JP2011012018A - Pharmaceutical composition for oral administration of paroxetine hydrochloride hydrate, having inhibited retardation of disintegration - Google Patents
Pharmaceutical composition for oral administration of paroxetine hydrochloride hydrate, having inhibited retardation of disintegration Download PDFInfo
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- JP2011012018A JP2011012018A JP2009157371A JP2009157371A JP2011012018A JP 2011012018 A JP2011012018 A JP 2011012018A JP 2009157371 A JP2009157371 A JP 2009157371A JP 2009157371 A JP2009157371 A JP 2009157371A JP 2011012018 A JP2011012018 A JP 2011012018A
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- hydrogen phosphate
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- AHOUBRCZNHFOSL-YOEHRIQHSA-N (+)-Casbol Chemical compound C1=CC(F)=CC=C1[C@H]1[C@H](COC=2C=C3OCOC3=CC=2)CNCC1 AHOUBRCZNHFOSL-YOEHRIQHSA-N 0.000 title claims abstract description 22
- 229960002296 paroxetine Drugs 0.000 title claims abstract description 22
- 239000008194 pharmaceutical composition Substances 0.000 title claims abstract description 15
- 239000000546 pharmaceutical excipient Substances 0.000 claims abstract description 28
- 239000011734 sodium Substances 0.000 claims abstract description 16
- 229910052708 sodium Inorganic materials 0.000 claims abstract description 16
- 229920002472 Starch Polymers 0.000 claims abstract description 15
- HUSUHZRVLBSGBO-UHFFFAOYSA-L calcium;dihydrogen phosphate;hydroxide Chemical compound O.[Ca+2].OP([O-])([O-])=O HUSUHZRVLBSGBO-UHFFFAOYSA-L 0.000 claims abstract description 15
- 239000008107 starch Substances 0.000 claims abstract description 15
- 235000019698 starch Nutrition 0.000 claims abstract description 15
- FBPFZTCFMRRESA-KVTDHHQDSA-N D-Mannitol Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-KVTDHHQDSA-N 0.000 claims abstract description 14
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 claims abstract description 13
- 229920002134 Carboxymethyl cellulose Polymers 0.000 claims abstract description 13
- VJHCJDRQFCCTHL-UHFFFAOYSA-N acetic acid 2,3,4,5,6-pentahydroxyhexanal Chemical compound CC(O)=O.OCC(O)C(O)C(O)C(O)C=O VJHCJDRQFCCTHL-UHFFFAOYSA-N 0.000 claims abstract description 13
- 239000011575 calcium Substances 0.000 claims abstract description 13
- 229910052791 calcium Inorganic materials 0.000 claims abstract description 13
- 235000010948 carboxy methyl cellulose Nutrition 0.000 claims abstract description 13
- 229950008138 carmellose Drugs 0.000 claims abstract description 13
- FUFJGUQYACFECW-UHFFFAOYSA-L calcium hydrogenphosphate Chemical compound [Ca+2].OP([O-])([O-])=O FUFJGUQYACFECW-UHFFFAOYSA-L 0.000 claims abstract description 12
- 239000011248 coating agent Substances 0.000 claims abstract description 12
- 238000000576 coating method Methods 0.000 claims abstract description 12
- 235000019700 dicalcium phosphate Nutrition 0.000 claims abstract description 12
- 239000001866 hydroxypropyl methyl cellulose Substances 0.000 claims abstract description 12
- 229920003088 hydroxypropyl methyl cellulose Polymers 0.000 claims abstract description 12
- 235000010979 hydroxypropyl methyl cellulose Nutrition 0.000 claims abstract description 12
- 229960003943 hypromellose Drugs 0.000 claims abstract description 12
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 7
- 235000010355 mannitol Nutrition 0.000 claims abstract description 7
- GUBGYTABKSRVRQ-XLOQQCSPSA-N Alpha-Lactose Chemical compound O[C@@H]1[C@@H](O)[C@@H](O)[C@@H](CO)O[C@H]1O[C@@H]1[C@@H](CO)O[C@H](O)[C@H](O)[C@H]1O GUBGYTABKSRVRQ-XLOQQCSPSA-N 0.000 claims abstract description 6
- 229920002261 Corn starch Polymers 0.000 claims abstract description 6
- GUBGYTABKSRVRQ-QKKXKWKRSA-N Lactose Natural products OC[C@H]1O[C@@H](O[C@H]2[C@H](O)[C@@H](O)C(O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@H]1O GUBGYTABKSRVRQ-QKKXKWKRSA-N 0.000 claims abstract description 6
- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 claims abstract description 6
- 229930006000 Sucrose Natural products 0.000 claims abstract description 6
- 229920002678 cellulose Polymers 0.000 claims abstract description 6
- 239000001913 cellulose Substances 0.000 claims abstract description 6
