Tunable Bifunctional Silyl Ether Cross-Linkers for the Design of Acid-Sensitive Biomaterials
Citations Over TimeTop 10% of 2010 papers
Abstract
Responsive polymeric biomaterials can be triggered to degrade using localized environments found in vivo. A limited number of biomaterials provide precise control over the rate of degradation and the release rate of entrapped cargo and yield a material that is intrinsically nontoxic. In this work, we designed nontoxic acid-sensitive biomaterials based on silyl ether chemistry. A host of silyl ether cross-linkers were synthesized and molded into relevant medical devices, including Trojan horse particles, sutures, and stents. The resulting devices were engineered to degrade under acidic conditions known to exist in tumor tissue, inflammatory tissue, and diseased cells. The implementation of silyl ether chemistry gave precise control over the rate of degradation and afforded devices that could degrade over the course of hours, days, weeks, or months, depending upon the steric bulk around the silicon atom. These novel materials could be useful for numerous biomedical applications, including drug delivery, tissue repair, and general surgery.
Related Papers
- → Selective monodeprotection of bis-silyl ethers(2004)136 cited
- → Selective deprotection of silyl ethers(2013)131 cited
- → Clay montmorillonite-catalysed Michael reactions of silyl ketene acetals and a silyl enol ether with α,β-unsaturated carbonyl compounds(1987)17 cited
- → A New Route to Preparations of Silyl Ethers by Reactions of Silyl Triflimides with Alcohol or Ether(2008)2 cited
- → ChemInform Abstract: THE 1,3 O → C SILYL REARRANGEMENT OF SILYL ENOL ETHER ANIONS ‐ SYNTHESIS OF α‐SILYL KETONES(1985)