The increasing accumulation of persistent nondegradable microplastics in the marine environment represents a global environmental problem. Among emerging approaches to tackle microplastics are micro- and nanomotors, tiny devices capable of autonomous propulsion powered by chemical fuels or light. These devices are capable of on-the-fly recognition, capture, and decomposition of pollutants. In the past, various micromotors were designed to efficiently remove and degrade soluble organic pollutants. Current effort is given to the rational design and surface functionalization to achieve micromotors capable of capturing, transporting, and releasing microplastics of different shapes and chemical structures. The catalytic micromotors performing photocatalysis and photo-Fenton chemistry hold great promise for the degradation of most common plastics. In this review, we highlight recent progress in the field of micromotors for microplastics treatment. These tiny self-propelled machines are expected to stimulate a quantum leap in environmental remediation.

• Publikační typ
• časopisecké články MeSH
• přehledy MeSH

Our previously-obtained impressive results of highly increased C2C12 mouse myoblast adhesion to amine plasma polymers (PPs) motivated current detailed studies of cell resistance to trypsinization, cell proliferation, motility, and the rate of attachment carried out for fibroblasts (LF), keratinocytes (HaCaT), rat vascular smooth muscle cells (VSMC), and endothelial cells (HUVEC, HSVEC, and CPAE) on three different amine PPs. We demonstrated the striking difference in the resistance to trypsin treatment between endothelial and non-endothelial cells. The increased resistance observed for the non-endothelial cell types was accompanied by an increased rate of cellular attachment, even though spontaneous migration was comparable to the control, i.e., to the standard cultivation surface. As demonstrated on LF fibroblasts, the resistance to trypsin was similar in serum-supplemented and serum-free media, i.e., medium without cell adhesion-mediating proteins. The increased cell adhesion was also confirmed for LF cells by an independent technique, single-cell force spectroscopy. This method, as well as the cell attachment rate, proved the difference among the plasma polymers with different amounts of amine groups, but other investigated techniques could not reveal the differences in the cell behaviour on different amine PPs. Based on all the results, the increased resistance to trypsinization of C2C12, LF, HaCaT, and VSMC cells on amine PPs can be explained most probably by a non-specific cell adhesion such as electrostatic interaction between the cells and amine groups on the material surface, rather than by the receptor-mediated adhesion through serum-derived proteins adsorbed on the PPs.

• MeSH
• aminy chemie   MeSH
• buněčná adheze účinky léků   MeSH
• buněčné linie MeSH
• lidé MeSH
• plazmové plyny chemie   MeSH
• polymery chemie   farmakologie   MeSH
• povrchové vlastnosti MeSH
• Check Tag
• lidé MeSH
• Publikační typ
• časopisecké články MeSH
• práce podpořená grantem MeSH
• Názvy látek
• aminy MeSH
• plazmové plyny MeSH
• polymery MeSH

Polycaprolactone composite nanofibers coated with a polydopamine layer are introduced as a new type of absorption material for on-line solid phase extraction (SPE) in chromatographic system. A hybrid technology combining the electrospinning and melt blowing was used for the preparation of 3D-structured microfiber/nanofibrous polycaprolactone composite. The dopamine coating was then applied to functionalize the micro/nanofibers. Polydopamine-coated polycaprolactone fibers were tested as an extraction phase in on-line SPE prior to HPLC separation and UV detection. Four groups of biologically active substances including bisphenols (Bisphenol S, Bisphenol AF, Bisphenol A, Bisphenol C, Bisphenol AP, Bisphenol Z, Bisphenol BP, and Bisphenol M), betablockers (Timolol, Metoprolol, Labetalol, and Propranolol), nonsteroidal antiphlogistic drugs (Salicylic acid, Ketoprofen, Naproxen, Indomethacin, Diclofenac, Ibuprophen, and Meclofenamic acid), and phenolic acids (Chlorogenic acid, Caffeic acid, Sinapic acid, m-Coumaric acid, Benzoic acid, and Cinnamic acid) were used as the model analytes. Neat and coated fibers were compared and applied as sorbents for the on-line extraction set-up. Both materials produced good extraction potential for the determination of bisphenols and nonsteroidal drugs in model biological and environmental samples including river water, human urine, and blood serum. However, the polydopamine layer significantly increased the extraction efficiency of polar drugs. Typical repeatability of on-line extraction procedure on polydopamine coated fibers was in the range 0.12-4.11% for bisphenols, 0.55-1.41% for antiphlogistic drugs, 0.59-2.52% for phenolic acids, and 1.01-1.65% for betablockers. Graphical abstract Schematic representation of polycaprolactone composite nanofibers coated with a polydopamine layer as an advanced absorption material for on-line solid phase extraction in chromatography.

