NZ613064B2 - Medical device containing a cake composition comprising aripiprazole as an active ingredient, and a cake composition comprising aripiprazole as an active ingredient - Google Patents
Medical device containing a cake composition comprising aripiprazole as an active ingredient, and a cake composition comprising aripiprazole as an active ingredient Download PDFInfo
- Publication number
- NZ613064B2 NZ613064B2 NZ613064A NZ61306412A NZ613064B2 NZ 613064 B2 NZ613064 B2 NZ 613064B2 NZ 613064 A NZ613064 A NZ 613064A NZ 61306412 A NZ61306412 A NZ 61306412A NZ 613064 B2 NZ613064 B2 NZ 613064B2
- Authority
- NZ
- New Zealand
- Prior art keywords
- cake composition
- cake
- aripiprazole
- syringe
- composition
- Prior art date
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- 239000000203 mixture Substances 0.000 title claims abstract description 349
- 229960004372 aripiprazole Drugs 0.000 title claims abstract description 113
- CEUORZQYGODEFX-UHFFFAOYSA-N Aripirazole Chemical compound ClC1=CC=CC(N2CCN(CCCCOC=3C=C4NC(=O)CCC4=CC=3)CC2)=C1Cl CEUORZQYGODEFX-UHFFFAOYSA-N 0.000 title claims abstract description 111
- 239000004480 active ingredient Substances 0.000 title claims abstract description 38
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- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 1
- 239000000825 pharmaceutical preparation Substances 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
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- 150000003904 phospholipids Chemical class 0.000 description 1
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- 229920005678 polyethylene based resin Polymers 0.000 description 1
- 229920005672 polyolefin resin Polymers 0.000 description 1
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- 235000010482 polyoxyethylene sorbitan monooleate Nutrition 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920005673 polypropylene based resin Polymers 0.000 description 1
- 229920000136 polysorbate Polymers 0.000 description 1
- 229920000053 polysorbate 80 Polymers 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 229910000160 potassium phosphate Inorganic materials 0.000 description 1
- 239000008057 potassium phosphate buffer Substances 0.000 description 1
- 235000011009 potassium phosphates Nutrition 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000003223 protective agent Substances 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
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- 239000011347 resin Substances 0.000 description 1
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- 238000004904 shortening Methods 0.000 description 1
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- 235000019698 starch Nutrition 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 229960004274 stearic acid Drugs 0.000 description 1
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- 230000008961 swelling Effects 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- OULAJFUGPPVRBK-UHFFFAOYSA-N tetratriacontyl alcohol Natural products CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCO OULAJFUGPPVRBK-UHFFFAOYSA-N 0.000 description 1
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- 235000010487 tragacanth Nutrition 0.000 description 1
- 239000000196 tragacanth Substances 0.000 description 1
- 229940116362 tragacanth Drugs 0.000 description 1
- LWIHDJKSTIGBAC-UHFFFAOYSA-K tripotassium phosphate Chemical compound [K+].[K+].[K+].[O-]P([O-])([O-])=O LWIHDJKSTIGBAC-UHFFFAOYSA-K 0.000 description 1
- LENZDBCJOHFCAS-UHFFFAOYSA-N tris Chemical compound OCC(N)(CO)CO LENZDBCJOHFCAS-UHFFFAOYSA-N 0.000 description 1
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- HEBKCHPVOIAQTA-SCDXWVJYSA-N xylitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)CO HEBKCHPVOIAQTA-SCDXWVJYSA-N 0.000 description 1
- 235000010447 xylitol Nutrition 0.000 description 1
- 229960002675 xylitol Drugs 0.000 description 1
Classifications
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/496—Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
-
- 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
- A61K9/0019—Injectable compositions; Intramuscular, intravenous, arterial, subcutaneous administration; Compositions to be administered through the skin in an invasive manner
-
- 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
- A61K9/0019—Injectable compositions; Intramuscular, intravenous, arterial, subcutaneous administration; Compositions to be administered through the skin in an invasive manner
- A61K9/0024—Solid, semi-solid or solidifying implants, which are implanted or injected in body tissue
-
- 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
- A61K9/10—Dispersions; Emulsions
-
- 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
- A61K9/14—Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
- A61K9/19—Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles lyophilised, i.e. freeze-dried, solutions or dispersions
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M5/00—Devices for bringing media into the body in a subcutaneous, intra-vascular or intramuscular way; Accessories therefor, e.g. filling or cleaning devices, arm-rests
- A61M5/178—Syringes
- A61M5/19—Syringes having more than one chamber, e.g. including a manifold coupling two parallelly aligned syringes through separate channels to a common discharge assembly
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M5/00—Devices for bringing media into the body in a subcutaneous, intra-vascular or intramuscular way; Accessories therefor, e.g. filling or cleaning devices, arm-rests
- A61M5/178—Syringes
- A61M5/28—Syringe ampoules or carpules, i.e. ampoules or carpules provided with a needle
- A61M5/284—Syringe ampoules or carpules, i.e. ampoules or carpules provided with a needle comprising means for injection of two or more media, e.g. by mixing
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M5/00—Devices for bringing media into the body in a subcutaneous, intra-vascular or intramuscular way; Accessories therefor, e.g. filling or cleaning devices, arm-rests
- A61M5/178—Syringes
- A61M5/31—Details
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/18—Antipsychotics, i.e. neuroleptics; Drugs for mania or schizophrenia
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B65—CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
- B65B—MACHINES, APPARATUS OR DEVICES FOR, OR METHODS OF, PACKAGING ARTICLES OR MATERIALS; UNPACKING
- B65B3/00—Packaging plastic material, semiliquids, liquids or mixed solids and liquids, in individual containers or receptacles, e.g. bags, sacks, boxes, cartons, cans, or jars
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F04—POSITIVE - DISPLACEMENT MACHINES FOR LIQUIDS; PUMPS FOR LIQUIDS OR ELASTIC FLUIDS
- F04C—ROTARY-PISTON, OR OSCILLATING-PISTON, POSITIVE-DISPLACEMENT MACHINES FOR LIQUIDS; ROTARY-PISTON, OR OSCILLATING-PISTON, POSITIVE-DISPLACEMENT PUMPS
- F04C2270/00—Control; Monitoring or safety arrangements
- F04C2270/04—Force
- F04C2270/042—Force radial
- F04C2270/0421—Controlled or regulated
Abstract
medical device in the form of a dual chamber syringe (1) is disclosed. The syringe (1) contains a separately prepared freeze-dried cake composition (8) comprising aripiprazole as an active ingredient. The syringe (1) includes a storage container where the inner wall of the container is treated with silicone and a space is provided between the inner wall of the storage container and the cake composition (8). The cake composition (8) has a cylindrical shape and a side surface of the cake composition (8) is sloped. h silicone and a space is provided between the inner wall of the storage container and the cake composition (8). The cake composition (8) has a cylindrical shape and a side surface of the cake composition (8) is sloped.
Description
DESCRIPTION
Title of Invention: MEDICAL DEVICE CONTAINING A CAKE COMPOSITION
COMPRISING ARIPIPRAZOLE AS AN ACTIVE INGREDIENT, AND A CAKE
COMPOSITION COMPRISING ARIPIPRAZOLE AS AN ACTIVE INGREDIENT
Technical Field
The present invention relates to a medical device
equipped with a storage container containing a separately
prepared freeze-dried cake composition comprising aripiprazole as
an active ingredient, wherein there is a space between an inner
wall of the storage container and the cake composition, and a
cake composition comprising aripiprazole as an active ingredient
and having a specific strength.
Background Art
Aripiprazole, which is used as an active ingredient in
pharmaceutical compositions, is known as an atypical
antipsychotic useful for the treatment of schizophrenia, and is
represented by the following structural formula:
A pharmaceutical composition comprising aripiprazole as
an active ingredient is used, for example, by the following
method: the pharmaceutical composition is suspended in a
dispersion medium, and the thus-obtained suspension is freeze-
dried, thereby preparing a cake composition. The cake composition
is mixed with a desired dispersion medium (injection liquid) and
thereby resuspended at the time of use. The resuspension is then
intramuscularly or subcutaneously injected (for example, see
Patent Literature 1 and 2).
Such a cake composition is produced by freeze-drying a
medical fluid in a medical device such as a syringe, which also
serves as a storage container (for example, see Patent Literature
3). Additionally, Patent Literature 3 employs a form, a so-called
dual-chamber syringe, in which after a solution is freeze-dried
to prepare a freeze-dried substance in a syringe, the syringe is
sealed by a stopper, and further, an injection liquid is enclosed
in a separate chamber in the syringe.
The medical device having a syringe-like shape has a
syringe tube whose inner wall is treated with silicone so as to
allow a sealing plug, such as a stopper, to smoothly slide in the
syringe tube.
However, when a freeze-dried substance is prepared in a
storage container by enclosing a medical fluid of a
pharmaceutical composition and freeze-drying the medical fluid in
the storage container, the freeze-dried substance comes into
contact with the silicone-treated inner wall of the storage
container, and the silicone used for treating the inner wall of
the storage container may be mixed into the freeze-dried
substance due to a long period (several months) of storage.
Citation List
Patent Literature
PTL 1: US Patent No. 5006528
PTL 2: Japanese Unexamined Patent Publication No. 2007-509148
PTL 3: Japanese Unexamined Patent Publication No. H8-112333
Summary of Invention
Technical Problem
When a freeze-dried substance was prepared in a storage
container whose inner wall had been treated with silicone by
enclosing a suspension (dispersion) of a pharmaceutical
composition comprising aripiprazole as an active ingredient and
freeze-drying the suspension (dispersion) in the storage
container, and when the silicone was mixed into the freeze-dried
substance due to a long period (several months) of storage and
the mixture was resuspended in a dispersion medium, the
phenomenon of agglomeration of aripiprazole in the suspension was
observed. Specifically, it became clear that there is a problem
in that the presence of silicone causes an increase in the mean
particle size of aripiprazole in the resuspension.
