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TEGDMA, or Triethylene Glycol Dimethacrylate, is a colorless, viscous liquid used as a monomer in the production of various polymers and resins. It functions as a cross-linking agent, helping to create a more stable and durable polymer structure.

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3 protocols using tegdma

1

Thermally Activated Polymer Network Formation

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Triethylene glycol dimethacrylate (TEGDMA; Tokyo Chemical Industry Co., Ltd., Tokyo, Japan) was used as the liquid monomer in this work (Figure 1a) together with di-t-hexyl peroxide (Peroxide H; Figure 1b) and di-t-butyl peroxide (Peroxide B; Figure 1c; NOF Corp., Tokyo, Japan). These compounds had initiation temperatures (that is, hour half-life temperatures) of 136.2 and 144.1 °C respectively. PANI Emeraldine Base (PANI-EB; Regulus Co., Ltd., Tokyo, Japan), a non-conductive polymer (Figure 1d), was also employed, together with DBSA (Kanto Chemical Co., Inc., Tokyo, Japan) as a liquid compound capable of acting as a dopant in response to a temperature increase (Figure 1e). TEGDMA was employed as the monomer because each molecule contains two reactive acrylate groups that are available for radical polymerization, and so this compound is suitable for the formation of a three-dimensional network in response to initiation by oxygen radicals (-O•) produced by the Peroxide H and Peroxide B as a result of thermal decomposition.
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2

Antibacterial Polymer Synthesis and Evaluation

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Unless otherwise stated, all compounds and solvents were used as received. 4-hydroxyazobenzene, 2’-dihydroxyazobenzene, and AIBN were acquired from Aldrich. AIBN was recrystallized in methanol prior to use. HEMA, MMA, and PMMA (≈35 k) were acquired from Acros Organics. TEGDMA, 2-hydroxybenzyl alcohol, and acyl chloride were acquired from Tokyo Chemical Industry. N,N-dimethylformamide (DMF), triethylamine, and silica gel were acquired from Fisher. THF was acquired from VWR. Dichloromethane (DCM) was acquired from Millipore. Rhodamine B was acquired from PolySciences.
S. mutans American Type Culture Collection (ATCC 25175), S. aureus (Herbert, 2010 HG001 or AH2183 or RN1HG), S. oralis (ATCC 9811), and A. actinomycetemcomitans (ATCC 43718), and E. coli (Mysorekar, 2013) were provided from the sources listed. BBL BHI media and Difco agar were acquired from Becton, Dickinson and Company. Sucrose for cell growth was acquired from MP Biomedicals, LLC. Phosphate-buffered saline (PBS) was acquired from Bioland Scientific. Dulbecco’s modified eagle medium (DMEM) media and fetal bovine serum (FBS) was acquired from Fisher. Penicillin-streptomycin and trypsin solution 10X (2.5%) was acquired from Aldrich.
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3

Silanization of YAG and SiO2 Nanoparticles

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Bis-GMA, ethyl-4-dimethylaminobenzoate (4-EDMAB), camphorquinone (CQ), and 3-methacryloxypropyltrimet hoxysilane (γ-MPS) were provided by Sigma-Aldrich (St. Louis, MO, USA). TEGDMA (95%) was purchased from Tokyo Chemical Industry (Tokyo, Japan). Microsized SiO 2 particles (average diameters: 50 nm and 1 µm) were supplied by Meryer Chemical Technology (Shanghai, China). Microsized YAG (Y 3Al5O12) particles with an average diameter of 500 nm were provided by Buwei Technology (Shanghai, China). Methods 1. Silanization of nanoparticles YAG powder was dried at 100°C in a vacuum oven overnight. Ten grams of the dried YAG powder and 500 mL of deionized water were added to a 1,000-mL round bottom flask and ultrasonicated for 10 min. Afterwards, 1.1 mL γ-MPS was added to the mixture, and its pH was adjusted to 8.5 by ammonia solution. The obtained mixture was magnetically stirred at a speed of 500 r/min and temperature of 26°C for 2 h and then at 100°C for additional 2 h. YAG was filtered and dried using a circulating water vacuum pump. During the filtration process, it was washed thrice with deionized water and twice with anhydrous ethanol. Finally, the obtained powder was dried at 80°C in a vacuum oven overnight. Microsized SiO 2 particles were modified by the same method.
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