• Klíčová slova
• Chromatography, Column switching, Degradation, Dopamine coating, Micro-column, Microfiber, Nanofiber, Polymerization, Solid phase extraction, Surface modification,
• MeSH
• antiflogistika nesteroidní analýza   izolace a purifikace   MeSH
• beta blokátory analýza   izolace a purifikace   MeSH
• chemické látky znečišťující vodu analýza   izolace a purifikace   MeSH
• cinnamáty analýza   izolace a purifikace   MeSH
• extrakce na pevné fázi metody   MeSH
• fenoly analýza   izolace a purifikace   MeSH
• indoly chemie   MeSH
• nanovlákna chemie   MeSH
• polyestery chemie   MeSH
• polymerizace MeSH
• polymery chemie   MeSH
• řeky chemie   MeSH
• reprodukovatelnost výsledků MeSH
• vysokoúčinná kapalinová chromatografie MeSH
• Publikační typ
• časopisecké články MeSH
• práce podpořená grantem MeSH
• Názvy látek
• antiflogistika nesteroidní MeSH
• beta blokátory MeSH
• chemické látky znečišťující vodu MeSH
• cinnamáty MeSH
• fenoly MeSH
• indoly MeSH
• polycaprolactone MeSH Prohlížeč
• polydopamine MeSH Prohlížeč
• polyestery MeSH
• polymery MeSH

For the first time, the combination of molecularly imprinted polymer (MIP) technology with laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) is presented with focus on an optimization of the LA-ICP-MS parameters such as laser beam diameter, laser beam fluence, and scan speed using CdS quantum dots (QDs) as a template and dopamine as a functional monomer. A non-covalent imprinting approach was employed in this study due to the simplicity of preparation. Simple oxidative polymerization of the dopamine that creates the self-assembly monolayer seems to be an ideal choice. The QDs prepared by UV light irradiation synthesis were stabilized by using mercaptosuccinic acid. Formation of a complex of QD-antibody and QD-antibody-antigen was verified by using capillary electrophoresis with laser-induced fluorescence detection. QDs and antibody were connected together via an affinity peptide linker. LA-ICP-MS was employed as a proof-of-concept for detection method of two types of immunoassay: 1) antigen extracted from the sample by MIP and subsequently overlaid/immunoreacted by QD-labelled antibodies, 2) complex of antigen, antibody, and QD formed in the sample and subsequently extracted by MIP. The first approach provided higher sensitivity (MIP/NIP), however, the second demonstrated higher selectivity. A mixture of proteins with size in range 10-250 kDa was used as a model sample to demonstrate the capability of both approaches for detection of IgG in a complex sample.

• MeSH
• elektroforéza kapilární MeSH
• fluorescence MeSH
• hmotnostní spektrometrie * MeSH
• imunoanalýza metody   MeSH
• imunoglobulin G analýza   MeSH
• kvantové tečky chemie   MeSH
• laserová terapie * MeSH
• molekulový imprinting * MeSH
• myši MeSH
• počítačové zpracování signálu MeSH
• polymery chemie   MeSH
• proteiny analýza   MeSH
• sloučeniny kadmia chemie   MeSH
• sulfidy chemie   MeSH
• zvířata MeSH
• Check Tag
• myši MeSH
• zvířata MeSH
• Publikační typ
• časopisecké články MeSH
• práce podpořená grantem MeSH
• Názvy látek
• cadmium sulfide MeSH Prohlížeč
• imunoglobulin G MeSH
• polymery MeSH
• proteiny MeSH
• sloučeniny kadmia MeSH
• sulfidy MeSH

A general high-yielding method for the preparation of monosubstituted β-cyclodextrin derivatives which have attached a thiol group in position 6 is described. The thiol group is attached through linkers of different lengths and repeating units (ethylene glycol or methylene). The target compounds were characterized by IR, MS and NMR spectra. A simple method for their complete conversion to the corresponding disulfides as well as a method for the reduction of the disulfides back to the thiols is presented. Both, thiols and disulfides are derivatives usable for well-defined covalent attachment of cyclodextrin to gold or polydopamine-coated solid surfaces.

• Klíčová slova
• cyclodextrins, disulfides, monosubstituted derivatives, thiols,
• Publikační typ
• časopisecké články MeSH

Protein-repulsive surfaces modified with ligands for cell adhesion receptors have been widely developed for controlling the cell adhesion and growth in tissue engineering. However, the question of matrix production and deposition by cells on these surfaces has rarely been addressed. In this study, protein-repulsive polydopamine-poly(ethylene oxide) (PDA-PEO) surfaces were functionalized with an RGD-containing peptide (RGD), with a collagen-derived peptide binding fibronectin (Col), or by a combination of these peptides (RGD + Col, ratio 1:1) in concentrations of 90 fmol/cm(2) and 700 fmol/cm(2) for each peptide type. When seeded with vascular endothelial CPAE cells, the PDA-PEO surfaces proved to be completely non-adhesive for cells. On surfaces with lower peptide concentrations and from days 1 to 3 after seeding, cell adhesion and growth was restored practically only on the RGD-modified surface. However, from days 3 to 7, cell adhesion and growth was improved on surfaces modified with Col and with RGD + Col. At higher peptide concentrations, the cell adhesion and growth was markedly improved on all peptide-modified surfaces in both culture intervals. However, the collagen-derived peptide did not increase the expression of fibronectin in the cells. The deposition of fibronectin on the material surface was generally very low and similar on all peptide-modified surfaces. Nevertheless, the RGD + Col surfaces exhibited the highest cell adhesion stability under a dynamic load, which correlated with the highest expression of talin and vinculin in the cells on these surfaces. A combination of RGD + Col therefore seems to be the most promising for surface modification of biomaterials, e.g. vascular prostheses.

