RESUMEN
Development of smart switchable surfaces to solve the inevitable bacteria attachment and colonization has attracted much attention; however, it proves very challenging to achieve on-demand regeneration for noncontaminated surfaces. We herein report a smart, host-guest interaction-mediated photo/temperature dual-controlled antibacterial surface, topologically combining stimuli-responsive polymers with nanobactericide. From the point of view of long-chain polymer design, the peculiar hydration layer generated by hydrophilic poly(2-hydroxyethyl methacrylate) (polyHEMA) segments severs the route of initial bacterial attachment and subsequent proliferation, while the synergistic effect on chain conformation transformation poly(N-isopropylacrylamide) (polyNIPAM) and guest complex dissociation azobenzene/cyclodextrin (Azo/CD) complex greatly promotes the on-demand bacterial release in response to the switch of temperature and UV light. Therefore, the resulting surface exhibits triple successive antimicrobial functions simultaneously: (i) resists â¼84.9% of initial bacterial attachment, (ii) kills â¼93.2% of inevitable bacteria attack, and (iii) releases over 94.9% of killed bacteria even after three cycles. The detailed results not only present a potential and promising strategy to develop renewable antibacterial surfaces with successive antimicrobial functions but also contribute a new antimicrobial platform to biomedical or surgical applications.
Asunto(s)
Antibacterianos/química , Compuestos Azo/química , Materiales Biocompatibles/química , Ciclodextrinas/química , Polímeros/química , Antibacterianos/farmacología , Compuestos Azo/farmacología , Bacterias/efectos de los fármacos , Infecciones Bacterianas/prevención & control , Materiales Biocompatibles/farmacología , Ciclodextrinas/farmacología , Humanos , Interacciones Hidrofóbicas e Hidrofílicas , Nanoestructuras/química , Polihidroxietil Metacrilato/química , Polihidroxietil Metacrilato/farmacología , Polímeros/farmacología , Temperatura , Rayos UltravioletaRESUMEN
Bone is a highly vascularized tissue with a unique and complex structure. Long bone consists of a peripheral cortical shell containing a network of channels for vascular penetration and an inner highly vascularized bone marrow space. Bioprinting is a powerful tool to enable rapid and precise spatial patterning of cells and biomaterials. Here we developed a two-step digital light processing technique to fabricate a bone-mimetic 3D hydrogel construct based on octacalcium phosphate (OCP), spheroids of human umbilical vein endothelial cells (HUVEC), and gelatin methacrylate (GelMA) hydrogels. The bone-mimetic 3D hydrogel construct was designed to consist of a peripheral OCP-containing GelMA ring to mimic the cortical shell, and a central GelMA ring containing HUVEC spheroids to mimic the bone marrow space. We further demonstrate that OCP, which is evenly embedded in the GelMA, stimulates the osteoblastic differentiation of mesenchymal stem cells. We refined the design of a spheroid culture device to facilitate the rapid formation of a large number of HUVEC spheroids, which were embedded into different concentrations of GelMA hydrogels. It is shown that the concentration of GelMA modulates the extent of formation of the capillary-like structures originating from the HUVEC spheroids. This cell-loaded hydrogel-based bone construct with a biomimetic dual ring structure can be potentially used for bone tissue engineering.
Asunto(s)
Vasos Sanguíneos/efectos de los fármacos , Desarrollo Óseo/efectos de los fármacos , Hidrogeles/farmacología , Neovascularización Fisiológica/efectos de los fármacos , Biomimética , Bioimpresión , Vasos Sanguíneos/crecimiento & desarrollo , Huesos/irrigación sanguínea , Huesos/efectos de los fármacos , Gelatina/química , Gelatina/farmacología , Células Endoteliales de la Vena Umbilical Humana , Humanos , Hidrogeles/química , Osteogénesis/efectos de los fármacos , Polihidroxietil Metacrilato/química , Polihidroxietil Metacrilato/farmacología , Impresión TridimensionalRESUMEN
A star-like hyperbranched polymer having hydrophilic poly(ethyleneoxide acrylate) arms (HB-PEO9A) was prepared by a core-first method based on atom transfer radical polymerization. The PEO9A layer coated on a solid substrate was dissolved by water, and effectively inhibited protein adsorption and cell adhesion.
