WO2023136797A2 - A bilayer tablet composition comprising amorphous dapagliflozin and metformin - Google Patents
A bilayer tablet composition comprising amorphous dapagliflozin and metformin Download PDFInfo
- Publication number
- WO2023136797A2 WO2023136797A2 PCT/TR2023/050022 TR2023050022W WO2023136797A2 WO 2023136797 A2 WO2023136797 A2 WO 2023136797A2 TR 2023050022 W TR2023050022 W TR 2023050022W WO 2023136797 A2 WO2023136797 A2 WO 2023136797A2
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- bilayer tablet
- tablet composition
- composition according
- layer
- pharmaceutical
- Prior art date
Links
Classifications
-
- 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
-
- 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
- A61K9/20—Pills, tablets, discs, rods
- A61K9/2004—Excipients; Inactive ingredients
- A61K9/2022—Organic macromolecular compounds
- A61K9/205—Polysaccharides, e.g. alginate, gums; Cyclodextrin
- A61K9/2054—Cellulose; Cellulose derivatives, e.g. hydroxypropyl methylcellulose
-
- 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
- A61K9/20—Pills, tablets, discs, rods
- A61K9/2072—Pills, tablets, discs, rods characterised by shape, structure or size; Tablets with holes, special break lines or identification marks; Partially coated tablets; Disintegrating flat shaped forms
- A61K9/2086—Layered tablets, e.g. bilayer tablets; Tablets of the type inert core-active coat
- A61K9/209—Layered tablets, e.g. bilayer tablets; Tablets of the type inert core-active coat containing drug in at least two layers or in the core and in at least one outer layer
Definitions
- the invention relates to a bilayer tablet composition
- a bilayer tablet composition comprising metformin hydrochloride and amorphous dapagliflozin, and at least one pharmaceutically acceptable excipient, wherein both layers comprising microcrystalline cellulose as a filler and at least one pharmaceutical acceptable excipient.
- the composition has immediate release layer and an extended release layer.
- Diabetes mellitus is a lifelong chronic disease resulting from the pancreas's inability to produce enough insulin or the body's ability to use insulin effectively, and it continues with the reduction of insulin-producing cells. Blood glucose rises with absent or non-functioning insulin hormone. The resulting high blood sugar causes classical symptoms such as polyuria (frequent urination), polydipsia (increased thirst) and polyphagia (increased hunger).
- type 1 diabetes type 1
- type 2 diabetes type 2 diabetes
- gestational diabetes is seen in pregnant women who develop high blood sugar levels. Type 1 diabetes is caused by the body's inability to produce insulin, requiring insulin injection.
- Type 2 diabetes the body either resists the effects of insulin or does not produce enough insulin to maintain a normal glucose level.
- Dapagliflozin is a sodium-glucose cotransporter 2 inhibitor (SGLT2).
- SGLT2 is a carrier responsible for the reabsorption of most of the glucose from the lumen of the renal tubule.
- SGLT2 is expressed in proximal renal tubules.
- dapagliflozin reduces the reabsorption of the filtered glucose and lowers the renal threshold for glucose. This improves urinary glucose excretion and blood glucose control.
- Dapagliflozin also known as (1S)-1 ,5- Anhydro-1-C-[4-chloro-3-[(4-ethoxyphenyl)methyl]phenyl]-D-glucitol or (2S,3R,4R,5S,6R)-2- (3-(4-etoxybenzyl)-4-chlorophenyl)-6-hydroxymethyltetrahydro-2H-pyran-3,4,5-triol is represented by the structure of Formula I.
- Metformin is an antihyperglycemic agent that improves glucose tolerance and lowers both basal and postprandial plasma glucose levels by different mechanisms than other oral antidiabetic agents. Metformin decreases hepatic gluconeogenesis, decreases intestinal absorption of glucose, and improves insulin sensitivity by increasing peripheral glucose uptake and utilization. With metformin therapy, insulin secretion remains unchanged while fasting insulin levels and day-long plasma insulin response may actually decrease. Metformin, also known as N, N-dimethylimidodicarbonimidic diamide or 1,1- Dimethylbiguanide or N, N-dimethyldiguanide or N, N-Dimethylguanylguanidine, is represented by the chemical structure in Formula II.
- EP2498758B1 discloses bilayer tablets comprising a first layer, wherein the first layer is extended-release metformin and a second layer, wherein the second layer is immediate release dapagliflozin molecule.
- EP2498759B1 discloses a process for the preparation of an immediate release formulation comprising a combination of dapagliflozin and metformin.
- WO 2017/098481 discloses an effervescent combination comprising metformin with retained carbon dioxide content of at least 90% of the input blend and a different antidiabetic agent.
- Unexamined patent TR2012/02948 discloses a tablet form comprising a combination of metformin hydrochloride and dapagliflozin and a core tablet coated with a coating solution containing extended-release metformin and dapagliflozin.
- bilayer tablet formulations comprising metformin hydrochloride and amorphous dapagliflozin compared to other drug forms is the immediate effect of the drug experienced by the target group of patients, which continues throughout the day. Thus, the target patient group does not need to use drugs repeatedly.
