CA2214343C - Liquid aqueous pharmaceutical compositions comprising sodium alginate and potassium bicarbonate - Google Patents
Liquid aqueous pharmaceutical compositions comprising sodium alginate and potassium bicarbonate Download PDFInfo
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- CA2214343C CA2214343C CA002214343A CA2214343A CA2214343C CA 2214343 C CA2214343 C CA 2214343C CA 002214343 A CA002214343 A CA 002214343A CA 2214343 A CA2214343 A CA 2214343A CA 2214343 C CA2214343 C CA 2214343C
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- sodium alginate
- potassium bicarbonate
- sodium
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/0012—Galenical forms characterised by the site of application
- A61K9/0053—Mouth and digestive tract, i.e. intraoral and peroral administration
- A61K9/0065—Forms with gastric retention, e.g. floating on gastric juice, adhering to gastric mucosa, expanding to prevent passage through the pylorus
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K33/00—Medicinal preparations containing inorganic active ingredients
- A61K33/06—Aluminium, calcium or magnesium; Compounds thereof, e.g. clay
- A61K33/10—Carbonates; Bicarbonates
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/0087—Galenical forms not covered by A61K9/02 - A61K9/7023
- A61K9/0095—Drinks; Beverages; Syrups; Compositions for reconstitution thereof, e.g. powders or tablets to be dispersed in a glass of water; Veterinary drenches
Abstract
The use of potassium bicarbonate for the preparation of an aqueous pourable liquid composition comprising at least 8 % sodium alginate for use as a pharmaceutical.
Description
V4'O 96/27368 PCT/GB96/00358 LIQUID AQUEOUS PHARMACEUTICAL COMPOSITIONS COMPRISING SODIUM ALGINATE AND
POTASSIUM BICARBONATE
This invention relates to the preparation of pourable liquid sodium alginate compositions and in particular to the preparation of such compositions for the treatment of reflux oesophagitis, gastritis, dyspepsia or peptic ulceration, or for use as sustained releasing compositions.
Reflux oesophagitis occurs when small amounts of gastric juice, food and/or bile acids pass into the lower part of the oesophagus and cause oesophageal inflammation accompanied by pain which may manifest itself in the form of heartburn.
One approach to the problem of reflux oesophagitis has been to administer a preparation which on contact with gastric acid generates a carbonated gelatinous foam or raft which floats on the stomach contents. When reflux occurs it is this raft which precedes the stomach contents into the oesophagus, thus protecting the mucosa from further irritation. Known preparations of this type include solid preparations in the form of powder or tablets containing alginic acid, sodium bicarbonate and antacid materials or liquid preparations containing sodium alginate, sodium bicarbonate and calcium carbonate marketed under the name GAVISCON (TM Reckitt & Colman Products Ltd). In our British Patent No. 1524740 we describe such liquid preparations.
GB 1524740 specifies that sodium bicarbonate is used as the effervescent agent to release carbon dioxide on contact with stomach acid, and most similar liquid products also use the sodium salt. Sodium bicarbonate is WO 96/27368 PC'T/GB96/00358 generally the salt of choice for many reasons, including its taste characteristics, its solubility and its general ~
pharmaceutical acceptability. Other bicarbonates, eg potassium bicarbonate have been avoided in the past r because of poor taste characteristics (brackish) and because of potential cardiac problems in high dosages.
A current problem with liquid alginate products of the above type is the size of the dose which must be taken (up to 20 ml four times daily). This results in large volumes of products which are not conveniently portable and which take up a lot of space in pharmacies, warehouses etc.
It is therefore an aim of the invention to provide more concentrated products thereby reducing the relative dosage volume.
On the one hand, we have found that merely doubling the concentration of all ingredients in conventional sodium alginate compositions leads to compositions which are too thick to dispense from a bottle and may even be too thick to comfortably swallow.
On the other hand we have found that reducing the sodium bicarbonate concentrations in such products will reduce the initial viscosity to apparently acceptable levels at which pouring may be achieved. However if the bicarbonate concentrations are reduced too far there will be inadequate carbon dioxide production in the stomach, which will lead to inadequate raft formation.
We have found moreover that the compositions having high concentrations of sodium alginate and low concentrations of sodium bicarbonate have a further serious defect. Their pouring properties are lost if storage temperatures drop too low. Specifically, if such compositions are stored at below 5°C for 48 hours or more they will remain too thick to pour, even after being restored to room temperature and vigorously shaken.
Temperatures of 5°C or lower are commonly encountered when commercial products are stored for long periods in warehouses or transported over long distances.
We have now unexpectedly found that using potassium bicarbonate in the above compositions alleviates these thickening problems.