Asunto(s)
Incrustaciones Biológicas/prevención & control , Polímeros/química , Adsorción , Animales , Adhesión Celular/efectos de los fármacos , Interacciones Hidrofóbicas e Hidrofílicas , Ratones , Células 3T3 NIH , Polihidroxietil Metacrilato/química , Polihidroxietil Metacrilato/farmacología , Polímeros/farmacología , Proteínas/químicaRESUMEN
Antimicrobial polymers and coatings are potent types of materials for fighting microbial infections, and as such, they have attracted increased attention in many fields. Here, a series of antimicrobial copolymers were prepared by radical copolymerization of 2-hydroxyethyl methacrylate (HEMA), which is widely employed in the manufacturing of biomedical devices, and the monomer 2-(4-methylthiazol-5-yl)ethyl methacrylate (MTA), which bears thiazole side groups susceptible to quaternization, to provide a positive charge. The copolymers were further quantitatively quaternized with either methyl or butyl iodide, as demonstrated by nuclear magnetic resonance (NMR) and attenuated total reflection Fourier-transform infrared spectroscopy (ATR-FTIR). Then, the polycations were characterized by zeta potential measurements to evaluate their effective charge and by differential scanning calorimetry (DSC) and thermogravimetric analysis (TGA) to evaluate their thermal properties. The ζ-potential study revealed that the quaternized copolymers with intermediate compositions present higher charges than the corresponding homopolymers. The cationic copolymers showed greater glass transition temperatures than poly(2-hydroxyethyl methacrylate) (PHEMA), with values higher than 100 °C, in particular those quaternized with methyl iodide. The TGA studies showed that the thermal stability of polycations varies with the composition, improving as the content of HEMA in the copolymer increases. Microbial assays targeting Gram-positive and Gram-negative bacteria confirmed that the incorporation of a low number of cationic units into PHEMA provides antimicrobial character with a minimum inhibitory concentration (MIC) of 128 µg mL-1. Remarkably, copolymers with MTA molar fractions higher than 0.50 exhibited MIC values as low as 8 µg mL-1.
Asunto(s)
Antibacterianos/farmacología , Polihidroxietil Metacrilato/farmacología , Polimerizacion , Tiazoles/farmacología , Rastreo Diferencial de Calorimetría , Cationes , Electrólitos/química , Pruebas de Sensibilidad Microbiana , Pseudomonas aeruginosa/efectos de los fármacos , Espectroscopía Infrarroja por Transformada de Fourier , Staphylococcus aureus/efectos de los fármacos , Electricidad Estática , Temperatura , TermogravimetríaRESUMEN
BACKGROUND: Non-adherent or ultra-low attachment three-dimensional (3D) culture, also called sphere formation assay, has been widely used to assess the malignant phenotype and stemness potential of transformed or cancer cells. This method is also popularly used to isolate the cancer stem-like cells (CSCs) or tumor-initiating cells based on their unique anchorage-independent growth or anoikis-resistant capacity. Different non-adhesive coating agents, such as poly-2-hydroxyethyl methacrylate (poly-HEMA) and synthetic hydrogels, have been used in this non-adherent 3D culture. However, preparation of non-adherent culture-ware is labor-intensive and technically demanding, and also costs of commercial non-adherent culture-ware prepared with various coating agents are relatively expensive and the culture-ware cannot be used repeatedly. METHODS: In this study, we developed a non-adherent 3D culture method based on agar coating for growing tumor spheres derived from various cancer cell lines and primary prostate cancer tissues under a non-adherent and serum-free condition. The tumor spheres generated by this 3D culture method were analyzed on their expression profiles of CSC-associated markers by reverse transcription quantitative polymerase chain reaction, presence and relative proportion of CSCs by fluorescence-activated cell sorting (CD133+/CD44+ cell sorting) and also a CSC-visualizing reporter system responsive to OCT4 and SOX2 (SORE6), and in vivo tumorigenicity. The repeated use of agar-coated plates for serial passages of tumor spheres was also evaluated. RESULTS: Our results validated that the multicellular tumor spheres generated by this culture method were enriched of CSCs, as evidenced by their enhanced expression profiles of CSC markers, presence of CD133+/CD44+ or SORE6+ cells, enhanced self-renewal capacity, and in vivo tumorigenicity, indicating its usefulness in isolation and enrichment of CSCs. The agar-coated plates could be used multiple times in serial passages of tumor spheres. CONCLUSIONS: The described agar-based 3D culture method offers several advantages as compared with other methods in isolation of CSCs, including its simplicity and low-cost and repeated use of agar-coated plates for continuous passages of CSC-enriched spheres.
