Storage-stable formulation of paracetamol in aqueous solution

• US 9,089,477 B2
• Filed: 02/10/2011
• Issued: 07/28/2015
• Est. Priority Date: 02/10/2011
• Status: Active Grant

• Current Assignee: Neogen Corporation
• Original Assignee: Neogen Corporation
• Inventors: Al Dandachi Atassi, Khaled
• Primary Examiner(s): Zarek, Paul
• Assistant Examiner(s): Kosturko, George W
• Application Number:
  US13/984,132
• Publication Number:
  US 20130317112A1
• Time in Patent Office: 1,629 Days
• Field of Search: 514/613, 514/615
• US Class Current: 1/1
• CPC Class Codes: A61K 31/166 having the carbon of a carboxamide group directly attached to the aromatic ring, e.g. procainamide, procarbazine, metoclopramide, labetalol
• CPC Class Codes: A61K 9/0019 Injectable compositions; Intramuscular, intravenous, arterial, subcutaneous administration; Compositions to be administered through the skin in an invasive manner non-active ingredients are additionally classified in A61K47/00
• CPC Class Codes: A61P 29/00 Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]

Abstract

The present invention relates to a method for the production of a formulation that is stable to oxidation and that is based on paracetamol in an aqueous solvent, comprising the steps of (i) dissolving paracetamol in an aqueous solvent comprising an isotonic agent that is sodium chloride and a buffer agent that is sodium citrate, having a temperature between 65° C. and 95° C. and having pH between 5.0 and 6.0 in a reaction vessel, (ii) replacing the remaining air in the vessel by an inert gas, such as nitrogen, and cooling the solution so formed to a temperature below 38° C., (iii) adding cysteine hydrochloride to the solution without mechanical agitation, and (iv) closing the reaction vessel and mechanically agitating the solution in a nitrogen atmosphere. The further relates to a formulation prepared according to the method.

Claims

1. Formulation that is stable to oxidation and hydrolysis, based on paracetamol in an aqueous solvent comprising:

between 0.25% and 2% (w/v) paracetamol,

between 0.5% and 0.9% (w/v) sodium chloride,

between 0.05% and 0.09% (w/v) monosodium citrate monohydrate,

between 0.015% and 0.035% (w/v) cysteine hydrochloride monohydrate, and

water for injection,

where the final pH of the formulation is between 5.0 and 6.0, and

wherein the water for injection is not degassed by bubbling with an inert gas, prepared according to a method comprising in given order the steps of;

(i) dissolving paracetamol in an aqueous solvent comprising an isotonic agent that is sodium chloride and a buffer agent that is sodium citrate, having a temperature between 65°

C. and 95°

C. and having pH between 5.0 and 6.0 in a reaction vessel,

(ii) replacing the remaining air in the vessel by an inert gas and cooling the solution so formed to a temperature below 38°

C.,

(iii) adding cysteine hydrochloride to the solution without mechanical agitation, and

(iv) closing the reaction vessel and mechanically agitating the solution in a nitrogen atmosphere;

wherein for at least 15 months from preparation impurity K<

0.05%;

impurity F <

0.05%, as determined by HPLC at 245 nm.

2. The formulation of claim 1, wherein the determination of impurities by HPLC is performed under the following conditions:

octylsilyl silica gel column for chromatography,

temperature of 35°

C.,

flow rate of 1.5 ml/minute, and

mobile phase comprising disodium hydrogen phosphate, sodium dihydrogen phosphate, methanol, and tetrabutylammonium hydroxide.

3. A method of preparing the formulation of claim 1, comprising the following steps in given order:

(i) dissolving paracetamol in an aqueous solvent comprising an isotonic agent that is sodium chloride and a buffer agent that is sodium citrate, having a temperature between 65°

C. and 95°

C. and having pH between 5.0 and 6.0 in a reaction vessel,

(ii) replacing the remaining air in the vessel by an inert gas and cooling the solution so formed to a temperature below 38°

C.,

(iii) adding cysteine hydrochloride to the solution without mechanical agitation, and

(iv) closing the reaction vessel and mechanically agitating the solution in a nitrogen atmosphere.

4. The method according to claim 3, wherein the aqueous solvent and/or solution is not purged with an inert gas.

5. The method according to claim 4, wherein the inert gas is nitrogen.

6. The method according to claim 3, wherein the aqueous solvent has a temperature between 70°

C. and 90°

C.

7. The method according to claim 3, wherein the aqueous solvent has a pH between 5.6 and 5.7.

8. The method according to claim 3, wherein the paracetamol is added to the aqueous solvent in step (i) without mechanical agitation.

9. The method according to claim 3 wherein the solution is stirred after replacing the remaining air in the vessel by the inert gas such as nitrogen in step (ii).

10. The method according to claim 3 wherein the solution in step (iv) is subsequently filtered prior to packaging in one or more vials.

11. The method according to claim 10, wherein the vials are closed under vacuum.