Skip to Main Content

Latest News

Advertisement
Advertise Here
December 6, 2010
Volume 88, Number 49
p. 11

Tuning Up For A Breakdown

Biomaterials: Acid-sensitive polymers permit tight control over degradation for in vivo drug delivery

Steve Ritter

Tunable Decay Stents made with methyl (from left), ethyl, isopropyl, and tert-butyl silyl ether cross-linkers look the same initially (T= 0), but after three days under acidic conditions (T = 3 days), only the methyl version degrades significantly. J. Am. Chem. Soc.
Tunable Decay Stents made with methyl (from left), ethyl, isopropyl, and tert-butyl silyl ether cross-linkers look the same initially (T= 0), but after three days under acidic conditions (T = 3 days), only the methyl version degrades significantly.
  • Print this article
  • Email the editor

Latest News



October 28, 2011

Speedy Homemade-Explosive Detector

Forensic Chemistry: A new method could increase the number of explosives detected by airport screeners.

Solar Panel Makers Cry Foul

Trade: U.S. companies complain of market dumping by China.

Novartis To Cut 2,000 Jobs

Layoffs follow similar moves by Amgen, AstraZeneca.

Nations Break Impasse On Waste

Environment: Ban to halt export of hazardous waste to developing world.

New Leader For Lawrence Livermore

Penrose (Parney) Albright will direct DOE national lab.

Hair Reveals Source Of People's Exposure To Mercury

Toxic Exposure: Mercury isotopes in human hair illuminate dietary and industrial sources.

Why The Long Fat?

Cancer Biochemistry: Mass spectrometry follows the metabolism of very long fatty acids in cancer cells.

Text Size A A

A scientific team based in North Carolina has used tunable silyl ether protecting groups to create a new class of bioabsorbable polymeric materials. These materials can be precisely programmed to degrade by hydrolysis in hours, days, weeks, or months under the acidic conditions found in target tissues, depending on the bulk of alkyl substituents on the silyl ether. This development lays the foundation for a new generation of biodegradable materials that can be shaped into drug-eluting particles, sutures, and coronary stents for medical applications.

Degradable methyl cross-linker

Silyl ethers are among the most popular protecting groups in organic synthesis because the rate of de­pro­tec­tion can be modulated by varying the size of the alkyl substituents on silicon. For example, a simple switch from methyl to tert-butyl groups alters the rate of hydrolytic deprotection by orders of magnitude. Matthew C. Parrott, Joseph M. DeSimone, and coworkers at the University of North Carolina, Chapel Hill, and North Carolina State University applied this chemistry to design easy-to-make materials that are nontoxic and controllably degrade under the acidic conditions in tumor tissue, inflammatory tissue, and diseased cells (J. Am. Chem. Soc., DOI: 10.1021/ja108568g).

The researchers used variously substituted silyl ethers as cross-linkers—in which the silyl group links two acrylate groups—to make different-shaped particles by a process developed earlier in De­Si­mone’s labs. When internalized in cells, the particles containing methyl-substituted silyl ether linkers degraded in a few hours; those containing the ethyl version showed minimal changes, and those with the isopropyl and tert-butyl versions remained unaltered during the same period. The researchers also made sutures and stents that showed similar patterns of degradation.

A key attribute of the new materials is their ability to resist enzymatic degradation, notes chemical engineer Mark E. Davis of California Institute of Technology. For example, in addition to acid hydrolysis, natural esterases break down polymeric biomaterials that contain ester bonds, like those in the silyl ether-based materials. This can be a problem in vivo, Davis says, because the esterases cause unwanted variations in the biomaterials’ degradation rate. Hydrolysis rates can be controlled by knowing the pH in cells or tissues, he explains, but esterase activity varies from test animals to people and individually from person to person.

“DeSimone’s group has come up with a clever idea in using the silyl ethers, which should shut down enzyme degradation to give highly controlled acid hydrolysis degradation rates, because there are no known esterases that degrade the silicon-based polymers,” Davis says.

The silyl ether technology has been licensed to Liquidia Technologies, a company spun off from DeSimone’s labs a few years ago. DeSimone says Liquidia is expected to use the new bioabsorbable materials to fabricate “Trojan horse” particles to deliver chemotherapy agents and vaccines, as well as drug-eluting coronary stents.

Chemical & Engineering News
ISSN 0009-2347
Copyright © 2011 American Chemical Society
  • Print this article
  • Email the editor

Services & Tools

ACS Resources

ACS is the leading employment source for recruiting scientific professionals. ACS Careers and C&EN Classifieds provide employers direct access to scientific talent both in print and online. Jobseekers | Employers

» Join ACS

Join more than 161,000 professionals in the chemical sciences world-wide, as a member of the American Chemical Society.
» Join Now!