Asunto(s)
Agar/química , Técnicas de Cultivo de Célula/métodos , Hidrogeles/farmacología , Células Madre Neoplásicas/patología , Antígeno AC133/genética , Adhesión Celular/efectos de los fármacos , Línea Celular Tumoral , Humanos , Receptores de Hialuranos/genética , Hidrogeles/química , Polihidroxietil Metacrilato/química , Polihidroxietil Metacrilato/farmacología , Esferoides CelularesRESUMEN
Caspase-dependent apoptosis, including its distinct cell death subroutine known as anoikis, perform essential roles during organogenesis, as well as in the maintenance and repair of tissues. To this effect, the continuous renewal of the human intestinal/colon epithelium is characterized by the exfoliation by anoikis of differentiated cells, whereas immature/undifferentiated cells may occasionally undergo apoptosis in order to evacuate daughter cells that are damaged or defective. Dysregulated epithelial apoptosis is a significant component of inflammatory bowel diseases. Conversely, the acquisition of a resistance to apoptosis represents one of the hallmarks of cancer initiation and progression, including for colorectal cancer (CRC). Furthermore, the emergence of anoikis resistance constitutes a critical step in cancer progression (including CRC), as well as a limiting one that enables invasion and metastasis.Considering the implications of apoptosis/anoikis dysregulation in gut physiopathology, it therefore becomes incumbent to understand the functional determinants that underlie such dysregulation-all the while having to monitor, assess, or evidence apoptosis and/or anoikis. In this chapter, methodologies that are typically used to assess caspase-dependent apoptosis and anoikis in intestinal/colonic normal and CRC cells, whether in vivo, ex vivo, or in cellulo, are provided.
Asunto(s)
Técnicas de Cultivo de Célula/métodos , Neoplasias Colorrectales/patología , Etiquetado Corte-Fin in Situ/métodos , Feto Abortado , Anoicis/efectos de los fármacos , Apoptosis/efectos de los fármacos , Apoptosis/genética , Western Blotting/instrumentación , Western Blotting/métodos , Caspasa 3/metabolismo , Técnicas de Cultivo de Célula/instrumentación , Línea Celular Tumoral , Colon/patología , Fragmentación del ADN/efectos de los fármacos , Dimetilsulfóxido/farmacología , Electroforesis en Gel de Poliacrilamida/instrumentación , Electroforesis en Gel de Poliacrilamida/métodos , Técnica del Anticuerpo Fluorescente Indirecta/instrumentación , Técnica del Anticuerpo Fluorescente Indirecta/métodos , Humanos , Etiquetado Corte-Fin in Situ/instrumentación , Mucosa Intestinal/patología , Polihidroxietil Metacrilato/farmacologíaRESUMEN
Well-organized composite formations such as hierarchical nested-network (NN) structure in bone tissue and reticular connective tissue present remarkable mechanical strength and play a crucial role in achieving physical and biological functions for living organisms. Inspired by these delicate microstructures in nature, an analogous scaffold of double network hydrogel was fabricated by creating a poly(2-hydroxyethyl methacrylate) (pHEMA) network in the porous structure of alginate hydrogels. The resulting hydrogel possessed hierarchical NN structure and showed significantly improved mechanical strength but still maintained high elasticity comparable to soft tissues due to a mutual strengthening effect between the two networks. The tough hydrogel is also self-lubricated, exhibiting a surface friction coefficient comparable with polydimethylsiloxane (PDMS) substrates lubricated by a commercial aqueous lubricant (K-Y Jelly) and other low surface friction hydrogels. Additional properties of this hydrogel include high hydrophilicity, good biocompatibility, tunable cell adhesion and bacterial resistance after incorporation of silver nanoparticles. Firm bonding of the hydrogel on silicone substrates could be achieved through facile chemical modification, thus enabling the use of this hydrogel as a versatile coating material for biomedical applications. STATEMENT OF SIGNIFICANCE: In this study, we developed a tough hydrogel by crosslinking HEMA monomers in alginate hydrogels and forming a well-organized structure of hierarchical nested network (NN). Different from most reported stretchable alginate-based hydrogels, the NN hydrogel shows higher compressive strength but retains comparable softness to alginate counterparts. This work further demonstrated the good integration of the tough hydrogel with silicone substrates through chemical modification and micropillar structures. Other properties including surface friction, biocompatibility and bacterial resistance were investigated and the hydrogel shows a great promise as a versatile coating material for biomedical applications.
