Fabrication of aggregation induced emission dye-based fluorescent organic nanoparticles via emulsion polymerization and their cell imaging applications
文献信息
Xiqi Zhang, Bin Yang, Meiying Liu, Wanyun Liu, Yiwang Chen, Yen Wei
Aggregation induced emission (AIE) dye-based fluorescent organic nanoparticles (FONs) have recently emerged as novel fluorescent bioprobes due to their remarkable optical properties, water solubility and biocompatibility. In this work, a novel strategy for the fabrication of AIE-based FONs was developed via emulsion polymerization for the first time. During this procedure, a polymerizable AIE dye (named as PhE) with a double bond end functional group was facilely incorporated into the hydrophobic core of polymer nanoparticles. The obtained polymer nanoparticles (named as PhE–Pst NPs) exhibited strong fluorescence and high water dispersibility owing to the partial aggregation of PhE and the surface covered with a hydrophilic shell. More importantly, these FONs showed spherical morphology, uniform size (about 200 nm) and excellent biocompatibility, making them promising for bioimaging applications.
期刊推荐
相关文献
Structure and solvation dynamics of the hydroxide ion in ice-like water clusters: a CCSD(T) and car–parrinello molecular dynamics study
DOI: 10.1039/D1CP02524D
Exploring the thermodynamic, kinetic and inhibitory mechanisms of 5-iTU targeting mitotic kinase haspin by integrated molecular dynamics
Qianqian Wang, Qinggao Zhang, Elaine Lai Han Leung, Yingqing Chen, Xiaojun Yao
DOI: 10.1039/D1CP02783B
Directed gas-phase preparation of the elusive phosphinosilylidyne (SiPH2, X2A′′) and cis/trans phosphinidenesilyl (HSiPH; X2A′) radicals under single-collision conditions
Chao He, Shane J. Goettl, Zhenghai Yang, Srinivas Doddipatla, Ralf I. Kaiser, Mateus Xavier Silva, Breno R. L. Galvão
DOI: 10.1039/D1CP02812J
Designing new ferromagnetic double perovskites: the coexistence of polar distortion and half-metallicity
Neda Rahmani, Mohammad Ebrahim Ghazi, Morteza Izadifard, Alireza Shabani, Jost Adam
DOI: 10.1039/D1CP02479E
Microscale pH inhomogeneity in frozen NaCl solutions
Shun Kataoka, Makoto Harada, Tetsuo Okada
DOI: 10.1039/D1CP01655E
Oxidation of HOSO˙ by Cl˙: a new source of SO2 in the atmosphere?
Amit Kumar, Subhasish Mallick, Pradeep Kumar
DOI: 10.1039/D1CP01048D
Fluorescence band exchange narrowing in a series of squaraine oligomers: energetic vs. structural disorder
Arthur Turkin, Pavel Malý
DOI: 10.1039/D1CP02136B
Characterization of the deformation behaviors under uniaxial stress for bicontinuous nanoporous amorphous alloys
Yuhang Zhang, Yiqun Hu, Suhang Ding, Fuying Du
DOI: 10.1039/D1CP04970D
Adsorption and reaction mechanisms of single and double H2O molecules on graphene surfaces with defects: a density functional theory study
Zeng Liang, Kejiang Li, Ziming Wang, Yushan Bu, Jianliang Zhang
DOI: 10.1039/D1CP02595C
Mechanistic insight into oxygen vacancy migration in SrFeO3−δ from DFT+U simulations
Musa Alaydrus
DOI: 10.1039/D1CP02452C
您可能还喜欢
如何储存1,2-环己二酮环乙缩醛(CAS号:4746-96-7)?
1,2-环己二酮环乙缩醛应储存在阴凉、干燥、通风良好的地方,避免阳光直射。建议使用密封容器保存,并保持环境温度在室温范围内,远离火源和热源。
Ecopladib(CAS号:381683-92-7)的市场或研究趋势如何?
