The fungal pathogen causes a variety of oral infections, including denture stomatitis, which is characterized by inflammation of the oral mucosa in direct contact with dentures and affects a significant number of otherwise healthy denture wearers. While antifungal treatment reduces symptoms, infections are often recurrent. One strategy to address this problem is to incorporate compounds with fungicidal activities into denture materials to prevent colonization. Our laboratory synthesized novel derivatives of 1,4-diazabicyclo[2.2.2]octane (DABCO), which is an organic compound typically used as a catalyst in polymerization reactions. DABCO derivatives with different aliphatic chain lengths (DC16, DC16F, DC18, and C6DC16), as well as methacrylate monomers conjugated to DABCO compounds (DC11MAF and C2DC11MAF), were synthesized and tested for antimicrobial activity. All the compounds exhibited fungicidal activity against several species at concentrations ranging between 2 and 4 μg/ml. Moreover, acrylic denture base resins fabricated to contain 1, 2, or 4 wt% DABCO compounds inhibited surface biofilm formation, as well as fungal growth, in disc diffusion assays. Remarkably, discs (4 wt%) aged for 2 months also exhibited approximately 100% growth-inhibitory activity. While some DABCO compounds exerted intermediate to high cytotoxicity against mammalian oral cell types, DC11MAF and denture base resin discs containing 2 or 4 wt% C2DC11MAF exhibited relatively low cytotoxicity against periodontal ligament (PDL) cell and gingival fibroblast (GF) lines, as well as primary oral epithelial cells. These studies demonstrate that DABCO derivatives can be incorporated into denture materials and exert fungicidal activity with minimal cytotoxicity to mammalian cells. DC11MAF and C2DC11MAF are considered strong candidates as therapeutic or preventive alternatives against -associated denture stomatitis.
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http://dx.doi.org/10.1128/AAC.02575-16 | DOI Listing |
Addressing the pressing need to develop affordable and efficient catalysts is essential. In this study, we successfully synthesized CuBiS nanostructures with a modified morphology using three different nitrogen bases: DBN, DBU, and DABCO a hydrothermal technique. These nanostructures were used for the electrochemical detection of organic nitro groups, a previously unexplored application for this material.
View Article and Find Full Text PDFChemMedChem
December 2024
IICT CSIR: Indian Institute of Chemical Technology, Department of Applied Biology, Hyderabad, INDIA.
An efficient and concise synthesis of highly functionalized bridged coumarins has been developed through a diastereoselective double Michael addition reaction of p-quinols with various 4-hydroxy coumarins under catalyst-free conditions in H2O-DMSO (8:2). The method has been applied to oxindoles for the synthesis of a variety of bridged-oxindoles and bridged-spiroxindoles in presence of a DABCO base using H2O-EtOH (8:2) as solvent medium. The strategy is simple, highly atom economical as there is no by-product and environmentally benign (E-factor = 0.
View Article and Find Full Text PDFMolecules
November 2024
Department of Applied Chemistry, Osaka Institute of Technology, 5-16-1 Omiya, Ashahi-ku, Osaka 535-8585, Japan.
The mixture of hexamethylene diisocyanate (HDI) and butanol (BuOH) with the intercalation compound of 1,4-diazabicyclo[2.2.2]octane (DABCO) with α-zirconium phosphate (α-ZrP) has been evaluated as a latent thermal catalyst at varying temperatures.
View Article and Find Full Text PDFDalton Trans
October 2024
Nikolaev Institute of Inorganic Chemistry, Siberian Branch of the Russian Academy of Sciences, 3 Acad. Lavrentiev Ave., 630090, Novosibirsk, Russia.
Three new three-dimensional (3D) metal-organic frameworks [M(ttdc)(dabco)] (M = Zn(II), 1-Zn; Cu(II), 1-Cu; and Zn/Cu, 1-ZnCu) based on thieno[3,2-]thiophene-2,5-dicarboxylate (ttdc) were synthesized and characterized by a combination of physicochemical methods (single crystal X-ray diffraction, powder X-ray diffraction, chemical and thermogravimetric analyses and IR spectroscopy). 1-Cu demonstrated permanent porosity ( = 0.790 cm g and = 1725 m g) and significant CO, CH, CH, CH and CH gas uptakes under ambient conditions.
View Article and Find Full Text PDFOrg Biomol Chem
August 2024
Department of Chemistry, Lishui University, No. 1, Xueyuan Road, Lishui City 323000, Zhejiang Province, P. R. China.
Alkynes are important in organic synthesis. This review mainly focuses on recent advances (2013-2023) on alkynes with C-S bond formation, based on more than 30 types of sulfur reagents. The reactions of alkynes with various sulfur-containing compounds including RSSR (disulfides), RSH (thiols), S (elemental sulphur), alkynyl thioethers, RSCN, AgSCF, KS, NaS, dithiane, RSCl, NFSI, RNCS, EtOCSK, thiocarbamate, RSONH, thiourea, sulfoxide, RSON, CS, RSONH, RSONHNH, RSOCl, RSOOar, RSOSR', DABCO·(SO), NaSO, KSO, RSOH, RSONa and related compounds are discussed.
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