According to the invention there is provided the use of potassium bicarbonate for the preparation of an aqueous pourable liquid composition comprising at least 8% w/w sodium alginate for use as a pharmaceutical.
Such aqueous pourable liquid compositions that 'result are pourable at room temperatures and furthermore this property is regained upon warming following prolonged storage below 5°C for up to six weeks or more (although reasonably vigorous shafting may be required).
By pourable we mean that the compositions of the 2$ invention will flow evenly at room temperature (possibly following reasonably vigorous shaking) such that doses of for example 5 ml may be measured out with reasonable accuracy. For example reproducible doses of as low as 5 ml may be dispensed from screw cap bottles having neck diameters of 1.5 cm, or from squeezable plastic bottles having dispensing outlets as small as 5 mm diameter.
Compositions of the invention, particularly those according to the preferred embodiments are liquid, or become liquid upon vigorous shaking, even after prolonged storage under low temperatures.
POTASSIUM BICARBONATE
This invention relates to the preparation of pourable liquid sodium alginate compositions and in particular to the preparation of such compositions for the treatment of reflux oesophagitis, gastritis, dyspepsia or peptic ulceration, or for use as sustained releasing compositions.
Reflux oesophagitis occurs when small amounts of gastric juice, food and/or bile acids pass into the lower part of the oesophagus and cause oesophageal inflammation accompanied by pain which may manifest itself in the form of heartburn.
One approach to the problem of reflux oesophagitis has been to administer a preparation which on contact with gastric acid generates a carbonated gelatinous foam or raft which floats on the stomach contents. When reflux occurs it is this raft which precedes the stomach contents into the oesophagus, thus protecting the mucosa from further irritation. Known preparations of this type include solid preparations in the form of powder or tablets containing alginic acid, sodium bicarbonate and antacid materials or liquid preparations containing sodium alginate, sodium bicarbonate and calcium carbonate marketed under the name GAVISCON (TM Reckitt & Colman Products Ltd). In our British Patent No. 1524740 we describe such liquid preparations.
GB 1524740 specifies that sodium bicarbonate is used as the effervescent agent to release carbon dioxide on contact with stomach acid, and most similar liquid products also use the sodium salt. Sodium bicarbonate is WO 96/27368 PC'T/GB96/00358 generally the salt of choice for many reasons, including its taste characteristics, its solubility and its general ~
pharmaceutical acceptability. Other bicarbonates, eg potassium bicarbonate have been avoided in the past r because of poor taste characteristics (brackish) and because of potential cardiac problems in high dosages.
A current problem with liquid alginate products of the above type is the size of the dose which must be taken (up to 20 ml four times daily). This results in large volumes of products which are not conveniently portable and which take up a lot of space in pharmacies, warehouses etc.
It is therefore an aim of the invention to provide more concentrated products thereby reducing the relative dosage volume.
On the one hand, we have found that merely doubling the concentration of all ingredients in conventional sodium alginate compositions leads to compositions which are too thick to dispense from a bottle and may even be too thick to comfortably swallow.
On the other hand we have found that reducing the sodium bicarbonate concentrations in such products will reduce the initial viscosity to apparently acceptable levels at which pouring may be achieved. However if the bicarbonate concentrations are reduced too far there will be inadequate carbon dioxide production in the stomach, which will lead to inadequate raft formation.
We have found moreover that the compositions having high concentrations of sodium alginate and low concentrations of sodium bicarbonate have a further serious defect. Their pouring properties are lost if storage temperatures drop too low. Specifically, if such compositions are stored at below 5°C for 48 hours or more they will remain too thick to pour, even after being restored to room temperature and vigorously shaken.
Temperatures of 5°C or lower are commonly encountered when commercial products are stored for long periods in warehouses or transported over long distances.
We have now unexpectedly found that using potassium bicarbonate in the above compositions alleviates these thickening problems.
According to the invention there is provided the use of potassium bicarbonate for the preparation of an aqueous pourable liquid composition comprising at least 8% w/w sodium alginate for use as a pharmaceutical.
Such aqueous pourable liquid compositions that 'result are pourable at room temperatures and furthermore this property is regained upon warming following prolonged storage below 5°C for up to six weeks or more (although reasonably vigorous shafting may be required).
By pourable we mean that the compositions of the 2$ invention will flow evenly at room temperature (possibly following reasonably vigorous shaking) such that doses of for example 5 ml may be measured out with reasonable accuracy. For example reproducible doses of as low as 5 ml may be dispensed from screw cap bottles having neck diameters of 1.5 cm, or from squeezable plastic bottles having dispensing outlets as small as 5 mm diameter.
Compositions of the invention, particularly those according to the preferred embodiments are liquid, or become liquid upon vigorous shaking, even after prolonged storage under low temperatures.
