Zhang Kun, Bai Yuxin, Wang Xiaofeng, Li Qian, Guan Fangxia, Li Jingan
School of Life Science, Zhengzhou University, 100 Science Road, Zhengzhou, 450001, PR China.
National Center for International Research of Micro-nano Molding Technology & Key Laboratory for Micro Molding Technology of Henan Province, Zhengzhou, PR China.
J Mater Sci Mater Med. 2017 Aug;28(8):125. doi: 10.1007/s10856-017-5939-y. Epub 2017 Jul 13.
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 × 10, 1 × 10, 2.5 × 10 and 7 × 10 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 × 10, 1 × 10, 2.5 × 10 and 7 × 10 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.
食管癌在全球范围内难以治愈且死亡率高,人们普遍认为诸如支架植入等姑息治疗是食管癌晚期的主要治疗方法。然而,肿瘤细胞和炎症细胞引起的再狭窄严重干扰了支架的临床应用并限制了其长期使用。为了解决这个问题,人们开发了一系列药物洗脱支架,并且在植入初期证明相当有效,但在药物释放结束后出现了更严重的再狭窄,危及患者生命。因此,赋予食管支架持续抗癌功能成为抑制再狭窄的理想策略。在本研究中,由聚多巴胺(PDA)和具有一系列分子量(MW,1.8×10、1×10、2.5×10和7×10 Da)的聚乙烯亚胺(PEI)组成的功能层被制备在食管支架材料317L不锈钢(317L SS)表面。包括胺定量、原子力显微镜(AFM)和水接触角测量在内的表面表征表明成功制备了PDA/PEI层。Eca109细胞培养结果证明,PDA/PEI层显著促进Eca109细胞凋亡和坏死,表明其具有优异的抗癌功能。此外,我们还发现PDA/PEI层的抗癌功能与固定化PEI的分子量呈正相关。所有结果证明了PDA/PEI层在食管支架表面改性以实现持续抗癌功能方面的潜在应用。人们普遍认为肿瘤细胞引起的再狭窄严重干扰了食管支架的临床应用。因此,赋予食管支架持续抗癌功能是抑制再狭窄的理想策略。在这项工作中,我们在食管支架材料317L不锈钢(317L SS)表面制备了由聚多巴胺(PDA)和具有一系列分子量(MW,1.8×10、1×10、2.5×10和7×10 Da)的聚乙烯亚胺(PEI)组成的功能层以抑制肿瘤细胞生长,并且这种功能与PEI的分子量有关。功能性PDA/PEI层有望潜在地应用于食管支架材料的表面改性。