Asunto(s)
Materiales Biocompatibles Revestidos , Hidrogeles , Ensayo de Materiales , Alginatos/química , Alginatos/farmacología , Adhesión Celular/efectos de los fármacos , Materiales Biocompatibles Revestidos/química , Materiales Biocompatibles Revestidos/farmacología , Dimetilpolisiloxanos/química , Dimetilpolisiloxanos/farmacología , Células HEK293 , Humanos , Hidrogeles/química , Hidrogeles/farmacología , Interacciones Hidrofóbicas e Hidrofílicas , Nylons/química , Nylons/farmacología , Polihidroxietil Metacrilato/química , Polihidroxietil Metacrilato/farmacologíaRESUMEN
The majority of patients with hydrocephalus are dependent on ventriculoperitoneal shunts for diversion of excess cerebrospinal fluid. Unfortunately, these shunts are failure-prone and over half of all life-threatening pediatric failures are caused by obstruction of the ventricular catheter by the brain's resident immune cells, reactive microglia and astrocytes. Poly(2-hydroxyethyl methacrylate) (PHEMA) hydrogels are widely used for biomedical implants. The extreme hydrophilicity of PHEMA confers resistance to protein fouling, making it a strong candidate coating for ventricular catheters. With the advent of initiated chemical vapor deposition (iCVD), a solvent-free coating technology that creates a polymer in thin film form on a substrate surface by introducing gaseous reactant species into a vacuum reactor, it is now possible to apply uniform polymer coatings on complex three-dimensional substrate surfaces. iCVD was utilized to coat commercially available ventricular catheters with PHEMA. The chemical structure was confirmed on catheter surfaces using Fourier transform infrared spectroscopy and X-ray photoelectron spectroscopy. PHEMA coating morphology was characterized by scanning electron microscopy. Testing PHEMA-coated catheters against uncoated clinical-grade catheters in an in vitro hydrocephalus catheter bioreactor containing co-cultured astrocytes and microglia revealed significant reductions in cell attachment to PHEMA-coated catheters at both 17-day and 6-week time points. © 2017 Wiley Periodicals, Inc. J Biomed Mater Res Part B: Appl Biomater, 106B: 1268-1279, 2018.
Asunto(s)
Catéteres , Adhesión Celular/efectos de los fármacos , Derivaciones del Líquido Cefalorraquídeo , Materiales Biocompatibles Revestidos , Polihidroxietil Metacrilato/farmacología , Animales , Astrocitos/efectos de los fármacos , Técnicas de Cocultivo , Falla de Equipo , Inmunohistoquímica , Ratones , Microglía/efectos de los fármacos , Espectroscopía de Fotoelectrones , Ratas , Espectroscopía Infrarroja por Transformada de Fourier , Derivación VentriculoperitonealRESUMEN
This study evaluated the effect of chitosan, poly vinyl alcohol (PVA) and poly (2-hydroxyethyl methacrylate) (pHEMA) on delaying the human fibroblast senescence. Cells could form suspending multicellular spheroids on these biomaterials, but only chitosan was capable of decreasing the SA ß-gal activity and increasing the proliferation ability of senescent fibroblasts. Therefore, in addition to the structure of multicellular spheroids, chitosan itself should play an important role in delaying fibroblast senescence. The main difference of senescence-related protein expressions for cells cultured on chitosan, PVA and pHEMA occurred on the TGF-ß signaling pathway. In addition to the intracellular TGF-ß expression, the extracellular TGF-ß expression was also downregulated. Chitosan with cationic amino structure was assumed to bind with anionic TGF-ß by forming polyelectrolyte complexes. This assumption was demonstrated by directly adding chitosan into the medium to downregulate the cell TGF-ß expression and further to delay cell senescence, indicating TGF-ß signaling pathway was involved in the chitosan-mediating fibroblast senescence process. Finally, the delaying cell senescence ability of chitosan increased with increasing the amount of amino groups in chitosan and its ionization degree. In summary, these results provide important information for considering the application of chitosan in the future cell therapy and regeneration medicine.
Asunto(s)
Senescencia Celular/efectos de los fármacos , Quitosano/farmacología , Regulación hacia Abajo/efectos de los fármacos , Fibroblastos/metabolismo , Transducción de Señal/efectos de los fármacos , Factor de Crecimiento Transformador beta/biosíntesis , Animales , Fibroblastos/citología , Humanos , Polihidroxietil Metacrilato/farmacología , Alcohol Polivinílico/farmacologíaRESUMEN
Polymeric, ceramic and hybrid material-based three-dimensional (3D) scaffold or matrix structures are important for successful tissue engineering. While the number of approaches utilizing the use of cell-based scaffold and matrix structures is constantly growing, it is essential to provide a framework of their typical preparation and evaluation for tissue engineering. This chapter describes the fabrication of 3D scaffolds using two-photon polymerization, decellularization and cell encapsulation methods and easy-to-use protocols allowing assessing the cell morphology, cytotoxicity and viability in these scaffolds.
