JP2016056154A - Chinese medicine jelly pharmaceutical composition - Google Patents
Chinese medicine jelly pharmaceutical composition Download PDFInfo
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- JP2016056154A JP2016056154A JP2014186623A JP2014186623A JP2016056154A JP 2016056154 A JP2016056154 A JP 2016056154A JP 2014186623 A JP2014186623 A JP 2014186623A JP 2014186623 A JP2014186623 A JP 2014186623A JP 2016056154 A JP2016056154 A JP 2016056154A
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- 239000003814 drug Substances 0.000 title claims abstract description 55
- 235000015110 jellies Nutrition 0.000 title claims abstract description 51
- 239000008274 jelly Substances 0.000 title claims abstract description 51
- 239000008194 pharmaceutical composition Substances 0.000 title claims abstract description 34
- 239000000284 extract Substances 0.000 claims abstract description 22
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims abstract description 18
- 229910052782 aluminium Inorganic materials 0.000 claims abstract description 18
- 239000000679 carrageenan Substances 0.000 claims abstract description 14
- 235000010418 carrageenan Nutrition 0.000 claims abstract description 14
- 229920001525 carrageenan Polymers 0.000 claims abstract description 14
- 229940113118 carrageenan Drugs 0.000 claims abstract description 14
- UHVMMEOXYDMDKI-JKYCWFKZSA-L zinc;1-(5-cyanopyridin-2-yl)-3-[(1s,2s)-2-(6-fluoro-2-hydroxy-3-propanoylphenyl)cyclopropyl]urea;diacetate Chemical compound [Zn+2].CC([O-])=O.CC([O-])=O.CCC(=O)C1=CC=C(F)C([C@H]2[C@H](C2)NC(=O)NC=2N=CC(=CC=2)C#N)=C1O UHVMMEOXYDMDKI-JKYCWFKZSA-L 0.000 claims abstract description 14
- 229920001817 Agar Polymers 0.000 claims abstract description 10
- 238000003860 storage Methods 0.000 claims abstract description 9
- 229940079593 drug Drugs 0.000 claims abstract description 7
- 239000010175 Yi-Gan San Substances 0.000 claims abstract description 6
- 239000000843 powder Substances 0.000 claims description 16
- 239000005022 packaging material Substances 0.000 claims description 15
- 235000003599 food sweetener Nutrition 0.000 claims description 13
- 239000003765 sweetening agent Substances 0.000 claims description 13
- 239000000463 material Substances 0.000 claims description 8
- 239000009181 shakuyaku-kanzoh-toh Substances 0.000 claims description 8
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 claims description 6
- 241000411851 herbal medicine Species 0.000 claims description 5
- HDTRYLNUVZCQOY-UHFFFAOYSA-N α-D-glucopyranosyl-α-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OC1C(O)C(O)C(O)C(CO)O1 HDTRYLNUVZCQOY-UHFFFAOYSA-N 0.000 claims description 3
- OWEGMIWEEQEYGQ-UHFFFAOYSA-N 100676-05-9 Natural products OC1C(O)C(O)C(CO)OC1OCC1C(O)C(O)C(O)C(OC2C(OC(O)C(O)C2O)CO)O1 OWEGMIWEEQEYGQ-UHFFFAOYSA-N 0.000 claims description 3
- WBZFUFAFFUEMEI-UHFFFAOYSA-M Acesulfame k Chemical compound [K+].CC1=CC(=O)[N-]S(=O)(=O)O1 WBZFUFAFFUEMEI-UHFFFAOYSA-M 0.000 claims description 3
- 108010011485 Aspartame Proteins 0.000 claims description 3
- 239000004386 Erythritol Substances 0.000 claims description 3
- UNXHWFMMPAWVPI-UHFFFAOYSA-N Erythritol Natural products OCC(O)C(O)CO UNXHWFMMPAWVPI-UHFFFAOYSA-N 0.000 claims description 3
- GUBGYTABKSRVRQ-PICCSMPSSA-N Maltose Natural products O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@@H]1O[C@@H]1[C@@H](CO)OC(O)[C@H](O)[C@H]1O GUBGYTABKSRVRQ-PICCSMPSSA-N 0.000 claims description 3
- 229920002472 Starch Polymers 0.000 claims description 3
- HDTRYLNUVZCQOY-WSWWMNSNSA-N Trehalose Natural products O[C@@H]1[C@@H](O)[C@@H](O)[C@@H](CO)O[C@@H]1O[C@@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 HDTRYLNUVZCQOY-WSWWMNSNSA-N 0.000 claims description 3
