Hydrogels reversible system

Richter S (2006) Contributions to the dynamical behavior of cross-linked and cross-linking systems stimulus-sensitive microgels and hydrogels, reversible and irreversible gelation processes. Habilitation thesis, TU Dresden... 

Finally, a new water-soluble polyphosphazene was recently synthesized that has the structure shown in 36 (46). This polymer has two attributes as a biomedical macromolecule. First, the pendent carboxylic acid groups are potential sites for condensation reactions with amines, alcohols, phenols, or other carboxylic acid units to generate amide, ester, or anhydride links to polypeptides or bioactive small molecules. Second, polymer forms ionic crosslinks when brought into contact with di- or trivalent cations such as Ca or Ai3+. The crosslinking process converts the water-soluble polymer to a hydrogel, a process that can be reversed when the system... 

Similarly to the phospholipid polymers, the MPC polymers show excellent biocompatibility and blood compatibility [43—48]. These properties are based on the bioinert character of the MPC polymers, i.e., inhibition of specific interaction with biomolecules [49, 50]. Recently, the MPC polymers have been applied to various medical and pharmaceutical applications [44-47, 51-55]. The crosslinked MPC polymers provide good hydrogels and they have been used in the manufacture of soft contact lenses. We have applied the MPC polymer hydrogel as a cell-encapsulation matrix due to its excellent cytocompatibility. At the same time, to prepare a spontaneously forming reversible hydrogel, we focused on the reversible covalent bonding formed between phenylboronic acid and polyol in an aqueous system. 

Sol-gel reversibility, of hydrogels, 13 730 Sol—gel silica—PDMS hybrids, 23 81 Sol—gel silica system, chemical additions to, 23 62... 

This was evidenced by cyclovoltammetric measurements. In both linear and crosslinked systems, there is a temperature-dependent switching of the Fc(CN)6l3 reduction peak current from high current at 25°C to low current at 45°C. However, while the process is fully reversible in the linear system, the reduction peak current values continuously increase cycle by cycle in the crosslinked system. This indicates that ions becoming entrapped in the collapsed hydrogel at elevated temperature accumulate in the hydrogel. 

Physical hydrogels were formed induced by self-assembled water-insoluble and crystalline polypseudorotaxane domains which act as physical crosslinking points. Such physical hydrogels include the polypseudorotaxane systems of a-CD threading on PEO or its copolymers, a-CD threaded on PEI, PL, or their copolymers, and even 3-CD or y-CD threaded PPO or PEI copolymers. The thermo-reversible and thixotropic properties of these supramolecular hydrogels have inspired their applications as injectable drug delivery systems. Physical hydrogels induced by physical interaction of threaded CD molecules in polyrotaxanes were also developed. 

PEO-PPO-PEO triblock copolymers (Pluronics or Poloxamers) form reversible physically cross-linked hydrogels under certain concentration range and temperature. The use of this system in tissue engineering is scarce because of its inability to degrade. Di- or tri-block copolymers of PEG with PLA have been developed to overcome this problem. Multiple blocks of PEG and PLA, synthesized by condensation reaction of L-lactic acid in the presence of succinic acid. 

---