Whilst simple numerical viscosity is not an accurate prediction of pourability in the compositions of the invention, a rough guide is that compositions having a viscosity of below 3500 mPa.s are preferred and more preferably compositions having a viscosity of below 2000 mPa.s. For the: purposes of this rough test the samples should be shaken vigorously before testing and viscosity should be measured at a shear rate of lODs-1 in a Bob and Cup Viscometer. Alternatively, to simulate vigorous shaking, the samples may be sheared at 50Ds'1 iW a viscometer before the viscosity is measured.
Sodium alginate mainly comprises the sodium salt of alginic acid which is a mixture of polyuronic acids composed of residues of D-mannuronic and L-guluronic acids. It may be obtained from algae belonging to the order Phaeophycae. Preferably, low viscosity grade sodium alginate is used to prepare the compositions according to the invention. These are grades of sodium alginate for which the viscosity of a 10% weight/volume aqueous solution, when determined on a Brookfield RVT
viscometer using spindle number 3 at 20 r.p.m. at 20°C, falls within the range 200 - 1500 mPa.s. An example of a suitable commercial grade of low viscosity sodium alginate is Protanal*LFR 5/60 (Pronova Biopol).
Preferably the sodium alginate has a high guluronic acid content. Guluronic acid content is expressed as gel strength(G). High guluronic acid grades of sodium alginate preferably have gel strengths of at least lOG.
The concentration of sodium alginate in compositions produced according to the invention is higher than in conventional compositions, i.e. at least 8% w/w.
Preferably the concentration is 8 to 14% w/v, more *Trade-mark preferably 9 to 14% w/v, even more preferably 10 to 13%
w/v and most preferably 10 to 12% w/v.
The concentration of potassium bicarbonate in compositions according to the invention is preferably 0.1 to 5% w/v, more preferably 0.5 to 5% w/v,~ even more preferably 1 to 3% w/v and most preferably 1.5 to 3% w/v.
Compositions prepared according to the invention may be used in the treatment of reflux oesophagitis, gastritis, dyspepsia or peptic ulceration. They may also be used as carriers of other active ingredients and so act as sustaiYied release compositions, or compositions delivering the actives specifically to the stomach (targeted delivery).
Further according to the invention there is provided the use of an orally effective amount of an aqueous pourable liquid composition comprising a) 8 to 14~ w/v low viscosity sodium alginate;
b) 0.1 to 5o w/v potassium bicarbonate for the treatment of reflux oesophagitis, gastritis, dyspepsia or peptic ulceration.
Further according to the invention there is therefore provided a pharmaceutical composition for the treatment of reflux oesophagitis, gastritis, dyspepsia or peptic ulceration, or for use as a sustained releasing or targeted delivery composition, in the form of an aqueous pourable liquid comprising a) 8 to 14 w/v low viscosity grade sodium alginate;
b) 0.1 to 5 w/v potassium bicarbonate.
Sodium alginate mainly comprises the sodium salt of alginic acid which is a mixture of polyuronic acids composed of residues of D-mannuronic and L-guluronic acids. It may be obtained from algae belonging to the order Phaeophycae. Preferably, low viscosity grade sodium alginate is used to prepare the compositions according to the invention. These are grades of sodium alginate for which the viscosity of a 10% weight/volume aqueous solution, when determined on a Brookfield RVT
viscometer using spindle number 3 at 20 r.p.m. at 20°C, falls within the range 200 - 1500 mPa.s. An example of a suitable commercial grade of low viscosity sodium alginate is Protanal*LFR 5/60 (Pronova Biopol).
Preferably the sodium alginate has a high guluronic acid content. Guluronic acid content is expressed as gel strength(G). High guluronic acid grades of sodium alginate preferably have gel strengths of at least lOG.
The concentration of sodium alginate in compositions produced according to the invention is higher than in conventional compositions, i.e. at least 8% w/w.
Preferably the concentration is 8 to 14% w/v, more *Trade-mark preferably 9 to 14% w/v, even more preferably 10 to 13%
w/v and most preferably 10 to 12% w/v.
The concentration of potassium bicarbonate in compositions according to the invention is preferably 0.1 to 5% w/v, more preferably 0.5 to 5% w/v,~ even more preferably 1 to 3% w/v and most preferably 1.5 to 3% w/v.
Compositions prepared according to the invention may be used in the treatment of reflux oesophagitis, gastritis, dyspepsia or peptic ulceration. They may also be used as carriers of other active ingredients and so act as sustaiYied release compositions, or compositions delivering the actives specifically to the stomach (targeted delivery).