- 239000008120 corn starch Substances 0.000 claims abstract description 6
- 239000008101 lactose Substances 0.000 claims abstract description 6
- 239000007884 disintegrant Substances 0.000 claims description 19
- AHOUBRCZNHFOSL-UHFFFAOYSA-N 3-(1,3-benzodioxol-5-yloxymethyl)-4-(4-fluorophenyl)piperidine Chemical compound C1=CC(F)=CC=C1C1C(COC=2C=C3OCOC3=CC=2)CNCC1 AHOUBRCZNHFOSL-UHFFFAOYSA-N 0.000 claims description 18
- 229940031703 low substituted hydroxypropyl cellulose Drugs 0.000 claims description 11
- 229960005183 paroxetine hydrochloride Drugs 0.000 claims description 9
- 229920000881 Modified starch Polymers 0.000 claims description 5
- 239000005720 sucrose Substances 0.000 claims description 5
- 239000007931 coated granule Substances 0.000 claims description 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 abstract description 5
- 229920002153 Hydroxypropyl cellulose Polymers 0.000 abstract description 3
- 239000001863 hydroxypropyl cellulose Substances 0.000 abstract description 3
- 235000010977 hydroxypropyl cellulose Nutrition 0.000 abstract description 3
- 238000002156 mixing Methods 0.000 abstract description 2
- 238000002360 preparation method Methods 0.000 abstract description 2
- 238000006467 substitution reaction Methods 0.000 abstract 2
- 239000008187 granular material Substances 0.000 abstract 1
- HQKMJHAJHXVSDF-UHFFFAOYSA-L magnesium stearate Chemical compound [Mg+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O HQKMJHAJHXVSDF-UHFFFAOYSA-L 0.000 description 10
- 239000003826 tablet Substances 0.000 description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 235000019359 magnesium stearate Nutrition 0.000 description 5
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 125000002057 carboxymethyl group Chemical group [H]OC(=O)C([H])([H])[*] 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 239000011230 binding agent Substances 0.000 description 2
- 238000002845 discoloration Methods 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- 230000005764 inhibitory process Effects 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000008213 purified water Substances 0.000 description 2
- 230000001629 suppression Effects 0.000 description 2
- 238000005550 wet granulation Methods 0.000 description 2
- 208000020401 Depressive disease Diseases 0.000 description 1
- 208000021384 Obsessive-Compulsive disease Diseases 0.000 description 1
- 229920000148 Polycarbophil calcium Polymers 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 238000013270 controlled release Methods 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000007941 film coated tablet Substances 0.000 description 1
- 239000000796 flavoring agent Substances 0.000 description 1
- 235000013355 food flavoring agent Nutrition 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 238000011835 investigation Methods 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 235000010981 methylcellulose Nutrition 0.000 description 1
- 239000012046 mixed solvent Substances 0.000 description 1
- 208000019906 panic disease Diseases 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229940059101 polycarbophil calcium Drugs 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 235000019422 polyvinyl alcohol Nutrition 0.000 description 1
- 238000005070 sampling Methods 0.000 description 1
- 229940124834 selective serotonin reuptake inhibitor Drugs 0.000 description 1
- 239000012896 selective serotonin reuptake inhibitor Substances 0.000 description 1
- 238000007873 sieving Methods 0.000 description 1
- 210000000813 small intestine Anatomy 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 238000013268 sustained release Methods 0.000 description 1
- 239000012730 sustained-release form Substances 0.000 description 1
- 229920003176 water-insoluble polymer Polymers 0.000 description 1
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- Medicinal Preparation (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
Description
本発明はパロキセチン塩酸塩水和物を含有し、崩壊遅延が抑制された経口投与用医薬組成物に関する。 The present invention relates to a pharmaceutical composition for oral administration containing paroxetine hydrochloride hydrate and having a suppressed decay delay.
