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基于玉米醇溶蛋白的纳米载体:口服给药的进展

Zein-Based Nanocarriers: Advances in Oral Drug Delivery.

作者信息

Liu Yuxin, An Dongyu, Meng Xiangjian, Deng Shiming, Liu Guijin

机构信息

Key Laboratory of Tropical Biological Resources of Ministry of Education, School of Pharmaceutical Sciences, Hainan University, Haikou 570228, China.

出版信息

Pharmaceutics. 2025 Jul 21;17(7):944. doi: 10.3390/pharmaceutics17070944.

Abstract

Oral administration remains the preferred drug delivery route but faces formidable gastrointestinal barriers, including enzymatic degradation, solubility limitations, and poor epithelial absorption. Zein-based nanocarriers (ZBNs), derived from maize prolamin, provide a transformative platform to address these challenges. This review synthesizes recent advances in ZBNs' design, highlighting their intrinsic advantages: structural stability across pH gradients, self-assembly versatility, and a surface functionalization capacity. Critically, we detail how engineered ZBNs overcome key barriers, such as enzymatic/chemical protection via hydrophobic encapsulation, the enhanced mucus penetration or adhesion through surface engineering, and improved epithelial transport via ligand conjugation. Applications demonstrate their efficacy in stabilizing labile therapeutics, enhancing the solubility of BCS Class II/IV drugs, enabling pH-responsive release, and significantly boosting oral bioavailability. Remaining challenges in scalability and translational predictability warrant future efforts toward multifunctional systems, bio-interfacial modeling, and continuous manufacturing. This work positions ZBNs as a potential platform for the oral delivery of BCS Class II-IV drugs' in the biopharmaceutics classification system.

摘要

口服给药仍然是首选的药物递送途径,但面临着巨大的胃肠道屏障,包括酶降解、溶解度限制和上皮吸收不良。源自玉米醇溶蛋白的玉米醇溶蛋白基纳米载体(ZBNs)提供了一个变革性平台来应对这些挑战。本综述总结了ZBNs设计的最新进展,突出了它们的内在优势:跨pH梯度的结构稳定性、自组装多功能性和表面功能化能力。至关重要的是,我们详细阐述了工程化ZBNs如何克服关键障碍,例如通过疏水包封实现酶促/化学保护、通过表面工程增强黏液渗透或黏附以及通过配体偶联改善上皮转运。应用实例证明了它们在稳定不稳定治疗药物、提高BCS II/IV类药物溶解度、实现pH响应释放以及显著提高口服生物利用度方面的功效。在可扩展性和转化可预测性方面仍然存在的挑战需要未来在多功能系统、生物界面建模和连续制造方面做出努力。这项工作将ZBNs定位为生物药剂学分类系统中口服递送BCS II-IV类药物的潜在平台。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b1f2/12300950/20d6044b74ea/pharmaceutics-17-00944-g001.jpg

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