- the immediate release layer does not diffuse fast enough, the polymers that release and control the release in extended release layers creates a diffusion barrier surrounding the tablet. This barrier prevents the immediate release layer, which does not release fast enough, from diffusing and the drug from reaching its desired efficiency. As a result, the desired release profile cannot be achieved.
- the present formulations require additional time for the onset of action. This is undesirable for the patient. The early onset of the treatment process directly affects the patient's quality of life.
- the dapagliflozin is hygroscopic in nature. It absorbs moisture and forms sticky lumps which are difficult to process and handle, and which may ultimately lead to content uniformity issues in the dosage form.
- the low solubility and stability of dapagliflozin base as compared to its solvates may lead to poor bioavailability of the drug.
- metformin is a very poorly compressible active substance and metformin presents in high amounts in a composition. The problem causes some homogeneity, flowability and dissolution profile.
- a bilayer tablet comprising metformin HCI and amorphous dapagliflozin is provided using both layers comprising microcrystalline cellulose as a filler. Also, the bilayer tablet has been developed by using standard techniques which is simple and cost-effective method.
- the main object of the present invention is to provide a bilayer tablet comprising metformin hydrochloride and amorphous dapagliflozin with high stability, having desired level of dissolution rate, homogeneity, flowability and compressibility which overcomes the abovedescribed problems of active agents in prior art and have additive advantages over them.
- the object of the present invention is to provide an improved bilayer tablet formulation comprising metformin HCI and amorphous dapagliflozin to be used in the treatment of type 2 diabetes, using suitable excipients.
- the object of the present invention is to combine metformin hydrochloride and amorphous dapagliflozin in a single dosage form while maintaining stability and improving the dissolution profile.
- Metformin hydrochloride is used big proportion that can lead to considerable problems during the manufacture of the composition with regard to homogenity of active agent in the individual composition units. It reflects that homogenity play important role in the dissolution of the drug. Using the right fillers in first layer helps to ensure homogeneity of metformin HCI. That is, the fillers play an important role for the dissolution profile.
- a pharmaceutical bilayer tablet composition comprises; a. first layer comprising metformin hydrochloride, b. second layer comprising amorphous dapagliflozin, wherein both layers comprising microcrystalline cellulose as a filler and at least one pharmaceutical acceptable excipient. It has been found that a bilayer tablet of excellent homogeneity, good flowability and showing improved dissolution can be obtained when microcrystalline cellulose is used as filler in both layers.
- the first layer has extended release formulation and the second layer has immediately release formulation.
- the amount of metformin hydrochloride is 25.0% to 50.0% by weight in the total composition.
- the amount of amorphous dapagliflozin is 0.05% to 5.0% by weight in the total composition.
- At least one pharmaceutically acceptable excipient is selected from fillers, binders, disintegrants, matrix agents, glidants/lubricants or mixtures thereof.
- Microcrystalline cellulose is used as filler in both layers.
- the composition may comprise one more filler is selected from the group comprising anhydrous lactose, lactose, starch, mannitol, calcium hydrogen phosphate dihydrate, dicalcium hydrogen phosphate anhydrate, calcium phosphate trihydrate, silicon dioxide, neutral pellets, magnesium carbonate, magnesium oxide, maltodextrin, maltose or mixtures thereof.
- microcrystalline cellulose in both layers ensures homogeneous distribution of dapagliflozin, which is used in small amounts in the composition.
- the composition comprises anhydrous lactose as filler.
- anhydrous lactose is used at second layer. So, the desired dissolution profile is provided.
- second layer also comprises anhydrous lactose as a filler.
- the amount of fillers is 15.0% to 40.0% by weight in the total composition. This ratio provides the desired dissolution profile and content uniformity and good flowability.
- Suitable binders are selected from the group comprising hydroxypropyl methylcellulose, carboxymethylcellulose sodium, polyvinylpyrrolidone (povidone), lactose anhydrous, pregelatinized starch, calcium carbonate, calcium phosphate dibasic, calcium phosphate tribasic, calcium sulphate, hydroxypropylcellulose, methyl cellulose, ethyl cellulose or mixtures thereof.
- the binder is hydroxypropyl methylcellulose (E5 LV) or carboxymethylcellulose sodium or mixtures thereof.
- the binders are used in the first layer.
- the amount of binders is 1.0% to 15.0% by weight in the total composition.
- the amount of binders is 2.0% to 8.0% by weight in the total composition. This provides the desired dissolution profile.
- Suitable disintegrants are selected from the group comprising croscarmellose sodium, crospovidone, sodium starch glycollate, sodium alginate, gums, starch and magnesium aluminum silicate or a mixture thereof.
- the weight ratio of disintegrant to amorphous dapagliflozin is 1.0 - 4.0, preferably 1.2 - 3.5 in the immediate release layer provides bilayer tablet composition of dapagliflozin with good dissolution and solubility, thus high bioavailability.
- the disintegrant is croscarmellose sodium. The disintegrant is used in the second layer.
- the amount of disintegrants is 0.1% to 5.0% by weight in the total composition. This amount of disintegrants provides the desired dissolution profile.
- Suitable glidants/lubricants are selected from group comprising colloidal silicon dioxide, sodium stearyl fumarate, magnesium oxide, starch, silica colloidal anhydrous, talc, polyethylene glycol, stearic acid, aluminum silicate, magnesium silicate, colloidal silica or mixtures thereof.
