Photodynamic antimicrobial activities of a series of meso-substituted 2,6-dibrominated 1,3,5,7-tetramethylBODIPY dyes

Author:

May Aviwe K.1,Ngoy Bokolombe P.2,Mack John1,Nyokong Tebello1

Affiliation:

1. Institute for Nanotechnology Innovation, Rhodes University, Makhanda 6140, South Africa

2. Département de Chimie, Université de Kinshasa, Kinshasa, Democratic Republic of the Congo

Abstract

The photodynamic antimicrobial chemotherapy (PACT) activities of seven 1,3,5,7-tetramethyl-2,6-dibromoBODIPY dyes with 4-acetamidophenyl (2a), 2-iodophenyl (2b), 3-iodophenyl (2c), 4-iodophenyl (2d), 2-bromophenyl (2e), 5-bromothien-2-yl (2f), and methylphenyl ester (2g) meso-substituents were studied against Staphylococcus aureus through irradiation with a 530 nm Thorlabs M530L3 light emitting diode (LED) (110 mW.cm[Formula: see text]) to identify structure-property relationships related to modifying the meso-substituent. Significant differences are observed in the log[Formula: see text] reduction values obtained with 1 [Formula: see text]M of 2a exhibiting the highest PACT activity with a value of 9.60 after 15 min of photoirradiation. In contrast, log[Formula: see text] reduction values [Formula: see text] 1.20 were obtained after 60 min of photoirradiation for iodophenyl dyes 2b-2d. The data demonstrate that the singlet oxygen quantum yield of the dye is not the most important factor determining the PACT activity properties.

Funder

National Research Foundation (NRF) of South Africa ISRR

Department of Science and Technology (DST) through the DST/NRF South African Research Chairs Initiative for Professors of Medicinal Chemistry and Nanotechnology

Publisher

World Scientific Pub Co Pte Ltd

Subject

General Chemistry

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