Such agglomeration of aripiprazole results in a reduced
dissolution rate because the contacted area of the particles does
not contribute to dissolving the particles. When the dissolution
rate changes as described above, it results in a dissolution
profile in which blood levels differ between the aripiprazole
dispersion in the suspension before being subjected to freeze-
drying and the aripiprazole dispersion in the suspension obtained
by resuspending the freeze-dried substance. This considerably
affects the drug efficacy, and poses serious problems as follows:
the medicinal properties of aripiprazole are unable to
sufficiently exhibit their efficacy; clogging occurs when the
drug is used in an injection form; and physical stimulus occurs
at the injection site due to increased particle size.
An object of the present invention is to provide, with
respect to the above problems, a medical device containing a cake
composition comprising aripiprazole as an active ingredient and
capable of suppressing the agglomeration of aripiprazole in a
suspension obtained by resuspending a freeze-dried substance; and
a cake composition comprising aripiprazole as an active
ingredient, and/or to at least provide the public with a useful
choice.
Solution to Problem
The present inventors conducted extensive studies in
order to solve the above problem and, as a result, found that
providing a space between the silicone-treated inner wall of the
storage container and the cake composition makes it possible to
reduce the frequency of contact between the silicone and the cake
composition, and to suppress the mixing of the silicone into the
suspension when the cake composition is resuspended. The present
inventors also found a cake composition that can inhibit the
breaking of the cake composition in the storage container, which
is caused by external physical impacts; reduce the frequency of
contact with the silicone used for treating the inner wall; and
quickly resuspend in a dispersion medium.
The present invention has been accomplished through
further studies based on the above findings.
Item 1. A medical device containing a separately
prepared freeze-dried cake composition comprising aripiprazole as
an active ingredient in a storage container whose inner wall is
treated with silicone, wherein there is a space between the inner
wall of the storage container and the cake composition, wherein
the cake composition has a cylindrical shape, and a side surface
of the cylindrical cake composition is sloped.
Item 2. The medical device containing the cake
composition according to Item 1, wherein the cake composition is
a mass that was freeze-dried in a container separate from the
storage container.
Item 3. The medical device containing the cake
composition according to Item 1 or 2, wherein the apparent volume
of the cake composition accounts for 30 to 99% of the volume of
the storage container.
Item 4. The medical device containing the cake
composition according to any one of Items 1 to 3, wherein the
cake composition has a cylindrical shape.
Item 5. The medical device containing the cake
composition according to Item 4, wherein a top surface of the
cylindrical cake composition is raised.
Item 6. The medical device containing the cake
composition according to Item 4 or 5, wherein a side surface of
the cylindrical cake composition is sloped.
Item 7. The medical device containing the cake
composition according to any one of Items 1 to 6, wherein the
storage container treated with silicone is a vial or syringe.
Item 8. The medical device containing the cake
composition according to Item 7, wherein the syringe has multiple
chambers and the cake composition is contained in at least one
chamber.
Item 9. The medical device containing the cake
composition according to Item 7, wherein the syringe has a first
chamber for containing the cake composition, and a second chamber
(for containing an injection liquid;
the first chamber is arranged on the side where a needle is
placed, and the second chamber is arranged on the side where a
plunger is placed; and
the cake composition is contained in the first chamber and
the injection liquid is contained in the second chamber.
Item 10. The medical device containing the cake
composition according to any one of Items 1 to 9, wherein the
cake composition has a strength of 5 to 100 N.
Item 11. A cake composition comprising aripiprazole as
an active ingredient and having a strength of 5 to 100 N, wherein
the cake composition has a cylindrical shape, and a side surface
of the cylindrical cake composition is sloped.
Item 12. The cake composition according to Item 11,
wherein the percentage of aripiprazole in the cake composition is
60 to 95% by mass.
Item 13. The cake composition according to Item 11 or
12, wherein the amount of aripiprazole in the cake composition is
0.1 to 0.6 g.
Item 14. The cake composition according to any one of
Items 11 to 13, obtained by freeze-drying 0.25 to 12 g of a
suspension having an aripiprazole solids content of 5 to 45% by
mass.
Item 15. The cake composition according to Item 14,
wherein a top surface of the cylindrical cake composition is
raised.
Item 16. The cake composition according to any one of
Items 11 to 15, wherein the cake composition is used for being
placed in a medical device.
Item 17. The cake composition according to Item 18,
wherein the cake composition is a mass that was freeze-dried in a
container separate from a storage container in the medical device.
Item 18. A method for producing a medical device
containing a cake composition comprising aripiprazole as an
active ingredient, the method comprising
a step of enclosing a separately prepared freeze-dried cake
composition comprising aripiprazole as an active ingredient in a
storage container whose inner wall is treated with silicone,
wherein there is a space between the inner wall of the storage
container and the cake composition, and the cake composition has
a cylindrical shape, and a side surface of the cylindrical cake
composition is sloped.
Item 19. The method for producing the medical device
according to Item 18, wherein the storage container treated with
silicone is a vial or syringe.
Item 20. The method for producing the medical device
according to Item 19, wherein the syringe has multiple chambers
and the cake composition is contained in at least one chamber.
Item 21. The method for producing the medical device
according to Item 20, wherein the syringe has a first chamber for
containing the cake composition, and a second chamber for
containing an injection liquid;
the first chamber is arranged on the side where a needle is
placed, and the second chamber is arranged on the side where a
plunger is placed; and
the cake composition is contained in the first chamber and
the injection liquid is contained in the second chamber.
The medical device recited in the above method for
producing a medical device is a medical device according to any
one of Items 1 to 10.
Item 22. A method for producing a cake composition
comprising aripiprazole as an active ingredient and having a
strength of 5 to 100 N, the method comprising
a step of freeze-drying a suspension comprising aripiprazole as
an active ingredient, wherein the cake composition has a
cylindrical shape, and a side surface of the cylindrical cake
composition is sloped.
The cake composition recited in the above method for
producing a cake composition is a cake composition according to
any one of Items 11 to 17.
The medical device containing a cake composition and
the cake composition of the present invention are described in
detail below.
The present invention relates to a medical device
containing a separately prepared freeze-dried cake composition
comprising aripiprazole as an active ingredient, in a storage
container whose inner wall is treated with silicone.
As used herein, the "cake" in the cake composition
means a dried solid that maintains the shape of the liquid before
being dried. For example, when a vial that has a columnar inner
shape is used, the cake is a dried solid that maintains the
columnar shape.
The cake composition of the present invention
comprising aripiprazole as an active ingredient can be produced
by freeze-drying a suspension comprising aripiprazole as an
active ingredient.
The cake composition is enclosed in a storage container
whose inner wall is treated with silicone, thereby allowing a
space to be provided between the storage container and the cake
composition. Providing a space between the silicone-treated inner
wall of the storage container and the cake composition as
described above makes it possible to suppress an increase in the
mean particle size of aripiprazole, which is caused by mixing of
the silicone into the cake composition when the cake composition
that has been stored for a long period of time is resuspended in
a dispersion medium. In other words, providing a space can
suppress the agglomeration of aripiprazole particles.
When a cake composition is produced by placing the
suspension in a conventional storage container and freeze-drying
the suspension therein, the cake composition adheres to the inner
wall of the storage container treated with silicone. Therefore,
when the cake composition is resuspended, a large amount of the
silicone is mixed into the suspension. This undesirably causes an
increase in the mean particle size of aripiprazole, which is an
active ingredient.
The treatment with silicone is performed on the inner
wall of the storage container. When the storage container is a
vial, for example, the inner wall of the storage container means
the inner side surface of the vial. When the storage container is
a syringe, the inner wall means the inner surface of the syringe
tube. In the vial, treating the inner wall with silicone provides
functions to reduce the amount of medical fluid remaining on the
inner surface of the vial and to minimize the amount of the
medical fluid inserted therein. Further, in the syringe, treating
the inner wall with silicone provides a function as a lubricant
for sliding a plunger and stoppers (sealing plugs) provided in
the syringe tube.
Treatment with silicone means to apply and adhere
silicone to the inner wall of the storage container and, if
necessary, dry the surface to which the silicone is applied.
A vial, syringe or the like is used as a storage
container that is treated with silicone. In the case of a syringe,
a prefilled syringe in which the cake composition is enclosed is
used. Therefore, the syringe itself also serves as a storage
container. Further, as a syringe, a single-chamber syringe or a
syringe having multiple chambers in which a cake composition is
contained in one of the chambers (hereinafter also referred to as
dual-chamber syringe) is used.
A dual-chamber syringe comprises a chamber (A) for
containing a cake composition and a chamber (B) for containing an
injection liquid (liquid for injection), and has a structure in
which the chamber (A) is arranged on the side where a needle is
placed and the chamber (B) is arranged on the side where a
plunger is placed. The dual-chamber syringe is described below,
with reference to the figures.
Fig. 1 is a cross-section view showing an embodiment of
a dual-chamber syringe. A dual-chamber syringe 1 comprises the
following stoppers (sealing plugs) in a syringe tube 2, in the
described order from the side where a needle is placed (i.e., an
end 6 side where a needle is placed): a front stopper 3, a middle
stopper 4 and an end stopper 5. The chamber A is defined by the
front stopper 3 and the middle stopper 4, and the chamber B is
defined by the middle stopper 4 and the end stopper 5. The front
stopper 3 may be dispensed with. A front assembly 12 that houses
the front stopper 3 when the syringe is used is provided to the
end 6 side. When the front stopper 3 is not provided, the syringe
1 may have a common shape in which the end of the syringe 1 but
not the front assembly is molded in a form to which a needle is
attached. When the front stopper 3 is provided, the front stopper
3 is housed in the front assembly 12, and a space is created
between the front stopper 3 and the front assembly 12, thereby
forming a passage for discharging a suspension obtained by
resuspending a cake composition 8 in an injection liquid 9
through the end 6.
