Effects of Papain Incorporation on the Photo-Transformation Stability of 5-Bromo-8-Methoxy-6-Nitro Bips

Abstract

Photochromism behaviors of a spiropyran dye namely 5-bromo-8-methoxy-6-nitro BIPS (BNM) has been investigated in the present of papain as anti-oxidant at different H+ ions conditions. BNM has been dissolved and diluted in ethanol (EtOH) to a concentration of 1.0 x 10-5M. The hydrochloric acid (HCL) was used to alter the acidity of the solution to be pH2 and pH7. The fine dispersed transparent solutions were exposed to UV light at 365nm for 5s and the absorption spectra were measured using UV-Vis spectrometer. Upon UV light irradiation, BNM exhibits photochromic behaviors by displaying coloration changes from transparent to light purplish with maximum absorbance spectrum, λmax at 552nm with and without present of papain in both acidic (pH2) and neutral (pH7) conditions. It was found that incorporation of papain in both different pH conditions slightly decreased the intensities of absorbance spectrum for BNM photo-transformation activities. However, detection in time drive mode at 522nm with 5s UV irradiation showed that the addition of papain stabilize and prolongs the absorbance intensity. Incorporation of anti-oxidant molecules is significant in order to obtain long-life activities of the spiropyran in the photo-reversible activity of open-form merocyanine state to closed-form spiro state. This study reveals that the photo-transformation stability of BNM molecules is increased with addition of papain in neutral condition that acts as anti-oxidant agent towards the BNM photo-reversible process.

Preparation of photoactive ZnS-composite porous polymer films: Fluorescent and morphological properties

“…Spiropyrans (SP), reported first by Fischer and Hirshberg in 1962 [18], are one of the most widely studied classes of photoswitchable compounds. The irradiation of SP compounds with near-UV light [19] or its electro-oxidation [20] induces the heterolytic cleavage of the spiro carbon-oxygen bond, which leads to its ringopening and converting into merocyanine (MC). The intense absorption in the visible region of the openform MC has led to the advanced study of SP compounds in photochromic [16], molecular optoelectronic [21] optobioelectronic fields [22], and chemical sensing [23].…”