- TVXBFESIOXBWNM-UHFFFAOYSA-N Xylitol Natural products OCCC(O)C(O)C(O)CCO TVXBFESIOXBWNM-UHFFFAOYSA-N 0.000 claims description 3
- 235000010358 acesulfame potassium Nutrition 0.000 claims description 3
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- HDTRYLNUVZCQOY-LIZSDCNHSA-N alpha,alpha-trehalose Chemical compound O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@@H]1O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 HDTRYLNUVZCQOY-LIZSDCNHSA-N 0.000 claims description 3
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- 239000000605 aspartame Substances 0.000 claims description 3
- 235000010357 aspartame Nutrition 0.000 claims description 3
- IAOZJIPTCAWIRG-QWRGUYRKSA-N aspartame Chemical compound OC(=O)C[C@H](N)C(=O)N[C@H](C(=O)OC)CC1=CC=CC=C1 IAOZJIPTCAWIRG-QWRGUYRKSA-N 0.000 claims description 3
- 229960003438 aspartame Drugs 0.000 claims description 3
- UNXHWFMMPAWVPI-ZXZARUISSA-N erythritol Chemical compound OC[C@H](O)[C@H](O)CO UNXHWFMMPAWVPI-ZXZARUISSA-N 0.000 claims description 3
- 235000019414 erythritol Nutrition 0.000 claims description 3
- 229940009714 erythritol Drugs 0.000 claims description 3
- HEBKCHPVOIAQTA-UHFFFAOYSA-N meso ribitol Natural products OCC(O)C(O)C(O)CO HEBKCHPVOIAQTA-UHFFFAOYSA-N 0.000 claims description 3
- 235000019698 starch Nutrition 0.000 claims description 3
- 239000008107 starch Substances 0.000 claims description 3
- 239000006188 syrup Substances 0.000 claims description 3
- 235000020357 syrup Nutrition 0.000 claims description 3
- HRXKRNGNAMMEHJ-UHFFFAOYSA-K trisodium citrate Chemical compound [Na+].[Na+].[Na+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O HRXKRNGNAMMEHJ-UHFFFAOYSA-K 0.000 claims description 3
- 239000000811 xylitol Substances 0.000 claims description 3
- 235000010447 xylitol Nutrition 0.000 claims description 3
- HEBKCHPVOIAQTA-SCDXWVJYSA-N xylitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)CO HEBKCHPVOIAQTA-SCDXWVJYSA-N 0.000 claims description 3
- 229960002675 xylitol Drugs 0.000 claims description 3
- 238000013329 compounding Methods 0.000 claims 1
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- 235000013355 food flavoring agent Nutrition 0.000 claims 1
- 238000007789 sealing Methods 0.000 claims 1
- 238000002360 preparation method Methods 0.000 abstract description 22
- 239000008272 agar Substances 0.000 abstract description 6
- 238000000034 method Methods 0.000 abstract description 6
- 238000004806 packaging method and process Methods 0.000 abstract description 4
- 235000008598 Paeonia lactiflora Nutrition 0.000 abstract 1
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- 238000003475 lamination Methods 0.000 abstract 1
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- 229940088679 drug related substance Drugs 0.000 description 10
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- 239000008186 active pharmaceutical agent Substances 0.000 description 6
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- 239000003755 preservative agent Substances 0.000 description 5
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- 239000004480 active ingredient Substances 0.000 description 4
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- 239000008203 oral pharmaceutical composition Substances 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- 239000003390 Chinese drug Substances 0.000 description 3
- 108010010803 Gelatin Proteins 0.000 description 3
- 229920002125 Sokalan® Polymers 0.000 description 3
- 235000019658 bitter taste Nutrition 0.000 description 3
- 238000011049 filling Methods 0.000 description 3
- 238000009472 formulation Methods 0.000 description 3
- 239000008273 gelatin Substances 0.000 description 3
- 229920000159 gelatin Polymers 0.000 description 3