Further according to the invention there is provided the use of an orally effective amount of an aqueous pourable liquid composition comprising a) 8 to 14~ w/v low viscosity sodium alginate;
b) 0.1 to 5o w/v potassium bicarbonate for the treatment of reflux oesophagitis, gastritis, dyspepsia or peptic ulceration.
Further according to the invention there is therefore provided a pharmaceutical composition for the treatment of reflux oesophagitis, gastritis, dyspepsia or peptic ulceration, or for use as a sustained releasing or targeted delivery composition, in the form of an aqueous pourable liquid comprising a) 8 to 14 w/v low viscosity grade sodium alginate;
b) 0.1 to 5 w/v potassium bicarbonate.
The compositions of the invention preferably also comprise a suspending agent. Suitable suspending agents include carrageenans, hypromellose, tragacanth, pectin, S pre-gelatinised potato starch, sodium starch glycolate, carbomer or mixtures thereof. Carbomer is a synthetic high molecular weight polymer of acrylic acid cross linked with either allyl esters of sucrose or pentaerythritol. Suitable commercially available grades of carbomer include Carbopol*934P or Carbopol*974P (BF
Goodrich).
For use in liquid products, carbomers must be neutralised after being pre-dispersed in water. The preferred neutralising agent is sodium hydroxide. The concentration of carbomer is given as the total amount of material used before neutralisation.
The choice of suspending agent and its concentration will depend upon the amount and grade of sodium alginate used in the compositions and upon the amount and type of extra insoluble ingredients used. Preferably the suspending agent is a carbomer. The preferred concentration of suspending agent is 0.1 to 1% w/v, most preferably 0.1 to 0.5% w/v.
The compositions of the present invention preferably further comprise a source of divalent or trivalent metal ions to strengthen the raft formed in the stomach. These ~ metal ions preferably become available when the compositions reach the stomach but must not be available before then or the compositions will gel too early.
Suitable metal ions are aluminium and, preferably, calcium ions. Most preferably the compositions comprise calcium carbonate.
*Trade-mark _7_ The compositions of the present invention therefore r preferably further comprise from 0.1 to 5°s w/v calcium ions, most preferably 0.5 to 3~ w/v calcium carbonate.
Still further according to the invention, there is provided a pharmaceutical composition for the treatment of reflex oesophagitis, gastritis, dyspepsia or peptic ulceration, or for use as a sustained releasing or targeted delivery composition, in the form of an aqueous pourable liquid comprising a) 8 to 14 w/v low viscosity sodium alginate;
b) 0.1 to 5 w/v potassium bicarbonate;
c) 0.1 to 1% w/v carbomer, neutralised with sodium hydroxide; and d) 0 to 5o w/v, preferably 0.5 to 5o w/v, calcium carbonate.
The compositions of the present invention preferably comprise substantially no source of sodium ions other than those provided by the sodium alginate and the sodium hydroxide used to neutralise the carbomer. Most preferably no sodium bicarbonate is added during the manufacture of the compositions of the invention.
The compositions of the present invention may further comprise preservatives to prevent contamination and subsequent deterioration by micro-organisms.
Examples of suitable preservatives are methyl, ethyl, propyl and butyl para-hydroxybenzoates and their salts, which are preferably used in combination eg methyl and propyl or ethyl and butyl.
W O 96!27368 CA 0 2 214 3 4 3 19 9 7 - 0 8 - 2 9 p~/GB96/00358 _g_ Preferred concentrations for the preservatives are 0.01 to 0.5% w/v. a The compositions of the present invention may also include one or more of the following ingredients, colouring, sweetening, flavouring or pH adjusting ingredients.
Where the compositions of the present invention are intended for use as sustained releasing compositions they will also contain active ingredients suitable for sustained administration in the stomach.
Where the compositions of the present invention are intended for use as targeted delivery compositions they will also contain active ingredients suitable for specific delivery to the stomach, for example local antimicrobial agents.
The compositions of the invention may be prepared by any conventional manufacturing process for compositions of this type. Preferably the compositions are prepared by the following process.
1) Dissolving the potassium bicarbonate in approximately 60~ of the water to be used in the composition and mixing in any of the preservatives, sweeteners and crosslinking aids (if used).
2) Adding the sodium alginate and stirring until dissolved.
3) Adding the suspending agents (if used). If the suspending agent is carbomer it should be pre neutralised with sodium hydroxide in approximately 30~ of the water to be used in the compositions.
v 4) Adding any flavourings or colouring agents and adjusting the volume.
The process is preferably carried out at approximately 20 to 25°C.
I
The invention will now be illustrated by reference to the following examples.