- the glidants/lubricants is colloidal silicon dioxide or sodium stearyl fumarate or mixtures thereof.
- the amount of glidants/lubricants is 0.2% to 10.0% by weight in the total composition.
- the extended release formulation in first layer is prepared using matrix agents.
- Suitable matrix agents are selected from the group comprising hydroxypropylmethyl cellulose, ethyl cellulose, polymethylmethacrylate derivatives’s, poloxamer, polyvinyl alcohol, xanthan gum, sodium alginate, polymethacrylates, polyacrylamide, hydroxypropyl cellulose, polyvinyl acetate, cellulose acetate phthalate, ethylene vinyl acetate, methyl aminoethyl methacrylate, neutral methacrylic acid esters, polylactide, polylactide co-glycolide, diethyl aminoethyl methacrylate or mixtures thereof.
- the matrix agent is hydroxypropyl methyl cellulose (K100 MCR/ K100M/ CN10T), it is used only at first layer.
- the amount of matrix agents is 20.0% to 35.0% by weight in the total composition.
- the amount of matrix agents is 26.0% to 30.0% by weight in the total composition.
- the bilayer tablet composition is coated with at least one film coating agent.
- suitable film coating agents are selected from the group comprising polymethacrylates, hydroxypropyl methylcellulose, lactose monohydrate, talc, hydroxypropyl cellulose, polyvinyl alcohol (PVA), polyethylene glycol (PEG), glycerin, polyvinyl alcohol-polyethylene glycol copolymers (Kollicoat® IR), ethylcellulose dispersions (Surelease®), polyvinylprolidone, polyvinylprolidone-vinyl acetate copolymer (PVP-VA), iron oxide yellow, iron oxides, all kinds of Opadry®, pigments, dyes, titanium dioxide, coloring agent or mixtures thereof.
- the film coating agents are selected from the group comprising polyvinyl alcohol, talc, titanium dioxide, polyethylene glycol, yellow iron oxide.
- the amount of film coating agents is 0.5% to 5.0% by weight in the total composition.
- the bilayer tablet composition comprising amorphous dapagliflozin and metformin HCI is stable.
- the combination does not show incompatibilities, degradation problems, or extraction problems with certain excipients such as amorphous dapagliflozin, metformin HCI, microcrystalline cellulose, anhydrous lactose, croscarmellose sodium, carboxymethylcellulose sodium (7 HF), hydroxypropylmethylcellulose (E5 LV), hydroxypropylmethylcellulose (K100 MCR/ K100M/ CN10T), colloidal silicon dioxide, sodium stearyl fumarate and coating agents.
- the present invention provides bilayer tablets comprising an extended release formulation, wherein the first layer comprises metformin HCI as active ingredient, microcrystalline cellulose as filler, hydroxypropylmethylcellulose (E5 LV) and carboxymethylcellulose sodium (7 HF) as binder, hydroxypropylmethylcellulose (K100 MCR/ K100M/ CN10T) as a matrix agent, sodium stearyl fumarate as glidant/lubricant, as well as an immediate release formulation of amorphous dapagliflozin wherein the second layer comprises amorphous dapagliflozin as active agent, microcrystalline cellulose and anhydrous lactose as a filler, croscarmellose sodium as disintegrant, colloidal silicon dioxide and sodium stearyl fumarate as glidant/ lubricant.
- the first layer comprises metformin HCI as active ingredient, microcrystalline cellulose as filler, hydroxypropylmethylcellulose (E5 LV) and carboxymethylcellulose sodium (7 HF) as binder,
- the first layer comprises metformin HCI as active ingredient, microcrystalline cellulose as filler, hydroxypropylmethylcellulose (E5 LV) and carboxymethylcellulose sodium as binder, hydroxypropylmethylcellulose (K100 MCR or K100M or CN10T) as a matrix agent, sodium stearyl fumarate as glidant/lubricant.
- the second layer comprises amorphous dapagliflozin as active agent, microcrystalline cellulose and anhydrous lactose as a filler, croscarmellose sodium as disintegrant, colloidal silicon dioxide and sodium stearyl fumarate as glidant/ lubricant.
- Example 1 Example 2:
- the above-mentioned pharmaceutical bilayer tablet at example 1 or 2 is prepared as follows: The first layer (extended release layer): a) Sieving metformin and grinding, b) Mixing metformin, carboxymethylcellulose sodium (7 HF), hydroxypropylmethylcellulose (E5 LV) in the granulator and obtained a dry mixture, c) Granulating the dry mixture with pure water and then obtained wet granules, d) Drying the wet granules at fluid bed dryer and then sieving, e) Mixing the granules and hydroxypropylmethylcellulose (K100 MCR/ K100M/ CN10T), f) Adding microcrystalline cellulose and then mixing, g) Adding sodium stearyl fumarate and then mixing.
