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介孔硅纳米粒子纳米通道内锌酞菁的间隔组装和解组装及光动力活性。

Spacer intercalated disassembly and photodynamic activity of zinc phthalocyanine inside nanochannels of mesoporous silica nanoparticles.

机构信息

Division of Chemistry and Biological Chemistry, School of Physical and Mathematical Sciences, Nanyang Technological University , 21 Nanyang Link, 637371 Singapore.

出版信息

ACS Appl Mater Interfaces. 2013 Dec 26;5(24):12860-8. doi: 10.1021/am404578h. Epub 2013 Dec 16.

Abstract

Hydrophobic photosensitizer zinc(II) phthalocyanine (ZnPc) was loaded into adamantane (Ad) modified nanochannels of mesoporous silica nanoparticles (MSNPs). The Ad units on the surface of MSNPs were complexed with amino-substituted β-cyclodextrin to enhance the solubility of the hybrid in aqueous solution. The amino groups on β-cyclodextrin also provide functional sites for further conjugation with targeting ligands toward targeted cancer therapy. Since the intercalation of the Ad spacer isolates loaded ZnPc and prevents its aggregation inside MSNPs, ZnPc exhibits its monomeric characteristics to effectively generate cytotoxic singlet oxygen ((1)O2) upon light irradiation (675 nm) in aqueous conditions, leading to efficient photodynamic activity for successful cancer treatment in vitro. Current research presents a convenient approach to maintain the monomeric state of hydrophobic photosensitizer ZnPc by rationally utilizing multifunctional MSNPs as the carriers. The novel hybrid with targeting capability achieves active photodynamic property of monomeric ZnPc in aqueous solution under light irradiation, which may find its way for practical photodynamic therapy in the future.

摘要

将疏水性光敏剂锌(II)酞菁(ZnPc)负载到介孔硅纳米粒子(MSNPs)的金刚烷(Ad)修饰的纳米通道中。MSNPs 表面上的 Ad 单元与氨基取代的β-环糊精络合,以提高该混合体在水溶液中的溶解度。β-环糊精上的氨基还提供了进一步与靶向配体结合的功能位点,以实现针对癌症的靶向治疗。由于 Ad 间隔物的嵌入将负载的 ZnPc 隔开,并防止其在 MSNPs 内聚集,因此 ZnPc 在光照(675nm)下表现出其单体特性,有效地在水相条件下生成细胞毒性单重态氧((1)O2),从而实现体外有效的光动力治疗。目前的研究提出了一种简便的方法,通过合理利用多功能 MSNPs 作为载体,来保持疏水性光敏剂 ZnPc 的单体状态。具有靶向能力的新型杂化物在光照下实现了水溶性单体 ZnPc 的主动光动力特性,这可能为未来的实际光动力治疗开辟道路。

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