Exa le 1 Sodium alginate LFR 5/60 100 g (Pronova Biopol*) ' Potassium bicarbonate 20 g Calcium carbonate 20 g Carbomer (Carbopol*974P) 1 g Sodium hydroxide 0.3 g Ethyl parahydroxybenzoate 2 g Sodium butyl parahydroxybenzoate 0.2 g Sodium Saccharin 2 g Flavour 2 g Deionised water to 1 litre 1. The carbomer was dispersed in 300 ml deionised water in a first vessel and neutralised with the sodium hydroxide.
2. In a second vessel the potassium bicarbonate, calcium carbonate, preservatives and saccharin were mixed with 600 ml deionised water.
3. The sodium alginate was added to the second vessel and stirred until fully dissolved.
4. The contents of the second vessel were added to the contents of the first vessel and stirred until fully dispersed.
5. The flavour was added and the volume adjusted to 1 litre by the addition of further deionised water. The mixture was stirred until fully dispersed.
*Trade-mark ales 2 to 12 The following further Examples were all produced by the method of Example 1.
Sodium alginate LFR
5/60 (Pronova 1008 1008 1008 1008 100g Biopol:) Potassium 20g 31g 31g 31g 31g uicarbonate Calcium carbonate 20g 32g 32g 32g 32g Carbomer (Carbopol*
974P) 2g 2g 4g 6g lg Sodium hydroxide 0.7g 0.7g 1.4g 2.1g 0:3g Ethyl parahydroxybenzoate 2g 2g 2g 2g 2g Sodium butyl parahydroxybenzoate 0.2g 0.2g 0.2g 0.2g 0.2g Sodium Saccharin 2g 2g 2g 2g 2g Flavour 2g 2g 2g 2g 2g Deionised Water to 1 ltr 1 ltr 1 ltr 1 ltr 1 ltr *Trade-mark Sodium alginate LFR 5/60 (Pronova Biopol*) 1008 1008 1008 Potassium bicarbonate 20g lOg 25g Calcium carbonate 32g 32g 32g Carbomer (Carbopol*974P) 2g 2g 2g Sodium hydroxide 0.7g 0.7g 0.7g Ethyl parahydroxybenzoate 2g 2g 2g Sodium butyl parahydroxybenzoate 0.2g 0.2g 0.2g Sodium saccharin 2g 2g 2g Flavour 2g 2g 2g Deionised Water to 1 ltr 1 ltr 1 ltr *Trade-mark Sodium alginate LFR 5/60 (Pronova Biopol) 100g 100g 1008 Potassium bicarbonate 31g 31g 31g Calcium carbonate 16g 8g 24g Carbomer (Carbopol~' 974P) lg. lg lg Sodium hydroxide 0.3g 0.3g 0.3g Ethyl parahydroxybenzoate 2g 2g 2g Sodium butyl parahydroxybenzoate 0.2g 0.2g 0.2g Sodium saccharin 2g 2g 2g Flavour 2g 2g 2g Deionised Water to 1 ltr 1 Itr 1 ltr Examples 2 to 12 may be repeated using 8 or 12% w/v sodium alginate instead of 10%.
Examples 2 to 12 may further be repeated using 0.5, 4 or 5% w/v potassium bicarbonate.
*Trade-mark All of Examples 1 to l2 have the capability o~ being stored for at least 48 hours below 4°C, and in the case where a gel forms can be made pourable at room temperature by reasonable shaking or stirring.
gxam~l_es 13-to 24 Sodium alginate LFR
5/60(Pronova Biopol) 100g 80g 1008 1008 Potassium bicarbonate 20g 20g IOg I5 Calcium carbonate 20g 20g 20g 20g Aluminium hydroxide - - - -Carbomer (Carbopol* 4g 4g 4g 4g 974P) Sodium hydroxide 1.4g 1.4g 1.4g 1.4g Ethyl 2g 2g 2g 2g parahydroxybenzoate Sodium butyl 0.228 0.22g 0.228 0.228 parahydroxybenzoate Sodium saccharin lg lg lg lg Flavour 0.7g 0.7g 0.7g 0.7g Deionised water to 1 ltr 1 ltr 1 ltr 1 ltr *Trade-mark Sodium alginate LFR 5/60 100g 100g ~100g 1008 (Pronova Biopol) Potassium bicarbonate 20g 20g 20g 20g Calcium carbonate - - 20g 20g Aluminium hydroxide - 20g - -Carbomer (Carbopol*974P) 4g 4g 4g -Sodium hydroxide 1.4g 1.4g 1.4g -Ethyl parahydroxybenzoate 2g 2g 5g 2g Sodium butyl parahydroxybenzoate 0.22g 0.22g 0.558 0.22g Sodium saccharin lg lg lg lg Flavour 0.7g 0.7g 0.7g 0.7g Deionised water to 1 ltr 1 ltr 1 ltr 1 ltr *Trade-mark Sodium alginate LFR 1208 I30g 100g 100g 5/60 (Pronova Biopol*) Potassium bicarbonate 20g 20g 5g 50g Calcium carbonate - - 20g 20g Aluminium hydroxide - - -Carbomer (Carbopol*974P) 4g 4g 4g 4g Sodium hydroxide 1.4g 1.4g 1.4g I.4g Ethyl 2g 2g 2g 2g parahydroxybenzoate Sodium butyl parahydroxybenzoate 0.228 0.228 0.228 0.228 Sodium saccharin lg lg lg lg Flavour 0.7g 0.7g 0.7g 0.7g Deionised water to 1 ltr 1 ltr 1 ltr 1 ltr Each of Examples 13 to 24 were manufactured by the general method of Example 1 (taking into account changes necessitated by the various formula differences).