- the first layer (extended release layer) a) Sieving metformin and grinding, b) Mixing metformin, carboxymethylcellulose sodium (7 HF), hydroxypropylmethylcellulose (E5 LV) in the granulator
- the second layer (immediate release layer): h) Mixing amorphous dapagliflozin and colloidal silicon dioxide, i) Adding anhydrous lactose, croscarmellose sodium and mixing, and then sieving, j) Adding the half of microcrystalline cellulose and mixing, then adding the remaining part of microcrystalline cellulose and then mixing and then sieving, k) Adding sodium stearyl fumarate and mixing,
- Tablet compression The first layer and second layer are compressed to form a bilayer tablet.
- a bilayer tablet formulation of metformin HCI and amorphous dapagliflozin with the desired release profile is obtained.
- the immediate release and extended release layers in the bilayer tablet have been used in such proportions, so that a formulation with suitable and desired properties could be obtained which provides up to 24 hours of release.
- the start of treatment is achieved at the desired level depending on the dissolution rate of the immediate release layer.
Abstract
The invention relates to a bilayer tablet composition comprising metformin hydrochloride and amorphous dapagliflozin, and at least one pharmaceutically acceptable excipient, wherein both layers comprising microcrystalline cellulose as a filler and at least one pharmaceutical acceptable excipient. Also, the composition has immediate release layer and an extended release layer.
Description
A BILAYER TABLET COMPOSITION COMPRISING AMORPHOUS DAPAGLIFLOZIN AND METFORMIN
Field of Invention
The invention relates to a bilayer tablet composition comprising metformin hydrochloride and amorphous dapagliflozin, and at least one pharmaceutically acceptable excipient, wherein both layers comprising microcrystalline cellulose as a filler and at least one pharmaceutical acceptable excipient. Also, the composition has immediate release layer and an extended release layer.
Background of the Invention
Diabetes mellitus, known as diabetes, is a lifelong chronic disease resulting from the pancreas's inability to produce enough insulin or the body's ability to use insulin effectively, and it continues with the reduction of insulin-producing cells. Blood glucose rises with absent or non-functioning insulin hormone. The resulting high blood sugar causes classical symptoms such as polyuria (frequent urination), polydipsia (increased thirst) and polyphagia (increased hunger). Currently, there are three types of diabetes: type 1 diabetes (type 1), type 2 diabetes (type 2) and gestational diabetes. Gestational diabetes is seen in pregnant women who develop high blood sugar levels. Type 1 diabetes is caused by the body's inability to produce insulin, requiring insulin injection. Finally, with type 2 diabetes, the body either resists the effects of insulin or does not produce enough insulin to maintain a normal glucose level.
Dapagliflozin is a sodium-glucose cotransporter 2 inhibitor (SGLT2). SGLT2 is a carrier responsible for the reabsorption of most of the glucose from the lumen of the renal tubule. SGLT2 is expressed in proximal renal tubules. By inhibiting SGLT2, dapagliflozin reduces the reabsorption of the filtered glucose and lowers the renal threshold for glucose. This improves urinary glucose excretion and blood glucose control. Dapagliflozin, also known as (1S)-1 ,5- Anhydro-1-C-[4-chloro-3-[(4-ethoxyphenyl)methyl]phenyl]-D-glucitol or (2S,3R,4R,5S,6R)-2- (3-(4-etoxybenzyl)-4-chlorophenyl)-6-hydroxymethyltetrahydro-2H-pyran-3,4,5-triol is represented by the structure of Formula I.
Formula I
Dapagliflozin was first disclosed in patent US 6515117 (2003, Bristol-Myers Squibb).
Metformin is an antihyperglycemic agent that improves glucose tolerance and lowers both basal and postprandial plasma glucose levels by different mechanisms than other oral antidiabetic agents. Metformin decreases hepatic gluconeogenesis, decreases intestinal absorption of glucose, and improves insulin sensitivity by increasing peripheral glucose uptake and utilization. With metformin therapy, insulin secretion remains unchanged while fasting insulin levels and day-long plasma insulin response may actually decrease. Metformin, also known as N, N-dimethylimidodicarbonimidic diamide or 1,1- Dimethylbiguanide or N, N-dimethyldiguanide or N, N-Dimethylguanylguanidine, is represented by the chemical structure in Formula II.
Formula II
Metformin was first disclosed in patent US 3174901 (1965, Jan Marcel Didier Aron-Samuel).
EP2498758B1 discloses bilayer tablets comprising a first layer, wherein the first layer is extended-release metformin and a second layer, wherein the second layer is immediate release dapagliflozin molecule.
EP2498759B1 discloses a process for the preparation of an immediate release formulation comprising a combination of dapagliflozin and metformin.
WO 2017/098481 discloses an effervescent combination comprising metformin with retained carbon dioxide content of at least 90% of the input blend and a different antidiabetic agent.
Unexamined patent TR2012/02948 discloses a tablet form comprising a combination of metformin hydrochloride and dapagliflozin and a core tablet coated with a coating solution containing extended-release metformin and dapagliflozin.
The main advantage of bilayer tablet formulations comprising metformin hydrochloride and amorphous dapagliflozin compared to other drug forms is the immediate effect of the drug experienced by the target group of patients, which continues throughout the day. Thus, the target patient group does not need to use drugs repeatedly.