塩酸パロキセチンはうつ病・うつ状態、パニック障害、強迫性障害の効能・効果を有する選択的セロトニン再取り込み阻害剤であり、我が国ではフィルムコート錠剤が販売されている。塩酸パロキセチンは水存在下においては変色することが知られており、これを防止することを目的として種々の検討が行われている。特許文献１では、塩酸パロキセチンを乾燥賦形剤と混合し、錠剤形態に直接打錠するか又は塩酸パロキセチンを乾燥賦形剤と混合し、乾燥造粒し、錠剤の形態に圧縮する、水の不存在下で湿式造粒法を用いない製造方法が記載されている。特許文献２ではエタノールまたはエタノールと水の混合溶媒を用いて湿式造粒することで、塩酸パロキセチンの変色が抑制され、かつ簡便な製造方法により含量均一性に優れた製剤が得られることが記載されている。海外においては、経口懸濁液や徐放剤も販売されており、特許文献３には水膨潤可能で水不溶性ポリマーであるポリカルボフィルカルシウム成分と、水との相互作用により形成される反応複合体を含む高分子制御放出組成物により、塩酸パロキセチンが小腸で徐々に放出される経口投与製剤が記載されている。塩酸パロキセチンの変色防止を目的とした検討は種々行われているものの、崩壊遅延の抑制について検討した例は見受けられない。 Paroxetine hydrochloride is a selective serotonin reuptake inhibitor having the effects and effects of depression / depressed state, panic disorder and obsessive compulsive disorder, and film-coated tablets are sold in Japan. Paroxetine hydrochloride is known to change color in the presence of water, and various studies have been conducted for the purpose of preventing this. In Patent Document 1, paroxetine hydrochloride is mixed with a dry excipient and compressed directly into a tablet form, or paroxetine hydrochloride is mixed with a dry excipient, dry granulated, and compressed into a tablet form. A production method is described that does not use wet granulation in the absence. Patent Document 2 describes that by wet granulation using ethanol or a mixed solvent of ethanol and water, discoloration of paroxetine hydrochloride is suppressed, and a preparation with excellent content uniformity can be obtained by a simple production method. ing. Overseas, oral suspensions and sustained-release agents are also sold, and Patent Document 3 discloses a reaction complex formed by the interaction between water and a polycarbophil calcium component that is a water-insoluble polymer and water. An oral dosage formulation is described in which paroxetine hydrochloride is gradually released in the small intestine by a polymeric controlled release composition comprising the body. Although various studies have been conducted for the purpose of preventing discoloration of paroxetine hydrochloride, there have been no examples of studying the suppression of decay delay.
本発明の課題は、崩壊遅延が抑制されたパロキセチン塩酸塩水和物の経口投与用医薬組成物を提供することである。 An object of the present invention is to provide a pharmaceutical composition for oral administration of paroxetine hydrochloride hydrate with suppressed decay delay.
