AU2011200289B2

AU2011200289B2 - Stable ready to use injectable paracetamol formulation

Info

Publication number: AU2011200289B2
Application number: AU2011200289A
Authority: AU
Inventors: Ioulia Tseti
Original assignee: Uni Pharma Kleon Tsetis Pharmaceutical Laboratories SA
Current assignee: Uni Pharma Kleon Tsetis Pharmaceutical Laboratories SA
Priority date: 2011-01-24
Filing date: 2011-01-24
Publication date: 2016-10-13
Anticipated expiration: 2031-01-24
Also published as: AU2011200289A1

Abstract

C:\NRPortbl\DCC\CRS\3426152_1.DOC-24 01.2D11 - 17 Stable ready to use injectable Paracetamol formulation Abstract s The invention concerns a stable aqueous paracetamol solution for use in IV infusion comprising at least one stabilizing-dissolving compound for paracetamol in solution selected from the group consisting of hydroxyalkyl-cyclodextrins and at least one stabilizing compound, being EDTA or monothioglycerol, alone or in combination, in a concentration between 0.001% and 20 % m/v.

Description

Stable ready to use injectable Paracetamol formulation

The present invention refers to a pharmaceutical composition comprising Paracetamol for parenteral administration by IV infusion, with an optimum pH 6.0 (ranging between 5.5 and 6.5) comprising at least one stabilizing and one dissolving substance of paracetamol in solution such as a cyclodextrin, EDTA, monothioglycerol (MTG), in a suitable concentration, able to stabilize and solubilize the paracetamol.

Description

Field of the Invention

The present invention relates to an injectable liquid paracetamol composition. Background of the Invention

Paracetamol is considered to be the main active metabolite of phenacetin and acetanidile having analgesic and antipyretic properties. Paracetamol has equivalent analgesic and antipyretic action to that of aspirin whilst it expresses weak antiinflammatory action therefore its use in inflammatory rheumatic diseases is limited. A large number of pharmaceutical preparations to be administered orally or even topically are known. However, it is difficult to obtain a pharmaceutical preparation for injection and particularly, a ready-to-use solution for intravenous perfusion, due to the fact that paracetamol is not very soluble in water and its solutions in aqueous medium are unstable in the presence of oxygen and/or light, being decomposed through a plurality of degradation pathways which are well known and are described for example in the article "Stability of aqueous solutions of N-acetyl-p-aminophenol", by K.T. Koshy and J.L. Lach, J. Pharmaceutical Sciences, Vol 50 (2) (February 1961), p. 113-118. This instability in aqueous medium is shown by the appearance of degradation substances causing a coloring in the solution. The different substances causing the coloring of the solution include benzoquinoimines which are hepatotoxic in humans.

However, the development of color in pharmaceutical solutions and especially in injectable formulations, which must be completely transparent, involves a serious problem, because the presence of said color is indicative of the existence of unwanted compounds in the formulation and therefore leads to the rejection of the injectable product without being used.

One of the causes of paracetamol degradation is based on chemical oxidation reactions in which the oxygen present in the solution is the main precursor of this degradation. The secondary cause of degradation may be the deacetylation of the amino group generating p-aminophenol which is also quickly degraded producing p-benzoquinoneimine. This deacetylation takes places both at acid pH and (much faster) at basic pH once the phenolate form is present.

Obtaining stable paracetamol solutions in aqueous medium can be solved by means of several joint actions. 1) Establishing an optimal pH in which the formation of 4-aminophenol is prevented or minimized, as has been indicated by K. Thomas Koshy and Jon L. Lach in the previous indicated reference "Stability of aqueous solutions of N-acetyl-p-aminophenol", J. of Phar. Sci., Vol 50 No. 2 (1961), 113-118, the hydrolysis of the acetate group of paracetamol is minimized between pH= 4.5 and pH 6.0. 2) Preventing the presence of oxygen in solution. This action is described in Spanish patent no. 2,201,316, from the validation in Spain of European patent EP 858,329 Bl, issued to Pharmatop SCR. This document discloses a process whereby paracetamol oxidation is prevented by means of eliminating the main element activating the reaction, oxygen, with nitrogen bubbling. By further keeping the solution in a completely hermetic bottle, the stability of paracetamol in solution is ensured for long time periods, with minimal impurity levels and the total absence of color in the solution. It may be presumed that this product of the prior art must be kept in suitable bottles preventing the incorporation of oxygen into the solution and therefore these solutions cannot be stored in individual oxygen-permeable bottles such as plastic materials.

