Dextran 70 in Sodium Chloride Injection
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This article is compiled based on the United States Pharmacopeia (USP) – 2025 Edition
Issued and maintained by the United States Pharmacopeial Convention (USP)
1 DEFINITION
Dextran 70 in Sodium Chloride Injection is a sterile solution of Dextran 70 and Sodium Chloride in Water for Injection. It contains, in each 100 mL, NLT 5.4 g and NMT 6.6 g of Dextran 70, and NLT 0.81 g and NMT 0.99 g of sodium chloride. It contains no bacteriostatic agents.
2 IDENTIFICATION
2.1 • A.
Diluent: Sodium chloride solution (0.9 in 100)
Sample solution: Injection, diluted with Diluent to 10 mg/mL of Dextran 70
Analysis: Using a capillary tube viscometer having dimensions such that the ow time of water is NLT 100 s, measure the times of the Sample solution and Diluent at 20°.
Calculate the intrinsic viscosity:
Result = {ln[(RD) × (t/t0)]}/C
RD = ratio of the density of the Sample solution to that of the Diluent
t = Sample solution ow time
t0 = Diluent ow time
C = concentration of Dextran 70 in the Sample solution (g/mL)
Acceptance criteria: 24–29 mL/g
3 ASSAY
3.1 Sodium Chloride
Sample solution: Pipet a volume of Injection, equivalent to 90 mg of chloride, into a porcelain casserole, and add 100 mL of water and 1 mL of dichlorouorescein TS.
Analysis: Titrate with 0.1 N silver nitrate VS until the silver chloride occulates and the mixture acquires a faint pink color. Each mL of 0.1 N silver nitrate VS is equivalent to 5.844 mg of sodium chloride.
Acceptance criteria: 0.81–0.99 g of sodium chloride per 100 mL
3.2 Dextran 70
Sample solution: To 25 mL of Injection add 1 drop of 5 N ammonium hydroxide.
Analysis: Determine the optical rotation (see Optical Rotation 〈781〉).
Calculate the concentration, in g per 100 mL, of Dextran 70 in the portion of Injection taken:
Result = (a/l) × (1/Av) × 100
a = observed optical rotation (°)
l = length of the polarimeter tube (dm)
Av = average value for the specic rotation of Dextran 70, 197.5
Acceptance criteria: 5.4–6.6 g of Dextran 70 per 100 mL
4 SPECIFIC TESTS
pH 〈791〉: 4.0–7.0
Bacterial Endotoxins Test 〈85〉: It contains NMT 0.5 USP Endotoxin Unit/mL.
Sterility Tests 〈71〉: It meets the requirements when tested as directed in Test for Sterility of the Product to Be Examined, Membrane Filtration.
Color of Solution: Its absorbance, determined at 375 nm against a water blank, is NMT 0.04.
Other Requirements: It meets the requirements in Injections 〈1〉 and Particulate Matter in Injections 〈788〉.
5 ADDITIONAL REQUIREMENTS
Packaging and Storage: Preserve in single-dose glass or plastic containers.
Labeling: The label states the total osmolar concentration in mOsmol/L. Where the contents are less than 100 mL, the label alternatively may state the total osmolar concentration in mOsmol/mL.