- 235000019322 gelatine Nutrition 0.000 description 3
- 235000011852 gelatine desserts Nutrition 0.000 description 3
- 229940069445 licorice extract Drugs 0.000 description 3
- 239000004584 polyacrylic acid Substances 0.000 description 3
- 230000002335 preservative effect Effects 0.000 description 3
- 239000005711 Benzoic acid Substances 0.000 description 2
- 239000002585 base Substances 0.000 description 2
- 235000010233 benzoic acid Nutrition 0.000 description 2
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
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- 230000007774 longterm Effects 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000000546 pharmaceutical excipient Substances 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 238000011160 research Methods 0.000 description 2
- WXMKPNITSTVMEF-UHFFFAOYSA-M sodium benzoate Chemical compound [Na+].[O-]C(=O)C1=CC=CC=C1 WXMKPNITSTVMEF-UHFFFAOYSA-M 0.000 description 2
- 235000010234 sodium benzoate Nutrition 0.000 description 2
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- 235000006200 Glycyrrhiza glabra Nutrition 0.000 description 1
- 235000017382 Glycyrrhiza lepidota Nutrition 0.000 description 1
- 229920000161 Locust bean gum Polymers 0.000 description 1
- 244000170916 Paeonia officinalis Species 0.000 description 1
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- 206010035669 Pneumonia aspiration Diseases 0.000 description 1
- 201000009807 aspiration pneumonia Diseases 0.000 description 1
- 239000000795 chinese herbal drug Substances 0.000 description 1
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- 238000007796 conventional method Methods 0.000 description 1
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- 238000009826 distribution Methods 0.000 description 1
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- 239000000321 herbal drug Substances 0.000 description 1
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- 229940010454 licorice Drugs 0.000 description 1
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- 230000007721 medicinal effect Effects 0.000 description 1
- 229940126601 medicinal product Drugs 0.000 description 1
- 239000000820 nonprescription drug Substances 0.000 description 1
- 229940124595 oriental medicine Drugs 0.000 description 1
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- Medicines Containing Plant Substances (AREA)
- Medicinal Preparation (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Abstract
Description
本発明は、漢方原薬と基剤とを含み、さらに甘味料及び矯味剤を混和して生成される漢方ゼリー医薬組成物を、一回服用量単位毎に小分け包装した漢方ゼリー医薬品に関するものである。 The present invention relates to a Kampo jelly pharmaceutical comprising a Kampo drug substance and a base, and further comprising a Chinese medicine jelly pharmaceutical composition produced by mixing a sweetener and a corrigent, and divided and packaged for each single dose unit. is there.
漢方製剤の医療用医薬品には散剤または顆粒剤としたものが多く、漢方製剤の一般用医薬品には散剤、顆粒剤に加え、錠剤、液剤などとしたものがある。該漢方製剤において漢方原薬は、一回の服用量が数百ミリグラムのものから数グラムを超えるものに及ぶ。
漢方製剤を散剤にする場合、吸湿性を有することから、漢方原薬の2〜3倍量の賦形剤を添加して製剤化しなければならない。特に、漢方原薬の一回の服用量が3gを超える漢方製剤は、散剤にすると一回の服用量が非常に多くなるので、服用しづらく、口中に広がってむせたり、苦味が残ったり、服用後長時間にわたって違和感が残ったりする等の問題があった。
漢方製剤を錠剤にする場合、上記散剤にする場合と同様に、漢方原薬の一回の服用量が3gを超えるものは、一錠あたりの重量が三百ミリグラムを超えてしまい、かつ必要な錠数も多くなるので、服用のしづらさが問題であった。
漢方製剤を液剤にする場合は、漢方特有の味や匂いを和らげるために、多くの場合、漢方原薬を希釈していることから、服用量が多くなり、また容器が比較的大きくその材質、形状も限定されるなど必ずしも利便性が高いとは言えず、服用コンプライアンス、易服用、利便性などから問題となっている。また液剤は、誤嚥を最も引き起こしやすく、誤嚥性肺炎に繋がることから、特に高齢者には敬遠されている。
Many medicinal drugs for Kampo preparations are powders or granules, and over-the-counter drugs for Kampo preparations are tablets, liquids, etc. in addition to powders and granules. In the Chinese medicine formulation, the Chinese medicine active ingredient ranges from several hundred milligrams to over several grams.
