CA2727477C

CA2727477C - Stable ready to use injectable paracetamol formulation

Info

Publication number: CA2727477C
Application number: CA2727477A
Authority: CA
Inventors: Ioulia Tseti
Original assignee: UNI-PHARMA KLEON TSETIS
Current assignee: UNI-PHARMA KLEON TSETIS
Priority date: 2011-01-11
Filing date: 2011-01-11
Publication date: 2017-11-21
Anticipated expiration: 2031-01-11
Also published as: CA2727477A1

Abstract

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 anti-inflammatory 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

2 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 6Ø

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 B1, 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.

The present invention concerns a stable aquous 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:

3 Ingredient Quantity/ 100 ml Paracetamol 1000 mg Hydroxypropyl-beta-cyclodextrin 666 mg Monothioglycerol 10 mg EDTA 10 mg NaCl 600 mg Disodium phosphate dihydrate 35.6 mg Water for Injection to 100 ml Final pH (HCI or NaOH) 1M 5.5-6.5 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 7Ø 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.

4 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 io 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-hydroxypropyl-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.

5 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.

i5 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

6 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 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.

The unit composition of a first formulation is provided in Table 1 below:
Table 1 Ingredient Quantity/100 ml Paracetamol 1000 mg Hydroxypropyl-(3-cyclodextrin 666 mg Disodium edetate (EDTA) 10 mg Monothioglycerol 10 mg NaCl 600 mg Disodium phosphate dihydrate 35.6 mg Water for Injection to 100 ml Final pH ( HCI or NaOH) 1M 5.5-6.5 The unit composition of a second formulation (Control , No additives) is provided in Table 2 below:

7 Table 2 Ingredient Quantity/ 100 ml Paracetamol 1000 mg Hydroxypropyl-o-cyclodextrin 666 mg NaCI 600 mg Disodium phosphate 35.6 mg dihydrate Water for Injection to 100 ml Final pH ( HCI or NaOH) 1M 5.5-6.5 s 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 io results obtained:

Table 3 Stability of 1000mg/100ml (Paracetamol- HPBCD) Batches at 40 C For 3 Months Antioxidant Chemical stability pH Appearance Comments Control (No additives) Acceptable level of Not stable Discolouration;
known degradant downward (continued to 6 physical instability months as control) Acceptable level of slightly Complies, trial Stable EDTA 10 mg known degradant downward continued Not stable, trial NAC 10 mg + Acceptable level of Discolouration;
downward continued EDTA 5 mg known degradant physical instability Monothioglycerol 20 mg Acceptable level of Complies, trial Stable Stable continued known degradant Monothioglycerol 10 Acceptable level of Complies, trial Stable Stable mg + EDTA 10 mg known degradant continued ,~ a) a) a) L
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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.

To produce 100 1000mg/100 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 NaCl and 3.56 g Disodium phosphate dihydrate. The solution is stirred until all the MTG, EDTA, NaCl and Disodium phosphate dihydrate is dissolved. The pH is then adjusted to 6 with HCI 1M. 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 1000mg/100 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.

Claims

1. A stable aqueous paracetamol solution for use in IV infusion comprising a 2-hydroxypropyl-beta-cyclodextrin as a stabilizing-dissolving compound wherein the molar ratio of paracetamol to 2-hydroxypropyl-beta-cyclodextrin is 100:1 to 0.1:1, further comprising EDTA and monothioglycerol as stabilizing compounds, wherein the concentration of EDTA is 0.0015 mg to 1 mg per ml solution and the concentration of monothioglycerol is 0.015 mg to 1 mg per ml solution, 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.

2. The stable aqueous paracetamol solution for use in IV infusion according to claim 1, wherein the aqueous solution comprises 2 mg to 200 mg of paracetamol per ml solution.

3. The stable aqueous paracetamol solution for use in IV infusion according to claim 1 or 2, wherein the buffer comprises phosphate or sodium citrate/acetate.