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Light-switchable nanoparticles based on amphiphilic diblock, triblock and heterograft polyoxazoline

机译:基于两亲性二嵌段,三嵌段和异接枝聚恶唑啉的光可转换纳米粒子

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Photo-active nanoparticles (NPD, NPT, NPH) were elaborated in water from amphiphilic diblock (D), triblock (T) and heterograft (H) copolymers based on a chromatic unit, coumarin, linked to an alkyl chain and a hydrophilic polyoxazoline chain. Under UV-exposure, for graft copolymers, the coumarin moieties crosslink the nanoparticle core (NPHx) while a simple chain by chain dimerization happens with linear diblock and triblock copolymers (NPDx and NPT). The self-assembly of these copolymers was examined as well as the UV-activity and UV-reversibility of the corresponding NPs by UV spectroscopy. Their stability under light exposure and temperature was also monitored by dynamic light scattering (DLS). Finally, the loading of a lipophilic fluorescent probe (Nile red) into the NP core was evaluated by fluorescence emission. All these data illustrate the tunable size, UV-activity, stability and loading efficiency of the NPs by the starting macromolecular architecture of the amphiphilic copolymers. Triblock copolymers seem to be a promising tool for switchable NPs characterized by two opposite states: NPs alternatively with and without a photo-dimerized core.
机译:光敏纳米粒子(NP D ,NP T ,NP H )在水中由基于色单元香豆素的两亲性二嵌段(D),三嵌段(T)和异质接枝(H)共聚物加工而成,香豆素与烷基链和亲水性聚恶唑啉链相连。在紫外线照射下,对于接枝共聚物,香豆素部分使纳米颗粒核(NP Hx )交联,而线性二嵌段和三嵌段共聚物(NP)则通过链二聚作用形成简单链 Dx 和NP T )。通过紫外光谱检查了这些共聚物的自组装以及相应NP的UV活性和UV可逆性。还通过动态光散射(DLS)监测了它们在光照和温度下的稳定性。最后,通过荧光发射评估了亲脂性荧光探针(尼罗红)在NP核中的负载。所有这些数据说明了通过两亲共聚物的起始大分子结构,NP的可调大小,UV活性,稳定性和负载效率。三嵌段共聚物似乎是用于以两种相反状态为特征的可转换NP的有前途的工具:具有或不具有光二聚核的NP。

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