Samples of each of Examples 13 to 24 were stored at 4°C
for 3 weeks and were all found to be easily pourable *Trade-mark W~ 96/27368 PCTlGB96100358 following warming to room temperature and shaking.
a s
Goodrich).
For use in liquid products, carbomers must be neutralised after being pre-dispersed in water. The preferred neutralising agent is sodium hydroxide. The concentration of carbomer is given as the total amount of material used before neutralisation.
The choice of suspending agent and its concentration will depend upon the amount and grade of sodium alginate used in the compositions and upon the amount and type of extra insoluble ingredients used. Preferably the suspending agent is a carbomer. The preferred concentration of suspending agent is 0.1 to 1% w/v, most preferably 0.1 to 0.5% w/v.
The compositions of the present invention preferably further comprise a source of divalent or trivalent metal ions to strengthen the raft formed in the stomach. These ~ metal ions preferably become available when the compositions reach the stomach but must not be available before then or the compositions will gel too early.
Suitable metal ions are aluminium and, preferably, calcium ions. Most preferably the compositions comprise calcium carbonate.
*Trade-mark _7_ The compositions of the present invention therefore r preferably further comprise from 0.1 to 5°s w/v calcium ions, most preferably 0.5 to 3~ w/v calcium carbonate.
Still further according to the invention, there is provided a pharmaceutical composition for the treatment of reflex oesophagitis, gastritis, dyspepsia or peptic ulceration, or for use as a sustained releasing or targeted delivery composition, in the form of an aqueous pourable liquid comprising a) 8 to 14 w/v low viscosity sodium alginate;
b) 0.1 to 5 w/v potassium bicarbonate;
c) 0.1 to 1% w/v carbomer, neutralised with sodium hydroxide; and d) 0 to 5o w/v, preferably 0.5 to 5o w/v, calcium carbonate.
The compositions of the present invention preferably comprise substantially no source of sodium ions other than those provided by the sodium alginate and the sodium hydroxide used to neutralise the carbomer. Most preferably no sodium bicarbonate is added during the manufacture of the compositions of the invention.
The compositions of the present invention may further comprise preservatives to prevent contamination and subsequent deterioration by micro-organisms.
Examples of suitable preservatives are methyl, ethyl, propyl and butyl para-hydroxybenzoates and their salts, which are preferably used in combination eg methyl and propyl or ethyl and butyl.
W O 96!27368 CA 0 2 214 3 4 3 19 9 7 - 0 8 - 2 9 p~/GB96/00358 _g_ Preferred concentrations for the preservatives are 0.01 to 0.5% w/v. a The compositions of the present invention may also include one or more of the following ingredients, colouring, sweetening, flavouring or pH adjusting ingredients.
Where the compositions of the present invention are intended for use as sustained releasing compositions they will also contain active ingredients suitable for sustained administration in the stomach.
Where the compositions of the present invention are intended for use as targeted delivery compositions they will also contain active ingredients suitable for specific delivery to the stomach, for example local antimicrobial agents.
The compositions of the invention may be prepared by any conventional manufacturing process for compositions of this type. Preferably the compositions are prepared by the following process.
1) Dissolving the potassium bicarbonate in approximately 60~ of the water to be used in the composition and mixing in any of the preservatives, sweeteners and crosslinking aids (if used).
2) Adding the sodium alginate and stirring until dissolved.
3) Adding the suspending agents (if used). If the suspending agent is carbomer it should be pre neutralised with sodium hydroxide in approximately 30~ of the water to be used in the compositions.
v 4) Adding any flavourings or colouring agents and adjusting the volume.
The process is preferably carried out at approximately 20 to 25°C.
I
The invention will now be illustrated by reference to the following examples.
