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用于胰岛素鼻腔给药的玉米醇溶蛋白/聚丙烯酸树脂复合纳米粒的研制与表征

Development and Characterization of Zein/Eudragit Composite Nanoparticles for Insulin Intranasal Delivery.

作者信息

Moreira Felipe Figueiredo, Ziebarth Jeferson, Babinski Tatiane Patricia, Mainardes Rubiana Mara

机构信息

Laboratory of Nanostructured Formulations, Universidade Estadual do Centro-Oeste, Élio Antonio Dalla Vecchia Aveniu, 838, 85040-167 Guarapuava, Paraná, Brazil.

Centro Universitário Campo Real, Comendador Norberto Street, 1299, 85015-420 Guarapuava, Paraná, Brazil.

出版信息

ACS Omega. 2025 May 21;10(21):21236-21249. doi: 10.1021/acsomega.4c10474. eCollection 2025 Jun 3.

Abstract

Diabetes mellitus (DM) is a chronic metabolic disorder characterized by elevated blood glucose levels, primarily due to impaired insulin secretion or action. The standard treatment for Type 1 Diabetes Mellitus still involves daily parenteral insulin administration, which presents several challenges including patient discomfort, reduced adherence, and the potential for peripheral hyperinsulinemia. Intranasal administration has emerged as a promising alternative due to the nasal cavity's high vascularization, ease of access, and significant absorption capacity, though certain physiological barriers remain. This study aimed to develop and characterize Zein-Eudragit nanoparticles (NPS) as carriers for insulin (ZEU/INS NPS) intended for intranasal administration. The NPS were prepared using a liquid-liquid dispersion method, and the production process was optimized through a 2 factorial design. The resulting NPS were evaluated in terms of physicochemical properties, including particle size, polydispersity index (PDI), zeta potential, Fourier-transform infrared spectroscopy (FTIR), differential scanning calorimetry (DSC), thermogravimetric analysis (TG), and morphology. Additionally, the physical stability of the NPS during storage, in vitro insulin release, and in vitro mucoadhesion were assessed. The optimized nanoparticle formulation exhibited a mean particle size below 200 nm, a PDI of less than 0.3, a zeta potential of approximately +30 mV, and an encapsulation efficiency of 42%. FTIR analysis confirmed the interaction between nanoparticle components following insulin encapsulation, and DSC/TG analysis demonstrated the thermal stability of the system. NPS stored under refrigerated conditions maintained their stability for up to 60 days. In vitro release studies revealed that about 60% of the encapsulated insulin was released over a 24 h period. The in vitro mucoadhesion assay further supported the potential of these NPS to enhance the residence time in the nasal cavity. Overall, ZEU/INS NPS successfully demonstrated favorable physicochemical characteristics for the intranasal delivery of insulin. These findings suggest that these NPS offer significant promise as an effective and noninvasive delivery system for insulin.

摘要

糖尿病(DM)是一种慢性代谢紊乱疾病,其特征是血糖水平升高,主要原因是胰岛素分泌或作用受损。1型糖尿病的标准治疗方法仍然包括每日进行肠胃外胰岛素给药,这带来了诸多挑战,包括患者不适、依从性降低以及外周高胰岛素血症的可能性。由于鼻腔血管丰富、易于给药且具有显著的吸收能力,鼻内给药已成为一种有前景的替代方法,尽管仍存在某些生理屏障。本研究旨在开发并表征玉米醇溶蛋白 - 丙烯酸树脂纳米粒(NPS)作为用于鼻内给药的胰岛素载体(ZEU/INS NPS)。使用液 - 液分散法制备纳米粒,并通过二因素设计优化生产过程。对所得纳米粒进行了物理化学性质评估,包括粒径、多分散指数(PDI)、zeta电位、傅里叶变换红外光谱(FTIR)、差示扫描量热法(DSC)、热重分析(TG)和形态学。此外,还评估了纳米粒在储存期间的物理稳定性、体外胰岛素释放以及体外黏膜黏附性。优化后的纳米粒制剂平均粒径低于200 nm,PDI小于0.3,zeta电位约为 +30 mV,包封率为42%。FTIR分析证实了胰岛素包封后纳米粒成分之间的相互作用,DSC/TG分析表明系统具有热稳定性。在冷藏条件下储存的纳米粒在长达60天内保持其稳定性。体外释放研究表明,约60%的包封胰岛素在24小时内释放。体外黏膜黏附试验进一步支持了这些纳米粒增强在鼻腔内停留时间的潜力。总体而言,ZEU/INS NPS成功展示了用于胰岛素鼻内递送的良好物理化学特性。这些发现表明,这些纳米粒作为一种有效且无创的胰岛素递送系统具有巨大潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/984a/12138680/91fddfe21eff/ao4c10474_0001.jpg

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