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1.
Mater Sci Eng C Mater Biol Appl ; 70(Pt 1): 824-831, 2017 Jan 01.
Article in English | MEDLINE | ID: mdl-27770960

ABSTRACT

The aim of this study is to explore the importance of the potentially competing effects of buffering effects of the calcium phosphate filler and particle-mediated water sorption on the degradation products of poly(d,l lactide-co-glycolide (50:50))(PLGA)/hydroxyapatite(HA) composites. Further the influence of type of HA on the mechanical properties of the composites was investigated. Phase pure HA was synthesised via a reaction between aqueous solutions of calcium hydroxide and orthophosphoric acid. The powder produced was either used as produced (uncalcined) or calcined in air or calcined in a humidified argon atmosphere. An in-vitro degradation study was carried out in phosphate buffered saline (PBS). The results obtained indicated that the degradation rate of the composite might be better understood if both the buffering effects and the rate of water sorption by the composites are considered.


Subject(s)
Durapatite/chemistry , Lactic Acid/chemistry , Polyglycolic Acid/chemistry , Calcium/analysis , Elastic Modulus , Hydrogen-Ion Concentration , Molecular Weight , Particle Size , Polylactic Acid-Polyglycolic Acid Copolymer , Powders , Solutions , Temperature , Water/chemistry , X-Ray Diffraction
2.
Mater Sci Eng C Mater Biol Appl ; 48: 642-50, 2015 Mar.
Article in English | MEDLINE | ID: mdl-25579967

ABSTRACT

This study investigates the influence of silanisation on the mechanical and degradation behaviour of PLGA/HA composites. Three different silanes (mercaptopropyl trimethoxy silane (MPTMS), aminopropyl trimethoxy silane (APTMS) and aminopropyltriethoxy silane (APTES)) were applied to HA substrates in order to study the effect of head group (which binds to the polymer) and tail group (which binds to the surface hydroxyl groups in HA). A composite of hydroxyapatite (HA) and poly(d,l lactide-co-glycolide (50:50)) (PLGA) was investigated. The influence of concentration, the reaction time, drying temperature and substrate surface on silanisation was examined. TGA was used to detect the degree of silanisation. HA with MPTMS (1wt.% MPTMS with reaction time of 1h) was used as filler in PLGA-30wt.% HA composites for an in-vitro degradation study carried out in PBS. In addition, the mechanical properties of the composites were studied. Silanisation affects the properties of the composite by improving the bonding at the interface and hence it was found to influence the plastic mechanical properties rather than the elastic mechanical properties or the degradation profile of the composite.


Subject(s)
Coated Materials, Biocompatible/chemistry , Durapatite/chemistry , Lactic Acid/chemistry , Polyglycolic Acid/chemistry , Silanes/chemistry , Elasticity , Polylactic Acid-Polyglycolic Acid Copolymer
3.
Indian Heart J ; 66(6): 663-71, 2014.
Article in English | MEDLINE | ID: mdl-25634402

ABSTRACT

Coronary artery disease (CAD) is the major cause of fatality and disability among all cardiovascular diseases (CVD). Intricate interactions of genes and environment dictate the outcomes of CAD. Technological advances in the different fields of genetics including linkage studies (LS), candidate gene studies (CGS) and genome-wide association studies (GWA studies) have augmented the knowledge of pathogenesis of CAD. LS were more successful in identifying genetic variants among monogenic disease. GWA studies were relatively popular in identification of variation in polygenic disease. Until now, GWA studies recognized about 50 loci determining around 6% of the heritability in CAD. Clinical utility of the above knowledge would result in better CAD management, but validation of the variants in native population is warranted for active adoption into the clinic. The major aim of this review is to provide an adequate perspective of our current understanding and advances of genetics in CAD.


Subject(s)
Coronary Artery Disease/genetics , Genetic Predisposition to Disease , Genome-Wide Association Study , Genotype , Humans , Phenotype , Polymorphism, Single Nucleotide , Risk
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