Summary

According to a first aspect of the invention there is provided a stable aqueous paracetamol solution for use in IV infusion comprising at least one stabilizing-dissolving compound for paracetamol in solution selected from the group consisting of hydroxyalkyl-cyclodextrins and at least two stabilizing compounds, being EDTA and monothioglycerol, wherein the concentrations of the at least two stabilizing compounds are each from 0.015 mg to 1 mg per ml solution.

Detailed Description of Embodiments of the Invention

The present invention concerns a stable aqueous paracetamol solution for use in IV infusion with an optimum pH comprising at least one stabilizing-dissolving compound for paracetamol in solution selected from the group consisting of hydroxyalkyl-cyclodextrins and at least one stabilizing compound, being EDTA or monthioglycerol, alone or in combination, in a concentration between 0.001% and 20% m/v. An optimum pH is typically a pH of 6.0, ranging between 5.5 and 6.5. A preferred pharmaceutical composition according to the invention comprises:

The preferred hydroxyalkyl-cyclodextrin is 2-hydroxypropyl-beta-cyclodextrin. Typically the cyclodextrin is provided in a concentration between 0.2% m/v and 20% m/v. Preferably the 2-hydroxypropyl-beta-cyclodextrin is present in a concentration between 0.2% m/v and 6.0% m/v, more preferably between 0.5% and 3.0% m/v.

The at least one stabilizing substance of paracetamol in solution is typically monothioglycerol in a concentration between 0.001% m/v and 0.002% m/v.

In addition, the aqueous solution may further comprise other chelating agents.

The chelating or complexing agent in solution may be EDTA in a concentration between 0.0001% m/v and 0.2% m/v.

The stable aqueous paracetamol solution according to the invention may have a pH between 4.0 and 7.0. Typically, the solution may be a buffer with a buffer composition selected from at least one of the acid form and the ionized form of: citric, malic, acetic, sorbic, phosphoric, fumaric, lactic, gluconic and tartaric acids or mixtures thereof. Preferably, the pH is between 5.5 and 6.5 and more preferably the pH is adjusted to 6. A typical buffer includes phosphate or sodium citrate/acetate.

The stable aqueous paracetamol solution according to the invention may further comprise isotonizing agents, preferably sodium chloride

The stable aqueous paracetamol solution for IV infusion may be sterilized by heat or by filtration. A typical concentration of paracetamol is between 0.20% and 10% m/v, preferably 0.5% and 1.5% m/v.

The aqueous medium of the solution according to the invention may have been deoxygenated by a water-insoluble inert gas (N2).

The compositions according to the invention will be administered intravenously and they are stable when stored for more than 24 months at room temperature. Moreover, the compositions may be even stable when stored for more than 3 months at elevated temperatures. A composition may be prepared in solution and stored in clear glass containers or bottles made of a polymer material such as polyethylene, or in soft material bags made from polyethylene, polyvinylchloride or polypropylene.

According to the invention, a stable aqueous solution is provided, comprising Paracetamol and 2-hydroxy propyl-beta-cyclodextrin with EDTA, and monothioglycerol, in a suitable concentrations.

The molar ratio of Paracetamol to 2-hydroxypropyl beta-cyclodextrin is preferably 100:1 to 0.1:1, most preferably 5:1.

Typically, the solution comprises 2 mg to 200 mg, preferably more than 5 mg, most preferably 10 mg, Paracetamol per millilitre solution.