In the state of the art, there are tablet configurations with layers that provide immediate and extended releases. Immediate release layers balance the amount of glucose in the blood immediately, while the extended release layers maintain the blood sugar balance over an extended period. But these configurations have undesired properties. Following administration, disintegration and dissolution begin in the immediate and extended release layers and the active substance diffuses into the environment. However, if the immediate release layer does not diffuse fast enough, the polymers that release and control the release in extended release layers creates a diffusion barrier surrounding the tablet. This barrier prevents the immediate release layer, which does not release fast enough, from diffusing and the drug from reaching its desired efficiency. As a result, the desired release profile cannot be achieved. The present formulations require additional time for the onset of action. This is undesirable for the patient. The early onset of the treatment process directly affects the patient's quality of life.
The dapagliflozin is hygroscopic in nature. It absorbs moisture and forms sticky lumps which are difficult to process and handle, and which may ultimately lead to content uniformity issues in the dosage form. The low solubility and stability of dapagliflozin base as compared to its solvates may lead to poor bioavailability of the drug. Also, as known, metformin is a very poorly compressible active substance and metformin presents in high amounts in a composition. The problem causes some homogeneity, flowability and dissolution profile.
The selection and proportion of excipients with appropriate release profile for the desired drug configuration, promoting the release from the immediate release layer at the desired rate is of critical importance.
In order to eliminate the mentioned problems, it is obvious that an innovation is needed in the art that will facilitate production of daily single-dose formulations with appropriate release profile comprising metformin HCI and amorphous dapagliflozin.
In this invention, to overcome these problems mentioned above, a bilayer tablet comprising metformin HCI and amorphous dapagliflozin is provided using both layers comprising microcrystalline cellulose as a filler. Also, the bilayer tablet has been developed by using standard techniques which is simple and cost-effective method.
Background and Description of the Invention
The main object of the present invention is to provide a bilayer tablet comprising metformin hydrochloride and amorphous dapagliflozin with high stability, having desired level of dissolution rate, homogeneity, flowability and compressibility which overcomes the abovedescribed problems of active agents in prior art and have additive advantages over them.
The object of the present invention is to provide an improved bilayer tablet formulation comprising metformin HCI and amorphous dapagliflozin to be used in the treatment of type 2 diabetes, using suitable excipients.
The object of the present invention is to combine metformin hydrochloride and amorphous dapagliflozin in a single dosage form while maintaining stability and improving the dissolution profile.
Metformin hydrochloride is used big proportion that can lead to considerable problems during the manufacture of the composition with regard to homogenity of active agent in the individual composition units. It reflects that homogenity play important role in the dissolution of the drug. Using the right fillers in first layer helps to ensure homogeneity of metformin HCI. That is, the fillers play an important role for the dissolution profile.
According to an embodiment of the present invention, a pharmaceutical bilayer tablet composition comprises; a. first layer comprising metformin hydrochloride, b. second layer comprising amorphous dapagliflozin, wherein both layers comprising microcrystalline cellulose as a filler and at least one pharmaceutical acceptable excipient. It has been found that a bilayer tablet of excellent homogeneity, good flowability and showing improved dissolution can be obtained when microcrystalline cellulose is used as filler in both layers.
According to one embodiment of the present invention, the first layer has extended release formulation and the second layer has immediately release formulation.
According to one embodiment of the present invention, the amount of metformin hydrochloride is 25.0% to 50.0% by weight in the total composition.
According to one embodiment of the present invention, the amount of amorphous dapagliflozin is 0.05% to 5.0% by weight in the total composition.
According to one embodiment of the present invention, at least one pharmaceutically acceptable excipient is selected from fillers, binders, disintegrants, matrix agents, glidants/lubricants or mixtures thereof.
Microcrystalline cellulose is used as filler in both layers. In addition, the composition may comprise one more filler is selected from the group comprising anhydrous lactose, lactose, starch, mannitol, calcium hydrogen phosphate dihydrate, dicalcium hydrogen phosphate
anhydrate, calcium phosphate trihydrate, silicon dioxide, neutral pellets, magnesium carbonate, magnesium oxide, maltodextrin, maltose or mixtures thereof.
According to one embodiment of the present invention, using microcrystalline cellulose in both layers ensures homogeneous distribution of dapagliflozin, which is used in small amounts in the composition. In addition, the composition comprises anhydrous lactose as filler. Preferably, anhydrous lactose is used at second layer. So, the desired dissolution profile is provided.
According to one embodiment of the present invention, second layer also comprises anhydrous lactose as a filler.
According to one embodiment of the present invention, the amount of fillers is 15.0% to 40.0% by weight in the total composition. This ratio provides the desired dissolution profile and content uniformity and good flowability.
Suitable binders are selected from the group comprising hydroxypropyl methylcellulose, carboxymethylcellulose sodium, polyvinylpyrrolidone (povidone), lactose anhydrous, pregelatinized starch, calcium carbonate, calcium phosphate dibasic, calcium phosphate tribasic, calcium sulphate, hydroxypropylcellulose, methyl cellulose, ethyl cellulose or mixtures thereof.
According to one embodiment of the present invention, the binder is hydroxypropyl methylcellulose (E5 LV) or carboxymethylcellulose sodium or mixtures thereof. The binders are used in the first layer.
According to one embodiment of the present invention, the amount of binders is 1.0% to 15.0% by weight in the total composition. Preferably, the amount of binders is 2.0% to 8.0% by weight in the total composition. This provides the desired dissolution profile.
