Self-assembly of mucoadhesive nanofibers

RSC Advances ◽  
2014 ◽  
Vol 4 (102) ◽  
pp. 58664-58673 ◽  
Author(s):  
P. Suvannasara ◽  
N. Praphairaksit ◽  
N. Muangsin

Here, we present an easy and stable one-step procedure to fabricate self-assembled nanofibers from modified chitosan.

2016 ◽  
Vol 4 (32) ◽  
pp. 5475-5485 ◽  
Author(s):  
Robabeh Gharaei ◽  
Giuseppe Tronci ◽  
Robert P. W. Davies ◽  
Caroline Gough ◽  
Reem Alazragi ◽  
...  

Peptide self-assembly during electrospinning while the solvent is evaporating and the fibres are forming.


Author(s):  
Abigail N. Eldridge ◽  
Anna Dubnisheva ◽  
William H. Fissell ◽  
Aaaron J. Fleischman ◽  
Shuvo Roy

A Poly (ethylene glycol) (PEG) self-assembled monolayer was solution phase coupled to common MEMS (microelectromechanical systems) substrates through a one step procedure in order to investigate the potential anti-fouling properties of the polymer for implantable biomedical MEMS applications.


2020 ◽  
Vol 44 (27) ◽  
pp. 11895-11900
Author(s):  
Shuang Li ◽  
Wen Xia ◽  
Yunqian Zhang ◽  
Zhu Tao

A novel class of cucurbit[n]urils–polyoxometalate (Q[n]–POM) hybrids and tetramethyl cucurbit[6]uril–phosphomolybdic acid (TMeQ[6]–PMA) nanocubes (NCs), are synthesized via a one-step self-assembly method.


RSC Advances ◽  
2014 ◽  
Vol 4 (102) ◽  
pp. 58307-58314 ◽  
Author(s):  
Yan Li ◽  
Hao-Yu Bi ◽  
Yong-Sheng Jin ◽  
Xiao-Qin Shi

A simple one-step process involving the self-assembly of organo-LDH and the removal of non-ionic dyes from dyeing wastewater was realized.


RSC Advances ◽  
2015 ◽  
Vol 5 (66) ◽  
pp. 53611-53617 ◽  
Author(s):  
Jeyoung Park ◽  
Changjun Park ◽  
Byoung Tak Yim ◽  
Myungeun Seo ◽  
Sang Youl Kim

Partially sulfonated poly(arylene ether sulfone)s was synthesized by one-step SNAr copolymerization and self-assembled into spherical micelles in aqueous solutions, which assisted formation of Cu2S nanowires on various substrates.


The Analyst ◽  
2020 ◽  
Vol 145 (1) ◽  
pp. 268-276 ◽  
Author(s):  
Guoning Chen ◽  
Hua Shu ◽  
Lu Wang ◽  
Kamran Bashir ◽  
Qun Wang ◽  
...  

The silane emulsion self-assembly MIPs can specifically immobilize HRP in a one-step process from a crude extract of horseradish (unpurified samples).


MRS Advances ◽  
2020 ◽  
Vol 5 (64) ◽  
pp. 3507-3520
Author(s):  
Chunhui Dai ◽  
Kriti Agarwal ◽  
Jeong-Hyun Cho

AbstractNanoscale self-assembly, as a technique to transform two-dimensional (2D) planar patterns into three-dimensional (3D) nanoscale architectures, has achieved tremendous success in the past decade. However, an assembly process at nanoscale is easily affected by small unavoidable variations in sample conditions and reaction environment, resulting in a low yield. Recently, in-situ monitored self-assembly based on ion and electron irradiation has stood out as a promising candidate to overcome this limitation. The usage of ion and electron beam allows stress generation and real-time observation simultaneously, which significantly enhances the controllability of self-assembly. This enables the realization of various complex 3D nanostructures with a high yield. The additional dimension of the self-assembled 3D nanostructures opens the possibility to explore novel properties that cannot be demonstrated in 2D planar patterns. Here, we present a rapid review on the recent achievements and challenges in nanoscale self-assembly using electron and ion beam techniques, followed by a discussion of the novel optical properties achieved in the self-assembled 3D nanostructures.


