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Dalteparin Sodium: GMP, COA, DMF available

Dalteparin Sodium: GMP, COA, DMF available
Product Detailed
Related Categories:Pharmaceutical
Dalteparin Sodium complies with 1. Speicfication: EP 7 2. Injectable Grade Passed Japan PMDA GMP compliance certificate

Definition

Dalteparin sodium is the sodium salt of low molecular weight heparin obtained by nitrous acid depolymerization of heparin from pork intestinal mucosa.

Usage

As a new antithrombotic class, it is indicated for thromboprophylaxis in conjuntion with surgery, treatment of acute deep venous thrombosis, prevention of clotting during hemodialysis and hemofiltration and so on.

Specifications

Test

Acceptance criteria

Origin

Porcine intestinal mucosa

Characters

White or almost white, hygroscopic powder

Identification

A. 13C-NMR

B. the mass-average relative molecular mass ranges between 5600 and 6400, with a characteristic value of about 6000.

Lower than 3000: not more than 13.0%

Higher than 8000: 15.0%~25.0%

Anti-factor  Xa activity

110 IU/mg~210 IU/mg

Anti-factor Ⅱa activity

35 IU/mg~100 IU/mg

The ratio of Anti-factor Xa / Anti-factor Ⅱa

1.9~3.2

Appearance of solution

Clear and not more intensely colored than intensity 5 of reference solution

pH

5.5~8.0

Nitrite

Not more than 5 ppm

Boron

Not more than 1 ppm

Nitrogen

1.5%~2.5%

Sodium

9.5%~12.5%

Nucleotide and protein impurities of the source material

260nm: not greater than 0.20

280nm: not greater than 0.15

Molar ratio of sulfate ions to carboxylate ions

Not less than 1.8

Heavy metals

Not more than 20 ppm

Loss on drying

Not more than 5.0%

Bacterial endotoxins

Less than 0.01 IU/AXaIU

Dalteparin Sodium: GMP, COA, DMF available



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