Exa le 1 Sodium alginate LFR 5/60 100 g (Pronova Biopol*) ' Potassium bicarbonate 20 g Calcium carbonate 20 g Carbomer (Carbopol*974P) 1 g Sodium hydroxide 0.3 g Ethyl parahydroxybenzoate 2 g Sodium butyl parahydroxybenzoate 0.2 g Sodium Saccharin 2 g Flavour 2 g Deionised water to 1 litre 1. The carbomer was dispersed in 300 ml deionised water in a first vessel and neutralised with the sodium hydroxide.
2. In a second vessel the potassium bicarbonate, calcium carbonate, preservatives and saccharin were mixed with 600 ml deionised water.
3. The sodium alginate was added to the second vessel and stirred until fully dissolved.
4. The contents of the second vessel were added to the contents of the first vessel and stirred until fully dispersed.
5. The flavour was added and the volume adjusted to 1 litre by the addition of further deionised water. The mixture was stirred until fully dispersed.
*Trade-mark ales 2 to 12 The following further Examples were all produced by the method of Example 1.
Sodium alginate LFR
5/60 (Pronova 1008 1008 1008 1008 100g Biopol:) Potassium 20g 31g 31g 31g 31g uicarbonate Calcium carbonate 20g 32g 32g 32g 32g Carbomer (Carbopol*
974P) 2g 2g 4g 6g lg Sodium hydroxide 0.7g 0.7g 1.4g 2.1g 0:3g Ethyl parahydroxybenzoate 2g 2g 2g 2g 2g Sodium butyl parahydroxybenzoate 0.2g 0.2g 0.2g 0.2g 0.2g Sodium Saccharin 2g 2g 2g 2g 2g Flavour 2g 2g 2g 2g 2g Deionised Water to 1 ltr 1 ltr 1 ltr 1 ltr 1 ltr *Trade-mark Sodium alginate LFR 5/60 (Pronova Biopol*) 1008 1008 1008 Potassium bicarbonate 20g lOg 25g Calcium carbonate 32g 32g 32g Carbomer (Carbopol*974P) 2g 2g 2g Sodium hydroxide 0.7g 0.7g 0.7g Ethyl parahydroxybenzoate 2g 2g 2g Sodium butyl parahydroxybenzoate 0.2g 0.2g 0.2g Sodium saccharin 2g 2g 2g Flavour 2g 2g 2g Deionised Water to 1 ltr 1 ltr 1 ltr *Trade-mark Sodium alginate LFR 5/60 (Pronova Biopol) 100g 100g 1008 Potassium bicarbonate 31g 31g 31g Calcium carbonate 16g 8g 24g Carbomer (Carbopol~' 974P) lg. lg lg Sodium hydroxide 0.3g 0.3g 0.3g Ethyl parahydroxybenzoate 2g 2g 2g Sodium butyl parahydroxybenzoate 0.2g 0.2g 0.2g Sodium saccharin 2g 2g 2g Flavour 2g 2g 2g Deionised Water to 1 ltr 1 Itr 1 ltr Examples 2 to 12 may be repeated using 8 or 12% w/v sodium alginate instead of 10%.
Examples 2 to 12 may further be repeated using 0.5, 4 or 5% w/v potassium bicarbonate.
*Trade-mark All of Examples 1 to l2 have the capability o~ being stored for at least 48 hours below 4°C, and in the case where a gel forms can be made pourable at room temperature by reasonable shaking or stirring.
gxam~l_es 13-to 24 Sodium alginate LFR
5/60(Pronova Biopol) 100g 80g 1008 1008 Potassium bicarbonate 20g 20g IOg I5 Calcium carbonate 20g 20g 20g 20g Aluminium hydroxide - - - -Carbomer (Carbopol* 4g 4g 4g 4g 974P) Sodium hydroxide 1.4g 1.4g 1.4g 1.4g Ethyl 2g 2g 2g 2g parahydroxybenzoate Sodium butyl 0.228 0.22g 0.228 0.228 parahydroxybenzoate Sodium saccharin lg lg lg lg Flavour 0.7g 0.7g 0.7g 0.7g Deionised water to 1 ltr 1 ltr 1 ltr 1 ltr *Trade-mark Sodium alginate LFR 5/60 100g 100g ~100g 1008 (Pronova Biopol) Potassium bicarbonate 20g 20g 20g 20g Calcium carbonate - - 20g 20g Aluminium hydroxide - 20g - -Carbomer (Carbopol*974P) 4g 4g 4g -Sodium hydroxide 1.4g 1.4g 1.4g -Ethyl parahydroxybenzoate 2g 2g 5g 2g Sodium butyl parahydroxybenzoate 0.22g 0.22g 0.558 0.22g Sodium saccharin lg lg lg lg Flavour 0.7g 0.7g 0.7g 0.7g Deionised water to 1 ltr 1 ltr 1 ltr 1 ltr *Trade-mark Sodium alginate LFR 1208 I30g 100g 100g 5/60 (Pronova Biopol*) Potassium bicarbonate 20g 20g 5g 50g Calcium carbonate - - 20g 20g Aluminium hydroxide - - -Carbomer (Carbopol*974P) 4g 4g 4g 4g Sodium hydroxide 1.4g 1.4g 1.4g I.4g Ethyl 2g 2g 2g 2g parahydroxybenzoate Sodium butyl parahydroxybenzoate 0.228 0.228 0.228 0.228 Sodium saccharin lg lg lg lg Flavour 0.7g 0.7g 0.7g 0.7g Deionised water to 1 ltr 1 ltr 1 ltr 1 ltr Each of Examples 13 to 24 were manufactured by the general method of Example 1 (taking into account changes necessitated by the various formula differences).
