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Glass fiber prefilters

Manufactured by Merck Group

Glass fiber prefilters are a type of laboratory equipment used to remove particulates and contaminants from liquid samples prior to further analysis or processing. They are designed to capture a wide range of particle sizes and are commonly used in various applications such as water treatment, sample preparation, and filtration processes.

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2 protocols using glass fiber prefilters

1

Polyelectrolyte-Based Ion-Exchange Membrane Preparation

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Poly(allylamine
hydrochloride) (PAH, Mw = 17 500
Da), poly(sodium 4-styrenesulfonate)
(PSS, Mw = 70 000 Da), sodium chloride
(NaCl, ≥99%), anhydrous magnesium chloride (MgCl2, ≥98%), and sodium 2-mercaptoethanesulfonate (MESNA, analytical
standard, ≥ 98.0) were purchased from Sigma-Aldrich. Hydrochloric
acid (36.5–28.0% NF grade) was purchased from VWR International.
Nitric acid (65%, for analysis) and ethanol (absolute) were purchased
from Merck Millipore. Acetone (HPLC grade, 99.9%) and dichloromethane
(stabilized with amylene) were purchased from BIOSELVE BV. All chemicals
were used as received without further purification. The inorganic
salts were kept in a vacuum oven overnight prior to use.
Neosepta
cation-exchange (CMX), anion-exchange (AMX), and monovalent cation-selective
(CIMS) membranes (Astom Corp., Japan) were soaked in a solution of
4 mM NaCl and 4 mM MgCl2 for at least 48 h before use.
The porous carbon electrodes, which were deposited on a graphite foil
substrate, were supplied by Voltea BV, Netherlands. Glass fiber prefilters
(25 mm in diameter) with a pore size of 2.0 μm (Merck Millipore)
were used as a spacer for MCDI experiments. Flat substrates of gold
sputtered on glass (1 × 1 cm) were purchased from ECsens. Milli-Q
water (18.2 MΩ·cm, Milli-Q Integral 3 system, Millipore)
was used to prepare salt and polyelectrolyte solutions.
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2

Collagen Extraction from Bone Samples

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Collagen was extracted from the bones following the Longin method70 (link). The chemical pretreatment consists of a demineralization with 2.4MHCl for 20 min. An alkaline washing with 0.25 M NaOH for 15 min is performed to remove contaminants like fulvic and humic acids that can be present in the bone matrix. A final rinse with 0.3 M HCl is performed to remove any calcium carbonate precipitation. Each treatment is followed by a Milli-Q water rinsing using an Ezee-Filter separator, allowing a better conservation of the sample and a faster process. The sample is then soaked in a closed test tube containing a pH = 3 (HCl 10 − 3 M) solution at 90 °C for 10 h to obtain the total extraction of the collagen protein. The remaining solid is separated from the solution with a Büchner funnel by vacuum suction with glass fiber prefilters (7 μm, Merck–Millipore). The solution containing the collagen protein is then freeze-dried for 10–15 h.
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