Hameed Amer Rashid, Majdoub Hatem, Jabrail Fawzi Habeeb
The State Company for Drugs Industry and Medical Appliances, Samaraa 34010, Iraq.
Laboratory of Interfaces and Advanced Materials, Faculty of Science of Monastir, University of Monastir, Monastir 5000, Tunisia.
Polymers (Basel). 2023 Jul 26;15(15):3173. doi: 10.3390/polym15153173.
The cross-linked microspheres were prepared and loaded with Favipiravir SARS-CoV-2 antiviral drug, by copolymerization of chitosan (CS) with a polysaccharide extracted from fresh pomegranate peels. Moreover, glutaraldehyde (Glu) has been used as a chemical cross-linker and sodium hexametaphosphate (SHMP) as a physical cross-linker. The extracted polysaccharide was analyzed, and different techniques have been used. The analyses lead to the conclusion that it is pectin. The surface morphology of the prepared microspheres was studied using a scanning electron microscope, where the size and shape factor (S) of the Glu microspheres showed high values (74.27 μm) and (0.852), respectively, meaning their surfaces tend to be rough, whereas the SHMP microspheres showed a smaller size particle (20.47 μm) and a smaller shape factor (0.748), which gives an indication that the SHMP microspheres have smooth surfaces. The swelling studies have shown that Glu microspheres have a higher degree of swelling, which means SHMP microspheres are more compact. The prepared microspheres have shown a higher loading percentage of Favipiravir antiviral drug in SHMP microspheres (37% /) in comparison with Glu microspheres (35% /), where the electrostatic interaction between the Favipiravir ions and SHMP anions helps for more loading. The microspheres prepared under different types of cross-linking have shown initial burst release of Favipiravir, followed by a step of controlled release for a certain period of time, whose period depends on the pH of the release medium. Both Glu and SHMP cross-linked microspheres have shown high controlled release times in buffered release solutions at pH = 7.4 and for shorter periods at pH = 1.3 and pH = 9.4, which may be related to the type of electrostatic interactions between drug and polymer systems and their reactions with release solution ions.
通过壳聚糖(CS)与从新鲜石榴皮中提取的多糖共聚,制备了交联微球并负载了法匹拉韦抗SARS-CoV-2病毒药物。此外,戊二醛(Glu)用作化学交联剂,六偏磷酸钠(SHMP)用作物理交联剂。对提取的多糖进行了分析,并使用了不同的技术。分析得出结论,它是果胶。使用扫描电子显微镜研究了制备的微球的表面形态,其中Glu微球的尺寸和形状因子(S)分别显示出高值(74.27μm)和(0.852),这意味着它们的表面趋于粗糙,而SHMP微球显示出较小的颗粒尺寸(20.47μm)和较小的形状因子(0.748),这表明SHMP微球具有光滑的表面。溶胀研究表明,Glu微球具有更高的溶胀度,这意味着SHMP微球更致密。与Glu微球(35% /)相比,制备的微球在SHMP微球中显示出更高的法匹拉韦抗病毒药物负载百分比(37% /),其中法匹拉韦离子与SHMP阴离子之间的静电相互作用有助于更多的负载。在不同类型交联下制备的微球显示出法匹拉韦的初始突释,随后是一段时间的控释步骤,其时间取决于释放介质的pH值。Glu和SHMP交联微球在pH = 7.4的缓冲释放溶液中均显示出高控释时间,而在pH = 1.3和pH = 9.4时控释时间较短,这可能与药物和聚合物系统之间的静电相互作用类型及其与释放溶液离子的反应有关。