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Irgacure 1173

Manufactured by Merck Group
Sourced in United States

Irgacure 1173 is a photoinitiator used in the formulation of ultraviolet (UV) and visible light-curable coatings, inks, and adhesives. It is a clear, colorless liquid that initiates the polymerization process when exposed to UV or visible light.

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5 protocols using irgacure 1173

1

Synthesis of Bioactive Hydrogel Composites

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The chemical 2-hydroxy-2-methyl-1-phenyl-1-propanone (IRGACURE 1173) was purchased from Sigma Aldrich (St. Louis, USA). Laponite XLG was purchased from BYK (UK). Glycerin (AR, 99%) and gelatin methacryloyl (GelMA) were obtained from Aladdin (Shanghai, China). N-acryloyl glycinamide (NAGA) was supplied by Zhengzhou Alfa Chemical Co., Ltd. (Zhengzhou, China).
Hydrogels were synthesized through a simple one-pot method. First, dried GelMA (0.5 ​g) and NAGA (3 ​g) were successively dispersed into ultrapure water (7 ​ml) by magnetic stirring for 30 ​min at 50 ​°C. Subsequently, Laponite (0.2 ​g) and glycerol (3 ​ml) were added to the above suspension under vigorous stirring for another 1 ​h. Then, 1173 reagent (0.1% of NAGA) was quickly added under stirring for 15 ​min. The uniform solution was promptly cast into molds. Polymerization of the hydrogel was preceded by UV light irradiation to obtain the NAGA/GelMA/Laponite/glycerol composite hydrogel. In this work, hydrogel was used as an abbreviation of the NAGA/GelMA/Laponite/glycerol hydrogels. The P-sEV concentration was adjusted to 2 ​mg/mL, and 50 ​μL of P-sEVs was dropped into the hydrogel and immediately used for wound healing.
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2

Smectic Liquid Crystal and Photoinitiator Interactions

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We used a common smectic LC component, 8CB (4-octyl-4′-cyanobiphenyl, by Frinton Laboratories, Inc.). At room temperature it exhibits the smectic A phase and has a phase transition to the nematic phase at 33 °C and to the isotropic phase at 40 °C. We cast the LC onto a glass slide with a needle, either in the shape of a circular drop or in the shape of a line. The LC was then put into contact with ultra-pure water containing 0.4 wt% of 2-hydroxy-2-methylpropiophenone photoinitiator (HMPP, Irgacure 1173 by Sigma Aldrich Co.). The aqueous solution was either cast on top of the LC drop or beside the LC line. The HMPP is a substance that is poorly soluble in water, with 1 wt% being close to a saturated solution. It is more soluble in the LC. That is why the HMPP starts to diffuse from the water medium into the LC, which causes a decrease in the LC’s order.
For the characterization of the flow we added 1.5-μm silica micro-spheres (from Bangs Laboratories, Inc.) into the LC as tracers. The microparticles were treated with DMOAP (Dimethyloctadecyl[3-(trimethoxysilyl)propyl]ammonium chloride, by ABCR GmbH) prior to use, to achieve homeotropic anchoring.
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3

Photocrosslinkable Hydrogel Precursors

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Poly (ethylene glycol) diacrylates (PEGDAs) of Mw 250 and 700, and a photoinitiator, 2-Hydroxy-2-methylpropiophenone (Irgacure 1173) were purchased from Sigma-Aldrich. The Gelatin methacryloyl (GelMA) and Lithium phenyl-2,4,6-trimethyl-benzoyl phosphinate (LAP) were purchased from Cellink and Allevi, respectively. PBS and DPBS were purchased from Fisher Scientific. Irgacure 1173 is soluble in pure PEGDA, whereas PEGDA 250 prepolymer solution is prepared with 1% v/v Irgacure 1173 added to the PEGDA 250 solution. For the PEGDA 700 prepolymer solution, different volumes of PEGDA 700 and PBS were mixed in a beaker to protect from the light. The 1% v/v Irgacure 1173 was added into the solution and stirred by magnetic rode until fully dissolved. The GelMA prepolymer solution consisted of 10% w/v GelMA and 1% LAP in DPBS.
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4

Hydrogel Printing for Tissue Engineering

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Sterile phosphate-buffered
saline (PBS) solution was mixed with a desired polymer and cooled
at 4 °C overnight to prepare a hydrogel (F127 hydrogels: 30 wt
%, PGE-DMA: 20 wt %). One liter of PBS (pH = 7.2) contained 8 g of
NaCl (Sigma-Aldrich), 1.44 g of Na2HPO4 (Fisher
Scientific), 0.24 g of KH2PO4, and 0.2 g of
KCl in Milli-Q water. To make a hydrogel ready for printing, 1.5 μL
g–1 hydrogel of the photoinitiator 2-hydroxy-2-methylpropiophenone
(Irgacure 1173; >97%, Sigma-Aldrich) was added at a temperature
of
4 °C. If needed, 105 or 106 spun-down cells
g–1 hydrogel were added. A short stirring of both
additives ensured an equal distribution, and after incubating for
30 min on ice, to make the solution bubble-free, it was poured into
a 10 mL dispensing barrel equipped with a 0.41 mm dispensing tip (both
Adhesive Dispensing, United Kingdom) and warmed to room temperature
to transform into a shear-responsive state for printing.
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5

Fabrication of PLGA-PVA Nanoparticles

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PLGA 50:50 (Mw 5 7,000-17,000, ester terminated), poly(vinyl alcohol) (PVA, Mw 5 13,000-23,000), bovine serum albumin (BSA), sucrose (>99.5%), magnesium hydroxide (95%), PEG (Mn < 3,400), stannous octoate, acryloyl chloride (98%), 3,6-dimethyl-1,4-dioxane-2,5-dione, triethylamine (99.5%), and 2-hydroxy-2-methylpropiophenone (Irgacure 1173) were obtained from Sigma-Aldrich (St. Louis, MO). Dichloromethane (DCM, 99.9%), poly (ethylene glycol) (PEG, Mw 5 8,000), sodium chloride (99.5%), magnesium sulfate anhydrous (97%), ethyl ether (anhydrous), and phosphate-buffered saline (PBS) were obtained from Fisher Scientific (Hampton, NH).
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