Method for preparing a pharmaceutical formulation of lanthanide chelate in powder form

Patent metadata

Field	Value
Publication number	US-2016243265-A1
Application number	US-201615147570-A
Country	US
Kind code	A1
Filing date	May 5, 2016
Priority date	May 13, 2009
Publication date	Aug 25, 2016
Grant date	—

Abstract

The present invention relates to a method for preparing a pharmaceutical formulation of lanthanide chelate in powder form, wherein the powder constitutes a mol/mol excess of free chelate of between 0.002 and 0.4%.

First claim

What is claimed is:

1 . A method for preparing a pharmaceutical formulation of a macrocyclic chelate of a lanthanide, said macrocyclic chelate being DOTA, said lanthanide being Gadolinium, said macrocyclic chelate of a lanthanide being DOTA-Gd complex, and said method comprising the following successive steps of:
(1) mixing in a solution a macrocyclic chelate and a lanthanide so as to obtain a complexation solution of the lanthanide by the macrocyclic chelate, the complexation solution comprising, in addition to the macrocyclic chelate-lanthanide complex, an excess amount X1 of free macrocyclic chelate, wherein a step (1) is carried out in a single step or in several successive steps by measuring and adjusting, so as to have an amount X1 of free macrocyclic chelate, and the step (1) comprises the following successive substeps of:
(1.1) complexing in solution the lanthanide with the macrocyclic chelate,
(1.2) measuring the macrocyclic chelate and/or the lanthanide that is free, and
(1.3) adding free macrocyclic chelate, so as to complex the free lanthanide if any remains at the end of step (1.1), and to obtain an amount X1 of free macrocyclic chelate;
(2) optionally measuring X1 and/or adjusting X1 so as to have X1 between 0.002 and 0.4% mol/mol; (3) precipitating or crystallizing the complexation solution obtained in step (1) from an organic solvent, so as to obtain a powder of the macrocyclic chelate-lanthanide complex, said powder containing an excess amount X2 of free macrocyclic chelate, wherein X2 represents the amount of free macrocyclic chelate obtained after precipitation or crystallization and X2 is less than X1; (4) optionally adjusting X2 by adding or removing free macrocyclic chelate or by adding or removing lanthanide so as to obtain:
(4.a) X2 between 0.002 and 0.4% mol/mol, and
(4.b) X2 corresponding to between 0.2 and 5 times X1,

wherein said powder obtained after step (4) comprises a mol/mol excess of free macrocyclic chelate of between 0.002 and 0.4%; and
(5) returning said powder to solution so as to form a pharmaceutical composition in liquid form, said pharmaceutical composition in liquid form being ready for administration to a patient.

2 . The method of claim 1 , wherein, in step 3), the precipitating or crystallizing of the complexation solution obtained in step (1) is carried out at a pH in the range 1 to 9.

3 . The method of claim 1 , wherein the solvent of step (3) is chosen from ethanol, methanol and propanol.

4 . The method of claim 1 , wherein the solvent of step 3) is used according to a ratio of from 10 to 20 volumes of solvent per volume of complexation solution

5 . The method of claim 1 , wherein the solvent of step 3) is used at a temperature included in the range [0; 80° C].

6 . The method of claim 1 , wherein the complexation solution of step (1) is a solution of [DOTA-Gd], further comprising a meglumine salt.

7 . The method of claim 1 , wherein in step (4), X2 is adjusted so as to be comprised between 0.02 and 0.3% mol/mol.

8 . The method of claim 1 , wherein in step (4), X2 is adjusted so as to be comprised between 0.025 and 0.25% mol/mol.

9 . The method of claim 1 , wherein in step (4), X2 is adjusted so as to belong to the range: [0.5−0.95]×X1.

10 . The method of claim 5 , wherein the temperature is included in the range of 30 to 70° C.

11 . The method of claim 1 , wherein any free gadolinium is removed by virtue of a chelex resin in the complexation solution S with a level X1 of free macrocyclic chelate obtained after step 1.3.

12 . The method of claim 11 , wherein a quantification of the free gadolinium is carried out by means of a colorimetric assay with Arsenazo (III) before and optionally also afterwards the removal of this free gadolinium.

13 . The method of claim 11 , wherein the said resin is removed by filtration.

Assignees

• Guerbet Sa

Inventors

• Port Marc

Classifications

• A61K49/108 Primary

  the metal complex being Gd-DOTA · CPC title

• A61K9/08

  Solutions {(composition of solutions A61K47/00)} · CPC title

• A61K49/06 Primary

  Nuclear magnetic resonance [NMR] contrast preparations; Magnetic resonance imaging [MRI] contrast preparations · CPC title