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Acetic acid solution

Manufactured by Avantor
Sourced in Poland

Acetic acid solution is a clear, colorless liquid that is commonly used in various laboratory applications. It serves as a basic chemical reagent with a core function of providing a source of acetic acid, which is a weak organic acid. The concentration of the acetic acid in the solution can vary depending on the specific product.

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3 protocols using acetic acid solution

1

Multifunctional Chitosan-Agarose-Nanohydroxyapatite Scaffolds

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chitosan/agarose/nanoHA scaffolds with low (40 wt%; material marked as chit/aga/HA_L) and high (70 wt%; material marked as chit/aga/HA_H) nanoHA content were synthesized via combining freeze-drying and gas foaming methods, using sodium bicarbonate as a source of CO2 gas. Briefly, 2 wt% chitosan (75%–85% deacetylation degree, 50–190 kDa molecular weight, viscosity ≤300 cP, Sigma-Aldrich Co., St Louis, MO, USA) and 5 wt% agarose (gel point 36±1.5°C, low EEO, Sigma-Aldrich Co.) were dissolved in 2% acetic acid solution (Avantor Performance Materials, Gliwice, Poland) and mixed with the appropriate quantity of nanoHA and sodium bicarbonate (Sigma-Aldrich Co.). Resultant paste was transferred into cylinder-shaped mold and subjected to heating at 95°C in a water bath, followed by sample cooling, freezing in a liquid nitrogen vapor phase, and freeze-drying (LYO GT2-Basic, SRK Systemtechnik GmbH, Riedstadt, Germany). The final scaffolds were neutralized in 1% NaOH solution (Avantor Performance Materials), washed with deionized water, and air-dried. In the case of X-ray photoelectron spectroscopy (XPS), chitosan/agarose, chitosan, and agarose matrices (without nanoHA) were additionally prepared in an analogous manner to the scaffold production. Before all experiments, the scaffolds were sterilized using ethylene oxide.
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2

Highly Porous Biomaterial Scaffold Production

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Highly macroporous biomaterials acting as a platform for cell growth were produced in accordance with the procedure described in the Polish Patent no. 235822 and with the method described previously19 (link),21 (link). Briefly, 2% (w/v) chitosan (50–190 kDa MW, Sigma-Aldrich Chemicals, Warsaw, Poland), 5% (w/v) agarose (gel point 36 ± 1.5 °C, Sigma-Aldrich Chemicals, Warsaw, Poland), and 40% (w/v) hydroxyapatite nanopowder (particle size < 200 nm, Sigma-Aldrich Chemicals, Warsaw, Poland) were suspended in acetic acid solution (Avantor Performance Materials, Gliwice, Poland) and mixed. Subsequently, sodium bicarbonate (Sigma-Aldrich Chemicals, Warsaw, Poland) was added. The obtained paste was transferred into cylinder-shaped forms and subjected to heating (95 °C), cooling, freezing, and then freeze-drying. Finally, the resultant biomaterials were immersed in sodium hydroxide solution (Avantor Performance Materials, Gliwice, Poland), washed with deionized water, and air-dried. The microstructure of the fabricated scaffold was visualized by a stereoscopic microscope (Olympus SZ61TR, Olympus Polska Sp. z o. o., Warsaw, Poland (Fig. 1). Prior to cell culture experiments, the scaffolds were sterilized using ethylene oxide.

Microstructure of the fabricated scaffold visualized by a stereoscopic microscope.

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3

Chitosan/Curdlan/HA Composite Synthesis

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The chitosan/curdlan/HA composite was produced according to the procedure described previously by [23 (link),46 (link),47 (link)] with some modifications. Krill chitosan (1174 kDa molecular weight, 73% deacetylation degree) was obtained from National Marine Fisheries Research Institute (Gdynia, Poland), whereas curdlan (β-1,3-glucan) was purchased from Wako Pure Chemicals Industries (Osaka, Japan). Suspension of various NPs (with and without FexOy) was prepared in distilled water at the following concentrations: 0.50 wt.%, 0.25 wt.%, and 0.10 wt.%. Then, 16 wt.% curdlan suspension was prepared in the appropriate NPs suspension or in distilled water (control biomaterial) and mixed 1:1 with 4 wt.% chitosan solution prepared in 1% acetic acid solution (Avantor Performance Materials, Gliwice, Poland). The final concentrations of the individual components in the blend were as follow: 8 wt.% curdlan, 2 wt.% chitosan, and 0.25 wt.%, 0.125 wt.% or 0.05 wt.% NPs. The 80 wt.% (w/v) hydroxyapatite granules (HA BIOCER, Chema Elektromet, Rzeszow, Poland) were added to the blend and the resultant paste was subjected to thermal gelation at 95 °C for 20 min., followed by neutralization in sodium hydroxide (Avantor Performance Materials, Gliwice, Poland).
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