The cake composition 8 is enclosed in the chamber (A),
and the injection liquid 9 for resuspending the cake composition
8 is enclosed in the chamber (B). Additionally, the inner wall of
the syringe tube 2 is treated with silicone 10. Further, a bypass
11 having a shape that externally protrudes from the inside of
the side surface of the syringe tube is provided to transfer the
injection liquid 9 to the chamber (A) in which the cake
composition 8 is enclosed. The bypass 11 is provided toward the
end 6 side from the middle stopper 4. During storage, the
injection liquid 9 is prevented from flowing into the chamber (A)
side.
The dual-chamber syringe 1 may comprise one bypass 11
or multiple bypasses 11.
The usage form of the dual-chamber syringe 1 when it is
used as a medical device of the present invention is explained
with reference to the attached Figs. 2 to 4.
A needle 13 is inserted into the end 6 of the dual-
chamber syringe 1, and a plunger 14 is inserted into an opening 7
(see Fig. 2).
The plunger 14 is pressed into the end 6 side from the
opening 7, and the end stopper 5 is thereby slid to the end 6
side. By further pressing in the plunger 14, the middle stopper 4
and the front stopper 3 are also slid as the end stopper 5 is
slid. When the middle stopper 4 reaches the bypass 11, the
injection liquid 9 is flowed through the bypass 11 into the
chamber (A) in which the cake composition 8 is enclosed (see Fig.
The cake composition in the chamber (A) is resuspended
by the injection liquid 9 that flowed therein, thereby giving a
suspension 15. Further, the front stopper 3 is housed in the
front assembly 12 as the plunger 14 is pressed in, and the
resuspension 15 is discharged from the end 6 into which the
needle 13 is inserted, through the space created between the
front stopper 3 and the front assembly 12 (see Fig. 4).
The length of the syringe tube in the syringe (the
length in which the stopper may be located) is preferably about
50 to 200 mm and more preferably about 70 to 110 mm.
Further, the distance from the center of the front
stopper to the center of the middle stopper is preferably about 5
to 40 mm and more preferably about 15 to 35 mm. The distance
between the center of the middle stopper to the center of the end
stopper is preferably about 2 to 50 mm and more preferably about
to 30 mm.
Further, the inner diameter of the syringe tube is
preferably about 5 to 30 mm and more preferably about 10 to 20 mm.
The thus-configured dual-chamber syringe is preferable
from the viewpoint that a cake composition and a dispersion
medium (injection liquid) for resuspending the cake composition
can be simultaneously enclosed in such a dual-chamber syringe and
the step of injecting a dispersion medium (injection liquid) can
therefore be omitted at the time of use.
When a single-chamber syringe is used as the storage
container, an injection liquid is introduced into the syringe
from the outside at the time of use, and the cake composition is
thereby resuspended for use.
The shape of the cake composition enclosed in the
storage container is not particularly limited, insofar as a space
is created between the inner wall of the storage container and
the cake composition. When the storage container is cylindrical
like a syringe tube, for example, the cake composition is
preferably formed in a cylindrical shape.
When the cake composition is cylindrical, it is
preferable that the container (which is separate from the storage
container) that is used for freeze-drying the cake composition be
molded using plastic so that the cake composition can be easily
removed from the container, and that the side of the container be
further sloped as shown in Fig. 5, for ease in molding the part
that will be in contact with a liquid. When the cake composition
is shaped so as to have the above-described slope, the angle ("a"
in Fig. 5) of the slope is preferably about 0.1 to 10 degrees and
more preferably about 0.5 to 3 degrees. The slope may be formed
partially or entirely around the circumference.
Further, as shown in Fig. 6, the top surface of the
cylindrical cake composition is raised. This provides an effect
of reducing the contact area with the storage container (for
example, in the case of the dual-chamber syringe, the contact
with the front stopper or the middle stopper is reduced). The
distance ("L" in Fig. 6) between the peak of the raised portion
and the top surface is preferably about 0.5 to 5 mm and more
preferably about 1 to 3 mm.
The cylindrical cake composition may have a raised
circumference to enable the contact area with the storage
container to be reduced (for example, in the case of the dual-
chamber syringe, to reduce the contact with the front stopper or
the middle stopper).
The apparent volume of the cake composition preferably
accounts for about 30% or more, more preferably about 40% or more
and still more preferably 50% or more of the volume of the
storage container, from the viewpoint of inhibiting the breaking
of the cake composition due to impact with the inner wall of the
storage container during production and transport of the medical
device of the present invention, and shortening the overall
length of the syringe. Further, the apparent volume of the cake
composition is preferably about 99% or less, more preferably
about 90% or less and still more preferably 80% or less, from the
viewpoint of reducing the frequency of adhesion of the cake
composition to the silicone used for treating the inner wall of
the storage container.
The term "apparent volume" means the volume of the cake
composition when the cake composition is regarded as a mass
without microscopic pores, spaces, cracks, and the like.
Further, the volume of the storage container refers to
the volume occupied by the portion in which the cake composition
is enclosed. For example, in the case of the below-described
dual-chamber syringe having multiple chambers, the volume of the
storage container means the volume of the chamber portion
(chamber (A)) in which the cake composition is enclosed.
The specific apparent volume of the cake composition is
preferably about 250 to 12,000 mm, more preferably about 500 to
5,000 mm and still more preferably 800 to 1,600 mm.
Further, the volume of the storage container is
preferably about 250 to 40,000 mm, more preferably about 500 to
17,000 mm and still more preferably 800 to 5,300 mm .
The cake composition is obtained in the following
manner: a cake composition is separately obtained by preparing a
suspension composition comprising aripiprazole as an active
ingredient and further freeze-drying the suspension composition,
and the separately obtained cake composition is transferred to
the storage container. Therefore, it is preferable to freeze-dry
the suspension in a container separate from the storage container
to produce a mass of the cake composition, and to transfer the
mass to the storage container.
Plastic is preferable as a material for the separate
container, with olefin-based resin and the like, for example,
being more preferable from the following viewpoints: although the
resulting cake composition slightly expands when freeze-dried in
the production of the cake composition, the expansion does not
result in strong adhesion between the cake composition and the
container, or even if adhesion occurs between the cake
composition and the container, the cake composition can be easily
removed from the container by deforming the container; when the
suspension must be aseptically prepared, the container can be
easily molded in an aseptic atmosphere and easily sterilized by
radiation; and such materials are low in cost and disposable.
Non-limiting examples of olefin resin include polyethylene-based
resin, polypropylene-based resin, and the like.
The shape of the container (which is separate from the
storage container), that is used for producing the cake
composition, is suitably determined depending on the shape of the
cake composition. Hereinbelow, a method for producing a
cylindrical cake composition is described with reference to the
figures, based on the shape of the container.
Fig. 7 is a schematic view showing the shape of the
container (which is separate from the storage container) used for
producing the cylindrical cake composition. The container 16 has
an opening 17 on the top. The suspension is poured through the
opening 17 and freeze-dried, thereby molding a cake composition
in the container 16. The molded cake composition can be easily
removed from the container 16 by pressing the bottom surface 18.
The inner surface of the container is preferably sloped to
facilitate removal of the cake composition. The angle (a’ in Fig.
7) is the same as the angle of the resulting cake composition.
The angle is preferably about 0.1 to 10 degrees and more
preferably about 0.5 to 3 degrees. The slope may be formed
partially or entirely around the circumference.
Further, the bottom surface of the container (which is
separate from the storage container) is preferably raised so that
the contact area with the storage container can be reduced (for
example, in the case of the dual-chamber syringe, the contact
with the front stopper or the middle stopper is reduced) and the
freeze-dried cake can be easily removed from the container (which
is separate from the storage container).
Further, in order to allow the resulting cake
composition to be easily removed by pressing the bottom surface
18, the container may be provided with an exterior frame 19 as
shown in the schematic view of Fig. 8 and in the cross-section
view of Fig. 9.
Examples of silicone applied to the inner surface of
the storage container include silicone oil or a silicone
derivative that is used in known medical applications.
Specifically, the silicone is a linear polymer having a siloxane
bond as a skeleton with a C alkyl group on the side chain. More
specifically, the silicone may be one with the repeating unit
represented by the following Formula (1):
Si O
In Formula (1), R and R are the same or different, and
each represents a hydrogen atom or a C hydrocarbon group, where
n is an integer of 1 to 1,000. Specific examples of the
hydrocarbon groups represented by R and R include a methyl group,
an ethyl group, a propyl group, a butyl group, a pentyl group,
and a hexyl group. When n is 2 or more, the repeating units may
be the same or different.
Specific examples of the silicone oil include dimethyl
polysiloxane. The silicone oil derivative may be one in which the
substituent on the side chain of the silicone, and/or some of the
terminal Si substituents are replaced with, for example, a
polyoxyalkylene group or a vinyl group.
The silicone oil and silicone oil derivative can be
obtained from commercially available products, for example, Shin-
Etsu Silicone KM72® and Shin-Etsu Silicone KF96ADF®, both
produced by Shin-Etsu Chemical Co., Ltd., and Dow Corning®
(produced by Dow Corning Corporation). An emulsion (Dow Corning®
365, 35% Dimethicone NF Emulsion (produced by Dow Corning
Corporation)) that contains a surfactant and water, can also be
used as the silicone oil.
The average molecular weight of the silicone is not
particularly limited, and is preferably from 10 to 100,000,000,
more preferably from 100 to 10,000,000, and still more preferably
from 200 to 10,000.
The mean particle size of the aripiprazole contained in
the cake composition that is stored in the storage container is
preferably 0.1 μm or larger, more preferably 0.5 μm or larger,
and still more preferably 1.5 μm or larger when it is used as a
sustained-release injectable preparation, because a sustained
release lasting as long as 1 month can be desirably obtained with
these ranges. From the standpoint of slowing settling, improving
ease of manufacture, and preventing needle clogging during
injection when, for example, a prefilled syringe is used as the
storage container, the mean particle size of the aripiprazole in
the cake composition is preferably smaller than 200 μm, more
preferably smaller than 10 μm, and still more preferably about 4
μm or smaller.