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Imagenología Tridimensional/métodos , Microscopía Confocal/métodos , Células Madre/ultraestructura , Ingeniería de Tejidos/métodos , Andamios del Tejido , Huesos/metabolismo , Huesos/ultraestructura , Cartílago Articular/metabolismo , Cartílago Articular/ultraestructura , Técnicas de Cultivo de Célula , Supervivencia Celular/efectos de los fármacos , Células Inmovilizadas , Quitosano/química , Quitosano/farmacología , Matriz Extracelular/metabolismo , Matriz Extracelular/ultraestructura , Adhesivo de Tejido de Fibrina/química , Humanos , Imagenología Tridimensional/instrumentación , Ácido Láctico/química , Ácido Láctico/farmacología , Microscopía Confocal/instrumentación , Ácido Poliglicólico/química , Ácido Poliglicólico/farmacología , Polihidroxietil Metacrilato/química , Polihidroxietil Metacrilato/farmacología , Copolímero de Ácido Poliláctico-Ácido Poliglicólico , Células Madre/efectos de los fármacos , Células Madre/metabolismoRESUMEN
The current study was aimed to develop a transparent wound dressing comprised of bacterial cellulose (BC) and poly (2-hydroxyethyl methacrylate) (PHEMA) hydrogel coated with silver (Ag) nanoparticles. Briefly, different concentrations of BC whiskers (BCWs) were added into the HEMA solution to form PHEMA/BCWs hydrogel with volume ratio of monomer HEMA and BCWs as 7:3 and 1:1. The addition of BCWs into PHEMA matrix improved its equilibrium water content and light transmittance about 20%-40% and 10%, respectively. The Young's modulus for PHEMA was found to be 0.72MPa, which was improved to 0.57MPa and 0.50MPa for PHEMA/BCWs 7:3 and PHEMA/BCWs 1:1, respectively. Further, immersion of PHEMA/BCWs hydrogel in the AgNO3 and NaBH4 solutions bestowed it with antibacterial property and produced inhibition zones of 0.5±0.15cm and 0.25±0.15cm against Escherichia coli and Staphylococcus aureus, respectively. Similarly, PHEMA/BCWs prepared with 0.001M AgNO3 and 0.001M NaBH4 solutions showed 99% and 90% reduction in colony forming unit (CFU) for E. coli and S. aureus, respectively, after 24h. The PHEMA/BCWs/Ag hydrogel facilitated the growth of NIH3T3 fibroblast, showing their low toxicity. These results demonstrate the suitability of PHEMA/BCWs/Ag hydrogel for its application as potential transparent wound dressing material for skin repair.
Asunto(s)
Antibacterianos/química , Vendajes , Celulosa/química , Gluconacetobacter xylinus/química , Polihidroxietil Metacrilato/química , Cicatrización de Heridas/efectos de los fármacos , Animales , Antibacterianos/farmacología , Vendajes/microbiología , Supervivencia Celular/efectos de los fármacos , Escherichia coli/efectos de los fármacos , Hidrogeles/química , Ensayo de Materiales , Fenómenos Mecánicos , Ratones , Células 3T3 NIH , Polihidroxietil Metacrilato/farmacología , Plata/química , Staphylococcus aureus/efectos de los fármacos , Agua/químicaRESUMEN
PURPOSE: To investigate the influence of the polymerization technique and the content of hydroxyl groups on the performance of new bile acid sequestrants based on PAMPMTA-co-PHEA (PAMPTMA: poly((3-acrylamidopropyl)trimethylammonium chloride); PHEA: poly(2-hydroxyethyl acrylate)) hydrogels. METHODS: PAMPMTA-co-PHEA hydrogels were prepared using either free radical polymerization or supplemental activator and reducing agent atom transfer radical polymerization. The chemical structure and composition of the hydrogels was confirmed by both FTIR and ssNMR. The binding of sodium cholate as the model bile salt was evaluated in simulated intestinal fluid using HPLC. The degradation of the polymers was evaluated in vitro in solutions mimicking the gastrointestinal tract environment. RESULTS: The binding showed that an increase of the amount of HEA in the hydrogel lead to a decrease of the binding capacity. In addition, it was demonstrated for the first time that the hydrogels produced by SARA ATRP presented a higher binding capacity than similar ones produced by FRP. Finally, it was observed that copolymers of PAMPTMA-co-PHEA showed no sign of degradation in solutions mimicking both the stomach and the intestine environment. CONCLUSIONS: The use of an advanced polymerization technique, such as the SARA ATRP, could be beneficial for the preparation of BAS with enhanced performance.