本発明は、
パロキセチン塩酸塩水和物；
乳糖、白糖、Ｄ−マンニトール、トウモロコシデンプン、部分アルファ化デンプン、結晶セルロース、無水リン酸水素カルシウムおよびリン酸水素カルシウム水和物よりなる群から選ばれた少なくとも１種の賦形剤；およびカルメロースカルシウム、低置換度ヒドロキシプロピルセルロースおよびカルボキシメチルスターチナトリウムよりなる群から選ばれた少なくとも１種の崩壊剤；
を含有する経口投与用医薬組成物であって、
ａ）無水リン酸水素カルシウムを賦形剤として選択し、前記崩壊剤の中から少なくとも任意の１種を選択するか、
ｂ）前記賦形剤の中から少なくとも任意の１種を選択し、カルメロースカルシウムまたは低置換度ヒドロキシプロピルセルロースまたはその両者を崩壊剤として選択する、
ことによって崩壊遅延が抑制されていることを特徴とするパロキセチン塩酸塩水和物の経口投与用医薬組成物を提供する。
また本発明は、
パロキセチン塩酸塩をヒプロメロースでコーティングして得たコーティング造粒物；
乳糖、白糖、Ｄ−マンニトール、トウモロコシデンプン、部分アルファ化デンプン、結晶セルロース、無水リン酸水素カルシウムおよびリン酸水素カルシウム水和物よりなる群から選ばれた少なくとも１種の賦形剤；および
カルメロースカルシウム、低置換度ヒドロキシプロピルセルロースおよびカルボキシメチルスターチナトリウムよりなる群から選ばれた少なくとも１種の崩壊剤を混合し、打錠してなる経口投与用医薬組成物であって、
ａ）リン酸水素カルシウム水和物を賦形剤として選択し、前記崩壊剤の中から少なくとも任意の１種を選択するか、
ｂ）前記賦形剤の中から少なくとも任意の１種を選択し、カルボキメチルスターチナトリウムを崩壊剤として選択するか、または
ｃ）賦形剤としてリン酸水素カルシウム水和物を選択し、崩壊剤としてカルボキシメチルスターチナトリウムを選択する、
ことによって崩壊遅延が抑制されていることを特徴とするパロキセチン塩酸塩水和物の経口投与用医薬組成物を提供する。
The present invention
Paroxetine hydrochloride hydrate;
At least one excipient selected from the group consisting of lactose, sucrose, D-mannitol, corn starch, partially pregelatinized starch, crystalline cellulose, anhydrous calcium hydrogen phosphate and calcium hydrogen phosphate hydrate; and carmellose At least one disintegrant selected from the group consisting of calcium, low substituted hydroxypropylcellulose and sodium carboxymethyl starch;
A pharmaceutical composition for oral administration comprising
a) selecting anhydrous calcium hydrogen phosphate as an excipient and selecting at least any one of the disintegrants;
b) selecting at least any one of the excipients and selecting carmellose calcium or low substituted hydroxypropylcellulose or both as disintegrants;
This provides a pharmaceutical composition for oral administration of paroxetine hydrochloride hydrate, characterized in that disintegration delay is suppressed.
The present invention also provides
Coated granules obtained by coating paroxetine hydrochloride with hypromellose;
At least one excipient selected from the group consisting of lactose, sucrose, D-mannitol, corn starch, partially pregelatinized starch, crystalline cellulose, anhydrous calcium hydrogen phosphate and calcium hydrogen phosphate hydrate; and carmellose A pharmaceutical composition for oral administration comprising at least one disintegrating agent selected from the group consisting of calcium, low-substituted hydroxypropylcellulose and sodium carboxymethyl starch mixed, and compressed into tablets.
a) selecting calcium hydrogen phosphate hydrate as an excipient and selecting at least any one of the disintegrants;
b) Select at least any one of the excipients and select sodium carboxymethyl starch as the disintegrant, or c) Select calcium hydrogen phosphate hydrate as the excipient and disintegrant Select sodium carboxymethyl starch as
This provides a pharmaceutical composition for oral administration of paroxetine hydrochloride hydrate, characterized in that disintegration delay is suppressed.
