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首页> 外文期刊>Journal of nanoscience and nanotechnology >Imine Bond-and Coordinate Bond-Linked pH-Sensitive Cisplatin Complex Nanoparticles for Active Targeting to Tumor Cells
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Imine Bond-and Coordinate Bond-Linked pH-Sensitive Cisplatin Complex Nanoparticles for Active Targeting to Tumor Cells

机译:亚胺键和坐标粘合链接的pH敏感的顺铂复合纳米颗粒用于肿瘤细胞的活性靶向

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摘要

Aldehyde hyaluronic acid-cisplatin (A-HA-CDDP) complex nanoparticles were readily prepared, and CDDP was stably loaded into the core of the NPs through imine bond and coordinate bond linkages. The results show that the NPs were prepared successfully by a chemical complexation reaction rather than by physical mixing. Compared to many CDDP and HA complex nanoparticles evaluated in other studies, A-HA-CDDP NPs with imine and coordinate bonds between the A-HA and CDDP displayed better sustained release behavior and pH sensitivity. Therefore, the acidic tumor environment could accelerate the release of CDDP from the NPs. MTT and AO/EB staining assays showed that A-HA-CDDP NPs had comparable cell inhibition with CDDP in HeLa cells as well as little toxicity to NIH3T3 cells. This result indicates that the chemical reaction between A-HA and CDDP had little effect on the antitumor activity of CDDP and that the NPs actively targeted CD44-rich tumor cells. Both a hemolysis test and a protein adsorption assay demonstrated that A-HA-CDDP NPs had good biocompatibility and blood circulation in vivo. Therefore, the NPs have the potential to be used for targeted CDDP delivery in vivo. A subsequent publication will describe the circulation, targeting and tumor inhibition experiments of these NPs in vivo.
机译:物容易地制备醛透明质酸 - 顺铂(A-HA-CDDP)复合纳米颗粒,和CDDP稳定地装载到NP的通过亚胺键芯和配位键键。该结果表明,该纳米颗粒是通过化学络合反应,而不是通过物理混合成功制备。的A-HA和CDDP之间相比在其他研究中,A-HA-CDDP的NP与亚胺评价许多CDDP和HA复合纳米颗粒和配位键显示更好的持续释放行为和pH敏感性。因此,酸性肿瘤环境可能会加速CDDP从纳米粒子释放。 MTT和AO / EB染色分析表明,A-HA-CDDP的NP不得不在HeLa细胞与CDDP可比细胞抑制以及毒性小到NIH3T3细胞。这一结果表明,A-HA与顺铂之间的化学反应对顺铂的抗肿瘤活性的影响不大,而且纳米粒子积极有针对性的丰富的CD44的肿瘤细胞。两者的溶血试验和蛋白质吸附测定表明A-HA-CDDP的NP具有在体内具有良好的生物相容性和血液循环。因此,纳米颗粒必须被用于体内靶向递送CDDP的电位。随后的出版物将描述循环,靶向和体内这些NP的肿瘤抑制实验。

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