Department of Chemistry, College of Natural Sciences, Can Tho University, Can Tho, Vietnam.
Department of Biology, College of Natural Sciences, Can Tho University, Can Tho, Vietnam.
PLoS One. 2024 May 23;19(5):e0303177. doi: 10.1371/journal.pone.0303177. eCollection 2024.
Silk fibroin nanoparticles (FNP) have been increasingly investigated in biomedical fields due to their biocompatibility and biodegradability properties. To widen the FNP versatility and applications, and to control the drug release from the FNP, this study developed the Eudragit S100-functionalized FNP (ES100-FNP) as a pH-responsive drug delivery system, by two distinct methods of co-condensation and adsorption, employing the zwitterionic furosemide as a model drug. The particles were characterized by sizes and zeta potentials (DLS method), morphology (electron microscopy), drug entrapment efficiency and release profiles (UV-Vis spectroscopy), and chemical structures (FT-IR, XRD, and DSC). The ES100-FNP possessed nano-sizes of ∼200-350 nm, zeta potentials of ∼ -20 mV, silk-II structures, enhanced thermo-stability, non-cytotoxic to the erythrocytes, and drug entrapment efficiencies of 30%-60%, dependent on the formulation processes. Interestingly, the co-condensation method yielded the smooth spherical particles, whereas the adsorption method resulted in durian-shaped ones due to furosemide re-crystallization. The ES100-FNP adsorbed furosemide via physical adsorption, followed Langmuir model and pseudo-second-order kinetics. In the simulated oral condition, the particles could protect the drug in the stomach (pH 1.2), and gradually released the drug in the intestine (pH 6.8). Remarkably, in different pH conditions of 6.8, 9.5, and 12, the ES100-FNP could control the furosemide release rates depending on the formulation methods. The ES100-FNP made by the co-condensation method was mainly controlled by the swelling and corrosion process of ES100, and followed the Korsmeyer-Peppas non-Fickian transport mechanism. Whereas, the ES100-FNP made by the adsorption method showed constant release rates, followed the zero-order kinetics, due to the gradual furosemide dissolution in the media. Conclusively, the ES100-FNP demonstrated high versatility as a pH-responsive drug delivery system for biomedical applications.
丝素纳米粒子(FNP)由于其生物相容性和可生物降解性而在生物医学领域得到了越来越多的研究。为了拓宽 FNP 的多功能性和应用范围,并控制 FNP 中的药物释放,本研究通过两种不同的共聚缩合和吸附方法,以两性离子呋塞米为模型药物,开发了 Eudragit S100 功能化 FNP(ES100-FNP)作为 pH 响应性药物递送系统。通过动态光散射法(DLS 法)测定粒径和zeta 电位,电子显微镜观察形态,紫外可见分光光度法测定药物包封率和释放曲线,傅里叶变换红外光谱(FT-IR)、X 射线衍射(XRD)和差示扫描量热法(DSC)测定化学结构。ES100-FNP 的粒径约为 200-350nm,zeta 电位约为 -20mV,具有丝素 II 结构,热稳定性增强,对红细胞无细胞毒性,药物包封率为 30%-60%,这取决于制剂工艺。有趣的是,共聚缩合法得到的是光滑的球形粒子,而吸附法则由于呋塞米再结晶而得到榴莲状粒子。ES100-FNP 通过物理吸附吸附呋塞米,符合 Langmuir 模型和拟二级动力学。在模拟口服条件下,该粒子可在胃(pH1.2)中保护药物,并在肠(pH6.8)中逐渐释放药物。值得注意的是,在不同的 pH 值条件 6.8、9.5 和 12 下,ES100-FNP 可以根据制剂方法控制呋塞米的释放速率。通过共聚缩合法制备的 ES100-FNP 主要受 ES100 的溶胀和腐蚀过程控制,符合 Korsmeyer-Peppas 非菲克扩散机制。而通过吸附法制备的 ES100-FNP 由于药物在介质中的逐渐溶解,表现出恒定的释放速率,符合零级动力学。总之,ES100-FNP 作为一种用于生物医学应用的 pH 响应性药物递送系统具有很高的多功能性。