Adsorption of 2,2 '-dithiodipyridine as a tool for the assembly of silver nanoparticles

Silver nanostructured thin films stabilized by 2,2’-dithiodipyridine (2dtpy) were prepared. The Ag nanoparticles were obtained by treating the complex [Ag(2dtpy)]NO3 with NaBH4 in a methanol–toluene mixture. The films were transferred to borosilicate glass slips by a dip-coating method and were found to consist of Ag nanoparticles possibly linked via 2dtpy molecules. Surface-enhanced Raman scattering (SERS) studies have offered the possibility of investigating the adsorption modes of 2dtpy at the Ag nanoparticle surfaces in the fil

Influence of a diene impurity on the molecular structure of phosphate-containing polymers with medical applications

We have demonstrated that the unacknowledged presence of almost 30% diene impurity in some commercial phosphate monomers had not only a significant effect on the molecular structure (topology) of a series of synthesized polymers but the instability of the ester functionalities during these polymerizations resulted in unexpectedly complex co-polymer chemistry

FT-IR Spectroscopy of Fluoro-Substituted Hydroxyapatite: Strengths and Limitations

Fluoro substituted hydroxyapatite (FHAp) samples were prepared by a cyclic pH method. Both calcined and uncalcined samples were subjected to elemental analysis (F, Ca, P) and X-ray diffraction (XRD) analysis to verify composition and phase purity. Good correlation between a-axis parameters and fluoride ion content was found for calcined samples, however, for uncalcined samples the fluoride ion content was higher than estimated from the a-axis values. Fourier transform infra red (FT-IR) spectroscopy analysis of the calcined samples showed OH band shifts and splitting in accordance with F-HO interactions affecting the OH vibration. We conclude that the OH libration (620–780 cm-1 range) is more suited for estimation of fluoride ion content than the OH stretching. In contrast, uncalcined samples all displayed FT-IR spectra similar to that of hydroxyapatite (HAp) despite the presence of fluoride ions (18–73%). FT-IR emission spectroscopy was used to probe the changes occurring in the FT-IR spectra of HAp and FHAp samples upon heating. Interpretation of the spectral changes occurring during heating to 1,000 degrees Celsius and subsequent cooling is given. Room temperature spectra of samples heated to various temperatures was used to determine the temperature necessary to produce FT-IR spectra displaying the expected OH bands. A model accounting for the combined observations is proposed

Calcium Phosphate Nucleation on Surface-Modified PTFE Membranes

Highly porous PTFE membranes are currently being used in facial reconstructive surgery. The present study aims at improving this biomaterial through creating a more bioactive surface by introducing ionic groups onto the surface. The unmodified PTFE membrane does not induce inorganic growth after immersion in simulated body fluid (SBF) for up to 4 weeks. Copolymeric grafting with acrylic acid (AAc) by means of gamma irradiation and subsequent in vitro testing in SBF reveals that this copolymer initially acts as an ion-exchange material and subsequently induces growth of a calcium phosphate phase (Ca/P = 2.7) when large amounts (15%) of pAAc are introduced onto the membrane surface. This copolymer is not expected to function well from a biomaterials perspective since SEM showed the pores on the surface to be partly blocked. In contrast, the surface of monoacryloxyethyl phosphate (MAEP) modified samples is altered at a molecular level only. Yet the modified materials are able to induce calcium phosphate nucleation when the external surface coverage is 44% or above. The initial inorganic growth on these membranes in SBF has a (Ca+Mg)/P ratio of 1.1 (presumably Brushite or Monetite). The secondary growth, possibly calcium-deficient apatite or tricalcium phosphate, has a (Ca+Mg)/P ratio of 1.5. This result is a promising indicator of a bioactive biomaterial

Carbodiimide-mediated synthesis of poly(l-lactide)-based networks

Poly(L-lactide-co-succinic anhydride) networks were synthesised via the carbodiimide-mediated coupling of poly(L-lactide) (PLLA) star polymers. When 4-(dimethylamino)pyridine (DMAP) alone was used as the catalyst gelation did not occur. However, when 4-(dimethylamino)pyridinium p-toluenesulfonate (DPTS), the salt of DMAP and p-toluenesulfonic acid (PTSA), was the catalyst, the networks obtained had gel fractions comparable to those which were reported for networks synthesised by conventional methods. Greater gel fractions and conversion of the prepolymer terminal hydroxyl groups were observed when the hydroxyl-terminated star prepolymers reacted with succinic anhydride in a one-pot procedure than when the hydroxyl-terminated star prepolymers reacted with presynthesised succinic-terminated star prepolymers. The thermal properties of the networks, glass transition temperature (Tg), melting temperature (Tm) and crystallinity (Xc) were all strongly influenced by the average molecular weights between the crosslinks ((M_c). The network with the smallest (M_c )(1400 g/mol) was amorphous and had a Tg of 59 °C while the network with the largest (M_c ) (7800 g/mol) was 15 % crystalline and had a Tg of 56 °C

Expanded poly (tetrafluoroethylene): From conception to biomedical device

Poly(tetrafluoroethylene) is ubiquitous in our daily lives. Applications range from non-stick cookware to artificial arteries and from wet weather apparel to high-altitude mountaineering ropes. Its serendipitous discovery is a story worth telling

In Vitro Bioactivity of MOEP Grafted ePTFE Membranes for Craniofacial Applications

Abstract The bioactivity of three methacryloyloxyethyl phosphate (MOEP) grafted expanded polytetrafluoroethylene (ePTFE) membranes with varying surface coverage as well as unmodified ePTFE was investigated through a series of in vitro tests: calcium phosphate growth in simulated body fluid (SBF), serum protein adsorption, and a morphology and attachment study of human osteoblast-like SaOS-2 cells. The graft copolymers were prepared by means of gamma irradiation induced grafting and displayed various surface morphologies and wettabilities depending on the grafting conditions used. Unmodified ePTFE did not induce nucleation of calcium phosphate minerals, whereas all the grafted membranes revealed the growth of calcium phosphate minerals after 7 days immersion in SBF. The sample with lowest surface grafting yield (24% coverage), a smooth graft morphology and relatively high hydrophobicity (θadv = 120º, θrec = 80º) showed carbonated hydroxyapatite growth covering the surface. On the other hand, the samples with high surface grafting yield (76 and 100%), a globular graft morphology and hydrophilic surfaces (θadv = 60º and 80º, θrec = 25º and 15º, respectively) exhibited irregular growth of non-apatitic calcium phosphate minerals. Irreversibly adsorbed protein measured after a 1 hour immersion in serum solution was quantified by the amount of nitrogen on the surface using XPS, as well as by weight increase. All grafted membranes adsorbed 3-6 times more protein than the unmodified membrane. The sample with the highest surface coverage adsorbed the most protein. Osteoblast-like SaOS-2 cells cultured for 3 hours revealed significantly higher levels of cell attachment on all grafted membranes compared to unmodified ePTFE. Although the morphology of the cells was heterogeneous, in general, the higher grafted surfaces showed a much better cell morphology than both the low surface-grafted and the control unmodified sample. The suite of in vitro tests confirms that a judicious choice of grafted monomer such as the phosphate-containing methacrylate monomer (MOEP) significantly improves the bioactivity of ePTFE in vitro