细胞毒性
化学
细胞
生物物理学
磁导率
紫杉醇
膜透性
细胞膜
药物输送
膜
体外
长时程增强
药品
体内
脉搏(音乐)
细胞生长
生物医学工程
核磁共振
膜电位
静磁学
磁场
跨膜蛋白
细胞培养
提拉帕扎明
电化学疗法
分子生物物理学
药理学
生物磁学
作者
Chi Ma,Fei Teng,Wei Zheng,Jiayu Chen,Yan Mi
摘要
Non-contact pulsed magnetic field (PMF) can alter cell membrane permeability, offering a novel pathway for the transmembrane delivery of exogenous substances. However, the dose–response characteristics of the relevant parameters remain unclear, and in vitro validation in combination with chemotherapeutic agents is still lacking. To address this gap, this study systematically evaluated the effects of magnetic induction intensity and pulse width on cell membrane permeability using a self-built, adjustable PMF generator, and further investigated, in a molecular size-oriented manner, the enhancement of cytotoxicity for different chemotherapeutic agents. The results showed that, within the tested parameter ranges, the cell permeabilization rate increased exponentially with magnetic induction intensity and followed a sigmoidal trend with pulse width. Moreover, the cytotoxicity of the small-molecular-size meisoindigo was markedly enhanced under the PMF (up to a 4.52-fold increase), whereas the larger-molecular-size paclitaxel showed only minimal potentiation. This Letter not only elucidates the parameter–dose relationships governing PMF-induced cell permeabilization, but also, for the first time, demonstrates the feasibility of PMF-synergized drug potentiation guided by drug molecular size. Together, these findings provide important theoretical and experimental support for parameter optimization and for expanding the applications of noninvasive magnetic field-assisted chemotherapy.
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