Instituto de Química de São Carlos, Universidade de São Paulo, Av. Trabalhador São-Carlense, 400, São Carlos 13566-590, SP, Brazil.
Departamento de Química, Universidade Federal de São Carlos, Rodovia Washington Luis, km 235, São Carlos, 13565-905, SP, Brazil.
Molecules. 2022 Sep 7;27(18):5801. doi: 10.3390/molecules27185801.
Salts of naproxen (NAP) with chitosan (CTS) and reticulated chitosan (CEP) were prepared under optimized conditions to maximize the yield of reaction. The objective was to evaluate the dissociation in water, which can guide studies of release of the drug from biopolymeric salts in pharmaceutical applications. Higher salification was found after 24 h of reaction at 60 °C in a molar ratio 1:1.05 (CTS:NAP, mol/mol), resulting in a degree of substitution (DS) of 17% according to C NMR, after neutralization of the -NH group of the biopolymer by the carboxylic group of the drug. The presence of NAP salt is evidenced by FTIR bands related to the -NH group at 856 cm, a decrease in crystallinity index in XRD diffractograms as well as changes in mass loss ratios (TG/DTG/DTA) and increased thermal stability of the salt regarding CTS itself. The CEPN crosslinked salt presented a DS = 3.6%, probably due to the shielding of the -NH groups. Dissociation studies revealed that at pH 2.00, dissociation occurred faster when compared to at pH 7.00 in the non-reticulated salt, while the opposite was observed for the reticulated one.
制备了在优化条件下与壳聚糖(CTS)和交联壳聚糖(CEP)的萘普生(NAP)盐,以最大化反应产率。目的是评估在水中的离解,这可以指导药物从药物应用中的生物聚合物盐中释放的研究。在 60°C 下以 1:1.05(CTS:NAP,摩尔/摩尔)的摩尔比反应 24 小时后,发现盐化程度更高,根据 C NMR,得到 17%的取代度(DS),这是由于生物聚合物的-NH 基团被药物的羧酸基团中和。通过与-NH 基团相关的 FTIR 带(856 cm 处),XRD 衍射图中的结晶度指数降低,以及质量损失比(TG/DTG/DTA)的变化和交联盐相对于 CTS 本身的热稳定性增加,可以证明 NAP 盐的存在。CEPN 交联盐的取代度为 3.6%,这可能是由于-NH 基团被屏蔽。离解研究表明,在 pH 2.00 时,与非交联盐相比,在 pH 7.00 时离解更快,而对于交联盐则相反。