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1.
Small ; 15(42): e1903784, 2019 10.
Artículo en Inglés | MEDLINE | ID: mdl-31448570

RESUMEN

Biodegradable polycaprolactone (PCL) has been widely applied as a scaffold material in tissue engineering. However, the PCL surface is hydrophobic and adsorbs nonspecific proteins. Some traditional antifouling modifications using hydrophilic moieties have been successful but inhibit cell adhesion, which is not ideal for tissue engineering. The PCL surface is modified with bioinspired zwitterionic poly[2-(methacryloyloxy)ethyl choline phosphate] (PMCP) via surface-initiated atom transfer radical polymerization to improve cell adhesion through the unique interaction between choline phosphate (CP, on PMCP) and phosphate choline (PC, on cell membranes). The hydrophilicity of the PCL surface is significantly enhanced after surface modification. The PCL-PMCP surface reduces nonspecific protein adsorption (e.g., up to 91.7% for bovine serum albumin) due to the zwitterionic property of PMCP. The adhesion and proliferation of bone marrow mesenchymal stem cells on the modified surface is remarkably improved, and osteogenic differentiation signs are detected, even without adding any osteogenesis-inducing supplements. Moreover, the PCL-PMCP films are more stable at the early stage of degradation. Therefore, the PMCP-functionalized PCL surface promotes cell adhesion and osteogenic differentiation, with an antifouling background, and exhibits great potential in tissue engineering.


Asunto(s)
Incrustaciones Biológicas , Diferenciación Celular/efectos de los fármacos , Osteogénesis/efectos de los fármacos , Fosforilcolina/análogos & derivados , Poliésteres/farmacología , Ácidos Polimetacrílicos/farmacología , Ingeniería de Tejidos , Adsorción , Animales , Animales Recién Nacidos , Materiales Biocompatibles/farmacología , Adhesión Celular/efectos de los fármacos , Proliferación Celular/efectos de los fármacos , Citocinas/metabolismo , Células Madre Mesenquimatosas/citología , Células Madre Mesenquimatosas/efectos de los fármacos , Fosforilcolina/síntesis química , Fosforilcolina/farmacología , Espectroscopía de Fotoelectrones , Poliésteres/síntesis química , Ácidos Polimetacrílicos/síntesis química , Ratas Sprague-Dawley , Propiedades de Superficie , Agua/química
2.
Langmuir ; 35(5): 1895-1901, 2019 02 05.
Artículo en Inglés | MEDLINE | ID: mdl-30145900

RESUMEN

Zwitterionic polymers are continually suggested as promising alternatives to tune the surface/interface properties of materials in many fields because of their unique molecular structures. Tremendous efforts have been devoted to immobilizing zwitterionic polymers (polyzwitterions, PZIs) on the material surfaces. However, these efforts usually suffer from cumbersome and time-consuming procedures. Herein we report a one-step strategy to facilely achieve the bioinspired polydopamine/polyzwitterion (PDA/PZI) coatings on various substrates. It requires only 30 min to form PDA/PZI coatings by mixing oxidant, dopamine, and zwitterionic monomers, including carboxybetaine methacrylate (CBMA), sulfobetaine methacrylate (SBMA), and 2-methacryloxyethyl phosphorylcholine (MPC). These bioinspired coatings display multifunctional properties such as underwater antioil-adhesion and antifreezing thanks to their high hydrophilicity and underwater superoleophobicity. The coatings even show the antiadhesion property for crude oil with high viscosity. Therefore, the PDA/PZI-coated meshes are efficient for separating both light oil and crude oil from oil/water mixtures. All these results demonstrate that the one-step strategy is a facile approach to design and exploit the bioinspired PDA/PZI coatings for diverse applications.


Asunto(s)
Betaína/química , Indoles/química , Metacrilatos/química , Petróleo , Fosforilcolina/análogos & derivados , Polímeros/química , Ácidos Polimetacrílicos/química , Betaína/síntesis química , Congelación , Indoles/síntesis química , Metacrilatos/síntesis química , Fosforilcolina/síntesis química , Fosforilcolina/química , Polímeros/síntesis química , Ácidos Polimetacrílicos/síntesis química , Extracción en Fase Sólida/instrumentación , Extracción en Fase Sólida/métodos , Propiedades de Superficie , Agua/química
3.
Langmuir ; 32(4): 1184-94, 2016 Feb 02.
Artículo en Inglés | MEDLINE | ID: mdl-26695478

