Humidity Effects on the Wetting Characteristics of Poly(N‑isopropylacrylamide) during a Lower Critical Solution Transition

• Published in: Langmuir Vol. 29; no. 25; pp. 8116 - 8124
• Main Authors: Chhabra, Arnav, Kanapuram, Ravitej R, Kim, Tae Jin, Geng, Jianxin, da Silva, Alexandre K, Bielawski, Christopher W, Hidrovo, Carlos H
• Format: Journal Article
• Language: English
• Published: Washington, DC American Chemical Society 25.06.2013
• Subjects: adsorption; Chemistry; drugs; Exact sciences and technology; General and physical chemistry; hydrogen bonding; molecular weight; polymers; relative humidity; Solid-liquid interface; solutes; solvents; Surface physical chemistry; temperature; tissue engineering; Wetting; Humidity effect
• ISSN: 0743-7463; 1520-5827; 1520-5827
• DOI: 10.1021/la401072d

Poly(N-isopropylacrylamide) (PNIPAM) is expected to find utility in tissue engineering and drug delivery, among other biomedical applications. These applications capitalize on the intrinsic lower critical solution temperature (LCST) of the polymer: below the LCST, enthalpic gain from intermolecular hydrogen bonding between PNIPAM and water molecules dominates the solvation; above the LCST, entropic effects resulting from the intramolecular hydrogen bonding between the carboxyl and amide groups of PNIPAM lead to water expulsion. The dependence of the LCST upon the molecular weight, solvent, and solution activity (i.e., solute concentration) has been studied extensively. However, what has not been previously explored is the effect of humidity on the characteristic properties of the polymer. Herein, we show that the relative humidity affects the water adsorption dynamics of PNIPAM as well as the magnitude of the transition that occurs at the LCST of the polymer. In short, the magnitude of the LCST transition decreases with an increasing relative humidity, and the time period over which adsorption occurs decreases with the temperature.