When a Chinese medicine preparation is used as a powder, it has a hygroscopic property, so it must be formulated by adding 2 to 3 times as much excipient as the Chinese medicine. In particular, Kampo medicines with a single dose of 3g or more in Chinese herbal medicines are very difficult to take when powdered, so it is difficult to take, spread in the mouth, and bitterness remains. There were problems such as a feeling of discomfort remaining for a long time after taking the medicine.
When making a Kampo preparation into a tablet, as in the case of the above powder, if the dose of Kampo medicine exceeds 3g, the weight per tablet exceeds 300 milligrams and is necessary. Since the number of tablets increases, the difficulty of taking was a problem.
In the case of using Kampo preparations as liquids, in order to relieve the taste and odor peculiar to Kampo, in many cases, the Kampo drug substance is diluted, so the dosage is increased, the container is relatively large, its material, Convenience is not necessarily high because the shape is limited, and it is a problem from taking compliance, easy taking, convenience and the like. In addition, the liquid agent is most likely to cause aspiration and leads to aspiration pneumonia.
上記のように、漢方製剤については種々の問題があり、こうした問題を解決するためにさまざまな漢方製剤の剤型検討がなされ、そうした中でもゼリー状製剤はその解決の為の有効な一手段と考えられている。しかし、特許文献1のように、ゼラチンを用いてゼリー製剤化したものについては、保存安定性が低く、冷所での保存が必要となる制限がある。また、医薬品としての長期安定性試験や、加速安定性試験に耐える組成物ではないことから、製品の流通面からもゼラチンを用いたゼリー状製剤は、医薬品レベル製品としては問題がある。
As described above, there are various problems with Kampo preparations, and in order to solve these problems, various types of Kampo preparations have been studied. Among them, jelly-form preparations are considered to be an effective means for solving them. It has been. However, as disclosed in
一方、ゼラチンを用いずゼリー状製剤を創製した例として、基剤にカラギーナン等を用いた方法が提案されている(例えば、特許文献2〜5)。一例を挙げると、八味地黄丸、葛根湯、及び五苓散を漢方原薬とし、カラギーナン、ローカストビーンガム、及び、ポリアクリル酸又はポリアクリル酸の部分中和物もしくはポリアクリル酸塩を含有し、加速安定性(40℃、75%RH、6ヶ月)及び長期安定性(室温3年間)を有するゼリー状経口医薬組成物や、更にリン酸塩の緩衝剤を加えたゼリー状経口医薬組成物がある。
On the other hand, as an example of creating a jelly-like preparation without using gelatin, methods using carrageenan or the like as a base have been proposed (for example,
ところが、上記従来のゼリー状とした漢方製剤は、服用コンプライアンスや易服用や利便性等の問題が解決された一方で、粘弾性などの点から工業生産の際に利用する充填機で不具合を起こす可能性があり、また服用感においても必ずしも満足できるレベルにないという問題があった。 However, the above conventional jelly-form Kampo preparations have solved problems such as compliance, easy use and convenience, but have problems with filling machines used in industrial production in terms of viscoelasticity. There is a problem that there is a possibility that it is possible and that the feeling of taking is not always satisfactory.
本発明は、上記従来技術に存在する問題点に着目してなされたものであり、本発明者等は鋭意研究を重ねた結果、漢方原薬、基剤、賦形剤、包装材料、包装形態などを的確に選択することにより医薬品として安定かつ有効な漢方ゼリー医薬組成物の創製が可能であることを見出し、本発明を完成させた。 The present invention has been made paying attention to the problems existing in the above-mentioned prior art, and as a result of intensive research, the present inventors have conducted research on Kampo medicines, bases, excipients, packaging materials, and packaging forms. Thus, the present inventors have found that a stable and effective Kampo jelly pharmaceutical composition can be created as a medicinal product by accurately selecting the above.
