Skip to main content
. 2019 Sep 4;85(11):2479–2486. doi: 10.1111/bcp.14081

Table 2.

Main chemical characteristics of low molecular weight (MW) heparins (LMWHs) [Minghetti et al.9]

Depolarization method LMWH Representative and residues MW mean Xa/IIa ratio Pharmacopeia specific assays Sulfatation degree

Deaminative cleavage Nitrous acid

Nadroparin

§

Nonreducing; 2‐O‐sulfo‐alfa‐L‐

idopyranosuric acid

Reducing

See Table 1

See Table 1

Ethanol; N‐NO groups; free sulfates

 

Nitrite, boron

2.5

 

 

 

 

1.8

Dalteparin

#

6‐O‐sulfo‐2,5‐anhydro‐D‐mannitol 2.5
Isoamyl‐nitrate

Reviparin

§

2–2.6

Certoparin

§

2

Beta‐eliminative cleavage benzylation and alkaline treatment

Enoxaparin

#

Nonreducing: 4‐enopyranose urinate Reducing: 1,6‐anhydro derivate

See Table 1 See Table 1

Benzylalcohol Content + % oligosaccharide chains that are cylizied in 1,6‐anhydro ring

Alkaline treatment with quarternary NH4‐salt

Bemiparin

§

 

Enzymatic treatment Heparinase

Tinzaparin

#

Nonreducing end: 2‐O‐sulfo‐4 enepyrano‐suric acid

Reducing end: 2‐N,6‐O‐disulfo‐D‐glucosamine

See Table 1 See Table 1

Radical‐catalysed depolymerization: peroxide + copper salt

Parnaparin

§

Nonreducing end: 2‐O‐sulafo‐alfa‐L‐idopyrano‐suric acid

Reducing end: 2‐N,6‐O‐disulfo‐D‐glucosamine

Copper
Market #USA + EU §EU