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Dextran 1
» Dextran 1 is a low molecular weight fraction of dextran, consisting of a mixture of isomaltooligosaccharides. It is obtained by controlled hydrolysis and fractionation of dextrans produced by fermentation of Leuconostoc mesenteroides (strain NRRL B-512; CIP 78.59, or its sub-strains, for example L. mesenteroides B-512F; NCTC, 10817), in the presence of sucrose. It is a glucose polymer in which the linkages between glucose units are almost exclusively
Packaging and storage
Store in well-closed containers at a temperature between 4
Labeling
Where it is intended for use in preparing injectable dosage forms, the label states that it is sterile or must be subjected to further processing during the preparation of injectable dosage forms.
Identification
A:
Infrared Absorption
B:
It meets the requirements of the test for Molecular weight distribution and average molecular weight.
Absorbance
Specific rotation
Microbial enumeration tests
Bacterial endotoxins
pH
Heavy metals, Method II
Limit of alcohol and related impurities
Test solution
Proceed as directed for Test solution in the test for Limit of alcohol and related impurities under Dextran 40, except to use 5.0 g of Dextran 1.
Standard solution, Chromatographic system, and Procedure
Proceed as directed in the test for Limit of alcohol and related impurities under Dextran 40. The total area of peaks from impurities in the Test solution does not exceed the area of the n-propyl alcohol solution peak.
Limit of sodium chloride
Dissolve 5 g of Dextran 1, accurately weighed, in 100 mL of water. Add 0.2 mL of potassium chromate TS, and titrate with 0.1 N silver nitrate VS (see Titrimetry
Limit of nitrogenous impurities
Sulfate solution
To 1000 mL sulfuric acid add 5 g of anhydrous cupric sulfate and 500 g of potassium sulfate. Dissolve by heating, and store at 60
Indicator
Dilute a mixture of 20 mL of a 0.1% solution of bromocresol green in alcohol and 4 mL of methyl red TS with water to 100 mL.
Procedure
Transfer 0.2 g Dextran 1, accurately weighed, to a micro-Kjeldahl flask. Add 4 mL of Sulfate solution. Heat until the solution exhibits a clear green color and the sides of the flask are free from carbonaceous material. Cool, cautiously add 30 mL of water, mix, and transfer the solution to a steam distillation unit. Rinse the Kjeldahl flask with three 5-mL portions of water, adding the washings to the solution. Add 15 mL of 45% sodium hydroxide solution, immediately close the distillation apparatus, and start steam distillation immediately. Receive the distillate in 1 mL of Indicator and sufficient water to cover the end of the condensing tube. Upon completion of the distillation, remove the receiving flask, and rinse the end of the condensing tube with a small quantity of water, adding the rinse to the distillate. Titrate the distillate with 0.010 N hydrochloric acid until the color changes from blue to reddish violet. Perform a blank determination, and make any necessary correction. The corrected volume of 0.010 N hydrochloric acid required to change the color does not exceed 0.15 mL (110 ppm of nitrogen).
Molecular weight distribution and average molecular weight
Mobile phase
Prepare a filtered and degassed solution of sodium chloride containing 2.9 g per L.
Calibration solution
Prepare a solution containing about 0.45 mg of isomaltotriose (3 glucose units) and 0.60 mg of sodium chloride per mL.
Reference solution
Prepare a solution of USP Dextran 1 RS in Mobile phase containing 6.0 to 6.5 mg per mL.
Test solution
Prepare a solution of Dextran 1 in Mobile phase containing 6.0 to 6.5 mg per mL.
Chromatographic system (see Chromatography
Procedure
Inject about 100 µL of the Calibration solution, record the chromatogram, and note the retention times of the peaks. Separately inject equal volumes (about 100 µL) of the Reference solution and Test solution, and record the chromatograms. Using the retention times in the chromatogram of Calibration solution, identify the peaks due to isomaltotriose and sodium chloride in the chromatograms of Reference solution and Test solution. Disregard the peak due to sodium chloride in Reference solution and Test solution. Calculate the weight-average molecular weight, MW, by the formula:
SWi Mi
in which Wi is the weight proportion of oligosaccharide i; and Mi is the molecular weight of oligosaccharide i. Use the following molecular weight values for calculation:
Auxiliary Information
Please check for your question in the FAQs before contacting USP.
Chromatographic Column
USP32NF27 Page 2097
Pharmacopeial Forum: Volume No. 29(6) Page 1866
Chromatographic columns text is not derived from, and not part of, USP 32 or NF 27.
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