すなわち本発明は、漢方原薬と、基剤としてカラギーナン及びカンテン末とを含み、更に甘味料及び矯味剤を混和して生成される漢方ゼリー医薬組成物を、一回服用量単位毎にスティック状のアルミラミネート包材に小分け包装してなる漢方ゼリー医薬品を提供するものである。
本発明によれば、粉末状または顆粒状の漢方製剤が服用し難い患者に対して服用し易いゼリー状経口医薬組成物、特に医薬品レベルの保存安定性が確保され、該患者が服用しやすい硬さで、喉ごし良く服用できる。
That is, the present invention provides a Chinese medicine jelly pharmaceutical composition containing a Chinese medicine active ingredient and carrageenan and agar powder as a base, and further mixed with a sweetener and a corrigent, in a stick form for each dose unit. Chinese medicine jelly medicines that are packaged in small quantities in aluminum laminate packaging materials.
According to the present invention, a jelly-form oral pharmaceutical composition that is easy to take for a patient who is difficult to take a powdered or granular Chinese medicine preparation, in particular, a storage stability at a pharmaceutical level is ensured, and the patient is hard to take. Now you can take your throat well.
より詳しくは、芍薬甘草湯エキス、あるいは抑肝散料エキスから選択される漢方原薬を含み、また基剤としてカラギーナン、カンテン末を含み、さらに甘味料、及び矯味剤を混和して生成される組成物を、先端の開封口が狭いスティック状のアルミラミネート包装材料に一回服用量単位毎1〜20gに小分け包装することを特徴とする漢方ゼリー医薬組成物に関するものである。 More specifically, it contains a Chinese herbal drug selected from Shakuyakukanzoto extract or Yokukansan extract, and contains carrageenan and agar powder as a base, and is further mixed with a sweetener and a corrigent. The present invention relates to a Kampo jelly pharmaceutical composition characterized in that the composition is packaged in a stick-shaped aluminum laminate packaging material having a narrow opening at the tip into 1 to 20 g per dose unit.
本発明において、漢方ゼリー医薬組成物の基剤であるカンテンとカラギーナンの配合組成は0.1〜1.0重量%であることが好ましく、より好ましくは0.3〜0.6重量%である。
甘味料は、粉末還元麦芽糖水飴、アセスルファムカリウム、アスパルテームからなる群から選択される少なくとも1種であり、その配合組成は、それぞれ1〜24重量%、0.001〜0.04重量%、0.01〜0.4重量%が好ましく、より好ましくは、それぞれ5〜18%、0.01〜0.03重量%、0.1〜0.3重量%である。
矯味剤は、キシリトール、エリスリトール、トレハロース、無水クエン酸、クエン酸ナトリウム水和物からなる群から選択される少なくとも1種であり、配合組成は、それぞれ1〜30重量%、1〜10重量%、1〜30重量%、0.01〜0.5重量%、0.01〜0.4重量%、が好ましく、より好ましくは、それぞれ5〜25重量%、2〜8重量%、5〜25重量%、0.1〜0.4重量%、0.05〜0.3重量%である。
In the present invention, the composition of Kanten and carrageenan, which is the base of the Kampo jelly pharmaceutical composition, is preferably 0.1 to 1.0% by weight, more preferably 0.3 to 0.6% by weight. .
The sweetener is at least one selected from the group consisting of powdered reduced maltose starch syrup, acesulfame potassium, and aspartame, and the blending composition thereof is 1 to 24% by weight, 0.001 to 0.04% by weight, and 0. 01 to 0.4% by weight is preferable, and more preferably 5 to 18%, 0.01 to 0.03% by weight, and 0.1 to 0.3% by weight, respectively.
The corrigent is at least one selected from the group consisting of xylitol, erythritol, trehalose, anhydrous citric acid, sodium citrate hydrate, and the blend composition is 1 to 30% by weight, 1 to 10% by weight, 1 to 30% by weight, 0.01 to 0.5% by weight, and 0.01 to 0.4% by weight are preferable, and more preferably 5 to 25% by weight, 2 to 8% by weight, and 5 to 25% by weight, respectively. %, 0.1 to 0.4% by weight, and 0.05 to 0.3% by weight.