Asunto(s)
Ácidos y Sales Biliares/metabolismo , Hidrogeles/química , Hidrogeles/farmacología , Polihidroxietil Metacrilato/análogos & derivados , Compuestos de Amonio Cuaternario/química , Compuestos de Amonio Cuaternario/farmacología , Sitios de Unión , Humanos , Hidrogeles/síntesis química , Oxidación-Reducción , Polihidroxietil Metacrilato/síntesis química , Polihidroxietil Metacrilato/química , Polihidroxietil Metacrilato/farmacología , Polimerizacion , Compuestos de Amonio Cuaternario/síntesis química , Colato de Sodio/metabolismoRESUMEN
The interactions of cells with the surface of materials is known to be influenced by a range of factors that include chemistry and roughness; however, it is often difficult to probe these factors individually without also changing the others. Here we investigate the role of roughness on cell adhesion while maintaining the same underlying chemistry. This was achieved by using a polymerization in mold technique to prepare poly(hydroxymethyl methacrylate) hydrogels with either a flat topography or a topography that replicated the microscale features of lotus leaves. These materials were then assessed for cell adhesion, and atomic force microscopy and contact angle analysis were then used to probe the physical reasons for the differing behavior in relation to cell adhesion.
Asunto(s)
Hidrogeles/química , Lotus/anatomía & histología , Hojas de la Planta/anatomía & histología , Animales , Adhesión Celular/efectos de los fármacos , Humanos , Hidrogeles/farmacología , Microscopía de Fuerza Atómica , Polihidroxietil Metacrilato/química , Polihidroxietil Metacrilato/farmacologíaRESUMEN
Thrombus formation presents a serious hindrance in the development of functional artificial blood vessels, especially those with a small diameter. Endothelialization can prevent thrombus formation; however, the adhesion of endothelial cells to existing polymer materials is generally weak. Therefore, polymers that have both anti-thrombotic and endothelialization properties do not currently exist. We previously reported that platelets do not adhere to poly(2-methoxyethyl acrylate) (PMEA) or poly(tetrahydrofurfuryl acrylate)(PTHFA). Here, we investigated whether endothelial cells and smooth muscle cells, both of which are blood vessel components, could adhere to these synthetic polymers. Polyethylene terephthalate films were coated with PMEA and PTHFA using a spin-coater. Human umbilical vein endothelial cells or aorta smooth muscle cells were seeded on the polymer surfaces, after which we analyzed the number of adherent cells, their morphologies and vinculin expression. We found that both endothelial and smooth muscle cells adhered to PMEA and PTHFA, while platelets did not. We propose that, by using PMEA and PTHFA with no modifications, it should be possible to develop artificial blood vessels with both anti-thrombotic and endothelialization properties. In addition, we discuss the mechanism of selective cell adhesion in PMEA and PTHFA.
Asunto(s)
Materiales Biocompatibles/farmacología , Células Endoteliales de la Vena Umbilical Humana/citología , Ensayo de Materiales , Miocitos del Músculo Liso/citología , Polihidroxietil Metacrilato/farmacología , Materiales Biocompatibles/química , Adhesión Celular/efectos de los fármacos , Recuento de Células , Proliferación Celular/efectos de los fármacos , Células Cultivadas , Células Endoteliales de la Vena Umbilical Humana/efectos de los fármacos , Humanos , Microscopía Confocal , Peso Molecular , Miocitos del Músculo Liso/efectos de los fármacos , Adhesividad Plaquetaria/efectos de los fármacos , Polihidroxietil Metacrilato/química , Propiedades de SuperficieRESUMEN
This study presents a custom-made in situ gelling polymeric precursor for cell encapsulation. Composed of poly((2-hydroxyethyl)methacrylate-co-(3-aminopropyl)methacrylamide) (P(HEMA-co-APM) mother backbone and RGD-mimicking poly(amidoamine) (PAA) moiteis, the comb-like structured polymeric precursor is tailored to gather the advantages of the two families of synthetic polymers, i.e., the good mechanical integrity of PHEMA-based polymers and the biocompatibility and biodegradability of PAAs. The role of P(HEMA-co-APM) in the regulation of the chemico-physical properties of P(HEMA-co-APM)/PAA hydrogels is thoroughly investigated. On the basis of obtained results, namely the capability of maintaining vital NIH3T3 cell line in vitro for 2 d in a 3D cell culture, the in vivo biocompatibility in murine model for 16 d, and the ability of finely tuning mechanical properties and degradation kinetics, it can be assessed that P(HEMA-co-APM)/PAAs offer a cost-effective valid alternative to the so far studied natural polymer-based systems for cell encapsulation.