Suitable disintegrants are selected from the group comprising croscarmellose sodium, crospovidone, sodium starch glycollate, sodium alginate, gums, starch and magnesium aluminum silicate or a mixture thereof.
According to one embodiment of the present invention, it has been surprisingly found that, the weight ratio of disintegrant to amorphous dapagliflozin is 1.0 - 4.0, preferably 1.2 - 3.5 in the immediate release layer provides bilayer tablet composition of dapagliflozin with good dissolution and solubility, thus high bioavailability.
According to one embodiment of the present invention, the disintegrant is croscarmellose sodium. The disintegrant is used in the second layer.
According to one embodiment of the present invention, the amount of disintegrants is 0.1% to 5.0% by weight in the total composition. This amount of disintegrants provides the desired dissolution profile.
Suitable glidants/lubricants are selected from group comprising colloidal silicon dioxide, sodium stearyl fumarate, magnesium oxide, starch, silica colloidal anhydrous, talc, polyethylene glycol, stearic acid, aluminum silicate, magnesium silicate, colloidal silica or mixtures thereof.
According to one embodiment of the present invention, the glidants/lubricants is colloidal silicon dioxide or sodium stearyl fumarate or mixtures thereof.
According to one embodiment of the present invention, the amount of glidants/lubricants is 0.2% to 10.0% by weight in the total composition.
According to one embodiment of the present invention, the extended release formulation in first layer is prepared using matrix agents.
Suitable matrix agents are selected from the group comprising hydroxypropylmethyl cellulose, ethyl cellulose, polymethylmethacrylate derivatives’s, poloxamer, polyvinyl alcohol, xanthan gum, sodium alginate, polymethacrylates, polyacrylamide, hydroxypropyl cellulose, polyvinyl acetate, cellulose acetate phthalate, ethylene vinyl acetate, methyl aminoethyl methacrylate, neutral methacrylic acid esters, polylactide, polylactide co-glycolide, diethyl aminoethyl methacrylate or mixtures thereof.
According to one embodiment of the present invention, the matrix agent is hydroxypropyl methyl cellulose (K100 MCR/ K100M/ CN10T), it is used only at first layer.
According to one embodiment of the present invention, the amount of matrix agents is 20.0% to 35.0% by weight in the total composition.
According to one embodiment of the present invention, the amount of matrix agents is 26.0% to 30.0% by weight in the total composition.
According to one embodiment of the present invention, the bilayer tablet composition is coated with at least one film coating agent.
Suitable film coating agents are selected from the group comprising polymethacrylates, hydroxypropyl methylcellulose, lactose monohydrate, talc, hydroxypropyl cellulose, polyvinyl alcohol (PVA), polyethylene glycol (PEG), glycerin, polyvinyl alcohol-polyethylene glycol copolymers (Kollicoat® IR), ethylcellulose dispersions (Surelease®), polyvinylprolidone, polyvinylprolidone-vinyl acetate copolymer (PVP-VA), iron oxide yellow, iron oxides, all kinds of Opadry®, pigments, dyes, titanium dioxide, coloring agent or mixtures thereof.
According to an embodiment of the present invention, the film coating agents are selected from the group comprising polyvinyl alcohol, talc, titanium dioxide, polyethylene glycol, yellow iron oxide.
According to an embodiment of the present invention, the amount of film coating agents is 0.5% to 5.0% by weight in the total composition.
In this invention, the bilayer tablet composition comprising amorphous dapagliflozin and metformin HCI is stable. The combination does not show incompatibilities, degradation problems, or extraction problems with certain excipients such as amorphous dapagliflozin, metformin HCI, microcrystalline cellulose, anhydrous lactose, croscarmellose sodium, carboxymethylcellulose sodium (7 HF), hydroxypropylmethylcellulose (E5 LV), hydroxypropylmethylcellulose (K100 MCR/ K100M/ CN10T), colloidal silicon dioxide, sodium stearyl fumarate and coating agents.
The present invention provides bilayer tablets comprising an extended release formulation, wherein the first layer comprises metformin HCI as active ingredient, microcrystalline cellulose as filler, hydroxypropylmethylcellulose (E5 LV) and carboxymethylcellulose sodium (7 HF) as binder, hydroxypropylmethylcellulose (K100 MCR/ K100M/ CN10T) as a matrix agent, sodium stearyl fumarate as glidant/lubricant, as well as an immediate release formulation of amorphous dapagliflozin wherein the second layer comprises amorphous dapagliflozin as active agent, microcrystalline cellulose and anhydrous lactose as a filler, croscarmellose sodium as disintegrant, colloidal silicon dioxide and sodium stearyl fumarate as glidant/ lubricant.
According to an embodiment of the present invention, the first layer comprises metformin HCI as active ingredient, microcrystalline cellulose as filler, hydroxypropylmethylcellulose (E5 LV) and carboxymethylcellulose sodium as binder, hydroxypropylmethylcellulose (K100 MCR or K100M or CN10T) as a matrix agent, sodium stearyl fumarate as glidant/lubricant.