本発明の漢方ゼリー医薬組成物は、防腐剤を含んでもよく、防腐剤は、安息香酸、安息香酸ナトリウム、パラオキシ安息香酸エチル、パラオキシ安息香酸プロピル、パラオキシ安息香酸ブチルなど、医薬品に配合できる防腐剤から任意に選んでよい。その配合量は基準に定める量の範囲で、任意の量を選択できる。また、香料も医薬品の基準の範囲内で添加することができる。 The Chinese medicine jelly pharmaceutical composition of the present invention may contain a preservative, and the preservative can be blended in a pharmaceutical such as benzoic acid, sodium benzoate, ethyl paraoxybenzoate, propyl paraoxybenzoate, butyl paraoxybenzoate, etc. You may choose from The blending amount can be selected within an amount range defined in the standard. In addition, fragrances can be added within the range of pharmaceutical standards.
本発明は漢方ゼリー状医薬組成物とその包装形態を一体化して一回毎の服用を適正にかつ容易にするものであるが、包装材として保存安定性の機能が高く、また誤用・誤嚥が起こりにくい1〜20gの漢方ゼリー医薬品組成物を個包装する形態として、アルミラミネートのスティック状のものが好ましく、また内容物を出しやすく、服用しやすい形状として、より好ましくはスティック状アルミラミネート包材の先端の開封口が狭く切り込みが入った形状のものが挙げられる。 The present invention integrates a Chinese medicine jelly-like pharmaceutical composition and its packaging form to make each dose properly and easily, but it has a high storage stability function as a packaging material, and is also misused / aspiration. As a form for individually packaging 1 to 20 g of Chinese medicine jelly pharmaceutical composition, which is less likely to occur, an aluminum laminate stick-like form is preferable, and as a form that is easy to take out the contents and easy to take, more preferably a stick-like aluminum laminate package A material having a narrow opening at the tip of the material and having a notch.
上記の問題点を解決する漢方製剤のゼリー製剤として、予め創製された漢方原薬エキスを用い、基剤としてカラギーナンとカンテン末を配合することで、保存安定性に優れた漢方ゼリー経口医薬組成物を得ることができる。更に、得られた漢方ゼリー医薬組成物を先端の開封口が狭いスティック状のアルミラミネート包装材料に一回服用量単位毎に封入することにより、服用しやすく、誤用を避けることができる。 Kampo jelly oral pharmaceutical composition with excellent storage stability by using carrageenan and kanteng powder as a base, using a pre-developed Kampo drug extract as a jelly formulation of a Kampo formulation that solves the above problems Can be obtained. Furthermore, by enclosing the obtained Chinese medicine jelly pharmaceutical composition in a stick-like aluminum laminate packaging material having a narrow opening at the tip for each dosage unit, it is easy to take and avoids misuse.
本発明における漢方ゼリー医薬組成物には、種々の薬効を得ることを目的として、漢方原薬が主成分として配合される。該漢方原薬には、液状、軟稠エキス状、乾燥エキス状のいずれの形態のものを使用してもよいが、例えば、日本薬局方カンゾウエキスの創製法にあるように、生薬を水抽出した後に濃縮し、エタノールを定量加え濾過、濃縮することで得られたエキス状の形態のものが望ましい。更に、本発明で使用する漢方原薬としては、ゼリー状漢方製剤としては上市されていない、芍薬甘草湯エキス、抑肝散料エキスが最も望ましい。 The Kampo jelly pharmaceutical composition of the present invention is blended with Kampo drug substance as the main component for the purpose of obtaining various medicinal effects. The herbal drug substance may be used in the form of liquid, soft extract, or dry extract. For example, as in the method of creating Japanese pharmacopoeia licorice extract, the crude drug is extracted with water. Then, it is concentrated, and an extract in the form of an extract obtained by quantitatively adding ethanol, filtering and concentrating is desirable. Further, as the Chinese herbal medicines used in the present invention, Shakuyakukanzoto extract and Yokukansan extract, which are not marketed as jelly-like Chinese medicine preparations, are most desirable.
本発明における漢方ゼリー医薬組成物には、該組成物をゼリー状にして飲みやすくすることを目的として、基剤が配合される。該基剤には、カラギーナン及びカンテン末が使用される。
上記漢方ゼリー医薬組成物中において、基剤であるカンテン末及びカラギーナンの各配合量は、それぞれ0.1〜1.0質量%であることが好ましく、0.3〜0.6質量%であることがより好ましい。漢方ゼリー医薬組成物中におけるカンテン末あるいはカラギーナンの配合量が0.1質量%に満たない場合、十分な服用感の改善に至らないおそれがあり、1.0質量%を超える場合、服用感の悪化を招くおそれがある。
In the Kampo jelly pharmaceutical composition of the present invention, a base is blended for the purpose of making the composition into a jelly form for easy drinking. As the base, carrageenan and agar powder are used.