The EDTA may comprise 0.001 to 5 mg, preferably 0.0015 to 1 mg, most preferably 0.1 mg, per millilitre solution.

The monothioglycerol may comprise 0.01 to 5 mg, preferably 0.015 to 1 mg, most preferably 0.1 mg, per millilitre solution.

Advantageously, the solution is in the form of a unit dose that does not exceed 100 millilitres.

The inventor has found a way to prepare a stable aqueous solution comprising Paracetamol and 2-hydroxypropyl-beta-cyclodextrin, which is not only capable of having a concentration of Paracetamol of more than 10 mg per millilitre of solution, but is also stable and does not need to be refrigerated when packed in clear glass sealed vials, or in stoppered glass vials or in bottles made of a polymer material such as polyethylene, or in soft material bags made from polyethylene, polyvinyl chloride or polypropylene.

By "stable" is meant that the solution can be stored for at least 24 months at room temperature and at least 3 months at elevated temperature (40°C) without the appearance of colour and particulate matter which is visible to the eye.

The use of monothioglycerol (MTG) and ETDA has been found to not only increase the Paracetamol solubility to the extent that it is possible to dissolve 1000 mg of Paracetamol into a final volume of 100 ml but also effectively stabilises the solution preventing the formation of particulate matter and colour at elevated temperature in ampoules, vials and bags.

The solution may be formulated in unit dose form, each unit dose containing from 100 mg to 1500 mg Paracetamol inclusive, more preferably from 600 mg to 1000 mg inclusive, most preferably 1000 mg, in a volume not exceeding 100 millilitres.

The 2-hydroxypropyl beta-cyclodextrin (HPBCD) is selected from derivatives with a degree of substitution of between 2.5 and 10 hydroxypropyl substituents per beta-cyclodextrin molecule, more preferably between 3.5 and 8 hydroxypropyl substitutents per beta-cyclodextrin molecule. The molar ratio of Paracetamol to 2-hydroxypropyl beta-cyclodextrin is preferably 100:1 to 0.1:1, more preferably 10:1, most preferably 5:1.

The injectable stabilised solution of the invention may be prepared by methods known in the art

The stabilised injectable solution of the invention may be packed into suitable containers known in the art (for example glass ampoules, vials, cartridges, glass sealed vials, or in stoppered glass vials or in bottles made of a polymer material such as polyethylene, or in soft material bags made from polyethylene, polyvinyl chloride or polypropylene). The glass should preferably be clear glass.

The stabilized injectable solution of the invention is suitable for intravenous use.

The stabilized injectable solution of the invention need not be stored under refrigerated conditions to provide a shelf life of at least 24 months, saving refrigeration costs during transport and storage, and alleviating patient discomfort during administration.

The antioxidants of the invention show advantages over a control solution containing no antioxidant and solutions containing other antioxidants, namely NAC.

Tables 3-6 below show stability evaluations of 1000 mg per 100 ml Paracetamol formulations prepared according to the process which is described in EXAMPLE 4 and stored at 40°C for 3 and 6 months respectively. It is evident from Tables 3-6 that all formulations, according to the invention, are stable after 3 months at 40°C and therefore possible formulations, except NAC which is not stable. The example which contains monothioglycerol and EDTA is the example concerning the present invention.

The invention will now be described in more detail with reference to the following non-limiting examples. EXAMPLE 1

The unit composition of a first formulation is provided in Table 1 below: .

Table 1

EXAMPLE 2

The unit composition of a second formulation (Control, No additives) is provided in Table 2 below:

Table 2

EXAMPLE 3

Laboratory-scale formulations given in Examples 1 and 2 of the present invention were manufactured and filled into clear glass vials and polymer material (soft material bags) and placed on a stability program. Tables 3 - 6 below summarizes the results obtained:

Table 3

Table 4

Table 5

Table 6

Control solutions at 40°C for 6 months showed coloured material.