According to an embodiment of the present invention, the second layer comprises amorphous dapagliflozin as active agent, microcrystalline cellulose and anhydrous lactose as
a filler, croscarmellose sodium as disintegrant, colloidal silicon dioxide and sodium stearyl fumarate as glidant/ lubricant.
The present invention is described in more detail by the following examples. The example is not to limit the scope of the invention but should be considered in the light of the details described above.
The above-mentioned pharmaceutical bilayer tablet at example 1 or 2 is prepared as follows: The first layer (extended release layer): a) Sieving metformin and grinding, b) Mixing metformin, carboxymethylcellulose sodium (7 HF), hydroxypropylmethylcellulose (E5 LV) in the granulator and obtained a dry mixture, c) Granulating the dry mixture with pure water and then obtained wet granules, d) Drying the wet granules at fluid bed dryer and then sieving, e) Mixing the granules and hydroxypropylmethylcellulose (K100 MCR/ K100M/ CN10T),
f) Adding microcrystalline cellulose and then mixing, g) Adding sodium stearyl fumarate and then mixing.
The second layer (immediate release layer): h) Mixing amorphous dapagliflozin and colloidal silicon dioxide, i) Adding anhydrous lactose, croscarmellose sodium and mixing, and then sieving, j) Adding the half of microcrystalline cellulose and mixing, then adding the remaining part of microcrystalline cellulose and then mixing and then sieving, k) Adding sodium stearyl fumarate and mixing,
Tablet compression: The first layer and second layer are compressed to form a bilayer tablet.
Film coating: Opadry II 85F230167 ORANGE (%20 a/a)
With the invention, surprisingly, a bilayer tablet formulation of metformin HCI and amorphous dapagliflozin with the desired release profile is obtained. The immediate release and extended release layers in the bilayer tablet have been used in such proportions, so that a formulation with suitable and desired properties could be obtained which provides up to 24 hours of release. The start of treatment is achieved at the desired level depending on the dissolution rate of the immediate release layer.
Claims
1. A pharmaceutical bilayer tablet composition comprising; a. first layer comprising metformin hydrochloride, b. second layer comprising amorphous dapagliflozin, wherein both layers comprising microcrystalline cellulose as a filler and at least one pharmaceutical acceptable excipient.
2. The pharmaceutical bilayer tablet composition according to claim 1, wherein the first layer has extended release formulation and the second layer has immediately release formulation.
3. The pharmaceutical bilayer tablet composition according to claim 1, wherein the amount of metformin hydrochloride is 25.0% to 50.0% by weight in the total composition.
4. The pharmaceutical bilayer tablet composition according to claim 1, wherein the amount of amorphous dapagliflozin is 0.05% to 5.0% by weight in the total composition.
5. The pharmaceutical bilayer tablet composition according to claim 1, wherein at least one pharmaceutically acceptable excipient is selected from fillers, binders, disintegrants, matrix agents, glidants/lubricants or mixtures thereof.
6. The pharmaceutical bilayer tablet composition according to claim 5, wherein one more filler is selected from the group comprising anhydrous lactose, lactose, starch, mannitol, calcium hydrogen phosphate dihydrate, dicalcium hydrogen phosphate anhydrate, calcium phosphate trihydrate, silicon dioxide, neutral pellets, magnesium carbonate, magnesium oxide, maltodextrin, maltose or mixtures thereof.
7. The pharmaceutical bilayer tablet composition according to claim 1, wherein second layer also comprising anhydrous lactose as a filler.
8. The pharmaceutical bilayer tablet composition according to claim 5, wherein the amount of fillers is 15.0% to 40.0% by weight in the total composition.
9. The pharmaceutical bilayer tablet composition according to claim 5, wherein binders are selected from the group comprising hydroxypropyl methylcellulose, carboxymethylcellulose sodium, polyvinylpyrrolidone, lactose anhydrous, pregelatinized starch, calcium carbonate, calcium phosphate dibasic, calcium
phosphate tribasic, calcium sulphate, hydroxypropylcellulose, methyl cellulose, ethyl cellulose or mixtures thereof. The pharmaceutical bilayer tablet composition according to claim 5, wherein disintegrants are selected from the group comprising croscarmellose sodium, crospovidone, sodium starch glycollate, sodium alginate, gums, starch and magnesium aluminum silicate or a mixture thereof. The pharmaceutical bilayer tablet composition according to claim 5, wherein glidants/lubricants are selected from group comprising colloidal silicon dioxide, sodium stearyl fumarate, magnesium oxide, starch, silica colloidal anhydrous, talc, polyethylene glycol, stearic acid, aluminum silicate, magnesium silicate, colloidal silica or mixtures thereof. The pharmaceutical bilayer tablet composition according to claim 5, wherein matrix agents are selected from the group comprising