Ecopladib作为一种新型的药物,主要应用于治疗高胆固醇等疾病。目前,市场和研究趋势显示,Ecopladib因其独特的药理作用而受到关注。随着对心血管疾病治...
2,3-Dimethyl-3H-imidazo[4,5-c]pyridine(CAS号:52538-09-7)通常如何合成?
2,3-二甲基-3H-咪唑[4,5-c]吡啶通常通过咪唑和2,3-二甲基吡啶的缩合反应合成。具体来说,将咪唑和2,3-二甲基吡啶在适当的溶剂中进行加热或加压反应...
2,3,4,5-tetrahydro-1H-3-苯并氮杂环;盐酸盐(CAS号:17379-01-0)的市场或研究趋势如何?
该化合物在药物化学和有机合成中有一定的应用。近年来,随着对新型药物化合物的需求增加,该化合物的研究趋势主要集中在探索其生物活性,尤其是其在神经系统疾病治疗中的潜...
如何储存盐酸甘氨酸丁酯(CAS号:13048-99-2)?
盐酸甘氨酸丁酯应储存在阴凉、干燥、通风良好的地方,避免阳光直射和高温环境,温度应控制在25℃以下。储存容器应密封,避免与空气中的水分和酸性物质接触,以防发生水解...
什么是2-Iodo-N,N-dimethylbenzamide(CAS号:54616-46-5)?
2-碘-N,N-二甲基苯胺是一种有机化合物,化学名为2-Iodo-N,N-dimethylbenzamide。其分子式为C<sub>9</sub>H<sub>1...
5-溴-2-(4H-1,2,4-三唑-4-基)吡啶(CAS号:959240-99-4)的市场或研究趋势如何?
随着医药、农药和新材料领域的发展,该化合物作为关键中间体的应用日益增多。特别是在药物合成中,由于其独特的化学性质,可以用于合成多种药物分子。未来的研究趋势可能集...
2,4-二溴-6-三氟甲基嘧啶(CAS号:785778-00-9)通常如何合成?
2,4-二溴-6-三氟甲基嘧啶通常通过溴化反应合成。首先,将6-三氟甲基嘧啶与溴化剂(如液溴)在适当的溶剂(如二氯甲烷、四氢呋喃)中反应,加入适当的催化剂(如四...
来源期刊
Polymer Chemistry

Polymer Chemistry welcomes submissions in all areas of polymer science that have a strong focus on macromolecular chemistry. Manuscripts may cover a broad range of fields, yet no direct application focus is required.










![[(1S,2S,3R,4S,7R,9S,10S,12R,15S)-4,12-Diacetyloxy-15-[(2R,3S)-3-benzamido-3-phenyl-2-(2,2,2-trichloroethoxycarbonyloxy)propanoyl]oxy-1,9-dihydroxy-10,14,17,17-tetramethyl-11-oxo-6-oxatetracyclo[11.3.1.03,10.04,7]heptadec-13-en-2-yl] benzoate structure [(1S,2S,3R,4S,7R,9S,10S,12R,15S)-4,12-Diacetyloxy-15-[(2R,3S)-3-benzamido-3-phenyl-2-(2,2,2-trichloroethoxycarbonyloxy)propanoyl]oxy-1,9-dihydroxy-10,14,17,17-tetramethyl-11-oxo-6-oxatetracyclo[11.3.1.03,10.04,7]heptadec-13-en-2-yl] benzoate structure](https://cnstatic.chemtradehub.com/structs/100/100431-55-8-7104.webp)
![(2E)-3-(3-Chlorophenyl)-N-{2-[4-(methylsulfonyl)-1-piperazinyl]-2-oxoethyl}acrylamide structure (2E)-3-(3-Chlorophenyl)-N-{2-[4-(methylsulfonyl)-1-piperazinyl]-2-oxoethyl}acrylamide structure](https://cnstatic.chemtradehub.com/structs/250/2505001-54-5-c1e9.webp)


