsion was assessed. Chitosan ionization degree was pH dependent and was fully ionized below 4.0. The milliequivalent points were estimated at 0.9 and 1.06 for the two crosslinkers and chitosan, respectively. The maximum turbidity observed during complex formation was 0.5 and 1.0 for the pyrophosphate-chitosan and tripolyphosphate-chitosan samples, respectively, showing a critical conductivity value of 1. FTIR showed the interaction between phosphate salts (PO) and chitosan amino groups (NH3+) in the region of 1200–1650 cm–1. SEM showed that the particle size decreased with ultrasonication. After ultrasonication, the particle size of the phosphate-chitosan microparticles decreased 17-fold but the zeta potential did not change. The phosphate-chitosan complexes did not present cytotoxic activity at concentrations lower than 1000 µg/mL. The pyrophosphate-chitosan and tripolyphosphate-chitosan microparticles have remarkable loading capacities for curcumin, making them promising carriers for nutraceutical and pharmaceutical applications.

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磷酸盐和超声波对磷酸盐壳聚糖微颗粒的形成和特性的影响
壳聚糖微粒的理化性质与交联盐有关。评估了焦磷酸钠或三聚磷酸钠和超声波对磷酸盐壳聚糖微颗粒形成的影响。通过亨德森-哈塞尔巴赫方程和毫当量,利用电位滴定曲线确定壳聚糖的电离度。在不同的磷酸盐-壳聚糖盐比例下,通过浊度和电导率验证了胶体的形成。通过视觉外观、ZETA电位、粒度、傅立叶变换红外光谱、扫描电镜和 EDS 分析,确定了超声处理的效果。此外,还评估了粒度对姜黄素微乳液的细胞毒性和封装特性的影响。壳聚糖的电离度与 pH 值有关,在 4.0 以下完全电离。据估计,两种交联剂和壳聚糖的毫当量点分别为 0.9 和 1.06。傅立叶变换红外光谱显示,磷酸盐(PO-)和壳聚糖氨基(NH3+)在 1200-1650 cm-1 区域相互作用。扫描电镜显示,粒径随超声处理而减小。超声处理后,磷酸盐-壳聚糖微颗粒的粒径减小了 17 倍,但 zeta 电位没有变化。磷酸盐-壳聚糖复合物在浓度低于 1000 µg/mL 时不具有细胞毒性。焦磷酸-壳聚糖和三聚磷酸-壳聚糖微颗粒具有显著的姜黄素负载能力,使其成为营养保健品和医药应用的理想载体。
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