Here, the “mean particle size” refers to a volume mean
diameter as measured by a laser diffraction scattering method.
The particle distribution is measured using a laser diffraction
scattering method, and the mean particle size is calculated based
on the particle distribution.
From the viewpoint of attaining sufficient strength to
allow the cake composition to be removed from the container used
for freeze drying, which is separate from the storage container,
the content of the aripiprazole in the cake composition is
preferably about 60% by mass or more, more preferably about 65%
by mass or more, and still more preferably about 70% by mass or
more. Furthermore, the content of the aripiprazole in the cake
composition is preferably about 95% by mass or less, more
preferably about 90% by mass or less, and still more preferably
about 80% by mass or less in order to stabilize the dispersion of
the aripiprazole in a liquid containing a suspending agent and
the like.
The amount of the aripiprazole contained in the cake
composition is preferably about 0.1 g or more, and more
preferably about 0.15 g or more, and still more preferably about
0.2 g or more from the viewpoint of the dose that is necessary to
maintain the effective blood concentration required in the
treatment after administration into the body. Furthermore, the
amount of the aripiprazole contained in the cake composition is
preferably about 0.6 g or less, more preferably about 0.55 g or
less, and still more preferably about 0.5 g or less from the
viewpoint of safety with respect to the physical stimulus to the
body when administered at one time.
The aripiprazole contained in the cake composition is
known to exist in a variety of crystal forms, including
monohydrates (aripiprazole hydrate A), and many anhydrous forms,
specifically, such as anhydrous crystal B, anhydrous crystal C,
anhydrous crystal D, anhydrous crystal E, anhydrous crystal F,
and anhydrous crystal G. All of these forms may be used in the
cake composition of the present invention.
The cake composition of the present invention may also
appropriately contain other components, such as a suspending
agent, a bulking agent, a buffer, a pH adjuster, an excipient, a
lubricant, a fluidizer, a disintegrant, a binder, a surfactant, a
preservative, a flavoring agent, an odor improving agent, and a
tonicity agent, in addition to the aripiprazole that is used as
an active ingredient.
The additives may be those disclosed in Japanese
Unexamined Patent Publication No. 2007-509148 (Translation of
WO2005/041937).
The content of the suspending agent in the cake
composition is preferably about 0.1 to 10% by mass and more
preferably about 1 to 5% by mass. Preferable examples of
suspending agents include sodium carboxymethylcellulose,
hydroxypropylcellulose, carboxymethylcellulose,
hydroxypropylethylcellulose, hydroxypropylmethylcellulose, and
polyvinylpyrrolidone, or a mixture of two or more of these.
However, the suspending agent is not limited to these, and sodium
carboxymethylcellulose and polyvinylpyrrolidone can preferably be
used.
Examples of other suspending agents suited for use as
the vehicle for the aripiprazole include various polymers, low
molecular oligomers, natural products, and surfactants (both
nonionic and ionic). Specific examples include cetylpyridinium
chloride, gelatin, casein, lecithin (phosphatide), dextran,
glycerol, gum acacia, cholesterol, tragacanth, stearic acid,
benzalkonium chloride, calcium stearate, glyceryl monostearate,
cetostearyl alcohol, cetomacrogol emulsifying wax, sorbitan ester,
polyoxyethylenealkyl ether (for example, a macrogol ether such as
cetomacrogol 1000), a polyoxyethylene castor oil derivative, and
a polyoxyethylenesorbitan fatty acid ester (for example,
commercially available Tweens®, including Tween20® and Tween80®
(produced by ICI Specialty Chemicals)). Other examples include
polyethylene glycols (for example, Carbowaxes 3350® and 1450®,
and Carbopol 934® (produced by Union Carbide)),
dodecyltrimethylammonium bromide, polyoxyethylene stearate,
colloidal silicon dioxide, phosphate, sodium dodecyl sulfate,
carboxymethylcellulose calcium, hydroxypropylcellulose (for
example, HPC, HPC-SL, and HPC-L), methylcellulose,
hydroxyethylcellulose, hydroxypropylcellulose,
hydroxypropylmethyl-cellulose phthalate, noncrystalline cellulose,
magnesium aluminum silicate, triethanolamine, polyvinyl alcohol
(PVA), ethylene oxide-formaldehyde 4-(1,1,3,3-tetramethylbutyl)-
phenol polymers (also known as tyloxapol, superione, and triton),
poloxamers (for example, Pluronics F68® and F108®, which are
block copolymers of ethylene oxide and propylene oxide);
poloxamine (also known as, for example, Tetronic 908® and
Poloxamine 908®, which are tetrafunctional block copolymers
derived from the continuous addition of propylene oxide and
ethylene oxide to ethylenediamine (produced by BASF Wyandotte
Corporation, Parsippany, N.J.); charged phospholipids, such as
dimyristoylphosphatidylglycerol and dioctylsulfosuccinate (DOSS);
Tetronic 1508® (T-1508; produced by BASF Wyandotte Corporation),
dialkyl esters of sodium sulfosuccinate (for example, Aerosol OT®,
which is a dioctyl ester of sodium sulfosuccinate (produced by
American Cyanamid)); Duponol P® (a sodium lauryl sulfate;
produced by DuPont); Tritons X-200® (an alkylarylpolyether
sulfonate; produced by Rohm and Haas); Crodestas F-110® (a
mixture of sucrose stearate and sucrose distearate; produced by
Croda Inc.); p-isononylphenoxypoly-(glycidol) (also known as
Olin-10G® or Surfactant 10-G® (Olin Chemicals, Stamford, Conn.));
Crodestas SL-40® (produced by Croda, Inc.); SA9OHCO
(C H CH (CON(CH ))-CH (CHOH) (CH OH) (produced by Eastman Kodak
18 37 2 3 2 4 2 2
Co.); decanoyl-N-methylglucamide; n-decyl-β-D-glucopyranoside; n-
decyl-β-D-maltopyranoside; n-dodecyl-β-D-glucopyranoside; n-
dodecyl-β-D-maltoside; heptanoyl-N-methylglucamide; n-heptyl-β-D-
glucopyranoside; n-heptyl-β-D-thioglucoside; n-hexyl-β-D-
glucopyranoside; nonanoyl-N-methylglucamide; n-nonyl-β-D-
glucopyranoside; octanoyl-N-methylglucamide; n-octyl-β-D-
glucopyranoside; and octyl-β-D-thioglucopyranoside.
Most of these suspending agents are known
pharmaceutical excipients, and are described in detail in the
Handbook of Pharmaceutical Excipients, co-published by the
American Pharmaceutical Association and The Pharmaceutical
Society of Great Britain (The Pharmaceutical Press, 1986), which
is specifically incorporated herein by reference. The suspending
agents are commercially available, and can be produced by
techniques known in the art.
The content of the bulking agent (also called a
cryogenic/lyophilize protecting agent) in the cake composition is
preferably about 5 to 40% by mass, more preferably about 10 to
% by mass, and still more preferably about 15 to 25% by mass.
The bulking agent may be selected from, for example, mannitol,
sucrose, maltose, xylitol, glucose, starch, and sorbitol, or a
mixture of two or more of these. However, the bulking agent is
not limited to these, and mannitol can be preferably used.
Preferable examples of buffers include sodium phosphate,
disodium hydrogen phosphate, sodium dihydrogen phosphate,
potassium phosphate, and TRIS buffer, or a mixture of two or more
of these. However, the buffer is not limited to these, and sodium
phosphate, disodium hydrogen phosphate, and sodium dihydrogen
phosphate are preferably used.
When the cake composition is formed into a suspension
by being dispersed in a dispersion medium at the time of use, the
pH adjuster is used to adjust the pH of the aripiprazole
suspension to about 6 to 7.5, preferably about 7. When the pH of
the suspension obtained by dispersing the cake composition in a
dispersion medium is higher than the desired value, i.e., about 7,
an acidic pH adjuster is used. When the pH of the suspension is
lower than the desired value, i.e., about 7, a basic pH adjuster
is used. As the acidic pH adjuster, hydrochloric acid or acetic
acid, preferably hydrochloric acid is used. Examples of basic
adjusters include sodium hydroxide, potassium hydroxide, calcium
carbonate, magnesium oxide, and magnesium hydroxide. Among these,
sodium hydroxide is preferably used.
The suspension comprising aripiprazole before freeze-
drying as an active ingredient, which is the suspension being
used for preparing the cake composition, can be obtained by
mixing a dispersion medium with a composition suitably comprising
the aripiprazole (i.e., the active ingredient), the
aforementioned suspending agent, bulking agent, buffer, pH
adjuster, excipient, lubricant, fluidizer, disintegrant, binder,
surfactant, preservative, flavoring agent, odor improving agent,
tonicity agent and the like in such a manner that the contents
thereof will be in the desirable ranges described above.
As the dispersion media, water, or a hydrous solvent
containing water and an organic solvent is used. The organic
solvent is one that is miscible with water. Examples thereof
include alcohols, such as methanol, ethanol, propanol, and
isopropanol; ketones, such as acetone; ethers, such as
tetrahydrofuran; dimethylformamide; and mixtures thereof. Of
these, ethanol is particularly preferred. The amount of water
used for the hydrous solvent is not particularly limited, and is,
for example, preferably at least 10% by mass of the solvent.
Preferably, a wet pulverization technique is used, and
the dispersed aripiprazole particles are subjected to
pulverization in the presence of a pulverization medium to have a
desired mean particle size.
Preferably, an antiseptic wet pulverization technique,
such as wet ball milling, high-pressure homogenization, or high-
shear homogenization is used. In addition to these pulverization
techniques, a low-energy or high-energy mill (for example, a
roller mill) can also be used.