hydroxypropylmethyl cellulose, ethyl cellulose, polymethylmethacrylate derivatives’s, poloxamer, polyvinyl alcohol, xanthan gum, sodium alginate, polymethacrylates, polyacrylamide, hydroxypropyl cellulose, polyvinyl acetate, cellulose acetate phthalate, ethylene vinyl acetate, methyl aminoethyl methacrylate, neutral methacrylic acid esters, polylactide, polylactide coglycolide, diethyl aminoethyl methacrylate or mixtures thereof. The pharmaceutical bilayer tablet composition according to claim 1, wherein the first layer comprising metformin HCI as active ingredient, microcrystalline cellulose as filler, hydroxypropylmethylcellulose and carboxymethylcellulose sodium as binder, hydroxypropylmethylcellulose as a matrix agent, sodium stearyl fumarate as glidant/lubricant. The pharmaceutical bilayer tablet composition according to claim 1, wherein the second layer comprising amorphous dapagliflozin as active agent, microcrystalline cellulose and anhydrous lactose as a filler, croscarmellose sodium as disintegrant, colloidal silicon dioxide and sodium stearyl fumarate as glidant/ lubricant.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
TR2022/000397 TR2022000397A2 (en) | 2022-01-13 | A TWO-LAYER TABLET COMPOSITION CONTAINING AMORPHOUS DAPAGLIFLOZIN AND METFORMIN | |
TR2022000397 | 2022-01-13 |
Publications (2)
Publication Number | Publication Date |
---|---|
WO2023136797A2 true WO2023136797A2 (en) | 2023-07-20 |
WO2023136797A3 WO2023136797A3 (en) | 2023-08-17 |
Family
ID=87278498
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/TR2023/050022 WO2023136797A2 (en) | 2022-01-13 | 2023-01-11 | A bilayer tablet composition comprising amorphous dapagliflozin and metformin |
Country Status (1)
Country | Link |
---|---|
WO (1) | WO2023136797A2 (en) |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
HUE040486T2 (en) * | 2009-11-13 | 2019-03-28 | Astrazeneca Ab | Bilayer tablet formulations |
TR201202948A2 (en) * | 2012-03-15 | 2012-07-23 | Ali̇ Rai̇f İlaç Sanayi̇ A.Ş. | Tablet formulation comprising dapaglyphlosin and prolonged release metaphormin. |
KR20200005320A (en) * | 2018-07-06 | 2020-01-15 | 한미약품 주식회사 | Pharmaceutical formulation including amorphous dapagliflozin l-proline and preparation method thereof |
-
2023
- 2023-01-11 WO PCT/TR2023/050022 patent/WO2023136797A2/en unknown
Also Published As
Publication number | Publication date |
---|---|
WO2023136797A3 (en) | 2023-08-17 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN110548026B (en) | Pharmaceutical composition containing glucokinase activator and K-ATP channel blocker, and preparation method and application thereof | |
CA2652712C (en) | Stabilized pharmaceutical compositions comprising fesoterodine | |
RU2377976C2 (en) | PHARMACEUTICAL MULTILAYERED TABLET FOR CONTROLLED RELEASED OF ACTIVE COMPONENTS WITH SOLUBILITY, HIGHLY DEPENDING ON pH | |
EP4051246A1 (en) | Bilayer tablet formulations comprising dapagliflozin and metformin | |
US9616027B2 (en) | Pramipexole sustained release tablet formulation and manufacturing method thereof and use thereof | |
KR20130078101A (en) | Fixed dose combination formulation comprising losartan, amlodipine and hydrochlorothiazide | |
WO2021254409A1 (en) | Pharmaceutical composition of complex and preparation method therefor | |
WO2023136797A2 (en) | A bilayer tablet composition comprising amorphous dapagliflozin and metformin | |
US20150250734A1 (en) | Stable pharmaceutical compositions of saxagliptin or salts thereof | |
EP4212150A1 (en) | A bilayer tablet composition comprising amorphous dapagliflozin and metformin | |
WO2022225489A1 (en) | A bilayer tablet formulation comprising amorphous dapagliflozin and metformin | |
WO2022115053A1 (en) | Multi-layered tablet formulation with extended release layer of metformin hydrochloride | |
TR2022000397A2 (en) | A TWO-LAYER TABLET COMPOSITION CONTAINING AMORPHOUS DAPAGLIFLOZIN AND METFORMIN | |
WO2022119543A1 (en) | A process for tablet formulations comprising amorphous dapagliflozin and metformin hydrochloride | |
WO2014096983A1 (en) | Stable pharmaceutical compositions of saxagliptin or salts thereof | |
TR2021006927A2 (en) | A DOUBLE-LAYER TABLET FORMULATION CONTAINING AMORPHOUS DAPAGLIFLOZIN AND METFORMIN | |
KR102258372B1 (en) | Release Controlled Oral Formulation of Bepotastine | |
WO2022036506A1 (en) | Composition and use of sglt-2 inhibitor and angiotensin receptor blockers | |
KR20090107960A (en) | Pharmaceutical formulation for treating cardiovascular disease | |
WO2022119541A1 (en) | A film coated tablet formulation comprising dapagliflozin and metformin hydrochloride | |
WO2022119540A2 (en) | A process for formulations of dapagliflozin and metformin hydrochloride | |
US20240122858A1 (en) | Modified-release dosage forms of ruxolitinib | |
WO2022119542A1 (en) | Solid pharmaceutical formulations of amorphous dapagliflozin | |
WO2023234899A1 (en) | A bilayer tablet formulation comprising empagliflozin and metformin | |
CN115804774A (en) | Oxagolide pharmaceutical composition, pharmaceutical preparation containing same and application of pharmaceutical composition |