Literature DB >> 28707137

Surface modification of esophageal stent materials by a polyethylenimine layer aiming at anti-cancer function.

Kun Zhang1,2, Yuxin Bai1, Xiaofeng Wang2, Qian Li2, Fangxia Guan1, Jingan Li3,4.   

Abstract

Esophageal cancer is difficult to cure globally and possesses high mortality rate, and it is generally accepted that palliative care such as stent implantation is the main therapy method for esophageal cancer in later period. However, the restenosis caused by tumor cells and inflammatory cells seriously interferes the stent clinical application and limits its long-term services. To solve this problem, series of drug delivery stents were developed and proven rather effective in the early stage of implantation, but more serious restenosis occurred after the drug delivery was over, which endangered the patients' life. Therefore, endowing the esophageal stent continuous anti-cancer function become an ideal strategy for inhibiting the restenosis. In this contribution, the functional layer composed of polydopamine (PDA) and Poly-ethylenimine (PEI) with series of molecular weights (MW, 1.8 × 103, 1 × 104, 2.5 × 104 and 7 × 104 Da) were fabricated onto the esophageal stent material 317L stainless steel (317L SS) surface. The surface characterization including amine quantitative, atomic force microscopy (AFM) and water contact angle measurement indicated successful preparation of the PDA/PEI layer. The Eca109 cells culture results proved that the PDA/PEI layers significantly improve Eca109 cells apoptosis and necrosis, suggesting excellent anti-cancer function. In addition, we also found that the anti-cancer function of the PDA/PEI layers was positively correlated to the immobilized PEIs' MW. All the results demonstrated the potential application of the PDA/PEI layers on the surface modification of esophageal stent for continuous anti-cancer function. It is generally accepted that the restenosis caused by tumor cells seriously interferes the esophageal stent clinical application. Thus, endowing the esophageal stent continuous anti-cancer function is the ideal strategy for inhibiting the restenosis. In this work, we fabricated functional layers composed of polydopamine (PDA) and Poly-ethylenimine (PEI) with series of molecular weights (MW, 1.8 × 103, 1 × 104, 2.5 × 104 and 7 × 104 Da) onto the esophageal stent material 317L stainless steel (317L SS) surface to inhibit the tumor cells growth, and this function was related to the PEIs' molecular weights. The functional PDA/PEI layers were expected potentially applied for surface modification of esophageal stent materials.

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Year:  2017        PMID: 28707137     DOI: 10.1007/s10856-017-5939-y

Source DB:  PubMed          Journal:  J Mater Sci Mater Med        ISSN: 0957-4530            Impact factor:   3.896


  28 in total

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2.  Minimally invasive esophagectomy in the treatment of esophageal cancer.

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10.  Cell adhesion and growth enabled by biomimetic oligopeptide modification of a polydopamine-poly(ethylene oxide) protein repulsive surface.

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  7 in total

1.  Cell response of flexible PMMA-derivatives: supremacy of surface chemistry over substrate stiffness.

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Journal:  J Mater Sci Mater Med       Date:  2017-10-12       Impact factor: 3.896

2.  Benlysta-Loaded Sodium Alginate Hydrogel and Its Selective Functions in Promoting Skin Cell Growth and Inhibiting Inflammation.

Authors:  Xujia Wang; Shuaimeng Guan; Kun Zhang; Jingan Li
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3.  Investigation of Mg-Zn-Y-Nd alloy for potential application of biodegradable esophageal stent material.

Authors:  Shuo Wang; Xueqi Zhang; Jingan Li; Changsheng Liu; Shaokang Guan
Journal:  Bioact Mater       Date:  2020-01-08

4.  Investigation of Mg-xLi-Zn alloys for potential application of biodegradable bone implant materials.

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5.  Preparing a novel magnesium-doped hyaluronan/polyethyleneimine nanoparticle to improve endothelial functionalisation.

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Review 7.  Futuristic Developments and Applications in Endoluminal Stenting.

Authors:  Joel Ferreira-Silva; Renato Medas; Mohit Girotra; Monique Barakat; James H Tabibian; Eduardo Rodrigues-Pinto
Journal:  Gastroenterol Res Pract       Date:  2022-01-11       Impact factor: 2.260

  7 in total

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