Use of, for example, controlled crystallization is also
possible.
A homogeneous suspension of aripiprazole having a
desired mean particle size can be obtained by using the above-
mentioned methods.
The mean primary particle size of the aripiprazole in
the suspension is preferably 0.1 μm or larger, more preferably
0.5 μm or larger, and still more preferably 1.5 μm or larger in a
sustained-release injectable preparation, because a sustained
release lasting as long as one month can be desirably obtained
with these ranges. From the standpoint of slowing settling,
improving ease of manufacture, and preventing needle clogging
during injections, the mean particle size of the aripiprazole in
the suspension is preferably smaller than 200 μm, more preferably
smaller than 10 μm, and still more preferably about 4 μm or
smaller.
The “mean particle size” can be measured using the same
method that was used to measure the cake composition. The term
“primary particle size” refers to the particle size of each
individual particle, not the particle size of agglomerated
particles.
The “mean particle size” refers to a volume mean
diameter as measured by a laser-light scattering method (LLS).
The particle distribution is measured by LLS, and the mean
particle size is calculated based on the particle distribution.
Aripiprazole with the desired mean primary particle
size can be produced by using preferably, for example, an
impinging jet crystallization method (see Japanese Unexamined
Patent Publication No. 2007-509153 (Translation of WO2005/041970)
filed by Bristol-Myers Squibb), or a wet pulverization method
that uses a high-pressure homogenizer (see Japanese Patent
Application No. 2007-200088 filed by Otsuka Pharmaceutical Co.,
Ltd.).
The crystal forms of the aripiprazole that is contained
in the suspension may be the same as those of the aripiprazole
contained in the cake composition.
The solids content of the aripiprazole in the
suspension is preferably about 5% by mass or more, more
preferably about 10% by mass or more, and still more preferably
about 20% by mass or more, since having such a solids content
reduces the size of the syringe by reducing the volume of the
cake after freeze-drying, imparts strength to the cake to resist
the generation of fine particles, and enables administration with
a smaller dose. Furthermore, the solids content of the
aripiprazole in the suspension is preferably about 45% by mass or
less, more preferably about 40% by mass or less, and still more
preferably about 35% by mass or less, since having such a solids
content achieves excellent production efficiency due to the good
fluidity of the liquid during production, and reduces the load on
manufacturing equipment due to the low viscosity.
The amount of aripiprazole contained in the suspension
is preferably about 0.1 g or more, more preferably about 0.15 g
or more, and still more preferably about 0.2 g or more, from the
viewpoint of the dose that is necessary to maintain the effective
blood concentration required in the treatment after
administration into the body. Furthermore, the amount of
aripiprazole contained in the suspension is preferably about 0.6
g or less, more preferably about 0.55 g or less, and still more
preferably about 0.5 g or less from the viewpoint of safety with
respect to the physical stimulus to the body when administered at
one time.
The cake composition can be prepared by freeze-drying
the suspension. The conditions for freeze-drying may be suitably
selected. For example, freeze-drying can be performed by freezing
the suspension at -50 to -30°C, followed by drying for 12 hours
under reduced pressure of preferably about 5 to 40 Pa and more
preferably about 5 to 20 Pa at a temperature of preferably about
-15 to 10°C and more preferably about -10 to 5°C.
The cake composition obtained by freeze-drying the
suspension does not break even if external physical impacts are
applied thereto, and is capable of maintaining its form as a mass.
The strength of the cake composition is preferably
about 5 N or more, more preferably about 10 N or more, and still
more preferably about 20 N or more from the following viewpoint.
That is, the cake composition does not break during production,
transport, or the like due to vibration from the outside, etc.;
the cake composition can be easily removed from the container
used for freeze drying, which is separate from the storage
container; etc. Furthermore, the strength of the cake composition
is preferably about 100 N or less, more preferably about 80 N or
less, and still more preferably about 50 N or less, from the
viewpoint, for example, that the cake composition can be quickly
suspended by a dispersion medium when used.
The strength of the cake composition can be measured
using an apparatus for measuring stress, such as an Autograph AG-
I Universal Testing Instruments (Shimazu Corporation). The
strength of the cake composition is measured, for example, by
pinching and pressing the cake composition in the vertical
direction (i.e., from the top and bottom) and measuring the
stress applied until it breaks.
When the cake composition is stored in a container
whose inner wall is treated with silicone, in order to reduce the
contact with the silicone, it is necessary to prevent the
generation of fine particles due to impacts applied during
transport, etc. Taking this into consideration, the amount of
fine particles formed by the breaking of the cake composition is
preferably about 100 mg or less, more preferably about 30 mg or
less, and still more preferably about 10 mg or less. Also from
the viewpoint of appearance, it is preferable that the generation
of fine particles be reduced. The weight of generated fine
particles is preferably about 25% or less, more preferably about
% or less, and still more preferably about 3% or less relative
to the total weight of the cake composition.
The breaking of the cake composition is evaluated in
the following manner. The cake composition is placed on a sieve
with a diameter of 80 mm and openings of 2 mm, and covered with a
lid at a location 22 mm above the sieve, and the sieve holding
the cake composition is secured in a Bioshaker V-BR-36 produced
by TAITEC Co., Ltd. After shaking at 300 rpm for 10 minutes, the
weight of the powder that has passed through the sieve is
measured.
The cake composition of the present invention may be
resuspended by adding the dispersion medium used to prepare the
suspension that was used before the freeze-drying. Examples of
the dispersion media used for this purpose include water
(preferably, distilled water), a polymer aqueous solution, and a
surfactant aqueous solution. The resulting resuspended solution
is used as an injection liquid.
The amount of the dispersion medium used for
resuspending the cake composition is not particularly limited as
long as it can be administered subcutaneously or intramuscularly.
The amount thereof is preferably 0.5 to 3 mL, and more preferably
1 to 2 mL.
The series of processes for obtaining a medical device
containing the cake composition of the present invention is
preferably conducted in a sterilized room.
The medical device containing the cake composition of
the present invention has a space between the cake composition
and the storage container whose inner wall is treated with
silicone. This prevents the cake composition from directly
contacting the silicone. Accordingly, it is possible to suppress
agglomeration of aripiprazole caused by the silicone applied to
the inner wall of the storage container when the freeze-dried
cake composition is resuspended after long-term storage.
The cake composition of the present invention that
comprises aripiprazole as an active ingredient has a specific
strength that prevents the cake composition from breaking when
external physical impacts are applied and allows the cake
composition to be quickly resuspended when mixed with a
dispersion medium at the time of use. Therefore, the cake
composition of the present invention is suitably used as a cake
composition enclosed in a medical device.
Advantageous Effects of Invention
The medical device containing the cake composition of
the present invention has a space between the cake composition
and the silicone-treated inner wall of the storage container.
This reduces the frequency that the cake composition will contact
the silicone, and lowers the risk that silicone will contaminate
the suspension when the cake composition is resuspended. This
allows the aripiprazole, which is an active ingredient contained
in the suspension after the resuspension, to be satisfactorily
redispersed without agglomerating.
Furthermore, because the cake composition of the
present invention containing aripiprazole as an active ingredient
has a specific strength, it will not break even when external
physical impacts are applied during production and transportation.
Moreover, the cake composition can be quickly dispersed without
agglomerating when resuspended in a dispersion medium at the time
of use.
Brief Description of Drawings
Fig. 1 is a sectional view illustrating one embodiment
of a dual chamber syringe.
Fig. 2 is a sectional view showing the dual chamber
syringe at the time of use.
Fig. 3 is a sectional view showing the dual chamber
syringe at the time of use.
Fig. 4 is a sectional view showing the dual chamber
syringe at the time of use.
Fig. 5 is a schematic diagram illustrating a
cylindrical cake composition having a sloped side surface.
Fig. 6 is a schematic diagram illustrating a
cylindrical cake composition having a sloped side surface and
raised top surface.
Fig. 7 is a schematic diagram illustrating one
embodiment of the shape of a container, which is separate from
the storage container, used for preparing the cylindrical cake
composition.
Fig. 8 is a schematic diagram illustrating one
embodiment of the shape of a container, which is separate from
the storage container, used for preparing the cake cylindrical
composition.
Fig. 9 is a sectional view of the schematic diagram
illustrating one embodiment of the shape of a container, which is
separate from the storage container, used for preparing the
cylindrical cake composition.
Fig. 10 is a photograph of the side surface of the cake
composition prepared in Example 1.
Fig. 11 is a photograph of the side surface of the cake
composition prepared in Example 6.
Description of Embodiments
Examples
The present invention is described below in more detail
with reference to Examples and Comparative Examples. It should be
understood, however, that the present invention is not limited to
the following embodiments.
• Example 1
The components shown below were individually dissolved
or suspended in water to prepare a dispersion containing the
components in the following amounts per 1 mL of the final
dispersion: 12.48 mg of carboxymethyl cellulose, 62.4 mg of
mannitol, 1.11 mg of sodium dihydrogen phosphate monohydrate, and
312.0 mg of aripiprazole hydrate. The pH was adjusted to about 7
with sodium hydroxide.
This suspension was preliminarily pulverized with a
high-shear rotary homogenizer (Clearmix, produced by M Technique
Co., Ltd.), and then repeatedly wet pulverized with a high-
pressure homogenizer (produced by Niro) at 550 bar to a mean
particle size of 3 μm or less to thereby produce a suspension of
about 30% aripiprazole.
About 1.7 mL of the suspension prepared above
(containing about 510 mg of aripiprazole) was inserted into a
polyethylene-molded plastic container having an inner side
surface sloped at an angle of 2° and having a bottom surface with
a thickness of 1 mm or less, the container being deformable so as
to allow ejection of a freeze-dried product therefrom when the
bottom surface is pressed from the outside. The container
containing the suspension was transferred to a freeze-dryer, and
freeze-dried according to the cycle described below to obtain a
cake composition. The theoretical content of aripiprazole in the
cake composition was about 77% by mass. The obtained cake
composition had an apparent volume that was substantially the
same as the volume originally inserted, with only a slight
increase being observed. Thus, the apparent volume was about
1,700 mm . Fig. 10 shows a photograph of the cake composition.
