Design of pH-responsive Nanocarriers for Controlled Delivery of Anti-allergic Corticosteroid Analogues.

Sergey Gupalo, Sutha Devaraj, Kyaw Zaw Win, Yuan Seng Wu, Phone Myint Htoo, Wana Hla Shwe, Rohini Karunakaran, Aravinda Wundavalli, Suprava Das, Manglesh Waran Udayah, Nazmul Mhm
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Abstract

Introduction: Allergic inflammation has become an important public health issue. If left uncontrolled, it can lead to serious health problems. Mast cells and the drugs that regulate the endosomal compartments in these cells have become central to addressing these problems. The aim of this project was to build a biological model capable of regulating the intracellular delivery of anti-allergic corticosteroids.

Methods: The nanocarrier was designed based on micellar swelling and pH-responsive acid-sensitive linkers. The model's functionality was evaluated through a range of physicochemical characterization and in silico tests. Mathematical modeling was incorporated to simulate the nanocarrier's behavior and diffusion control. Models representing mucosal and mast cell-relevant environments were used to evaluate the designed system in a simulated microenvironment.

Results: The nanocarriers showed clear micellar swelling and a pronounced positive surface charge, with high drug encapsulation efficiency, and displayed both pH- and time-dependent behavior, as supported by physicochemical characterization and computational modeling. Mathematical modeling showed that charge dissolution was controlled and that drug release was governed by the rate of proton-dependent drug degradation. The system exhibited minimal drug release under physiological pH conditions, ensuring stability, while enabling controlled and enhanced drug release under acidic conditions relevant to mast cell-associated microenvironments. The system has low hemolysis, low cellular epithelial cytotoxicity, prolonged drug diffusive release, and favorable diffusive release.

Discussion: The collected data confirm that the design enables both time- and space-controlled release of the drug from the nanocarrier system within endolysosomal compartments associated with the allergic inflammatory response. The noted control of mast cell secretions illustrates immunomodulation and the control of side effects from systemic/extended use of corticosteroids.

Conclusion: This study demonstrates that the system is not only safe and effective for the delivery of drugs into cells but also capable of targeting cells involved in the allergic inflammatory pathway. The emerging pH-sensitive nanocarriers have strong therapeutic potential.

抗过敏皮质类固醇类似物控制递送ph响应纳米载体的设计。
导读:过敏性炎症已成为一个重要的公共卫生问题。如果不加以控制,可能会导致严重的健康问题。肥大细胞和调节这些细胞内体腔室的药物已成为解决这些问题的核心。本项目的目的是建立一个能够调节抗过敏皮质类固醇细胞内递送的生物学模型。方法:基于胶束膨胀和ph响应酸敏连接剂设计纳米载体。该模型的功能通过一系列物理化学表征和计算机测试进行了评估。采用数学模型对纳米载体的行为和扩散控制进行了模拟。代表粘膜和肥大细胞相关环境的模型用于在模拟微环境中评估设计的系统。结果:纳米载体胶束膨胀明显,表面带明显的正电荷,具有较高的药物包封效率,并具有pH和时间依赖性,物理化学表征和计算模型支持。数学模型表明,电荷溶解受控制,药物释放受质子依赖性药物降解速率的控制。该系统在生理pH条件下表现出最小的药物释放,确保了稳定性,同时在与肥大细胞相关的微环境相关的酸性条件下能够控制和增强药物释放。该系统溶血率低,细胞上皮细胞毒性低,药物弥散释放时间长,弥散释放有利。讨论:收集的数据证实,该设计能够在与过敏性炎症反应相关的内溶酶体腔室内的纳米载体系统中实现时间和空间控制的药物释放。肥大细胞分泌的显著控制说明了免疫调节和控制全身/长期使用皮质类固醇的副作用。结论:本研究表明,该系统不仅能够安全有效地将药物递送到细胞内,而且能够靶向参与过敏性炎症通路的细胞。新兴的ph敏感纳米载体具有很强的治疗潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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