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Alanina/análogos & derivados , Hidrogeles/química , Polihidroxietil Metacrilato/química , Acrilamidas/química , Alanina/química , Alanina/farmacología , Animales , Técnicas de Cultivo de Célula/métodos , Hidrogeles/farmacología , Cinética , Ensayo de Materiales , Metacrilatos/química , Ratones , Células 3T3 NIH/efectos de los fármacos , Polihidroxietil Metacrilato/farmacologíaRESUMEN
Thin polymer films that prevent the adhesion of bacteria are of interest as coatings for the development of infection-resistant biomaterials. This study investigates the influence of grafting density and film thickness on the adhesion of Staphylococcus epidermidis to poly(poly(ethylene glycol)methacrylate) (PPEGMA) and poly(2-hydroxyethyl methacrylate) (PHEMA) brushes prepared via surface-initiated atom transfer radical polymerization (SI-ATRP). These brushes are compared with poly(ethylene glycol) (PEG) brushes, which are obtained by grafting PEG onto an epoxide-modified substrate. Except for very low grafting densities (ρ = 1%), crystal violet staining experiments show that the PHEMA and PPEGMA brushes are equally effective as the PEG-modified surfaces in preventing S. epidermis adhesion and do not reveal any significant variations as a function of film thickness or grafting density. These results indicate that brushes generated by SI-ATRP are an attractive alternative to grafted-onto PEG films for the preparation of surface coatings that resist bacterial adhesion.
Asunto(s)
Adhesión Bacteriana/efectos de los fármacos , Materiales Biocompatibles/farmacología , Infecciones/tratamiento farmacológico , Staphylococcus epidermidis/efectos de los fármacos , Materiales Biocompatibles/química , Compuestos Epoxi/química , Humanos , Infecciones/microbiología , Metacrilatos/química , Metacrilatos/farmacología , Polietilenglicoles/química , Polietilenglicoles/farmacología , Polihidroxietil Metacrilato/química , Polihidroxietil Metacrilato/farmacología , Polimerizacion , Polímeros/química , Polímeros/farmacología , Ácidos Polimetacrílicos , Staphylococcus epidermidis/patogenicidad , Propiedades de SuperficieRESUMEN
Hydrogels are widely used in the biomedical field. Their main purposes are either to deliver biological active agents or to temporarily fill a defect until they degrade and are followed by new host tissue formation. However, for this latter application, biodegradable hydrogels are usually not capable to sustain any significant load. The development of biodegradable hydrogels presenting load-bearing capabilities would open new possibilities to utilize this class of material in the biomedical field. In this work, an original formulation of biodegradable photo-crosslinked hydrogels based on hydroxyethyl methacrylate (HEMA) is presented. The hydrogels consist of short-length poly(2-hydroxyethyl methacrylate) (PHEMA) chains in a star shape structure, obtained by introducing a tetra-functional chain transfer agent in the backbone of the hydrogels. They are cross-linked with a biodegradable N,O-dimethacryloyl hydroxylamine (DMHA) molecule sensitive to hydrolytic cleavage. We characterized the degradation properties of these hydrogels submitted to mechanical loadings. We showed that the developed hydrogels undergo long-term degradation and specially meet the two essential requirements of a biodegradable hydrogel suitable for load bearing applications: enhanced mechanical properties and low molecular weight degradation products. © 2015 Wiley Periodicals, Inc. J Biomed Mater Res Part B: Appl Biomater, 104B: 1161-1169, 2016.