(a) Thermal treatment: The product was frozen by being maintained
at about -40°C for at least 3 hours.
(b) Primary drying: Primary drying was continued for at least 24
hours at an increased shelf temperature of about -5°C under a
pressure of about 20 Pa or less.
The obtained cake composition was removed from the
plastic container. The cake composition had a shape such that the
top surface was raised by 2 mm from the inserted liquid level,
and the side surface was sloped at an angle of 1° or more. Other
cake compositions prepared simultaneously were also measured. The
results showed that all of the cake compositions were raised by
0.5 mm or more.
The strength of the obtained cake composition was
measured using an Autograph AG-I Universal Testing Instruments
(Shimadzu Corporation) by sandwiching and pressing the cake
composition of Fig. 6 from the top and bottom. The cake
composition had a strength of 49 N.
Results and Discussion
The cake composition obtained in Example 1 had a
relatively high strength of 49 N. Therefore, the freeze-dried
cake composition was easily removed from the container without
being broken when ejected from the container.
The cake composition obtained in Example 1 was
characterized by slight swelling when freeze-dried. In Example 1,
the inner side surface of the plastic container was sloped.
Therefore, by using a container that could be deformed by
pressing the bottom surface, the freeze-dried cake composition
was easily removed from the container without the necessity of
using other movable parts for ejecting the cake composition from
the container or applying a release agent to the inner surface of
the container, while retaining its freeze-dried shape from within
the container.
• Examples 2-1 to 2-9
1. Production of Siliconized Syringe
Dow Corning365, 35% Dimethicone NF Emulsion (produced
by Dow Corning Corporation) was diluted to various concentrations
with purified water. The silicone oil emulsion thus prepared was
applied to a glass syringe (inner diameter Φ 14.0 x length 106
mm; inner area 4,660 mm, capacity 16,309 mm ), and the water was
evaporated to dryness at about 300°C.
The silicone oil applied to the inner surface of the
glass was quantified by washing the inner surface of the glass
tube with methyl isobutyl ketone, and then measuring the solution
using an atomic absorption spectrometer with an Si measurement
lamp under the following conditions.
Measurement wavelength: 251.6 nm
Drying: From 50 to 80°C, 40 sec
Ashing: 1,000°C, 20 sec
Atomization: 2,700°C, 5 sec
Cleaning: 2,800°C, 15 sec
Cooling: 17 sec
2. Resuspension of the Cake Composition
A suspension containing about 30% aripiprazole with a
mean particle size of 2.1 μm was prepared and freeze-dried in the
same manner as in Example 1 to obtain a cake composition.
The cake composition was transferred from the plastic
container to a siliconized syringe produced as described above in
1. A stopper was disposed within the syringe. To maintain
airtightness during storage, the stopper was characterized by
being slightly larger than the inner diameter of the syringe and
being slidable due to silicone oil applied to the inner side
surface of the syringe. The cake composition was transferred into
the syringe, and then stored at room temperature for about 1
month. The amount of silicone oil in the cake composition was
determined by extracting a resuspension of the cake composition
in water with methyl isobutyl ketone, and then measuring the
methyl isobutyl ketone solution using an atomic absorption
spectrometer.
After storage for about 1 month, the cake composition
was resuspended in about 2 mL of water, and the particle size in
the suspension was measured using a laser diffraction particle
size analyzer produced by Shimadzu Corporation (SALD-3000J or
SALD-3100). The measurement was done at a refractive index of
2.00 to 0.20i, using water as the measurement medium in a
circulation cell. Separately, the suspension was sonicated for 1
minute with an ultrasonic wave generator attached to the particle
size analyzer, and the mean particle size of the sonicated
suspension was measured in the same manner as described above.
Table 1 shows the mean particle size of aripiprazole
before freeze-drying, the concentration of silicone oil applied
to the syringe, the amount of silicone oil on the syringe, the
amount of silicone oil after 1-month storage of the syringe
containing the cake composition at room temperature and
resuspension of the cake composition, and the mean particle size
of aripiprazole after resuspension.
Table 1
One-month storage at room temperature
Mean
Amount of Mean particle size of
particle size
Concentration Amount of silicone oil aripiprazole (μm)
of silicone oil silicone oil in the cake
aripiprazole
Example in the on the
composition
in the
No. emulsion syringe after
suspension
Without With
(% by mass) (μg/100 mm resuspension
before
Ultrasonic ultrasonic
) (μg/100 mg
freeze-
treatment treatment
of the
drying (μm)
active
ingredient)
2-1 35 75 22 2.1 2.1
2-2 20 45 6 2.1 2.1
2-3 15 36 7 2.1 2.0
2-4 10 24 4 2.1 2.0
2-5 7 14 4 2.1 2.1
2-6 5 11 3 2.1 2.0
2-7 2 3 5 2.0 2.0
2-8 1 2 4 2.0 2.0
2-9 0.5 1 5 2.1 2.1
Reference
0 0 2 2.0 2.1
Example
Results and Discussion
As shown in Table 1, the amount of silicone oil in the
resuspended cake compositions varied according to the
concentration of silicone oil in the emulsion applied.
In addition, even when the concentration of silicone
oil in the emulsion applied was 0%, silicone oil was detected in
the cake composition (Reference Example). This was probably
because the silicone oil originally contained in the stopper had
transferred to the cake composition. However, because the cake
composition had a convex, i.e., raised, top surface as described
in Example 1, which minimized the contact of the cake composition
with the stopper, the amount of silicone oil mixed into the cake
composition was extremely small.
No change in the mean particle size of aripiprazole was
observed in any of the syringes prepared using various
concentrations of the silicone oil emulsions in Examples 2-1 to
2-9. Agglomeration of particles due to silicone oil can be
confirmed by a reduction of the particle size in the measurement
under ultrasonic irradiation. The particle size was measured
before and after ultrasonic irradiation, and no change was
observed in the particle size therebetween. Accordingly, it was
determined that no agglomeration had occurred.
Example 3
A suspension containing about 30 mass% aripiprazole was
prepared in the same manner as in Example 1, and freeze-dried to
obtain a cake composition.
A dual chamber syringe with an inner diameter of 14 mm
as shown in Fig. 1 (capacity of the chamber in which the cake
composition was enclosed: about 3,000 mm ) was used as the syringe,
and a middle stopper 4 as shown in Fig. 1 was fitted using the
sleeve cap method. After about 1.7 mL of water was inserted into
the syringe, an end stopper 5 was fitted using the sleeve cap
method.
The aripiprazole-containing cake composition obtained
by freeze-drying in a plastic container was removed from the
plastic container by pressing the bottom surface of the plastic
container, and directly transferred to a space on a middle
stopper 4 as shown in Fig. 1 in the syringe in which water was
inserted. A front stopper 3 as shown in Fig. 1 was fitted using
the sleeve cap method. A front assembly 12 as shown in Fig. 1 was
fitted onto the syringe to obtain a prefilled syringe containing
the cake composition with aripiprazole as an active ingredient.
The apparent volume of the cake composition was about
60% of the capacity of the storage container of the prefilled
syringe (the capacity of the chamber in which the cake
composition was enclosed). The end stopper was pressed by a
plunger to allow water as a redispersion medium to flow into the
chamber A in which the cake composition was enclosed. After
mixing, the syringe was vigorously shaken to achieve complete
resuspension. The end stopper was pressed to the end to expel the
medicinal fluid from the syringe. The amount of medicinal fluid
remaining in the syringe was measured and found to be about 36 to
40 mg (about 38 mg on average).
This is the amount of medicinal fluid remaining in the
gaps of the stopper and the front assembly, i.e., the so-called
dead space of the outlet. It was considered that the prefilled
syringe obtained by this method fully performed the functions
required for administration.
Likewise, using a prefilled syringe in which the cake
composition containing aripiprazole as an active ingredient was
enclosed, the end stopper was slowly pressed to allow water as a
redispersion medium to flow into a front chamber for about 5
seconds. Without shaking the syringe at all, the end stopper was
pressed to the end to expel the suspension from the syringe.
The amount of medicinal fluid remaining in the syringe
was measured and found to be about 74 to 95 mg (about 85 mg on
average). The amount of medicinal fluid remaining in the gaps of
the stopper and the front assembly, i.e., the so-called dead
space of the outlet, was about 38 mg on average. Since the
syringe was not shaken, about 47 mg, which was obtained by
subtracting 38 mg from 85 mg, remained in the syringe. However,
it was considered that the prefilled syringe obtained by this
method was satisfactory to perform the functions required for
administration.
• Example 4
The components shown below were individually dissolved
or suspended in water to prepare a dispersion containing the
components in the following amounts per 1 mL of the final
dispersion: 8.32 mg of carboxymethyl cellulose, 4.16 mg of
mannitol, 0.74 mg of sodium dihydrogen phosphate monohydrate, and
208.0 mg of aripiprazole hydrate. The pH was adjusted to about 7
with sodium hydroxide.
This suspension was preliminarily pulverized with a
high-shear rotary homogenizer (Clearmix, produced by M Technique
Co., Ltd.), and then repeatedly wet pulverized with a high-
pressure homogenizer (produced by Niro) at 550 bar to a mean
particle size of 3 μm or less to thereby produce a suspension
containing about 20 mass% aripiprazole.