本発明者らは、パロキセチン塩酸塩水和物を有効成分とする医薬組成物の崩壊性について検討を行った結果、賦形剤としてリン酸水素カルシウム水和物を使用し、崩壊剤としてカルボキシメチルスターチナトリウムを使用した場合に崩壊遅延が引き起こされるという知見を得た。崩壊遅延の抑制を目的として種々検討を行った結果、崩壊剤としてカルボキシメチルスターチナトリウムに代えて、カルメロースカルシウム又は低置換度ヒドロキシプロピルセルロースを使用することで崩壊遅延が抑制されることを見出した。また、リン酸水素カルシウム水和物に代えて無水リン酸水素カルシウムを使用することで崩壊遅延が抑制されることが分かった。 As a result of examining the disintegration of a pharmaceutical composition containing paroxetine hydrochloride hydrate as an active ingredient, the present inventors have used calcium hydrogen phosphate hydrate as an excipient and carboxymethyl starch as a disintegrant. It was found that decay delay is caused when sodium is used. As a result of various investigations for the purpose of suppressing disintegration delay, it was found that disintegration delay is suppressed by using carmellose calcium or low-substituted hydroxypropylcellulose instead of carboxymethyl starch sodium as a disintegrant. . It was also found that the decay delay was suppressed by using anhydrous calcium hydrogen phosphate instead of calcium hydrogen phosphate hydrate.
一方、本発明者らは、リン酸水素カルシウム水和物及びカルボキシメチルスターチナトリウムを使用する場合においても、パロキセチン塩酸塩水和物をヒプロメロースでコーティングして造粒することで崩壊遅延が抑制されることを見出し、本発明を完成させた。 On the other hand, even when the present inventors use calcium hydrogen phosphate hydrate and sodium carboxymethyl starch, the delay of disintegration is suppressed by granulating by coating paroxetine hydrochloride hydrate with hypromellose. The present invention was completed.
パロキセチン塩酸塩水和物がヒプロメロースでコーティングされていればよく、パロキセチン塩酸塩水和物と賦形剤等の他の医薬添加物との混合物をヒプロメロースでコーティングすることによっても、目的とする崩壊遅延抑制効果を得ることができる。また、得られた造粒物は、他の医薬添加物と混合して通常用いられる方法により錠剤の形態とすることもできる。 It is only necessary that paroxetine hydrochloride hydrate is coated with hypromellose, and the desired disintegration-inhibiting effect can be achieved by coating a mixture of paroxetine hydrochloride hydrate and other pharmaceutical additives such as excipients with hypromellose. Can be obtained. Further, the obtained granulated product can be mixed with other pharmaceutical additives to form a tablet by a commonly used method.
パロキセチン塩酸塩水和物をコーティングするヒプロメロースの量は、本発明の効果が得られる範囲の量であれば特に限定はされないが、パロキセチン塩酸塩水和物に対して２０％以上、８０％以下、好ましくは３０％以上、７０％以下、特に好ましくは４０％以上、６０％以下である。 The amount of hypromellose that coats paroxetine hydrochloride hydrate is not particularly limited as long as the effect of the present invention is obtained, but is 20% or more and 80% or less, preferably with respect to paroxetine hydrochloride hydrate. It is 30% or more and 70% or less, particularly preferably 40% or more and 60% or less.
医薬添加物としては特に限定されることはなく、通常用いられる賦形剤、結合剤、崩壊剤、可塑剤、滑沢剤、着色剤、矯味剤などから適宜選択することができる。 The pharmaceutical additive is not particularly limited, and can be appropriately selected from commonly used excipients, binders, disintegrants, plasticizers, lubricants, coloring agents, flavoring agents, and the like.
賦形剤としては、乳糖、白糖、Ｄ−マンニトール、トウモロコシデンプン、部分アルファ化デンプン、結晶セルロースなどが挙げられる。
結合剤としては、ヒドロキシプロピルセルロース、ヒプロメロース、メチルセルロース、ポリビニルアルコールなどが挙げられる。
崩壊剤として、カルメロースカルシウム、低置換度ヒドロキシプロピルセルロースに加え、カルボキシメチルスターチナトリウムを使用することができる。
Examples of the excipient include lactose, sucrose, D-mannitol, corn starch, partially pregelatinized starch, and crystalline cellulose.
Examples of the binder include hydroxypropyl cellulose, hypromellose, methyl cellulose, polyvinyl alcohol and the like.
In addition to carmellose calcium and low-substituted hydroxypropylcellulose, sodium carboxymethyl starch can be used as a disintegrant.
