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首页> 外文期刊>Langmuir: The ACS Journal of Surfaces and Colloids >Internal Structure of Nanometer-Sized Droplets Prepared by Antisolvent Precipitation
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Internal Structure of Nanometer-Sized Droplets Prepared by Antisolvent Precipitation

机译:抗溶剂沉淀制备的纳米尺寸液滴的内部结构

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摘要

Antisolvent precipitation (AP) is a low-cost and less-invasive preparation alternative for organic nano-particles compared to top-down methods such as high-pressure homogenization or milling. Here we report on particularly small organic nanoparticles (NPs) prepared by AP. It has been found for various materials that these NPs in their liquid state exhibit a significant degree of molecular order at their interface toward the dispersion medium including ubiquinones (coenzyme Q10), triglycerides (trimyristin, tripalmitin), and alkanes (tetracosane). This finding is independent of the use of a stabilizer in the formulation. While this is obviously a quite general interfacial structuring effect, the respective structural details of specific NPs systems might differ. Here, a detailed structural characterization of very small liquid coenzyme Q10 (Q10) NPs is presented as a particular example for this phenomenon. The Q10 NPs have been prepared by AP in the presence of two different stabilizers, sodium dodecyl sulfate (SDS) and pentaethylene glycol monododecyl ether (C12E5), respectively, and without any stabilizer. The NPs' size is initially analyzed by photon correlation spectroscopy (PCS). The SDS-stabilized Q10 NPs have been studied further by differential scanning calorimetry (DSC), small-angle X-ray and neutron scattering (SAXS, SANS), wide-angle X-ray scattering (WAXS), and cryogenic transmission electron microscopy (CryoTEM). A simultaneous analysis of SAXS and contrast variation SANS studies revealed the molecular arrangement within the interface between the NPs and the dispersion medium. The Q10 NPs stabilized by SDS and C12E5, respectively, are small (down to 19.9 nm) and stable (for at least 16 months) even when no stabilizer is used. The SDS-stabilized Q10 NPs reported here, are therewith, to the best of our knowledge, the smallest organic NPs which have been reported to be prepared by AP so far. In particular, these NPs exhibit a core-shell structure consisting of an amorphous Q10 core and a surrounding shell, which is mainly composed of oriented Q10 molecules and aligned SDS molecules. This structure suggests a significant amphiphilic behavior and a rather unexpected stabilizing role of Q10 molecules.
机译:抗溶剂沉淀(AP)是与高压均质化或研磨等自上而下方法相比的有机纳米颗粒的低成本和较少侵入的制剂。在这里,我们报告了通过AP制备的特别小的有机纳米颗粒(NPS)。已经发现,对于各种材料,这些材料在其液态中,它们的液态具有显着程度的分子序,其界面朝向包括泛醌(辅酶Q10),甘油三酯(Trigyristin,Tripalmitin)和烷烃(四骨烷烃)的分散介质。该发现与配方中的稳定剂的使用无关。虽然这显然是一个相当一般的界面结构效果,但特定NPS系统的各个结构细节可能不同。这里,将非常小的液体辅酶Q10(Q10)NP的详细结构表征作为这种现象的特定示例。通过AP在两种不同的稳定剂,十二烷基硫酸钠(SDS)和五亚乙二醇单癸基醚(C12E5)存在下,Q10 NPS已经通过AP制备,并且没有任何稳定剂。最初通过光子相关光谱(PC)分析NPS的尺寸。通过差示扫描量热法(DSC),小角X射线和中子散射(SAXS,SAN),广角X射线散射(蜡)和低温透射电子显微镜()进一步研究了SDS稳定的Q10NPS。 Cryotem)。同时分析萨克斯和对比变异SANS研究显示NPS和分散介质之间的界面内的分子布置。通过SDS和C12E5稳定的Q10NPS分别稳定(下降至19.9nm),即使在不使用稳定剂时,也稳定(下降至19.9nm)和稳定(至少16个月)。据我们所知,这里报道的SDS稳定的Q10 NPS是据报道的最小有机NPS,据报道是通过AP准备的。特别地,这些NPS表现出由无定形Q10核和周围壳体组成的核壳结构,其主要由取向的Q10分子和对准的SDS分子组成。该结构表明了Q10分子的显着又意外的稳定作用。

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    Friedrich Alexander Univ Erlangen Nurnberg FAU Inst Crystallog &

    Struct Phys Staudtstr 3 D-91058 Erlangen Germany;

    Friedrich Alexander Univ Erlangen Nurnberg FAU Inst Crystallog &

    Struct Phys Staudtstr 3 D-91058 Erlangen Germany;

    Friedrich Alexander Univ Erlangen Nurnberg FAU Inst Crystallog &

    Struct Phys Staudtstr 3 D-91058 Erlangen Germany;

    Friedrich Alexander Univ Erlangen Nurnberg FAU Inst Crystallog &

    Struct Phys Staudtstr 3 D-91058 Erlangen Germany;

    Friedrich Alexander Univ Erlangen Nurnberg FAU Inst Crystallog &

    Struct Phys Staudtstr 3 D-91058 Erlangen Germany;

    Forschungszentrum Julich JCNS Heinz Maier Leibnitz Zentrum MLZ Lichtenbergstr 1 D-85748 Garching Germany;

    ESRF 71 Ave Martyrs CS40220 F-38042 Grenoble 9 France;

    Jena Univ Hosp Ctr Electron Microscopy Ziegelmuhlenweg 1 D-07743 Jena Germany;

    Friedrich Alexander Univ Erlangen Nurnberg FAU Chair Chem Engn &

    React Engn 1 Egerlandstr 3 D-91058 Erlangen Germany;

    Friedrich Alexander Univ Erlangen Nurnberg FAU Inst Crystallog &

    Struct Phys Staudtstr 3 D-91058 Erlangen Germany;

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  • 正文语种 eng
  • 中图分类 物理化学(理论化学)、化学物理学 ; 化学 ;
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