Polyketals: A New Acid-Sensitive Biomaterial for Drug Delivery

Wednesday, November 19, 2008: 4:35 PM
Room 108-A (Pennsylvania Convention Center)

Sungmun Lee, Biomedical Engineering, Georgia Institute of Technology, Atlanta, GA
Stephen Yang, Biomedical Engineering, Georgia Institute of Technology, Atlanta, GA
Michael Heffernan, Biomedical Engineering, Georgia Institute of Technology, Atlanta, GA
Niren Murthy, Biomedical Engineering, Georgia Institute of Technology, Atlanta, GA

There is currently great interest in developing acid-sensitive materials for drug delivery because of their ability to hydrolyze in the acidic environment of phagosomes and release drugs into the cytoplasm. In this presentation, we introduce a new acid-sensitive polymer for drug delivery, poly(cyclohexane-1,4-diyl acetone dimethylene ketal) (PCADK), which is ideal for treating inflammatory diseases because of its biocompatible degradation products. PCADK was synthesized using the acetal exchange reaction between 1,4-cyclohexanedimethanol and 2,2-dimethoxypropane. PCADK hydrolyzes into innocuous compounds, 1,4-cyclohexanedimethanol and acetone, which have FDA approval for human use. The hydrolysis half-life of PCADK is 24.1 days at pH 4.5 and over 4 years at pH 7.4, which is suitable for targeting chronic diseases. The therapeutic enzyme superoxide dismutase (SOD), which scavenges reactive oxygen species, was encapsulated into PCADK-based microparticles using a double emulsion procedure. Cell culture experiments demonstrated that PCADK-based microparticles significantly improved the ability of SOD to scavenge reactive oxygen species produced by macrophages. We anticipate the use of PCADK to treat a wide variety of chronic inflammatory diseases such as lung fibrosis, arthritis, and congestive heart failure.
Extended Abstract: File Not Uploaded
See more of this Session: Biomaterials for Drug Delivery III
See more of this Group/Topical: Materials Engineering and Sciences Division