ABSTRACT
Titanium (Ti) is widely used in biomedical devices due to its recognized biocompatibility. However, implant failures and subsequent clinical side effects are still recurrent. In this context, improvements can be achieved by designing biomaterials where the bulk and the surface of Ti are independently tailored. The conjugation of biomolecules onto the Ti surface can improve its bioactivity, thus accelerating the osteointegration process. Ti was modified with TiO2, two different spacers, 3-(4-aminophenyl) propionic acid (APPA) or 3-mercaptopropionic acid (MPA) and dentin matrix protein 1 (DMP1) peptides. X-ray photoelectron spectroscopy analysis revealed the presence of carbon and nitrogen for all samples, indicating a success in the functionalization process. Furthermore, DMP1 peptides showed an improved coverage area for the samples with APPA and MPA spacers. Biological tests indicated that the peptides could modulate cell affinity, proliferation, and differentiation. Enhanced results were observed in the presence of MPA. Moreover, the immobilization of DMP1 peptides through the spacers led to the formation of calcium phosphate minerals with a Ca/P ratio near to that of hydroxyapatite. Corrosion and tribocorrosion results indicated an increased resistance to corrosion and lower mass loss in the functionalized materials, showing that this new type of functional material has attractive properties for biomaterials application.
Subject(s)
Biocompatible Materials/chemistry , Biocompatible Materials/pharmacology , Materials Testing , Osteogenesis/drug effects , Peptides/chemistry , Titanium/chemistry , Cell Adhesion/drug effects , Cell Differentiation/drug effects , Cell Proliferation/drug effects , Corrosion , Electrochemistry , Humans , Mesenchymal Stem Cells/cytology , Mesenchymal Stem Cells/drug effects , Osteoblasts/cytology , Osteoblasts/drug effects , Surface PropertiesABSTRACT
The effect of (60)Co gamma rays irradiation on the polymetallayne [-Pt(PBu(3))-C≡C-C(6)H(4)-C(6)H(4)-C≡C-](n) (Pt-DEBP) of defined chain length corresponding to 10 repeat units, has been studied in detail. The UV-vis absorption spectra of Pt-DEBP have been recorded in solution upon exposure of the polymetallayne at increasing radiation doses in the range up to 90 Gy, with special care to the features related to low doses. Complex modifications of the chemical structure of Pt-DEBP could be accessed through NMR, FTIR, GPC, and XPS characterizations, which support the attack of Cl and H radicals coming from the radiolysis of the solvent, CHCl(3), to the triple C≡C bonds of the backbone, leading to the formation of chlorinated double and single C-C bonds, with a concomitant increase of the molecular weight due to a recombinant effect of oligomer fragments upon irradiation. The presence of vinyl and single chlorinated moieties has been sustained from the simulation of the UV-vis spectra based on theoretical calculations.
Subject(s)
Alkynes/chemistry , Gamma Rays , Organoplatinum Compounds/chemistry , Chloroform/chemistry , Models, Molecular , Molecular ConformationABSTRACT
The effect of (60)Co γ irradiation on the absorption and emission spectra of the organometallic polymer [-Pt(PBu(3))(2)-C≡C-C(6)H(4)-C(6)H(4)-C≡C-](n) (Pt-DEBP) in chloroform and toluene solutions for dosimetry applications has been studied. The system Pt-DEBP/chloroform can be used for dosimetric applications in two different ways: (i) monitoring of absorption spectra changes for higher doses (higher than 1 Gy), and (ii) monitoring of emission spectra changes for low doses (below 1 Gy). The response of the polymer solution to γ ray doses has been interpreted with the aid of theoretical studies based on time dependent density functional theory (TD-DFT) calculations on the absorption bands of a model complex and of the possible fragments coming from the degradation of the polymer backbone. It has been proposed that the observed changes are promoted by the attack of radicals, from the radiolysis of the solvent, on the polymer triple bonds.
Subject(s)
Gamma Rays , Organoplatinum Compounds/chemistry , Polymers/chemistry , Absorption , Chloroform/chemistry , Models, Theoretical , Spectrophotometry, Ultraviolet , Toluene/chemistryABSTRACT
Fragmentation reactions of beta-hydroxymethyl-, beta-acetoxymethyl- and beta-benzyloxymethyl-butenolides and the corresponding gamma-butyrolactones were investigated by electrospray ionization tandem mass spectrometry (ESI-MS/MS) using collision-induced dissociation (CID). This study revealed that loss of H(2)O [M+H-8](+) is the main fragmentation process for beta-hydroxymethylbutenolide (1) and beta-hydroxymethyl-gamma-butyrolactone (2). Loss of ketene ([M+H-42](+)) is the major fragmentation process for protonated beta-acetoxymethyl-gamma-butyrolactone (4), but not for beta-acetoxymethylbutenolide (3). The benzyl cation (m/z 91) is the major ion in the ESI-MS/MS spectra of beta-benzyloxymethylbutenolide (5) and beta-benzyloxymethyl-gamma-butyrolactone (6). The different side chain at the beta-position and the double bond presence afforded some product ions that can be important for the structural identification of each compound. The energetic aspects involved in the protonation and gas-phase fragmentation processes were interpreted on the basis of thermochemical data obtained by computational quantum chemistry.
