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Cellulose fiber

Manufactured by Merck Group
Sourced in United States

Cellulose fiber is a naturally occurring, biodegradable polymer derived from plant cell walls. It is composed of glucose units linked in a linear chain. Cellulose fibers have a high tensile strength and are often used in the manufacturing of various lab equipment.

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5 protocols using cellulose fiber

1

Reflux Device for Lateral Flow Assay

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Example 2

FIG. 7 shows a non-limiting example of an interior of a reflux device, which is included in embodiments of the present invention. Samples flow from A to B. Test strips for lateral flow assay are composed of (in this order): a sample pad (VF2; Whatman); a second pad (ReliaFlow, Ahlstrom); a membrane (UniSart CN 95, Sartorius); an absorbent pad (Cellulose fiber, Millipore). 1, 100 μl 0.9% NaCl dispensed upstream from the blood sample, at position A; 2, 100 μl of buffer (10 mM phosphate buffer pH 7.4, plus 137 mM NaCl, plus 0.02% triton-X-100) was dispensed immediately downstream from the blood sample in an angle and contrary to the direction of sample flow; 3, 100 μl of 0.9% NaCl was dispensed immediately downstream from the blood sample in an angle, and contrary to the direction of sample flow. Although the sample pad is composed of a bibulous material design to retain blood cells, the flow in (1) causes red blood cells to move into the membrane when liquid is applied above or upstream the sample. Dispensing of the liquid in (2) and (3) created a reflux compelling cells to the edge (position A) prior to resuming liquid flow towards the membrane. The leakage is more accentuated as the blood volume increases.

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2

Lateral Flow Assay for Anti-Adalimumab Detection

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Example 4

FIG. 10 shows a non-limiting example of an interior of a device, which is included in embodiments of the present invention. Samples flow from A to B. Test strips for lateral flow assay are composed of (in this order): a sample pad (LF1, GE Healthcare); a second pad (ReliaFlow, Ahlstrom) containing latex-labeled goat anti-human IgG; a membrane (Hi-Flow HF075, Millipore) where both a control antibody (rabbit anti-goat IgG, Thermo Fisher) and a chimeric antibody (chimeric-adalimumab) were immobilized, the latter being composed of the adalimumab variable region fused with mouse IgG2a constant region (Anti-hTNF-α-mlg2a, InvivoGen); an absorbent pad (cellulose fiber, Millipore). 1, no anti-adalimumab antibody in the buffer sample (10 mM phosphate buffer pH 7.4, plus 137 mM NaCl, plus 0.02% triton-X-100); 2, 5 μl of sheep blood; 3, 1 μl of anti-adalimumab antibody (HCA204, 500 m/ml, AbD Serotec) spiked on 5 μl of sheep blood; 4, 1 μl of anti-adalimumab antibody (HCA204, 500 m/ml, AbD Serotec) spiked on 5 μl of sheep blood. Following sample application, 50 μl of buffer (10 mM phosphate buffer pH 7.4, plus 137 mM NaCl, plus 0.02% triton-X-100) was added downstream of the sample application in an angle, and contrary to the direction of sample flow, to create a reflux. Sheep blood was obtained from Rockland Inc. (Limerick, Pa.).

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3

Reflux Device for Lateral Flow Assays

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Example 3

FIG. 8 shows a non-restrictive example of an interior of a reflux device, which is included in embodiments of the present invention. Samples flow from A to B. The test strips for lateral flow were composed of (in this order): a sample pad (CytoSep HV, Ahlstrom); a second pad (ReliaFlow, Ahlstrom); a membrane (HF075, Millipore); an absorbent pad (cellulose fiber, Millipore). Tests were performed with sheep blood obtained from Rockland Inc. (Limerick, Pa.); blood volumes of 5 μl, 10 μl, 15 μl, and 20 μl were dispensed at the end of the sample pad (position A), followed by 60 μl of buffer (10 mM phosphate buffer pH 7.4, plus 137 mM NaCl, plus 0.02% triton-X-100), said buffer dispensed in an angle and contrary to the direction of sample flow, to create a reflux. The corresponding drops of blood are shown to the right of the figure.

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4

Synthesis and Cellulose Dissolution in Ionic Liquids

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1-ethyl-3-methylimidazolium phosphorous methyl ester (EmimMeOPO2H) ionic liquids (ILs) were synthesized using a previously reported method11 . One part by weight of dimethyl phosphite reacted with 1.15 parts by weight of N-ethylimidazole in THF at 80 °C for 48 h under an argon atmosphere. The resultant was then washed with ether followed by a purification process using dichloromethane and activated, neutral alumina. 0.2 g of cellulose fibers (Sigma-Aldrich (Shanghai) Trading Co., Ltd, China, 99% purity, and medium fiber size) were separately dissolved in 5 ml of ILs at 85 °C through continuous stirring under the anhydrous condition. The process to fully dissolve the cellulose fibers in the ILs took about 16 min.
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5

Purification of modified mRNA via Cellulose Chromatography

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The purification of the cellulose was carried out according to a previously described method.[35 (link)
] Cellulose purification was used to remove the dsRNA by‐products from unmodified or chemically (Ψ‐, 5mC‐, or Ψ, 5mC) modified IVT mRNA. The cellulose fibers (Sigma–Aldrich, USA) were suspended in chromatography buffer (10 mm HEPES (pH 7.2), 0.1 mm EDTA, 125 mm NaCl, and 16% (v/v) ethanol) to create a cellulose slurry. This slurry was then subjected to centrifugation for 1 min at 14 000 RCF in a spin column, with this process being repeated twice as a prewashing step. The IVT mRNA, which was dissolved in 500 µL chromatography buffer, was placed into the prewashed cellulose fiber spin column for 30 min and then centrifuged at 14 000 RCF within the spin column for 1 min. This procedure effectively separated the dsRNA contaminants from the ssRNA and was repeated twice for thorough purification. Finally, the chromatography buffer was removed from the separated ssRNA via filtration using an Amicon Ultra system (Merck Millipore, USA), and the IVT mRNA dissolving buffer was changed to sterile‐filtered water treated with diethyl pyrocarbonate (DEPC water).
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