Samples of each of Examples 13 to 24 were stored at 4°C
for 3 weeks and were all found to be easily pourable *Trade-mark W~ 96/27368 PCTlGB96100358 following warming to room temperature and shaking.
a s
Claims (10)
1. Use of potassium bicarbonate for the preparation of an aqueous pourable liquid medicament composition comprising at least 8% w/v sodium alginate.
2. The use according to claim 1 in which the concentration of potassium bicarbonate in the medicament composition is 0.1 to 5% w/v.
3. A pharmaceutical composition for the treatment of reflux oesophagitis, gastritis, dyspepsia or peptic ulceration, or for use as a sustained releasing or targeted delivery composition, in the form of an aqueous pourable liquid comprising a) 8 to 14% w/v low viscosity grade sodium alginate; and b) 0.1 to 5% w/v potassium bicarbonate.
4. The pharmaceutical composition according to claim 3 which further comprises a suspending agent, selected, in the alternative, from carrageenans, hypromellose, tragacanth, pectin, pre-gelatinised potato starch, sodium starch glycolate, carbomer or mixtures thereof.
5. The pharmaceutical composition according to claim 3 or claim 4 which further comprises a source of divalent or trivalent metal ions to strengthen the raft formed in the stomach.
6. The pharmaceutical composition according to claim 5 wherein the source of metal ions is calcium carbonate.
7. Use of an orally effective amount of an aqueous pourable liquid composition comprising a) 8 to 14% w/v low viscosity sodium alginate; and b) 0.1 to 5% w/v potassium bicarbonate, for the treatment of reflux oesophagitis, gastritis, dyspepsia or peptic ulceration.
8. A pharmaceutical composition for the treatment of reflux oesophagitis, gastritis, dyspepsia or peptic ulceration, or for use as a sustained releasing or targeted delivery composition, in the form of an aqueous pourable liquid comprising a) 8 to 14% w/v low viscosity sodium alginate;
b) 0.1 to 5% w/v potassium bicarbonate;
c) 0.1 to 1% w/v carbomer, neutralised with sodium hydroxide; and d) 0 to 5% w/v calcium carbonate.
b) 0.1 to 5% w/v potassium bicarbonate;
c) 0.1 to 1% w/v carbomer, neutralised with sodium hydroxide; and d) 0 to 5% w/v calcium carbonate.
9. The pharmaceutical composition of claim 8 wherein the calcium carbonate is present in a concentration of 0.5 to 5% w/v.
10. The pharmaceutical composition of any one of claims 3, 4, 5, 6, 8 or 9 which is free of sodium bicarbonate.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB9504599.3 | 1995-03-03 | ||
GBGB9504599.3A GB9504599D0 (en) | 1995-03-03 | 1995-03-03 | Improvements in or relating to organic compositions |
PCT/GB1996/000358 WO1996027368A1 (en) | 1995-03-03 | 1996-02-16 | Liquid aqueous pharmaceutical compositions comprising sodium alginate and potassium bicarbonate |
Publications (2)
Publication Number | Publication Date |
---|---|
CA2214343A1 CA2214343A1 (en) | 1996-09-12 |
CA2214343C true CA2214343C (en) | 2007-05-01 |
Family
ID=38051353
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CA002214343A Expired - Fee Related CA2214343C (en) | 1995-03-03 | 1996-02-16 | Liquid aqueous pharmaceutical compositions comprising sodium alginate and potassium bicarbonate |
Country Status (1)
Country | Link |
---|---|
CA (1) | CA2214343C (en) |
-
1996
- 1996-02-16 CA CA002214343A patent/CA2214343C/en not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
CA2214343A1 (en) | 1996-09-12 |
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