Comprehensive studies on the interactions between chitosan nanoparticles and some live cells

被引:0
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作者
Ai-ping Zheng
Hui-xue Liu
Lan Yuan
Meng Meng
Jian-cheng Wang
Xuan Zhang
Qiang Zhang
机构
[1] School of Pharmaceutical Sciences,The State Key Laboratory of Natural and Biomimetic Drugs
[2] Peking University,The State Key Laboratory of Natural and Biomimetic Drugs
[3] Beijing Institute of Pharmacology and Toxicology,undefined
[4] School of Pharmaceutical Sciences,undefined
[5] Peking University,undefined
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关键词
Nanoparticles; Polycationic polymers; Thymopentin; Polymer interactions; Caco-2 Cells; C6 Cells; Nanomedicine;
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摘要
As more and more oral formulations of nanoparticles are used in clinical contexts, a comprehensive study on the mechanisms of interaction between polymer nanoparticles and live cells seems merited. Such a study was conducted and the results were compared to the polymer itself in order to demonstrate different kinds of effects that are brought into the cell by polymer and its nanoparticles, especially the effects on the biomembrane. Several techniques, including surface plasmon resonance (SPR), Fourier transformed infrared spectroscopy (FTIR), Raman spectroscopy, fluorescence polarization spectroscopy (FP), flow cytometry (FCM) with quantitative analysis, and confocal images with antibody staining were employed toward this end. The cytotoxicity in vitro was also evaluated. Chitosan (CS), a polycationic polymer, was used to prepare the nanoparticles. We demonstrate that chitosan nanoparticles (CS-NP) induce strong alterations in the distribution of membrane proteins, fluidity of membrane lipids, and general membrane structure. Furthermore, the uptake of CS-NP into Caco-2 cells was found to have a similar mechanism to that of CS molecules, but the differences in degree were noted. These results indicate that positive charge and nanoscale size were the factors that most significantly affected the interactions between the nanoparticles of polycationic polymers and live cells. However, no difference in cytotoxicity toward the Caco-2 cells was found between CS and CS-NP. This supports the idea that CS-NP is an effective and safe carrier for oral drug delivery.
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页码:4765 / 4776
页数:11
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