Department of Organic and Inorganic Chemistry, Federal University of Ceará, Fortaleza, Brazil.
Faculty of Medicine, Federal University of Ceará, Sobral, Ceará, Brazil.
Int J Biol Macromol. 2021 May 15;179:314-323. doi: 10.1016/j.ijbiomac.2021.03.011. Epub 2021 Mar 3.
Polysaccharide based copolymers have been the focus of several research, particularly for the development of drug delivery systems. This study reports on the preparation of nanoparticles from an amphiphilic copolymer obtained by the poly(ε-caprolactone) graft in the structure of cashew gum, via ring-opening polymerization. The synthesis of copolymers was confirmed by Fourier transform infrared spectroscopy and nuclear magnetic resonance. The copolymers exhibit self-organization capability in water, with critical association concentration of 42 and 50 μg mL. The nanoparticle hydrodynamic diameters (212 and 202 nm) revealed a decreasing trend with increasing poly(ε-caprolactone) graft percentage. Epirubicin was used as an anticancer drug model and incorporated into the nanoparticles. The encapsulation efficiency reached 50% and 5.0% drug load. Nanoparticles showed an epirubicin controlled release profile, with maximum release of 93.0 ± 4.0% in 72 h, as well as excellent biocompatibility, according to hemolysis and cytotoxicity assays.
多糖基共聚物一直是许多研究的焦点,特别是在药物传递系统的开发方面。本研究报告了通过开环聚合在腰果酚结构中接枝聚(ε-己内酯)制备两亲性共聚物纳米粒子。共聚物的合成通过傅里叶变换红外光谱和核磁共振得到证实。共聚物在水中具有自组织能力,临界聚集浓度为 42 和 50μg/mL。纳米颗粒的水动力直径(212 和 202nm)随聚(ε-己内酯)接枝百分比的增加呈现出减小的趋势。表阿霉素被用作抗癌药物模型并掺入纳米颗粒中。包封效率达到 50%和 5.0%的药物负载。纳米颗粒显示出表阿霉素的控制释放曲线,在 72 小时内最大释放 93.0±4.0%,并且根据溶血和细胞毒性测定具有优异的生物相容性。