Asunto(s)
Plásticos Biodegradables , Condrocitos/metabolismo , Hidrogeles , Metacrilatos , Plásticos Biodegradables/química , Plásticos Biodegradables/farmacocinética , Plásticos Biodegradables/farmacología , Células Cultivadas , Condrocitos/citología , Humanos , Hidrogeles/química , Hidrogeles/farmacocinética , Hidrogeles/farmacología , Metacrilatos/química , Metacrilatos/farmacocinética , Metacrilatos/farmacología , Polihidroxietil Metacrilato/química , Polihidroxietil Metacrilato/farmacocinética , Polihidroxietil Metacrilato/farmacologíaRESUMEN
The development of bioartificial liver (BAL) is expected because of the shortage of donor liver for transplantation. The substrates for BAL require the following criteria: (a) blood compatibility, (b) hepatocyte adhesiveness, and (c) the ability to maintain hepatocyte-specific functions. Here, we examined blood-compatible poly(2-methoxyethyl acrylate) (PMEA) and poly(tetrahydrofurfuryl acrylate) (PTHFA) (PTHFA) as the substrates for BAL. HepG2, a human hepatocyte model, could adhere on PMEA and PTHFA substrates. The spreading of HepG2 cells was suppressed on PMEA substrates because integrin contribution to cell adhesion on PMEA substrate was low and integrin signaling was not sufficiently activated. Hepatocyte-specific gene expression in HepG2 cells increased on PMEA substrate, whereas the expression decreased on PTHFA substrates due to the nuclear localization of Yes-associated protein (YAP). These results indicate that blood-compatible PMEA is suitable for BAL substrate. Also, PMEA is expected to be used to regulate cell functions for blood-contacting tissue engineering.
Asunto(s)
Materiales Biocompatibles/química , Hígado Artificial , Polihidroxietil Metacrilato/química , Proteínas Adaptadoras Transductoras de Señales/metabolismo , Adsorción , Materiales Biocompatibles/farmacología , Adhesión Celular/efectos de los fármacos , Células Hep G2 , Factor Nuclear 4 del Hepatocito/genética , Factor Nuclear 4 del Hepatocito/metabolismo , Humanos , Integrinas/química , Integrinas/metabolismo , Fosfoproteínas/metabolismo , Polihidroxietil Metacrilato/farmacología , ARN Mensajero/metabolismo , Reacción en Cadena en Tiempo Real de la Polimerasa , Albúmina Sérica/genética , Albúmina Sérica/metabolismo , Ingeniería de Tejidos , Factores de Transcripción , Proteínas Señalizadoras YAPRESUMEN
To determine whether PHEMA [poly(2-hydroxyethylmethacrylate)] is suitable for portal vein embolization in patients scheduled to right hepatectomy and whether it is as effective as the currently used agent (a histoacryl/lipiodol mixture). Two groups of nine patients each scheduled for extended right hepatectomy for primary or secondary hepatic tumor, had right portal vein embolization in an effort to induce future liver remnant (FLR) hypertrophy. One group had embolization with PHEMA, the other one with the histoacryl/lipiodol mixture. In all patients, embolization was performed using the right retrograde transhepatic access. Embolization was technically successful in all 18 patients, with no complication related to the embolization agent. Eight patients of either group developed FLR hypertrophy allowing extended right hepatectomy. Likewise, one patient in each group had recanalization of a portal vein branch. Histology showed that both embolization agents reach the periphery of portal vein branches, with PHEMA penetrating somewhat deeper into the periphery. PHEMA has been shown to be an agent suitable for embolization in the portal venous system comparable with existing embolization agent (histoacryl/lipiodol mixture).
Asunto(s)
Embolización Terapéutica/métodos , Hepatectomía/métodos , Hígado/efectos de los fármacos , Polihidroxietil Metacrilato/uso terapéutico , Vena Porta/efectos de los fármacos , Anciano , Enbucrilato/farmacología , Enbucrilato/uso terapéutico , Aceite Etiodizado/farmacología , Aceite Etiodizado/uso terapéutico , Femenino , Humanos , Masculino , Persona de Mediana Edad , Polihidroxietil Metacrilato/farmacologíaRESUMEN
The water structure and platelet compatibility of poly(methyl methacrylate (MMA)-block-2-hydroxyethyl methacrylate (HEMA)) were investigated. The molecular weight (Mn) of the polyHEMA segment was kept constant (average: 9600), while the Mn of the polyMMA segment was varied from 1340 to 7390. The equilibrium water content of the copolymers was found to be mainly governed by the HEMA content. The water structure in the copolymers was characterized in terms of the amounts of non-freezing and freezing water (abbreviated as Wnf and Wfz, respectively) using differential scanning calorimetry. It was found that the Wnf for the copolymers were higher than those estimated from the Wnf for the HEMA and MMA homopolymers and that the amount of excess non-freezing water depended on the polyMMA segment length. In addition, X-ray diffraction analysis revealed that some of the copolymers had cold-crystallizable water. These facts suggested that the polyMMA segments were involved in determining the water structures in the copolymers. Furthermore, the platelet compatibility of the copolymers was improved as compared to that of the HEMA homopolymer. It was therefore concluded that the platelet compatibility of the copolymer was related to the amount of excess non-freezing water.