About 2 mL of the suspension prepared above (containing
about 400 mg of aripiprazole) was inserted into a polyethylene-
molded plastic container having an inner side surface sloped at
an angle of 2° and having a bottom surface with a thickness of 1
mm or less, the container being deformable so as to allow
ejection of a freeze-dried product therefrom when the bottom
surface was pressed from the outside. The container containing
the suspension was transferred to a freeze-dryer, and freeze-
dried according to the cycle described below to obtain a cake
composition. The theoretical content of aripiprazole in the cake
composition was about 77% by mass. The obtained cake composition
had an apparent volume that was substantially the same as the
volume originally inserted, with only a slight increase being
observed. Thus, the apparent volume was about 2,000 mm .
(a) Thermal treatment: The product was frozen by being maintained
at about -40°C for at least 3 hours.
(b) Primary drying: Primary drying was continued for at least 24
hours at an increased shelf temperature of about -5°C under a
pressure of about 20 Pa or less.
The obtained cake composition was removed from the
plastic container by pressing the bottom surface of the plastic
container. The cake composition was easily removed from the
container while retaining its freeze-dried shape from within the
container, without the necessity of using other movable parts for
ejecting the cake composition from the container or applying a
release agent to the inner surface of the container.
Examples 5-1 to 5-3
A suspension containing about 30 mass% aripiprazole was
prepared in the same manner as in Example 1. This suspension was
diluted with purified water to suspensions containing about 10
mass%, 20 mass%, and 30 mass% aripiprazole. These suspensions
were freeze-dried in the same manner as in Example 1 to obtain
cake compositions. Table 2 shows the ease of removal of the
obtained cake compositions from the containers.
Table 2
Concentration of
Example Strength
aripiprazole Removal from the container
No. (N)
(% by mass)
-1 10.5 6.90 Smoothly removed from the container.
-2 20.8 42.29 Smoothly removed from the container.
-3 32.5 48.98 Smoothly removed from the container.
Results and Discussion
Each of the aripiprazole-containing cake compositions
obtained by freeze-drying in a plastic container was removed from
the plastic container by pressing the bottom surface of the
plastic container. All of the cake compositions obtained in
Examples 5-1 to 5-3 were easily removed from the containers. The
strength of the cake compositions obtained by freeze-drying was
measured using an Autograph AG-I Universal Testing Instruments
(Shimadzu Corporation) in the same manner as in Example 1. The
cake composition produced by using the suspension containing
about 10 mass% aripiprazole prepared in Example 5-1 had a
strength of about 7 N. Even when the container is configured to
allow easy removal, the cake composition must have some strength.
• Example 6
A container as described in Example 1 was produced
using polypropylene, and a cake composition was produced in the
same manner as in Example 1.
The cake composition obtained by freeze-drying in the
plastic container was removed from the plastic container by
pressing the bottom surface of the plastic container, and
directly transferred to a syringe. The cake composition was
easily removed from the container while retaining its freeze-
dried shape from within the container, without the necessity of
using other movable parts for ejecting the cake composition from
the container or applying a release agent to the inner surface of
the container. Fig. 11 shows a photograph of the cake composition
obtained.
It was confirmed that the obtained cake composition had
an elevated portion on the circumference of the upper surface.
The obtained cake composition was raised by 0.5 mm or more on the
circumference of the upper surface, although the shape was
different from that of the cake composition obtained using the
polyethylene container described above in Example 1.
The cake composition was enclosed in a syringe to
produce a prefilled syringe (capacity of the chamber in which the
cake composition was enclosed: about 3,500 mm). The apparent
volume of the cake composition was about 50% of the capacity of
the storage container of the prefilled syringe (the capacity of
the chamber in which the cake composition was enclosed). The
syringe used was a so-called single chamber type having only one
space for containing a medicinal agent. The freeze-dried cake
composition was easily resuspended by drawing water as a
redispersion medium into the syringe during the resuspension.
• Example 7
A suspension containing about 30 mass% aripiprazole was
obtained in the same manner as in Example 1. About 1.5 mL to
about 1.7 mL of this suspension was inserted into a polyethylene-
molded plastic container, and freeze-dried to obtain a cake
composition. The obtained cake composition weighed about 600 mg.
This cake composition was placed on a sieve with 2 mm openings
and a diameter of 80 mm, and covered with a lid that was 22 mm
above the sieve. The sieve was secured in a Bioshaker V-BR-36
produced by TAITEC Co., Ltd., and shaken at 300 rpm for 10
minutes. The amount of powder passing through the sieve openings
was about 1 to 9 mg.
Results and Discussion
The results of Example 7 showed that in spite of being
produced by freeze-drying, this cake composition was not brittle
and was less likely to break and generate fine powder due to
impacts during transportation, etc. Freeze-dried cake
compositions are generally brittle, and often break due to strong
impacts as in the above test. If fine powder is generated from
this pharmaceutical preparation, it may come into contact with
the silicone on the inner surface A in Fig. 1 and thereby
increase the particle size, etc.; furthermore, the generation of
fine powder would cause an undesirable appearance. The above
results showed that this production method can produce a cake
composition whose surface is not brittle and from which it is
unlikely to generate fine powder.
• Examples 8-1 to 8-3
A suspension containing about 30% aripiprazole was
obtained in the same manner as in Example 1 except that sucrose
was used in place of mannitol. The suspension was diluted with
purified water in the same manner as in Example 5 to suspensions
containing about 10 mass%, 20 mass%, and 30 mass% aripiprazole.
Using plastic containers, the suspensions were freeze-dried. As
in Example 1, without the necessity of using other movable parts
for ejecting the cake composition from the container or applying
a release agent to the inner surface of the container, each cake
composition was easily removed from the container while retaining
its freeze-dried shape from within the container. Table 3 shows
the ease of removal of the obtained cake compositions from the
containers.
Table 3
Concentration of
Example Strength
aripiprazole (% by mas Removal from the container
No. (N)
8-1 11.2 11.01 Smoothly removed from the container
8-2 21.4 33.04 Smoothly removed from the container.
8-3 32.8 48.72 Smoothly removed from the container.
Results and Discussion
Even when mannitol was used in place of sucrose, the
cake composition produced using a suspension containing about 10
mass% aripiprazole had a strength of about 11 N.
• Comparative Examples 1-1 to 1-9
A suspension containing about 30 mass% aripiprazole
with a mean particle size of 2.2 μm was prepared in the same
manner as in Example 1. Into syringes produced by applying
silicone oil emulsions of various concentrations prepared in
Example 2 and drying, a middle stopper with an outer diameter
slightly larger than the inner diameter of the syringe was fitted
using the sleeve cap method. About 1.5 mL of the suspension was
inserted into the space on the middle stopper, and freeze-dried
as is within the syringe. After the freeze-drying, a front
stopper was fitted using the sleeve cap method.
After freeze-drying, the syringes were stored at room
temperature for about 1 month, and the amount of silicone oil in
the cake composition was measured in the same manner as in
Example 2. In each of the syringes containing the cake
composition, the cake composition adhered to the syringe tube,
and there was no space between the inner wall of the syringe and
the cake composition.
Table 4 shows the mean particle size of aripiprazole
before freeze-drying, the concentration of silicone oil applied
to the syringe, the amount of silicone oil on the syringe, the
amount of silicone oil after 1-month storage of the syringe
containing the cake composition at room temperature and re-
suspension of the cake composition, and the mean particle size of
aripiprazole after resuspension.
Table 4
One-month storage at room temperature
Mean
particle size
Amount of Mean particle size of
Concentration silicone oil aripiprazole (μm)
Amount of
Com- aripiprazole of silicone oil
in the cake
silicone oil
parative in the in the composition
on the
Example suspension emulsion after
syringe Without With
before
No. (% by mass) resuspension
(μg/100mm ) ultrasonic ultrasonic
freeze-
(μg/100mg
treatment treatment
drying
of the
active
(μm)
ingredient)
1-1 35 75 49 3.5 2.5
1-2 20 45 41 3.1 2.3
1-3 15 36 49 3.1 2.4
1-4 10 24 38 3.1 2.4
1-5 7 14 27 2.9 2.4
1-6 5 11 24 2.8 2.3
1-7 2 3 26 2.7 2.2
1-8 1 2 16 2.6 2.3
1-9 0.5 1 19 2.5 2.3
Reference
0 0 14 2.3 2.2
Example
Results and Discussion
The results shown in Table 4 indicate that the higher
the concentration of silicone oil emulsion applied to the syringe,
the higher the silicone oil content of the cake composition; and
the higher the concentration of silicone oil applied to the
syringe, the greater the change in the mean particle size.
Compared to a prefilled syringe preparation using the cake
composition obtained by freeze-drying in a storage container
different from that described in Example 2, different results
were obtained even at the same concentration of silicone oil
emulsion applied.
Even when the concentration of silicone oil in the
emulsion applied was 0%, silicone oil was detected in the cake
composition. This was probably because the silicone oil
originally contained in the stopper had transferred to the cake
composition.
When agglomerated particles are measured under
ultrasonic irradiation, the size of loose particles changes. When
the particle size was measured under ultrasonic irradiation in
this Comparative Example, a reduction in particle size was
observed. This result indicates that according to the method
comprising freeze-drying in a syringe, silicone oil causes
agglomeration.
• Comparative Examples 2-1 to 2-12
Suspensions containing about 20 mass% aripiprazole with
a mean particle size of 2.0 μm and 2.4 μm were individually
prepared in the same manner as in Example 4. Into syringes
produced by applying the silicone oil emulsions of various
concentrations prepared in Example 2, a middle stopper with an
outer diameter slightly larger than the inner diameter of the
syringe was fitted using the sleeve cap method. About 2 mL of the
suspension was inserted into the space on the middle stopper, and
freeze-dried as is within the syringe. In each of the syringes
containing the cake composition, the cake composition adhered to
the syringe tube, and there was no space between the inner wall
of the syringe and the cake composition.
