RESUMEN
(Bis)furan-telechelic, low-molar-mass polybutadienes and polyisoprenes are synthesized by controlled degradation of high molar mass polymers and chain-end modifications yielding difunctional, trifunctional, or tetrafunctional polymers. Addition of a bismaleimide to the liquid-modified polymer leads to the formation of a thermoreversible elastomeric network based on the Diels-Alder chemistry for the trifunctional or tetrafunctional polymers, whereas only chain extension occurs for the bifunctional one. Dynamic mechanical analyses or tensile tests are performed on the networks and reveal a similar behavior for polyisoprene and polybutadiene with nevertheless quite different Young modulus or strain at break. The retro Diels-Alder reaction occurs upon heating, allowing the remolding of the used elastomer. The remolded network exhibits the same mechanical properties as the initial network, showing an efficient material recyclability.
Asunto(s)
Butadienos/química , Elastómeros/química , Reacción de Cicloadición , Módulo de Elasticidad , Elastómeros/síntesis química , Furanos/química , Maleimidas/química , Resistencia a la TracciónRESUMEN
Controlling the behavior of stem cells through the supramolecular architecture of the extracellular matrix remains an important challenge in the culture of stem cells. Herein, we report on a new generation of low-molecular-weight gelators (LMWG) for the culture of isolated stem cells. The bola-amphiphile structures derived from nucleolipids feature unique rheological and biological properties suitable for tissue engineering applications. The bola-amphiphile-based hydrogel scaffold exhibits the following essential properties: it is nontoxic, easy to handle, injectable, and features a biocompatible rheology. The reported glycosyl-nucleoside bola-amphiphiles (GNBA) are the first examples of LMWG that allow the culture of isolated stem cells in a gel matrix. The results (TEM observations and rheology) suggest that the supramolecular organizations of the matrix play a role in the behavior of stem cells in 3D environments.
Asunto(s)
Materiales Biocompatibles/química , Hidrogel de Polietilenoglicol-Dimetacrilato/química , Nucleósidos/química , Células Madre/citología , Tensoactivos/química , Células Cultivadas , Glicosilación , Humanos , Peso Molecular , Reología , Ingeniería de Tejidos , Andamios del Tejido/químicaRESUMEN
This article presents BEPO®, an in situ forming depot (ISFD) technology mediated by a solvent-exchange mechanism. The matrix of the in situ formed drug delivery depot is composed of the combination of a diblock (DB) and a triblock (TB) polyethylene glycol-polyester copolymer. This combination offers a broad capability to tune the release of a wide variety of drugs to the desired pharmacokinetics. The work described in the present article demonstrates that the delivery rate and profile can be adjusted by changing the composition of either TB or DB or the relative ratio between them, among other parameters. It has been shown that the polymeric composition of the formulation has a substantial impact on the solvent exchange rate between the organic solvent and the surrounding aqueous medium which subsequently determines the internal structure of the resulting depot and the delivery of the therapeutic cargo. This has been demonstrated studying the in vitro release of two model molecules: bupivacaine and ivermectin. Formulations releasing these drugs have been administered to animal models to show the possibility of delivering therapeutics from weeks to months by using BEPO® technology.