本発明によれば、崩壊剤としてカルメロースカルシウム又は低置換度ヒドロキシプロピルセルロースを使用することで崩壊遅延を抑制することができる。カルメロースカルシウムと低置換度ヒドロキシプロピルセルロースは同時に使用してもよい。また、リン酸水素カルシウム水和物に代えて無水リン酸水素カルシウムを選択することでも崩壊遅延の抑制が可能である。本発明によると、パロキセチン塩酸塩水和物をヒプロメロースでコーティングして造粒する工程を含むことで崩壊遅延が抑制された医薬組成物の製造が可能である。 According to the present invention, decay delay can be suppressed by using carmellose calcium or low-substituted hydroxypropylcellulose as a disintegrant. Carmellose calcium and low-substituted hydroxypropylcellulose may be used simultaneously. In addition, the decay delay can be suppressed by selecting anhydrous calcium hydrogen phosphate instead of calcium hydrogen phosphate hydrate. According to the present invention, it is possible to produce a pharmaceutical composition in which the delay of disintegration is suppressed by including a step of granulating by coating paroxetine hydrochloride hydrate with hypromellose.
以下、本発明の実施例及び比較例により、内容を詳細に説明するが、これらに限定されるものではない。 Hereinafter, the present invention will be described in detail by way of examples and comparative examples of the present invention, but the present invention is not limited thereto.
実施例１、２及び比較例１
崩壊剤の選択による崩壊遅延の抑制
表１の処方に従って、ステアリン酸マグネシウム以外を袋混合した後、ステアリン酸マグネシウムを加え、更に袋混合し、ロータリー打錠機で打錠した。
Examples 1 and 2 and Comparative Example 1
Inhibition of disintegration delay by selection of disintegrant According to the prescription in Table 1, after mixing bags other than magnesium stearate, magnesium stearate was added, the bags were further mixed, and tableted with a rotary tableting machine.
７０℃の密閉条件で苛酷試験を行い、試験開始時（０日）、４日、１０日に測定した錠剤の崩壊時間（分）の結果を表２に示した。 Table 2 shows the results of disintegration time (minutes) of the tablets measured at the start of the test (0 day), 4 days, and 10 days after conducting a severe test under a sealed condition of 70 ° C.
表２より、崩壊剤としてカルボキシメチルスターチナトリウムの代わりにカルメロースカルシウム又は低置換度ヒドロキシプロピルセルロースを使用した錠剤は崩壊遅延が抑制されることが認められた。 From Table 2, it was recognized that the disintegration delay was suppressed in the tablets using carmellose calcium or low-substituted hydroxypropylcellulose instead of carboxymethyl starch sodium as a disintegrant.
実施例３及び比較例２
賦形剤の選択による崩壊遅延の抑制
表３の処方に従って、ステアリン酸マグネシウム以外を袋混合した後、ビーカー内で精製水を用いて造粒し、５５℃下で２時間乾燥を行った。乾燥後３０Ｍ篩過を行い、ステアリン酸マグネシウムを加えて袋混合し、ロータリー打錠機で打錠した。
Example 3 and Comparative Example 2
Inhibition of Disintegration Delay by Selection of Excipients According to the formulation in Table 3, bags other than magnesium stearate were mixed, granulated with purified water in a beaker, and dried at 55 ° C. for 2 hours. After drying, 30M sieving was carried out, magnesium stearate was added and the bags were mixed, and tableted with a rotary tableting machine.
製造した錠剤は実施例１と同様にして苛酷試験を行った後に崩壊時間（分）を測定し、結果を表４に示した。 The tablets produced were subjected to a severe test in the same manner as in Example 1, and then the disintegration time (minutes) was measured. The results are shown in Table 4.
表４より、リン酸水素カルシウム水和物に代えて無水リン酸水素カルシウムを使用することで崩壊遅延が抑制されることが認められた。 From Table 4, it was recognized that the decay delay was suppressed by using anhydrous calcium hydrogen phosphate instead of calcium hydrogen phosphate hydrate.