2019 ◽  
Author(s):  
Mark Workentin ◽  
François Lagugné-Labarthet ◽  
Sidney Legge

In this work we present a clean one-step process for modifying headgroups of self-assembled monolayers (SAMs) on gold using photo-enabled click chemistry. A thiolated, cyclopropenone-caged strained alkyne precursor was first functionalized onto a flat gold substrate through self-assembly. Exposure of the cyclopropenone SAM to UV-A light initiated the efficient photochemical decarbonylation of the cyclopropenone moiety, revealing the strained alkyne capable of undergoing the interfacial strain-promoted alkyne-azide cycloaddition (SPAAC). Irradiated SAMs were derivatized with a series of model azides with varied hydrophobicity to demonstrate the generality of this chemical system for the modification and fine-tuning of the surface chemistry on gold substrates. SAMs were characterized at each step with polarization-modulation infrared reflection-absorption spectroscopy (PM-IRRAS) to confirm successful functionalization and reactivity. Furthermore, to showcase the compatibility of this approach with biochemical applications, cyclopropenone SAMs were irradiated and modified with azide-bearing cell adhesion peptides to promote human fibroblast cell adhesion, then imaged by live cell fluorescence microscopy. Thus, the “photoclick” methodology reported here represents an improved, versatile, catalyst-free protocol that allows for a high degree of control over the modification of material surfaces, with applicability in materials science as well as biochemistry.<br>


2020 ◽  
Author(s):  
Daniel B. Straus ◽  
Robert J. Cava

The design of new chiral materials usually requires stereoselective organic synthesis to create molecules with chiral centers. Less commonly, achiral molecules can self-assemble into chiral materials, despite the absence of intrinsic molecular chirality. Here, we demonstrate the assembly of high-symmetry molecules into a chiral van der Waals structure by synthesizing crystals of C<sub>60</sub>(SnI<sub>4</sub>)<sub>2</sub> from icosahedral buckminsterfullerene (C<sub>60</sub>) and tetrahedral SnI4 molecules through spontaneous self-assembly. The SnI<sub>4</sub> tetrahedra template the Sn atoms into a chiral cubic three-connected net of the SrSi<sub>2</sub> type that is held together by van der Waals forces. Our results represent the remarkable emergence of a self-assembled chiral material from two of the most highly symmetric molecules, demonstrating that almost any molecular, nanocrystalline, or engineered precursor can be considered when designing chiral assemblies.


2021 ◽  
Vol 11 (7) ◽  
pp. 3254
Author(s):  
Marco Pisco ◽  
Francesco Galeotti

The realization of advanced optical fiber probes demands the integration of materials and structures on optical fibers with micro- and nanoscale definition. Although researchers often choose complex nanofabrication tools to implement their designs, the migration from proof-of-principle devices to mass production lab-on-fiber devices requires the development of sustainable and reliable technology for cost-effective production. To make it possible, continuous efforts are devoted to applying bottom-up nanofabrication based on self-assembly to decorate the optical fiber with highly ordered photonic structures. The main challenges still pertain to “order” attainment and the limited number of implementable geometries. In this review, we try to shed light on the importance of self-assembled ordered patterns for lab-on-fiber technology. After a brief presentation of the light manipulation possibilities concerned with ordered structures, and of the new prospects offered by aperiodically ordered structures, we briefly recall how the bottom-up approach can be applied to create ordered patterns on the optical fiber. Then, we present un-attempted methodologies, which can enlarge the set of achievable structures, and can potentially improve the yielding rate in finely ordered self-assembled optical fiber probes by eliminating undesired defects and increasing the order by post-processing treatments. Finally, we discuss the available tools to quantify the degree of order in the obtained photonic structures, by suggesting the use of key performance figures of merit in order to systematically evaluate to what extent the pattern is really “ordered”. We hope such a collection of articles and discussion herein could inspire new directions and hint at best practices to fully exploit the benefits inherent to self-organization phenomena leading to ordered systems.


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