After 24 months at 25°C the solution containing 10 mg EDTA & 10 mg Monothioglycerol remained clear and colourless (both in Clear glass vials and soft material bags), free from visible particulate matter. The associated solution containing NAC 10 mg + EDTA 5 mg was clear but more coloured than the monothioglycerol /EDTA solution. EXAMPLE 4

To produce 100 lOOOmg/lOO ml paracetamol units for IV injection, 8000 ml water for injection (WFI) is purged with nitrogen gas to reduce the oxygen. The water was heated to 50°C. Processing continues under a nitrogen gas blanket. 66.675g of HPBCD (DS 4.69) is added to 60 % of the WFI batch volume and is mixed until dissolved. The solution is then allowed to cool to room temperature. The solution is pre-filtered with a 0.45Pg filter, followed by the addition of 1 g MTG, 1 g EDTA, 60 g NaCI and 3.56 g Disodium phosphate dihydrate. The solution is stirred until all the MTG, EDTA, NaCI and Disodium phosphate dihydrate is dissolved. The pH is then adjusted to 6 with HCI1M. 100 g paracetamol is added to the solution and stirred until dissolved. pH is adjusted to 6, should it be required and made up to 100% volume with WFI. The resultant lOOOmg/lOO ml paracetamol solution is sterilized by filtration with 0.22Pm filters and filled into pre-sterilized vials or bags, under aseptic conditions. The vials or bags are sealed aseptically under nitrogen. The formulation contains 1000 mg/100 ml paracetamol, as determined by validated HPLC.

Throughout this specification and the claims which follow, unless the context requires otherwise, the word "comprise", and variations such as "comprises" or "comprising", will be understood to imply the inclusion of a stated integer or step or group of integers or steps but not the exclusion of any other integer or step or group of integers or steps.

The reference in this specification to any prior publication (or information derived from it), or to any matter which is known, is not, and should not be taken as, an acknowledgement or admission or any form of suggestion that that prior publication (or information derived from it) or known matter forms part of the common general knowledge in the field of endeavour to which this specification relates.

Claims

The claims defining the invention are as follows:

1. A stable aqueous paracetamol solution for use in IV infusion comprising at least one stabilizing-dissolving compound for paracetamol in solution selected from the group consisting of hydroxyalkyl-cyclodextrins, and at least two stabilizing compounds, being EDTA and monothioglycerol, wherein the concentrations of the at least two stabilizing compounds are each from 0.015 mg to 1 mg per ml solution.
2. The stable aqueous paracetamol solution according to claim 1 wherein the concentration of the hydroxyalkyl-cyclodextrins is between 0.2% m/v - 20% m/v.
3. The stable aqueous paracetamol solution according to claim 1 or 2 wherein the at least one stabilizing - dissolving compound for paracetamol in solution is 2-hydroxypropyl-beta-cyclodextrin in a concentration between 0.2% m/v and 20% m/v.
4. The stable aqueous paracetamol solution according to claim 3 wherein the 2-hydroxypropyl-beta-cyclodextrin is present in a concentration between 0.2% m/v and 6.0% m/v.
5. The stable aqueous paracetamol solution according to claim 4, wherein the 2-hydroxypropyl-beta-cyclodextrin is present in a concentration between 0.5% m/v and 3.0% m/v.
6. The stable aqueous paracetamol solution according to any one of claims 1 to 5, wherein the pH is between 4.0 and 7, and the solution is buffered with a buffer composition selected from at least one of the acid form and the ionized form of: citric, malic, acetic, sorbic, phosphoric, fumaric, lactic, gluconic and tartaric acids, or mixtures thereof.
7. The stable aqueous paracetamol solution according to any one of claims 1 to 6, wherein the concentration of paracetamol is between 0.20% and 10% m/v.
8. The stable aqueous paracetamol solution according to any one of claims 1 to 7, wherein the concentration of paracetamol is between 0.5% and 1.5% m/v.