Polymer Research Laboratory, Department Of Chemistry, Sharif University of Technology, Azadi Avenue, P.O.Box11365-9516, Tehran, Iran.
Mater Sci Eng C Mater Biol Appl. 2016 Apr 1;61:782-90. doi: 10.1016/j.msec.2015.12.096. Epub 2016 Jan 8.
Novel bilayer coated mesoporous silica nanoparticle (MCM-41) based on pH sensitive poly(acrylic acid-co-itaconic acid) and human serum albumin (HSA) was designed for controlled delivery of gemcitabine (anticancer drug) to cancer cells. The shell around the mesoporous silica has bilayer structure. Poly(acrylic acid-co-itaconic acid) was used as pH-sensitive inner shell and human serum albumin, HSA, was used as outer shell. The core-shell structure was formed due to electrostatic interaction between ammonium groups of modified MCM-41 and carboxylate groups of copolymer. Also, the albumin layer was wrapped around the copolymer coated nanoparticle by electrostatic interaction between ammonium groups from protein and carboxylate ions of copolymer shell. Moreover, the maximum release occurred at pH 5.5 (pH of endosomes) because the bilayer shell collapsed at this pH. The drug nanocarrier would be a good candidate for tumor therapy due to its biocompatibility, controlled release and pH responsive behavior.
基于 pH 敏感的聚(丙烯酸-co-衣康酸)和人血清白蛋白 (HSA) 的新型双层包覆介孔硅纳米粒子 (MCM-41) 被设计用于控制吉西他滨 (抗癌药物) 递送到癌细胞。介孔硅周围的壳具有双层结构。聚(丙烯酸-co-衣康酸)被用作 pH 敏感的内壳,人血清白蛋白 (HSA) 被用作外壳。由于改性 MCM-41 的铵基团与共聚物的羧酸盐基团之间的静电相互作用,形成了核壳结构。此外,由于来自蛋白质的铵基团与共聚物壳的羧酸盐离子之间的静电相互作用,白蛋白层被包裹在共聚物包覆的纳米粒子周围。此外,在 pH 5.5(内涵体的 pH)时发生最大释放,因为双层壳在此 pH 下坍塌。由于其生物相容性、控制释放和 pH 响应行为,药物纳米载体将是肿瘤治疗的良好候选物。