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基于层层技术的羧基化金纳米粒子与不同链长脂质体相互作用的光谱研究及其控释药物

Spectroscopic Study of the Interaction of Carboxyl-Modified Gold Nanoparticles with Liposomes of Different Chain Lengths and Controlled Drug Release by Layer-by-Layer Technology.

机构信息

Discipline of Chemistry, Indian Institute of Technology Indore , Indore, Madhya Pradesh, India 453552.

出版信息

J Phys Chem B. 2017 Dec 21;121(50):11333-11343. doi: 10.1021/acs.jpcb.7b08455. Epub 2017 Dec 7.

Abstract

In this article, we investigate the interactions of carboxyl-modified gold nanoparticles (AuC) with zwitterionic phospholipid liposomes of different chain lengths using a well-known membrane probe PRODAN by steady-state and time-resolved spectroscopy. We use three zwitterionic lipids, namely, dipalmitoylphosphatidylcholine (DPPC), 1,2-dimyristoyl-sn-glycero-3-phosphocholine (DMPC), and 1,2-dilauroyl-sn-glycero-3-phosphocholine (DLPC), which are widely different in their phase transition temperatures to form liposome-AuC assemblies. The steady-state and time-resolved studies indicate that the AuC brings in stability toward liposomes by local gelation. We observe that the bound AuC detach from the surface of the liposomes under pH ≈ 5 due to protonation of the carboxyl group, thus eliminating the electrostatic interaction between nanoparticles and head groups of liposomes. The detachment rate of AuC from the liposome-AuC assemblies is different for the aforementioned liposomes due to differences in their fluidity. We exploited the phenomena for the controlled release of a prominent anticancer drug Doxorubicin (DOX) under acidic conditions for different zwitterionic liposomes. The drug release rate was further optimized by coating of liposome-AuC assemblies with oppositely charged polymer (P), polydiallyldimethylammonium chloride, followed by a mixture of lipids L (DMPC:DMPG) and again with a polymer in a layer-by-layer fashion to obtain capsule-like structures. This system is highly stable for weeks, as confirmed by field-emission scanning electron microscopy (FE-SEM) and confocal laser scanning microscopy (CLSM) imaging, and inhibits premature release. The layer coating was confirmed by hydrodynamic size and zeta potential measurements of the systems. The capsules obtained are of immense importance as they can control release of the drug from the systems to a large extent.

摘要

在本文中,我们使用一种众所周知的膜探针 PRODAN 通过稳态和时间分辨光谱研究了带负电荷的金纳米粒子(AuC)与不同链长的两性离子磷脂脂质体的相互作用。我们使用三种两性离子脂质,即二棕榈酰磷脂酰胆碱(DPPC)、1,2-二肉豆蔻酰-sn-甘油-3-磷酸胆碱(DMPC)和 1,2-二月桂酰基-sn-甘油-3-磷酸胆碱(DLPC),它们在相变温度方面差异很大,用于形成脂质体-AuC 组装体。稳态和时间分辨研究表明,AuC 通过局部凝胶化使脂质体稳定。我们观察到由于羧基的质子化,在 pH ≈ 5 时,AuC 从脂质体表面脱离,从而消除了纳米粒子和脂质体头部基团之间的静电相互作用。由于其流动性的差异,上述脂质体从脂质体-AuC 组装体上脱离 AuC 的速率不同。我们利用该现象在不同的两性离子脂质体条件下进行了在酸性条件下对著名抗癌药物阿霉素(DOX)的控制释放。通过带相反电荷的聚合物(P)聚二烯丙基二甲基氯化铵对脂质体-AuC 组装体进行涂层,然后将脂质 L(DMPC:DMPG)混合并再次用聚合物以层层方式进行涂层,以获得胶囊状结构,从而进一步优化了药物释放速率。正如场发射扫描电子显微镜(FE-SEM)和共聚焦激光扫描显微镜(CLSM)成像所证实的那样,该系统数周内高度稳定,并抑制了过早释放。通过系统的水动力粒径和 Zeta 电位测量证实了层涂层。所获得的胶囊具有重要意义,因为它们可以在很大程度上控制药物从系统中的释放。

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