実施例４〜６
薬物コーティングによる崩壊遅延の抑制
パロキセチン塩酸塩水和物とＤ−マンニトールをマルチプレックスに仕込み（２００ｇ）混合した。ヒプロメロースを精製水で５％になるように溶解させこれをコーティング液とした。表５に示したコーティング率になるように途中でサンプリングし、最終的に６０％までコーティングを行った。
Examples 4-6
Suppression of disintegration delay by drug coating Paroxetine hydrochloride hydrate and D-mannitol were charged into a multiplex (200 g) and mixed. Hypromellose was dissolved in purified water to 5% and used as a coating solution. Sampling was performed halfway so as to achieve the coating rate shown in Table 5, and finally coating was performed to 60%.
コーティング造粒物を３０Ｍ篩過後、直打用リン酸水素カルシウム水和物とカルボキシメチルスターチナトリウムを加えて袋混合した。ステアリン酸マグネシウムを加えてさらに混合し、ロータリー打錠機で打錠した。 The coated granulated product was passed through a 30M sieve, and then calcium hydrogen phosphate hydrate for direct hitting and sodium carboxymethyl starch were added and mixed in a bag. Magnesium stearate was added and further mixed, and tableted with a rotary tableting machine.
コーティング率はパロキセチン塩酸塩水和物に対するヒプロメロース量として算出した。 The coating rate was calculated as the amount of hypromellose relative to paroxetine hydrochloride hydrate.
実施例４〜６で製造した錠剤について、実施例１と同様にして崩壊時間（分）を測定し、結果を表６に示した。表７に示した比較例２との比較により、パロキセチン塩酸塩水和物を予めヒプロメロースでコーティングすることで崩壊遅延が抑制されることが認められた。 About the tablet manufactured in Examples 4-6, disintegration time (minutes) was measured like Example 1, and the result was shown in Table 6. By comparison with Comparative Example 2 shown in Table 7, it was confirmed that the disintegration delay was suppressed by previously coating paroxetine hydrochloride hydrate with hypromellose.
Claims (2)
乳糖、白糖、Ｄ−マンニトール、トウモロコシデンプン、部分アルファ化デンプン、結晶セルロース、無水リン酸水素カルシウムおよびリン酸水素カルシウム水和物よりなる群から選ばれた少なくとも１種の賦形剤；およびカルメロースカルシウム、低置換度ヒドロキシプロピルセルロースおよびカルボキシメチルスターチナトリウムよりなる群から選ばれた少なくとも１種の崩壊剤；
を含有する経口投与用医薬組成物であって、
ａ）無水リン酸水素カルシウムを賦形剤として選択し、前記崩壊剤の中から少なくとも任意の１種を選択するか、
ｂ）前記賦形剤の中から少なくとも任意の１種を選択し、カルメロースカルシウムまたは低置換度ヒドロキシプロピルセルロースまたはその両者を崩壊剤として選択する、
ことによって崩壊遅延が抑制されていることを特徴とするパロキセチン塩酸塩水和物の経口投与用医薬組成物。 Paroxetine hydrochloride hydrate;
At least one excipient selected from the group consisting of lactose, sucrose, D-mannitol, corn starch, partially pregelatinized starch, crystalline cellulose, anhydrous calcium hydrogen phosphate and calcium hydrogen phosphate hydrate; and carmellose At least one disintegrant selected from the group consisting of calcium, low substituted hydroxypropylcellulose and sodium carboxymethyl starch;
A pharmaceutical composition for oral administration comprising
a) selecting anhydrous calcium hydrogen phosphate as an excipient and selecting at least any one of the disintegrants;
b) selecting at least any one of the excipients and selecting carmellose calcium or low substituted hydroxypropylcellulose or both as disintegrants;
The pharmaceutical composition for oral administration of paroxetine hydrochloride hydrate characterized by the fact that disintegration delay is suppressed.
