Poly(lactide-co-ε-caprolactone) (PLCL) has been reported to be a good candidate for tissue engineering because of its good biocompatibility. Particularly, a braided PLCL scaffold (PLL/PCL ratio = 85/15) has been recently designed and partially validated for ligament tissue engineering. In the present study, we assessed the in vivo biocompatibility of acellular and cellularised scaffolds in a rat model. We then determined its in vitro biocompatibility using stem cells issued from both bone marrow and Wharton Jelly. From a biological point of view, the scaffold was shown to be suitable for tissue engineering in all these cases. Secondly, while the initial mechanical properties of this scaffold have been previously reported to be adapted to load-bearing applications, we studied the evolution in time of the mechanical properties of PLCL fibres due to hydrolytic degradation. Results for isolated PLCL fibres were extrapolated to the fibrous scaffold using a previously developed numerical model. It was shown that no accumulation of plastic strain was to be expected for a load-bearing application such as anterior cruciate ligament tissue engineering. However, PLCL fibres exhibited a non-expected brittle behaviour after two months. This may involve a potential risk of premature failure of the scaffold, unless tissue growth compensates this change in mechanical properties. This combined study emphasises the need to characterise the properties of biomaterials in a pluridisciplinary approach, since biological and mechanical characterisations led in this case to different conclusions concerning the suitability of this scaffold for load-bearing applications.

The purpose of this paper is to display the influence of isoalkanes on the structure and mechanical properties of waxes. This work was carried out by means of X-ray diffraction, differential thermal analyses, and dynamic mechanical analyses. Isoalkanes coming from an industrial wax were added in different quantities to a synthetic mixture of linear alkanes. The disorder generated by this addition was estimated by X-ray diffraction; it modifies the structural transformations versus temperature and therefore the mechanical properties. The branched chains of isoalkanes hinder the molecules motions, especially the rotation along the long axis. Thus, some phases usually formed at high temperature are not observed when increasing the temperature. With regard to the mechanical properties, the effect of the branched alkanes was studied using two industrial waxes with Gaussian distribution composition. The dynamic mechanical analyses have shown that the storage modulus (E′) is also affected by the isoalkane quantity.

The purpose of this paper is to compare the structure and the mechanical properties of several model mixtures exclusively constituted of pure linear alkanes so as to better understand the conditions in which disorder appears within real systems. The molar distribution of all the studied mixtures is of "normal logarithmic type", and the only statistical parameter varying from one mixture to the other is the standard deviation (σ) of the distribution. This work was carried out by means of X-ray diffraction, differential scanning calorimetry (DSC), and dynamical mechanical analysis (DMA) according to temperature. The obtained results show that the number of crystallized phases increases with the standard deviation and that the structural evolution versus temperature of the mixtures also depends on this statistical parameter. With regard to the mechanical properties, the results of the dynamic mechanical analyses show that the storage modulus (E 0 ) and the loss factor (tan δ) are also affected by the standard deviation of the distribution.