Wei Guangfei, Zong Bin, He Quan, Su Shiying, Li Yu, Zheng Jiawen, Qian Yuanxia, Cao Peng, Li Zhongxing
Clinical Medical Research Center, Zhenjiang Hospital of Chinese Traditional and Western Medicine, Zhenjiang, 212004, China.
Affiliated Zhenjiang Integrated Hospital of Traditional Chinese and Western Medicine of Xinglin College, Nantong University, Zhenjiang, 212004, China.
Small. 2024 Dec;20(51):e2405948. doi: 10.1002/smll.202405948. Epub 2024 Oct 2.
A monolayer encapsulation is a new opportunity for engineering a system with high drug loading, but immobilizing polymer molecules on the surface of individual peptide nanoparticles is still an ongoing challenge. Herein, an individual peptide nanoparticle encapsulation strategy is proposed via surface adsorption, in which peptide molecules undergo granulation and subsequently aggregate with polymer molecules, forming a network via electrostatic interactions. Under the water phase, surplus polymer molecules dissolve, leading to a single nanoparticle encapsulation with a core-shell structure. As expected, the dense interfacial layer on the peptide nanoparticle surface achieves a superior loading degree of up to 95.4%. What's more, once the core-shell structure is established, the peptide mass fraction in individual encapsulation always exceeds 90% even under fierce external force. Following the individual nanoparticle encapsulation, the insulin-polycation complex (InsNp@PEI) reduces the inflammation from polymer and displays an effective glycemic control in type 1 diabetes. Overall, the newly developed single surface decoration encapsulates peptides with ultrahigh efficiency and opens up the possibility for further encapsulation.
单层封装是构建高载药量系统的新契机,但将聚合物分子固定在单个肽纳米颗粒表面仍是一项持续的挑战。在此,提出了一种通过表面吸附的单个肽纳米颗粒封装策略,其中肽分子经历造粒过程,随后与聚合物分子聚集,通过静电相互作用形成网络。在水相中,多余的聚合物分子溶解,形成具有核壳结构的单个纳米颗粒封装。正如预期的那样,肽纳米颗粒表面致密的界面层实现了高达95.4%的优异载药量。此外,一旦建立核壳结构,即使在强大外力作用下,单个封装中的肽质量分数也始终超过90%。在单个纳米颗粒封装之后,胰岛素-聚阳离子复合物(InsNp@PEI)减轻了聚合物引起的炎症,并在1型糖尿病中显示出有效的血糖控制。总体而言,新开发的单表面修饰以超高效率封装肽,并为进一步封装开辟了可能性。