Oligo(p-phenyleneethynylene) embedded amphiphiles: synthesis, photophysical properties and self-assembled nanoparticles with high structural stability and photostability for cell imaging
Literature Information
Chao Yin, Wenli Song, Rongcui Jiang, Wenbo Hu, Qingming Shen, Xiang Li, Jie Li, Quli Fan
Novel amphiphilic organic asymmetrically oligo(p-phenyleneethynylene) (OPE) conjugated molecules, ending with a hydrophobic alkyl chain and a hydrophilic methoxypolyethyleneglycol (MPEG) segment, were designed and synthesized. Due to the hydrophilic–hydrophobic nature of the asymmetrically amphiphilic OPE conjugated molecules, monodispersed fluorescent nanoparticles were obtained easily by self-assembly in aqueous solution. Through adjusting the length of MPEG chains in amphiphilic OPE, a series of nanoparticles with different water solubility were prepared. The aggregation behaviors of these dyes were investigated by dynamic light scattering (DLS) and transmission electron microscopy (TEM), which indicated that when the MPEG chains bonding with amphiphilic OPE are longer, smaller sized nanoparticles will be formed at the same concentration of 10−5 mol L−1. Besides, taking OPE–PEG1900 as an example, diversified aggregation behaviors under different concentrations can be inferred through DLS and TEM, which were also supported by ultraviolet absorption (UV) and photoluminescence (PL) analyses. Compared with previously reported conjugated-polymer nanoparticles consisting of amphiphiles without photoelectric features and oil-soluble conjugated-polymers through non-covalent encapsulation, the introduction of OPE chromophores into amphiphiles by covalent linkage efficiently enhanced the structural stability of nanoparticles. A photobleaching test under UV excitation revealed the high photostability of these OPE nanoparticles. In view of the good water solubility, biocompatibility, structural stability, photostability, and excellent photoelectric features of these nanoparticles, cellular imaging of human pancreatic cancer cells (PANC-1 cells) was conducted. Confocal microscopy results showed that the nanoparticles (OPE–PEG1000 and OPE–PEG1900) were located specifically within the cell cytoplasm. We believe that the OPE nanoparticles would play an important role as fluorescent biomarkers for long-term bioimaging, and offer new opportunities for good applicability in cell imaging and sensing in biomedical science.
Recommended Journals
Related Literature
Mechanisms and kinetic studies of OH-initiated atmospheric oxidation of methoxyphenols in the presence of O2 and NOx
Xiaofan Li, Qingzhu Zhang, Yuanxiang Gu
DOI: 10.1039/C9CP03246K
Dissociative chemisorption of O2 on Agn and Agn−1Ir (n = 3–26) clusters: a first-principle study
Chuangchuang Wang, Yongpeng Yang, Xiaojing Liu, Yuanjie Li, Dandan Song, Yun Tian, Zhaojun Zhang
DOI: 10.1039/D0CP01005G
Enhanced carrier mobility and tunable electronic properties in α-tellurene monolayer via an α-tellurene and h-BN heterostructure
Xingtao Jia, Yujin Liu, Weiyang Yu, Baoji Wang, Xuefeng Yang, Qin Wang
DOI: 10.1039/D0CP00269K
Length-scale dependence of protein hydration-shell density
Andrea Amadei, Isabella Daidone
DOI: 10.1039/C9CP06214A
The electron–phonon scattering and carrier mobility in monolayer AsSb
Ying Luo, Guojun Zhao, Shudong Wang
DOI: 10.1039/C9CP06945C
Formation of resonances and anionic fragments upon electron attachment to benzaldehyde
E. Arthur-Baidoo, J. Pereira-da-Silva, M. Ryszka, I. Carmichael, L. M. Cornetta, M. T. do N. Varella, F. Ferreira da Silva, S. Denifl
DOI: 10.1039/D0CP00029A
Photoelectron spectroscopy and computational investigations of the electronic structures and noncovalent interactions of cyclodextrin-closo-dodecaborate anion complexes χ-CD·B12X122− (χ = α, β, γ; X = H, F)
Yanrong Jiang, Qinqin Yuan, Jonas Warneke, Zhubin Hu, Yan Yang, Xue-Bin Wang
DOI: 10.1039/D0CP00700E
The mechanism of thiophene oxidation on metal-free two-dimensional hexagonal boron nitride
Naixia Lv, Linghao Sun, Linlin Chen, Yujun Li, Jinrui Zhang, Peiwen Wu, Hongping Li, Wenshuai Zhu, Huaming Li
DOI: 10.1039/C9CP03758F
A revised model of silicon oxidation during the dissolution of silicon in HF/HNO3 mixtures
Anja Rietig, Thomas Langner, Jörg Acker
DOI: 10.1039/C9CP04429A
You might also like
What are the main uses of 4-Nitrophenyl phosphate disodium salt hexahydrate (CAS: 333338-18-4)?
4-Nitrophenyl phosphate disodium salt hexahydrate is primarily used as a substra...
What are the main uses of 2-(Trifluoromethyl)-1,3-oxazole-4-carboxylic Acid (CAS: 1060816-01-4)?
2-(Trifluoromethyl)-1,3-oxazole-4-carboxylic Acid (CAS: 1060816-01-4) is widely ...
How should 2-Fluoro-4-biphenylcarboxylic acid (CAS: 137045-30-8) be stored?
2-Fluoro-4-biphenylcarboxylic acid should be stored in a cool, dry place at room...
What industries use Prednisolone-21-Carboxylic Acid (CAS: 61549-70-0)?
Prednisolone-21-Carboxylic Acid is primarily used in the pharmaceutical industry...
How should 4-(Hydrazinomethyl)-1,2,3-benzenetriol (CAS: 3614-72-0) be stored?
4-(Hydrazinomethyl)-1,2,3-benzenetriol (CAS: 3614-72-0) should be stored in a co...
What industries use 4-Amino-1-methyl-1H-pyrazole-5-carboxylic acid hydrochloride (CAS: 92534-70-8)?
4-Amino-1-methyl-1H-pyrazole-5-carboxylic acid hydrochloride (CAS: 92534-70-8) i...
What regulatory guidelines apply to dehydropachymic acid (CAS: 77012-31-8)?
Dehydropachymic acid (CAS: 77012-31-8) is regulated by various agencies. It fall...
What is the market or research trend for 6-[(2,2-Dimethylpropanoyl)amino]nicotinic acid (CAS: 898561-66-5)?
The market and research trends for 6-[(2,2-Dimethylpropanoyl)amino]nicotinic aci...
How should 1,10-Phenanthroline-2,9-dicarbaldehyde (CAS: 57709-62-3) be stored?
1,10-Phenanthroline-2,9-dicarbaldehyde should be stored in a cool, dry place awa...
How is 5-Carbamoyl-11-oxo-10,11-dihydro-5H-dibenzo[b,f]azepin-10-yl acetate (CAS: 113952-21-9) typically synthesized?
5-Carbamoyl-11-oxo-10,11-dihydro-5H-dibenzo[b,f]azepin-10-yl acetate can be synt...
Source Journal
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.














