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用于生物医学成像的树枝状磁性纳米颗粒修饰的微泡:通过氟相互作用实现有效稳定化

Microbubbles decorated with dendronized magnetic nanoparticles for biomedical imaging: effective stabilization via fluorous interactions.

作者信息

Shi Da, Wallyn Justine, Nguyen Dinh-Vu, Perton Francis, Felder-Flesch Delphine, Bégin-Colin Sylvie, Maaloum Mounir, Krafft Marie Pierre

机构信息

Institut Charles Sadron (CNRS), University of Strasbourg, 23 rue du Loess, 67034 Strasbourg, France.

Institut de Physique et de Chimie des Matériaux de Strasbourg (IPCMS), University of Strasbourg, 23 rue du Loess, 67034 Strasbourg, France.

出版信息

Beilstein J Nanotechnol. 2019 Oct 31;10:2103-2115. doi: 10.3762/bjnano.10.205. eCollection 2019.

DOI:10.3762/bjnano.10.205
PMID:31728258
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6839566/
Abstract

Dendrons fitted with three oligo(ethylene glycol) (OEG) chains, one of which contains a fluorinated or hydrogenated end group and bears a bisphosphonate polar head (C X OEGDen, X = F or H; = 2 or 4), were synthesized and grafted on the surface of iron oxide nanoparticles (IONPs) for microbubble-mediated imaging and therapeutic purposes. The size and stability of the dendronized IONPs (IONP@C X OEGDen) in aqueous dispersions were monitored by dynamic light scattering. The investigation of the spontaneous adsorption of IONP@C X OEGDen at the interface between air or air saturated with perfluorohexane and an aqueous phase establishes that exposure to the fluorocarbon gas markedly increases the rate of adsorption of the dendronized IONPs to the gas/water interface and decreases the equilibrium interfacial tension. This suggests that fluorous interactions are at play between the supernatant fluorocarbon gas and the fluorinated end groups of the dendrons. Furthermore, small perfluorohexane-stabilized microbubbles (MBs) with a dipalmitoylphosphatidylcholine (DPPC) shell that incorporates IONP@C X OEGDen (DPPC/Fe molar ratio 28:1) were prepared and subsequently characterized using both optical microscopy and an acoustical method of size determination. The dendrons fitted with fluorinated end groups lead to smaller and more stable MBs than those fitted with hydrogenated groups. The most effective result is already obtained with CF, for which MBs of ≈1.0 μm in radius reach a half-life of ≈6.0 h. An atomic force microscopy investigation of spin-coated mixed films of DPPC/IONP@CXOEGDen combinations (molar ratio 28:1) shows that the IONPs grafted with the fluorinated dendrons are located within the phospholipid film, while those grafted with the hydrocarbon dendrons are located at the surface of the phospholipid film.

摘要

合成了带有三条聚乙二醇(OEG)链的树枝状分子,其中一条链含有氟化或氢化端基并带有双膦酸酯极性头(CₓOEGDen,x = F或H; = 2或4),并将其接枝到氧化铁纳米颗粒(IONPs)表面,用于微泡介导的成像和治疗目的。通过动态光散射监测树枝状化IONPs(IONP@CₓOEGDen)在水分散体中的尺寸和稳定性。对IONP@CₓOEGDen在空气或全氟己烷饱和空气与水相之间的界面上的自发吸附研究表明,暴露于碳氟化合物气体显著提高了树枝状化IONPs吸附到气/水界面的速率,并降低了平衡界面张力。这表明上清液中的碳氟化合物气体与树枝状分子的氟化端基之间存在氟相互作用。此外,制备了具有二棕榈酰磷脂酰胆碱(DPPC)壳且包含IONP@CₓOEGDen(DPPC/Fe摩尔比为28:1)的小型全氟己烷稳定微泡(MBs),随后使用光学显微镜和声学尺寸测定方法对其进行了表征。带有氟化端基的树枝状分子比带有氢化端基的树枝状分子导致更小且更稳定的MBs。对于CF已经获得了最有效的结果,其半径约为1.0μm的MBs半衰期约为6.0小时。对DPPC/IONP@CXOEGDen组合(摩尔比28:1)的旋涂混合膜进行的原子力显微镜研究表明,接枝有氟化树枝状分子的IONPs位于磷脂膜内,而接枝有烃基树枝状分子的IONPs位于磷脂膜表面。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7343/6839566/9db79e78486a/Beilstein_J_Nanotechnol-10-2103-g013.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7343/6839566/24e5655a62a1/Beilstein_J_Nanotechnol-10-2103-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7343/6839566/1632f2fba1ee/Beilstein_J_Nanotechnol-10-2103-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7343/6839566/454681603c4c/Beilstein_J_Nanotechnol-10-2103-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7343/6839566/55553f2a8875/Beilstein_J_Nanotechnol-10-2103-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7343/6839566/bbfdf528ca22/Beilstein_J_Nanotechnol-10-2103-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7343/6839566/ac03ef2be1c1/Beilstein_J_Nanotechnol-10-2103-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7343/6839566/6bcc2a6a9927/Beilstein_J_Nanotechnol-10-2103-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7343/6839566/d09f539bdb1f/Beilstein_J_Nanotechnol-10-2103-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7343/6839566/703dd394a5b5/Beilstein_J_Nanotechnol-10-2103-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7343/6839566/66c64425a53d/Beilstein_J_Nanotechnol-10-2103-g011.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7343/6839566/579d265ed326/Beilstein_J_Nanotechnol-10-2103-g012.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7343/6839566/9db79e78486a/Beilstein_J_Nanotechnol-10-2103-g013.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7343/6839566/24e5655a62a1/Beilstein_J_Nanotechnol-10-2103-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7343/6839566/1632f2fba1ee/Beilstein_J_Nanotechnol-10-2103-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7343/6839566/454681603c4c/Beilstein_J_Nanotechnol-10-2103-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7343/6839566/55553f2a8875/Beilstein_J_Nanotechnol-10-2103-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7343/6839566/bbfdf528ca22/Beilstein_J_Nanotechnol-10-2103-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7343/6839566/ac03ef2be1c1/Beilstein_J_Nanotechnol-10-2103-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7343/6839566/6bcc2a6a9927/Beilstein_J_Nanotechnol-10-2103-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7343/6839566/d09f539bdb1f/Beilstein_J_Nanotechnol-10-2103-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7343/6839566/703dd394a5b5/Beilstein_J_Nanotechnol-10-2103-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7343/6839566/66c64425a53d/Beilstein_J_Nanotechnol-10-2103-g011.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7343/6839566/579d265ed326/Beilstein_J_Nanotechnol-10-2103-g012.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7343/6839566/9db79e78486a/Beilstein_J_Nanotechnol-10-2103-g013.jpg

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