乳糖、白糖、Ｄ−マンニトール、トウモロコシデンプン、部分アルファ化デンプン、結晶セルロース、無水リン酸水素カルシウムおよびリン酸水素カルシウム水和物よりなる群から選ばれた少なくとも１種の賦形剤；および
カルメロースカルシウム、低置換度ヒドロキシプロピルセルロースおよびカルボキシメチルスターチナトリウムよりなる群から選ばれた少なくとも１種の崩壊剤を混合し、打錠してなる経口投与用医薬組成物であって、
ａ）リン酸水素カルシウム水和物を賦形剤として選択し、前記崩壊剤の中から少なくとも任意の１種を選択するか、
ｂ）前記賦形剤の中から少なくとも任意の１種を選択し、カルボキメチルスターチナトリウムを崩壊剤として選択するか、または
ｃ）賦形剤としてリン酸水素カルシウム水和物を選択し、崩壊剤としてカルボキシメチルスターチナトリウムを選択する、
ことによって崩壊遅延が抑制されていることを特徴とするパロキセチン塩酸塩水和物の経口投与用医薬組成物。 Coated granules obtained by coating paroxetine hydrochloride with hypromellose;
At least one excipient selected from the group consisting of lactose, sucrose, D-mannitol, corn starch, partially pregelatinized starch, crystalline cellulose, anhydrous calcium hydrogen phosphate and calcium hydrogen phosphate hydrate; and carmellose A pharmaceutical composition for oral administration comprising at least one disintegrating agent selected from the group consisting of calcium, low-substituted hydroxypropylcellulose and sodium carboxymethyl starch mixed, and compressed into tablets.
a) selecting calcium hydrogen phosphate hydrate as an excipient and selecting at least any one of the disintegrants;
b) Select at least any one of the excipients and select sodium carboxymethyl starch as the disintegrant, or c) Select calcium hydrogen phosphate hydrate as the excipient and disintegrant Select sodium carboxymethyl starch as
The pharmaceutical composition for oral administration of paroxetine hydrochloride hydrate characterized by the fact that disintegration delay is suppressed.
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| Publication number | Priority date | Publication date | Assignee | Title |
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| JP2014129238A (en) * | 2012-12-28 | 2014-07-10 | Lion Corp | Solid preparation including etodolac |
| JP2014129239A (en) * | 2012-12-28 | 2014-07-10 | Lion Corp | Solid preparation including etodolac |
| CN112641750A (en) * | 2021-01-12 | 2021-04-13 | 江苏睿实生物科技有限公司 | Paroxetine hydrochloride tablet and preparation method thereof |
| CN115350157A (en) * | 2022-09-21 | 2022-11-18 | 南京海纳医药科技股份有限公司 | Tablet containing paroxetine hydrochloride and preparation method thereof |
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| CN1853631A (en) * | 2005-04-27 | 2006-11-01 | 上海秀新臣邦医药科技有限公司 | Fast disintegrant containing paroxetine |
| JP2007186450A (en) * | 2006-01-13 | 2007-07-26 | Nichi-Iko Pharmaceutical Co Ltd | Paroxetine hydrochloride-containing preparation and method for producing the same |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20060216345A1 (en) * | 2005-03-24 | 2006-09-28 | Sun Pharmaceutical Industries Limited | Oral pharmaceutical composition including paroxetine |
| CN1853631A (en) * | 2005-04-27 | 2006-11-01 | 上海秀新臣邦医药科技有限公司 | Fast disintegrant containing paroxetine |
| JP2007186450A (en) * | 2006-01-13 | 2007-07-26 | Nichi-Iko Pharmaceutical Co Ltd | Paroxetine hydrochloride-containing preparation and method for producing the same |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2014129238A (en) * | 2012-12-28 | 2014-07-10 | Lion Corp | Solid preparation including etodolac |
| JP2014129239A (en) * | 2012-12-28 | 2014-07-10 | Lion Corp | Solid preparation including etodolac |
| CN112641750A (en) * | 2021-01-12 | 2021-04-13 | 江苏睿实生物科技有限公司 | Paroxetine hydrochloride tablet and preparation method thereof |
| CN115350157A (en) * | 2022-09-21 | 2022-11-18 | 南京海纳医药科技股份有限公司 | Tablet containing paroxetine hydrochloride and preparation method thereof |
| CN115350157B (en) * | 2022-09-21 | 2024-05-07 | 南京海纳医药科技股份有限公司 | Tablet containing paroxetine hydrochloride and preparation method thereof |
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