RESUMEN

A functional copolymer platform, namely, poly[(propargyl methacrylate)-ran-(2-methacryloyloxyethyl phosphorylcholine)] (PPgMAMPC), was synthesized by reversible addition-fragmentation chain-transfer polymerization. In principle, the alkyne moiety of propargyl methacrylate (PgMA) should serve as an active site for binding azide-containing molecules via a click reaction, i.e., Cu-catalyzed azide/alkyne cycloaddition (CuAAC), and 2-methacryloyloxyethyl phosphorylcholine (MPC), the hydrophilic monomeric unit, should enable the copolymer to suppress nonspecific adsorption. The copolymers were characterized using Fourier transform infrared (FTIR) and (1)H NMR spectroscopies. Thiol-terminated, PPgMAMPC-SH, obtained by aminolysis of PPgMAMPC, was immobilized on a gold-coated substrate using a "grafting to" approach via self-assembly. Azide-containing species, namely, biotin and peptide nucleic acid (PNA), were then immobilized on the alkyne-containing copolymeric platform via CuAAC. The potential use of surface-attached PPgMAMPC in biosensing applications was shown by detection of specific target molecules, i.e., streptavidin (SA) and DNA, by the developed sensing platform using a surface plasmon resonance technique. The copolymer composition strongly influenced the performance of the developed sensing platform in terms of signal-to-noise ratio in the case of the biotin-SA system and hybridization efficiency and mismatch discrimination for the PNA-DNA system.


Asunto(s)
Técnicas Biosensibles/métodos , Metacrilatos/química , Fosforilcolina/análogos & derivados , Azidas/química , Disparidad de Par Base , Biotina/análogos & derivados , Biotina/química , Química Clic , ADN Complementario/análisis , Oro/química , Metacrilatos/síntesis química , Ácidos Nucleicos de Péptidos/química , Fosforilcolina/síntesis química , Fosforilcolina/química , Estreptavidina/análisis , Resonancia por Plasmón de Superficie
4.
Biomacromolecules ; 12(6): 1973-82, 2011 Jun 13.
Artículo en Inglés | MEDLINE | ID: mdl-21553908

RESUMEN

This Review is focused on the growing interest brought to phosphorus-containing organic materials for applications in the biomedical field, mainly because of their properties such as biocompatibility, hemocompatibility, and protein adsorption resistance. It mainly describes relevant works achieved on these materials for various applications: dentistry, regenerative medicine, and drug delivery. Special attention was given to 2-methacryloyloxyethyl phosphorylcholine (MPC) monomer as the latter appeared of great importance because of its biomimetic structure due to the presence of the phospholipid group on its structure. As a result, much research effort is currently concentrated on the development of phosphorylcholine-containing (co)polymers that represent a promising class of materials.


Asunto(s)
Materiales Biocompatibles/síntesis química , Odontología/métodos , Sistemas de Liberación de Medicamentos/métodos , Metacrilatos/síntesis química , Fósforo/química , Fosforilcolina/análogos & derivados , Medicina Regenerativa/métodos , Ingeniería de Tejidos/métodos , Materiales Biocompatibles/metabolismo , Humanos , Hidrogeles/química , Hidrogeles/metabolismo , Metacrilatos/metabolismo , Fosfatos/química , Fosfatos/metabolismo , Fosfolípidos/química , Fosfolípidos/metabolismo , Fósforo/metabolismo , Fosforilcolina/síntesis química , Fosforilcolina/metabolismo , Polímeros/química , Proteínas/química , Proteínas/metabolismo , Propiedades de Superficie
6.
Biochem Biophys Res Commun ; 172(2): 855-61, 1990 Oct 30.
Artículo en Inglés | MEDLINE | ID: mdl-2241973

RESUMEN

A novel metabolite of choline, phosphorylcholine methyl ester, has been identified in the eggs of S. purpuratus wherein it is present at approximately 1 mM concentration. To the best of our knowledge, this is the first instance of a phosphoryl-methyl-ester to be observed in nature. The compound appears to be species specific, since it has not been observed in other species such as L. pictus and P. depressus. In S. purpuratus its distribution is confined to the ovary, eggs and embryos, and is absent from young animals following metamorphosis.


Asunto(s)
Ovario/química , Óvulo/química , Fosforilcolina/análogos & derivados , Animales , Isótopos de Carbono , Embrión no Mamífero , Femenino , Hidrógeno , Espectroscopía de Resonancia Magnética/métodos , Fósforo , Fosforilcolina/síntesis química , Fosforilcolina/aislamiento & purificación , Erizos de Mar/embriología
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