Synthesis of degradable poly(l-lactide-co-ethylene glycol) porous tubes by liquid–liquid centrifugal casting for use as nerve guidance channels
Source abstract
Abstract
Biodegradable nerve guidance channels are advantageous, obviating the need for their removal after regeneration; however, most channels lack the appropriate mechanical properties for soft tissue implantation and/or degrade too quickly, resulting in reduced regeneration and necessitating the need for the design of polymers with tunable degradation profiles and mechanical properties. We designed a series of biodegradable polymeric hydrogel tubes consisting of L-lactide (LLA) and polyethylene glycol (PEG) where both the ratio of LLA to PEG and PEG molar mass were varied. By adjusting the PEG:LLA ratio and the molecular weight of the PEG oligomer we were able to control degradation and mechanical properties of our polymers. By incorporating methacrylate (MA) groups on both termini of the linear oligomers, porous tubes were synthesized by a redox-initiated free radical mechanism during a liquid-liquid centrifugal casting process. The tube wall had a bead-like morphology, as determined by SEM, which was reminiscent of previous porous hydrogel tubes synthesized by the same method. Tubes swelled with degradation to 160 vol%, or 640 wt%, and an increased radius calculated at 1.26 times. Those tubes with greater PEG content and PEG molar mass degraded faster than those with greater LLA content, as was expected. Interestingly, the wall morphology changed with degradation to a fiber-like structure and the mechanical properties decreased with degradation. By correlating the accelerated degradation study to a physiologic one, these porous hydrogel tubes were stable for an equivalent of 1.5 months, after which the mechanical properties began to deteriorate. This study demonstrates how porous hydrogel tubes can be designed to meet tissue regeneration criteria by tuning the formulation chemistry and specifically how the ratio of hydrophobic/crystalline LLA and hydrophilic/amorphous PEG impact tube properties.
Source: europepmc · Quality: candidate unverified · Source record ↗
Research context
OpenAlex topics: Nerve injury and regeneration · Neuroscience and Neural Engineering · Advanced Drug Delivery Systems
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
References (29)
Show source-provided references
1. Peripheral nerve injury: a review and approach to tissue engineered constructs10.1002/ar.1120 ↗
2. In vitro degradation and biocompatibility of poly(d,l-lactide-ε-caprolactone) nerve guides10.1002/jbm.a.10157 ↗
3. Berkowitz · 1998
4. Enhancement of peripheral nerve regeneration10.1002/mus.880130904 ↗
5. Increased rate of peripheral nerve regeneration using bioresorbable nerve guides and a laminin-containing gel10.1016/0014-4886(85)90087-1 ↗
6. Manufacture of poly(2-hydroxyethyl methacrylate–co–methylmethacrylate) hydrogel tubes for use as nerve guidance channels10.1016/S0142-9612(02)00120-5 ↗
7. Long-term in vivo biomechanical properties and biocompatibility of poly(2-hydroxyethyl methacrylate–co–methyl methacrylate) nerve conduits10.1016/j.biomaterials.2004.05.031 ↗
8. Coil-reinforced hydrogel tubes promote nerve regeneration equivalent to that of nerve autografts
9. Bioartificial nerve grafts based on absorbable guiding filament structures–early observations
10. Clinical nerve reconstruction with a bioabsorbable polyglycolic acid tube
11. Design of macroporous biodegradable polymer scaffolds for cell transplantation10.4028/www.scientific.net/MSF.250.15 ↗
12. Shalaby · 1994 · 1
13. More about the polymerization of lactides in the presence of stannous octoate10.1002/(SICI)1099-0518(19971130)35:16<3431::AID-POLA10>3.0.CO;2-G ↗
14. Reversible kinetics and thermodynamics of the homopolymerization of l-lactide with 2-ethylhexanoic acid Tin(II) salt10.1021/ma970631m ↗
15. Resorbable initiators for polymerizations of lactones10.1002/masy.19991440124 ↗
16. Kinetics and mechanism of cyclic esters polymerization initiated with tin(II) octoate, 1. Polymerization of η-caprolactone
17. Polylactones 48. SnOct2-initiated polymerizations of lactide: a mechanistic study10.1021/ma991181w ↗
18. Mechanism of cyclic ester polymerization initiated with tin(II) octoate. 2
19. Polymerizations of—caprolactone and l,l-dilactide initiated with stannous octoate and stannous butoxide—a comparison10.1002/1521-3900(200003)153:1<41::AID-MASY41>3.0.CO;2-I ↗
20. Synthesis of polylactides in the presence of co-initiators with different numbers of hydroxyl groups10.1016/S0032-3861(01)00150-1 ↗
21. Synthesis of polymer network scaffolds from l-lactide and poly(ethylene glycol) and their interaction with cells10.1021/ma970302u ↗
22. Synthesis of acrylate functional telechelic poly(lactic acid) oligomer by transesterification10.1023/A:1008948325177 ↗
23. Ring opening polymerization of d,l-lactide in the presence of zinc metal and zinc lactate10.1002/(SICI)1097-0126(199807)46:3<177::AID-PI937>3.0.CO;2-S ↗
24. Wenz · 1998 · 132
25. Biodegradable polymer networks based on oligolactide macromers: synthesis, properties and biomedical applications10.1016/S1389-0344(02)00034-5 ↗
26. Mackinnon · 1988
27. In vitro and in vivo degradation studies for development of a biodegradable patch based on poly(3-hydroxybutyrate)10.1016/S0142-9612(01)00405-7 ↗
28. Synthesis, characterization, and polymerization of glycidyl methacrylate derivatized dextran10.1021/ma00122a044 ↗
29. A new class of polymerizable dextrans with hydrolysable groups: hydroxyethyl methacrylated dextran with and without oligolactate spacer10.1016/S0032-3861(97)00189-4 ↗