ORCID Profile
0000-0003-2110-7299
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Publisher: Wiley
Date: 18-04-2023
Abstract: Cell‐based therapies comprising the administration of living cells to patients for direct therapeutic activities have experienced remarkable success in the clinic, of which macrophages hold great potential for targeted drug delivery due to their inherent chemotactic mobility and homing ability to tumors with high efficiency. However, such targeted delivery of drugs through cellular systems remains a significant challenge due to the complexity of balancing high drug‐loading with high accumulations in solid tumors. Herein, a tumor‐targeting cellular drug delivery system (MAGN) by surface engineering of tumor‐homing macrophages (M φ s) with biologically responsive nanosponges is reported. The pores of the nanosponges are blocked with iron‐tannic acid complexes that serve as gatekeepers by holding encapsulated drugs until reaching the acidic tumor microenvironment. Molecular dynamics simulations and interfacial force studies are performed to provide mechanistic insights into the “ON‐OFF” gating effect of the polyphenol‐based supramolecular gatekeepers on the nanosponge channels. The cellular chemotaxis of the M φ carriers enabled efficient tumor‐targeted delivery of drugs and systemic suppression of tumor burden and lung metastases in vivo. The findings suggest that the MAGN platform offers a versatile strategy to efficiently load therapeutic drugs to treat advanced metastatic cancers with a high loading capacity of various therapeutic drugs.
Publisher: Elsevier BV
Date: 05-2021
Publisher: AIP Publishing
Date: 03-2022
DOI: 10.1063/5.0083099
Abstract: One-dimensional (1D) nanoscale objects abundant in nature commonly possess hierarchical structures and are generally constructed via bottom-up self-assembly strategies. The unique high aspect ratio morphology of the assembled nanofibrillar materials, such as collagen, cellulose, and silk, together with highly ordered architectures, endows a range of remarkable functionalities in nature. Inspired by this hierarchical building principle, block copolymers (BCPs) have been developed and employed to engineer man-made functional 1D nanostructures and as models to study the self-assembly process. The rapid development of advanced polymerization techniques allows for the precise design of BCPs and the resulting assemblies with intensive studies on distinct structure–property–function relationships. In this Review, we summarize and discuss the formation of fiber-like micelles from the perspectives of fundamental driving forces and molecular interactions involved in the solution self-assembly process. Three main formation mechanisms are highlighted, including covalent bonding, volume exclusion, and crystallization, which are involved in the corresponding domains of coronal, interfacial, and core segments of BCPs. Two spatiotemporal levels of fiber-like assemblies are discussed. In addition, the emerging applications and a general guidance for the rational design of advanced BCPs are proposed in light of the unique traits of fiber-like micelles.
No related grants have been discovered for Jiaojiao Shang.