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Powdered Cellulose
» Powdered Cellulose is purified, mechanically disintegrated cellulose prepared by processing alpha cellulose obtained as a pulp from fibrous plant materials.
Packaging and storage
Preserve in tight containers.
Labeling
The labeling indicates the nominal degree of polymerization value. Degree of polymerization compliance is determined using Identification test B.
Identification
A:
Prepare iodinated zinc chloride solution by dissolving 20 g of zinc chloride and 6.5 g of potassium iodide in 10.5 mL of water. Add 0.5 g of iodine, and shake for 15 minutes. Place about 10 mg of Powdered Cellulose on a watch glass, and disperse in 2 mL of iodinated zinc chloride solution: the substance takes on a violet-blue color.
B:
Transfer 0.25 g of Powdered Cellulose, accurately weighed to 0.1 mg, to a 125-mL conical flask. Add 25.0 mL of water and 25.0 mL of 1.0 M cupriethylenediamine hydroxide solution. Immediately purge the solution with nitrogen, insert the stopper, and shake on a wrist action shaker or other suitable mechanical shaker until completely dissolved. Transfer an appropriate volume of the solution to a calibrated number 150 Cannon-Fenske, or equivalent, viscosimeter. Allow the solution to equilibrate at 25 ± 0.1
t1(k1)
in which k1 is the viscosimeter constant (see Viscosity
t2(k2)
in which k2 is the viscosimeter constant. Determine the relative viscosity, (KV)1 / (KV)2
Determine the intrinsic viscosity, [(95)[
in which WS is the weight, in g, of the Powdered Cellulose taken; and % LOD is the value obtained from the test for Loss on drying. The degree of polymerization is greater than 440.
Microbial enumeration tests
pH
Loss on drying
Residue on ignition
Water-soluble substances
Mix 6.0 g with 90 mL of recently boiled and cooled water, and allow to stand with occasional stirring for 10 minutes. Filter, with the aid of vacuum, discard the first 10 mL of the filtrate, and pass the filtrate through the same filter a second time, if necessary, to obtain a clear filtrate. Evaporate a 15.0-mL portion of the filtrate in a tared evaporating dish to dryness without charring, dry at 105
Ether-soluble substances
Place 10.0 g in a chromatography column having an internal diameter of about 20 mm, and pass 50 mL of peroxide-free ether through the column. Evaporate the eluate to dryness in a previously dried and tared evaporating dish with the aid of a current of air in a fume hood. After all the ether has evaporated, dry the residue at 105
Heavy metals, Method II
Auxiliary Information
Please check for your question in the FAQs before contacting USP.
Chromatographic Column
USP32NF27 Page 1201
Pharmacopeial Forum: Volume No. 31(5) Page 1421
Chromatographic columns text is not derived from, and not part of, USP 32 or NF 27.
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