Method of stabilizing aqueous pyrazoloacridone derivative...

Organic compounds -- part of the class 532-570 series – Organic compounds – Heterocyclic carbon compounds containing a hetero ring...

Reexamination Certificate

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C546S062000

Reexamination Certificate

active

06552198

ABSTRACT:

TECHNICAL FIELD
The present invention relates to a method for stabilizing aqueous solutions containing a pyrazoloacridone derivative or a pharmaceutically acceptable salt thereof, and well-closed containers containing the aqueous solution.
BACKGROUND ART
Antioxidants are used to prevent drugs from oxidative decomposition. However, it is known that the antioxidants cannot be added to some drugs, since they would react with active ingredients or other additives in preparations (
J. Pharm. Sci.,
61, 708 (1972)).
It is known that pyrazoloacridone derivatives have a DNA intercalation activity and exhibit an antitumor effect (
J. Med. Chem.,
37, 1028 (1994)). Specific examples of such pyrazoloacridone derivatives are disclosed in Japanese Published Unexamined Patent Application No. 1064/93.
Pyrazoloacridone derivatives or pharmaceutically acceptable salts thereof are liable to decompose due to oxidation in aqueous solutions. Thus, there have been required stable aqueous solution preparations containing a pyrazoloacridone derivative or a pharmaceutically acceptable salt thereof which can be stored over a long period of time.
DISCLOSURE OF THE INVENTION
An object of the present invention is to provide a method for stabilizing aqueous solutions containing a pyrazoloacridone derivative or a pharmaceutically acceptable salt thereof, and well-closed containers containing the aqueous solution.
The present invention relates to a method for stabilizing aqueous solutions containing a pyrazoloacridone derivative or a pharmaceutically acceptable salt thereof, comprising adding an acid to an aqueous solution containing a pyrazoloacridone derivative represented by the following formula (I) (hereinafter referred to as Compound (I)):
wherein R
1a
, R
1b
, R
1c
and R
1d
independently represent hydrogen, a lower alkyl group, —(CH
2
)
p
—X (wherein p is an integer of 1 to 6; and X represents a hydroxyl group, a lower alkoxy group, or —NR
2a
R
2b
(wherein R
2a
and R
2b
independently represent hydrogen, a lower alkyl group, —(CH
2
)
m
—Y (wherein m is an integer of 1 to 6; and Y represents a hydroxyl group, a lower alkoxy group, or —NR
3a
R
3
b (wherein R
3a
, and R
3b
independently represent hydrogen or a lower alkyl group)), or R
2a
and R
2b
form a heterocyclic group together with the nitrogen atom adjacent thereto)), or —CH((CH
2
)
n
OH)
2
(wherein n is an integer of 1 to 5) or a pharmaceutically acceptable salt thereof; substituting the air in a well-closed container containing the aqueous solution with an inert gas; and sealing the container.
The present invention further relates to well-closed containers containing an aqueous solution containing Compound (I) or a pharmaceutically acceptable salt thereof and an acid, wherein the air in the well-closed container is substituted with an inert gas.
The lower alkyl group and the alkyl moiety in the lower alkoxy group in the definition of formula (I) include linear or branched alkyl groups having from 1 to 6 carbon atoms, such as methyl, ethyl, propyl, isopropyl, butyl, isobutyl sec-butyl, tert-butyl, pentyl, hexyl, and the like. The heterocyclic group formed together with the adjacent nitrogen atom includes pyrrolidinyl, piperidino, piperazinyl, morpholino, thiomorpholino, quinolyl, pyrimidinyl, pyridazinyl, pyridyl, pyrrolyl, imidazolyl, pyrazolyl, and the like. Among these, pyrrolidinyl, piperidino, piperazinyl and morpholino are preferred.
Examples of the pharmaceutically acceptable salt of Compound (I) include inorganic acid salts, such as hydrochlorides, hydrobromides, sulfates, phosphates, and the like, and organic acid salts, such as acetates, oxalates, malonates, maleates, fumarates, tartrates, succinates, citrates, and the like.
Compounds (I) are known compounds, which can be produced by, for example, the production method described in Japanese Published Unexamined Patent Application No. 1064/93.
The concentration of Compound (I) in the aqueous solution is preferably from 0.1 to 1,000 mM, more preferably from 1 to 100 mM, and particularly preferably from 10 to 50 mM.
Examples of Compound (I) are shown in Table 1.
TABLE 1
(I)