After the freeze-drying, the syringes were stored at
room temperature for 1 month, 2 months and 3 months. After the
storage, the cake composition within the syringes was resuspended
in about 2 mL of water, and the mean particle size was measured
in the same manner as in Example 2. Table 5 shows the
concentration of silicone oil applied to the syringe, the mean
particle size of aripiprazole before freeze-drying, and the mean
particle size of aripiprazole after storage at room temperature
for 1 month, 2 months, and 3 months, and resuspension.
Table 5
Mean particle Mean particle size
size of
(measurement without ultrasonic treatment) (μm)
Concentration
Com- aripiprazole
of silicone oil
in the
parative One-month Two-month Three-month
in the
suspension
Example storage at storage at storage at
emulsion
No. before
room room room
(% by mass)
freeze-drying
temperature temperature temperature
(μm)
2-1 35 3.7 3.6 5.3
2-2 30 3.3 3.8 3.6
2-3 25 2.0 2.6 2.9 3.1
2-4 20 3.3 3.4 4.5
2-5 15 2.6 3.0 2.6
2-6 10 3.3 3.6 3.5
2-7 7 3.1 3.1 3.1
2-8 5 2.9 2.9 2.9
2-9 2 2.4 2.6 2.7 2.7
2-10 1 2.5 2.7 2.6
2-11 0.5 2.5 2.6 2.5
2-12 0.2 2.5 2.6 2.6
Results and Discussion
As shown in Table 5, the results indicate that the
higher the concentration of silicone oil emulsion applied to the
syringe, the greater the change in the particle size. As in
Comparative Example 1, even with the use of a suspension
containing about 20 mass% aripiprazole, if the cake composition
obtained by freeze-drying within a syringe was resuspended as is,
changes in the mean particle size of aripiprazole were observed.
• Comparative Example 3
A suspension containing about 30 mass% aripiprazole
was prepared in the same manner as in Example 1. Into a syringe
produced by applying a 5 mass% silicone oil emulsion in the same
manner as in Example 2, a middle stopper with an outer diameter
slightly larger than the inner diameter of the syringe was fitted
using the sleeve cap method. About 1.5 mL of the suspension was
inserted into the space on the middle stopper, and the syringe
was transferred to a freeze-dryer. The suspension was freeze-
dried according to the cycle described below to prepare a syringe
in which the cake composition was enclosed. In the syringe
containing the cake composition, the cake composition adhered to
the syringe tube, and there was no space between the inner wall
of the syringe and the cake composition.
(a) Thermal treatment: The product was frozen by being maintained
at about -40°C for about 3 hours.
(b) Primary drying: Primary drying was continued for at least 24
hours at an increased shelf temperature of about -5°C under a
pressure of about 20 Pa or less.
A front stopper was fitted above the cake composition
within the obtained syringe (on the needle side, at the position
of front stopper 3 shown in Fig. 1) using the sleeve cap method.
About 1.7 mL of water as a redispersion medium was inserted into
chamber B, which is defined by the middle stopper and the end
stopper of the prefilled syringe. The end stopper was fitted
using the sleeve cap method. A front assembly was incorporated
into the syringe tip ejection portion. The end stopper was slowly
pressed to allow water as a redispersion medium to flow into a
front chamber for about 5 seconds. Without shaking the syringe at
all, the end stopper was pressed to the end to expel the
medicinal fluid from the syringe. The amount of medicinal fluid
remaining in the syringe was measured and found to be about 159
Results and Discussion
A dual chamber prefilled syringe preparation is
generally prepared by being freeze-dried within a syringe as
described in Comparative Example 3. Similar to the above, after
water was allowed to flow into a front chamber over a period of
about 5 seconds, a medicinal fluid was expelled without shaking
the syringe at all. The amount of medicinal fluid remaining was
measured and found to be about 159 mg, i.e., a very large amount.
Thus, the results show that compared to the method of Example 3,
in which about 85 mg of medicinal fluid remained, the general
method described in Comparative Example 3 exhibited poor
redispersibility.
The term ‘comprising’ as used in this specification
and claims means ‘consisting at least in part of’. When
interpreting statements in this specification and claims which
include the term ‘comprising’, other features besides the
features prefaced by this term in each statement can also be
present. Related terms such as ‘comprise’ and ‘comprised’ are to
be interpreted in a similar manner.
Reference Signs List
A: Chamber
B: Chamber
1: Dual chamber syringe
2: Syringe tube
3: Front stopper
4: Middle stopper
: End stopper
6: Tip
7: Opening
8: Cake composition
9: Injection liquid
: Silicone
11: Bypass
12: Front assembly
13: Hypodermic needle
14: Plunger
: Suspension
a: Angle
a’: Angle
L: Length from the raised top point to the top surface
16: Container
17: Opening
18: Bottom surface
19: Outer frame
Claims (26)
- [Claim 1] A medical device containing a separately prepared freeze-dried cake composition comprising aripiprazole as an 5 active ingredient in a storage container whose inner wall is treated with silicone, wherein there is a space between the inner wall of the storage container and the cake composition, wherein the cake composition has a cylindrical shape, and a side surface of the cylindrical cake composition is sloped.
- [Claim 2] The medical device containing the cake composition according to claim 1, wherein the cake composition is a cake composition that was freeze-dried in a container separate from 15 the storage container.
- [Claim 3] The medical device containing the cake composition according to claim 1 or 2, wherein the apparent volume of the 20 cake composition accounts for 30 to 99% of the volume of the storage container.
- [Claim 4] The medical device containing the cake composition 25 according to any one of claims 1-3, wherein a top surface of the cylindrical cake composition is raised.
- [Claim 5] The medical device containing the cake composition 30 according to any one of claims 1 to 4, wherein the storage container treated with silicone is a vial or syringe.
- [Claim 6] The medical device containing the cake composition according to claim 5, wherein the syringe has multiple chambers and the cake composition is contained in at least one chamber.
- [Claim 7] The medical device containing the cake composition according to claim 5, wherein the syringe has a first chamber for containing the cake composition, and a second chamber for 10 containing an injection liquid; the first chamber is arranged on the side where a needle is placed, and the second chamber is arranged on the side where a plunger is placed; and the cake composition is contained in the first chamber and 15 the injection liquid is contained in the second chamber.
- [Claim 8] The medical device containing the cake composition according to any one of claims 1 to 7, wherein the cake 20 composition has a strength of 5 to 100 N.
- [Claim 9] A cake composition comprising aripiprazole as an active ingredient and having a strength of 5 to 100 N, wherein the cake 25 composition has a cylindrical shape, and a side surface of the cylindrical cake composition is sloped.
- [Claim 10] The cake composition according to claim 9, wherein the 30 percentage of aripiprazole in the cake composition is 60 to 95% by mass.
- [Claim 11] The cake composition according to claim 9 or 10, wherein the amount of aripiprazole in the cake composition is 0.1 to 0.6 g.
- [Claim 12] The cake composition according to any one of claims 9 to 11, obtained by freeze-drying 0.25 to 12 g of a suspension having an aripiprazole solids content of 5 to 45% by mass.
- [Claim 13]
- The cake composition according to claim 12, wherein a top surface of the cylindrical cake composition is raised.
- 15 [Claim 14] The cake composition according to any one of claims 9 to 13, wherein the cake composition is used for being placed in a medical device. 20 [Claim 15] The cake composition according to claim 14, wherein the cake composition is a mass that was freeze-dried in a container separate from a storage container in the medical device. 25 [
- Claim 16] A method for producing a medical device containing a cake composition comprising aripiprazole as an active ingredient, the method comprising: a step of enclosing a separately prepared freeze-dried cake 30 composition comprising aripiprazole as an active ingredient in a storage container whose inner wall is treated with silicone, wherein there is a space between the inner wall of the storage container and the cake composition, and the cake composition has a cylindrical shape, and a side surface of the cylindrical cake 35 composition is sloped.
- [Claim 17] The method for producing the medical device according to claim 16, wherein the storage container treated with silicone 5 is a vial or syringe.
- [Claim 18] The method for producing the medical device according to claim 17, wherein the syringe has multiple chambers and the 10 cake composition is contained in at least one chamber.
- [Claim 19] The method for producing the medical device according to claim 18, wherein the syringe has a first chamber for 15 containing the cake composition, and a second chamber for containing an injection liquid; the first chamber is arranged on the side where a needle is placed, and the second chamber is arranged on the side where a plunger is placed; and 20 the cake composition is contained in the first chamber and the injection liquid is contained in the second chamber.
- [Claim 20] A method for producing a cake composition comprising 25 aripiprazole as an active ingredient and having a strength of 5 to 100 N, the method comprising: a step of freeze-drying a suspension comprising aripiprazole as an active ingredient, wherein the cake composition has a cylindrical shape, and a side surface of the cylindrical cake 30 composition is sloped.
- [Claim 21] The medical device comprising the cake composition according to claim 1, substantially as herein described with 35 reference to any embodiment disclosed.
- [Claim 22] A medical device comprising a separately prepared freeze-dried cake composition, substantially as herein described 5 with reference to any embodiment shown in the accompanying drawings.
- [Claim 23] The cake composition according to claim 9, 10 substantially as herein described with reference to any embodiment shown.
- [Claim 24] A cake composition substantially as herein described 15 with reference to any embodiment disclosed.
- [Claim 25] The method for producing a medical device according to claim 16, substantially as herein described with reference to any 20 embodiment disclosed.
- [Claim 26] The method for producing a cake composition of claim 20, substantially as herein described with reference to any 25 embodiment disclosed. [
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2011-011711 | 2011-01-24 | ||
JP2011011711 | 2011-01-24 | ||
PCT/JP2012/051285 WO2012102216A1 (en) | 2011-01-24 | 2012-01-17 | Medical device containing a cake composition comprising aripiprazole as an active ingredient, and a cake composition comprising aripiprazole as an active ingredient |
Publications (2)
Publication Number | Publication Date |
---|---|
NZ613064A NZ613064A (en) | 2015-10-30 |
NZ613064B2 true NZ613064B2 (en) | 2016-02-02 |
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