• MeSH
• adsorpce MeSH
• biomimetika * MeSH
• buněčná adheze * MeSH
• exprese genu MeSH
• fibronektiny chemie   genetika   MeSH
• indoly chemie   MeSH
• kultivované buňky MeSH
• lidé MeSH
• molekulární sekvence - údaje MeSH
• oligopeptidy chemie   MeSH
• polyethylenglykoly chemie   MeSH
• polymery chemie   MeSH
• povrchové vlastnosti MeSH
• sekvence aminokyselin MeSH
• talin genetika   MeSH
• vinkulin genetika   MeSH
• Check Tag
• lidé MeSH
• Publikační typ
• časopisecké články MeSH
• práce podpořená grantem MeSH
• Názvy látek
• fibronektiny MeSH
• indoly MeSH
• oligopeptidy MeSH
• polydopamine MeSH Prohlížeč
• polyethylenglykoly MeSH
• polymery MeSH
• talin MeSH
• vinkulin MeSH

Composite materials based on a titanium support and a thin, alginate hydrogel could be used in bone tissue engineering as a scaffold material that provides biologically active molecules. The main objective of this contribution is to characterize the activation and the functionalization of titanium surfaces by the covalent immobilization of anchoring layers of self-assembled bisphosphonate neridronate monolayers and polymer films of 3-aminopropyltriethoxysilane and biomimetic poly(dopamine). These were further used to bind a bio-functional alginate coating. The success of the titanium surface activation, anchoring layer formation and alginate immobilization, as well as the stability upon immersion under physiological-like conditions, are demonstrated by different surface sensitive techniques such as spectroscopic ellipsometry, infrared reflection-absorption spectroscopy and X-ray photoelectron spectroscopy. The changes in morphology and the established continuity of the layers are examined by scanning electron microscopy, surface profilometry and atomic force microscopy. The changes in hydrophilicity after each modification step are further examined by contact angle goniometry.

• Klíčová slova
• XPS, alginate, biomimetic surfaces, bisphosphonates, neridronate, poly(dopamine), spectroscopic ellipsometry, surface characterization, surface modification, titanium,
• Publikační typ
• časopisecké články MeSH

Nonfouling surfaces capable of reducing protein adsorption are highly desirable in a wide range of applications. Coating of surfaces with poly(ethylene oxide) (PEO), a water-soluble, nontoxic, and nonimmunogenic polymer, is most frequently used to reduce nonspecific protein adsorption. Here we show how to prepare dense PEO brushes on virtually any substrate by tethering PEO to polydopamine (PDA)-modified surfaces. The chain lengths of hetero-bifunctional PEOs were varied in the range of 45-500 oxyethylene units (M(n) = 2000-20,000). End-tethering of PEO chains was performed through amine and thiol headgroups from reactive polymer melts to minimize excluded volume effects. Surface plasmon resonance (SPR) was applied to investigate the adsorption of model protein solutions and complex biologic medium (human blood plasma) to the densely packed PEO brushes. The level of protein adsorption of human serum albumin and fibrinogen solutions was below the detection limit of the SPR measurements for all PEO chains end-tethered to PDA, thus exceeding the protein resistance of PEO layers tethered directly on gold. It was found that the surface resistance to adsorption of lysozyme and human blood plasma increased with increasing length and brush character of the PEO chains end-tethered to PDA with a similar or better resistance in comparison to PEO layers on gold. Furthermore, the chain density, thickness, swelling, and conformation of PEO layers were determined using spectroscopic ellipsometry (SE), dynamic water contact angle (DCA) measurements, infrared reflection-absorption spectroscopy (IRRAS), and vibrational sum-frequency-generation (VSFG) spectroscopy, the latter in air and water.

• MeSH
• adsorpce MeSH
• bioznečištění prevence a kontrola   MeSH
• indoly chemie   MeSH
• lidé MeSH
• muramidasa chemie   MeSH
• polyethylenglykoly chemie   MeSH
• polymery chemie   MeSH
• sérový albumin chemie   MeSH
• voda chemie   MeSH
• vzduch MeSH
• zlato chemie   MeSH
• Check Tag
• lidé MeSH
• Publikační typ
• časopisecké články MeSH
• práce podpořená grantem MeSH
• Research Support, N.I.H., Extramural MeSH
• Názvy látek
• indoly MeSH
• muramidasa MeSH
• polydopamine MeSH Prohlížeč
• polyethylenglykoly MeSH
• polymery MeSH
• sérový albumin MeSH
• voda MeSH
• zlato MeSH