Compound No.
NR
1a
R
1b
NR
1c
R
1d
1
NH(CH
2
)
2
NH
2
NH(CH
2
)
2
NH
2
2
N(C
2
H
5
)
2
NH(CH
2
)
2
NH
2
3
N(C
2
H
5
)
2
NH(CH
2
)
2
N(CH
3
)
2
4
NH(CH
2
)
2
OH
NH(CH
2
)
2
NH
2
5
NH(CH
2
)
2
OH
NH(CH
2
)
3
NH
2
6
NH(CH
2
)
2
OH
NH(CH
2
)
2
NH(CH
2
)
2
OH
7
NH(CH
2
)
2
OH
NH(CH
2
)
2
NHCH
3
8
NH(CH
2
)
2
OH
NH(CH
2
)
2
N(CH
3
)
2
9
N[(CH
2
)
2
OH]
2
NH(CH
2
)
2
N(CH
3
)
2
10
NHCH(CH
2
OH)
2
NH(CH
2
)
2
NH
2
11
NH(CH
2
)
2
OCH
3
NH(CH
2
)
2
NH
2
12
NHCH(CH
2
OH)
2
NH(CH
2
)
2
NH(CH
2
)
2
OH
13
NHCH(CH
2
OH)
2
NH(CH
2
)
3
NH
2

14
NHCH(CH
2
OH)
2
Examples of the acid include inorganic acids, organic acids, and inorganic salts thereof.
Examples of the inorganic acid include phosphoric acid, hydrochloric acid, sulfuric acid, nitric acid, and the like.
Examples of the organic acid include organic acids represented by the following formula (II) (hereinafter referred to as Compound (II)):
R
4
R
5
CH—COOH  (II)
wherein R
4
represents hydrogen or hydroxy; and R
5
represents hydrogen, carboxy, or alkyl having from 1 to 3 carbon atoms which may be substituted with hydroxy or carboxy. Examples of the alkyl having from 1 to 3 carbon atoms in the definition of formula (II) include methyl, ethyl, propyl, isopropyl, and the like. The substitution number of the hydroxy or carboxy is 1 or 2. Examples of Compound (II) include lactic acid, glyceric acid, tartronic acid, malic acid, tartaric acid, and the like. Lactic acid is particularly preferred as the organic acid.
Examples of the inorganic acid salt include alkali metal salts, such as lithium salts, sodium salts, potassium salts, and the like; and alkaline earth metal salts, such as beryllium salts, magnesium salts, calcium salts, and the like.
The concentration of the acid in the aqueous solution is preferably from 1 to 1,000 mM, more preferably from 5 to 500 mM, and particularly preferably from 10 to 200 mM.
The material and shape of the well-closed container is not particularly limited, so long as it can prevent the permeation of oxygen. Examples of such material include glass, metals, resins, and the like. Examples of the resin include polyethylene, polystyrene, polycarbonate, polypropylene, polyvinyl chloride, 6-nylon, polyethylene terephthalate, and the like, with a resin having a small coefficient of oxygen permeation being preferred. Examples of the resin having a small coefficient of oxygen permeation include resins having a coefficient of oxygen permeation less than 0.1×10
−11
cm
3
(STP) cm
−1
s
−1
cmHg
−1
, such as polyvinyl alcohol, polyacrylonitrile, polyvinylidene chloride, and the like. Examples of such shape of the container include an ampul, a vial, a syringe, and the like.
The pH of the aqueous solution is from 1 to 7, preferably from 2 to 6, and particularly preferably from 3 to 5. The pH can be adjusted using an alkali, such as sodium hydroxide, potassium hydroxide, or the like, or an inorganic acid, such as hydrochloric acid, sulfuric acid, or the like.
The aqueous solution can contain a pharmaceutically acceptable antioxidant, solubilizing agent, isotonizing agent, surfactant, soothing agent, and the like, if desired. Examples of the antioxidant include ascorbic acid, vitamin E, L-cysteine, and the like. Examples of the solubilizing agent include polyethylene glycol and the like. Examples of the isotonizing agent include glycerine, glucose, sodium chloride, and the like. Examples of the surfactant include HCO-60 (manufactured by Nikko Chemicals Co., Ltd.), and the like. Examples of the soothing agent include benzyl alcohol, lidocaine, and the like.
Examples of the inert gas include a nitrogen gas, an argon gas, a helium gas, carbon dioxide, and the like. Among these, a nitrogen gas is preferred.
The substitution of the air in the well-closed container with the inert gas can be carried out by a conventional method. For example, the inert gas may be poured after the well-closed container is depressuriz

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