In the above-mentioned Kampo jelly pharmaceutical composition, the blending amounts of Kanten powder and carrageenan as the base are each preferably 0.1 to 1.0% by mass, and 0.3 to 0.6% by mass. It is more preferable. If the blending amount of Kanteng powder or carrageenan in the Kampo jelly pharmaceutical composition is less than 0.1% by mass, there is a risk that the feeling of sufficient administration may not be improved. If it exceeds 1.0% by mass, May cause deterioration.
本発明における漢方ゼリー医薬組成物にあっては、更なる服用感の向上を図るべく、甘味料及び矯味剤が混和される。
上記甘味料は、漢方ゼリー医薬組成物に甘みをつけるためのものであって、上記漢方原薬による苦味を緩和するものである。該甘味料としては、粉末還元麦芽糖水飴、アセスルファムカリウム、およびアスパルテームが挙げられ、これらの群から選択される少なくとも1種が使用される。
上記矯味剤は、上記漢方原薬のような苦味を有するものを服用しやすくするものである。該矯味剤としては、キシリトール、エリスリトール、トレハロース水和物、無水クエン酸、およびクエン酸ナトリウム水和物が挙げられ、これらの群から選択される少なくとも1種が使用される。
In the Kampo jelly pharmaceutical composition of the present invention, a sweetener and a corrigent are mixed in order to further improve the feeling of dosing.
The sweetener is for sweetening the traditional Chinese medicine jelly pharmaceutical composition, and alleviates the bitter taste caused by the traditional Chinese medicine. Examples of the sweetener include powdered reduced maltose starch syrup, acesulfame potassium, and aspartame, and at least one selected from these groups is used.
The taste-masking agent makes it easy to take a bitter taste like the above-mentioned Chinese medicine drug substance. Examples of the corrigent include xylitol, erythritol, trehalose hydrate, anhydrous citric acid, and sodium citrate hydrate, and at least one selected from these groups is used.
本発明の漢方ゼリー医薬組成物において、上記漢方原薬、上記基剤、上記甘味料及び上記矯味剤は、何れも工業的に生産されたものを利用することができる。
また、本発明の漢方ゼリー医薬組成物には、上記漢方原薬、上記基剤、上記甘味料及び上記矯味剤の他に、防腐剤、香料などの成分を混和してもよい。
上記防腐剤は、安息香酸、安息香酸ナトリウム、パラオキシ安息香酸エチル、パラオキシ安息香酸プロピル、パラオキシ安息香酸ブチルなど、医薬品に配合できる防腐剤から任意に選んでよく、配合量は基準に定める量の範囲で、任意の量を選択できる。
また、香料も医薬品の基準の範囲内で添加することができる。
In the traditional Chinese medicine jelly pharmaceutical composition of the present invention, any of the above-mentioned traditional Chinese medicines, the above-mentioned base, the above-mentioned sweetener, and the above-mentioned corrigent can be produced industrially.
In addition, the Kampo jelly pharmaceutical composition of the present invention may contain ingredients such as preservatives and perfumes in addition to the above-mentioned Kampo drug substance, the above-mentioned base, the above-mentioned sweetener and the above-mentioned corrigent.
The preservative may be arbitrarily selected from preservatives that can be added to pharmaceuticals such as benzoic acid, sodium benzoate, ethyl paraoxybenzoate, propyl paraoxybenzoate, butyl paraoxybenzoate, etc. You can select any amount.
In addition, fragrances can be added within the range of pharmaceutical standards.
本発明の漢方ゼリー医薬組成物を製造する方法は特に制限されないが、通常の製造機器を利用することで製造することが可能である。
また、本発明の漢方ゼリー医薬組成物は、上記漢方原薬に基剤を配合してゼリー状とすることの他には、従来公知の方法で調製される。例えば、ゼリー状とするための基剤であるカラギーナン及びカンテン末を適当な温度で分散媒に分散させ、温度を調節しながらこれに上記漢方原薬を分散させ、更に甘味料及び矯味剤を混和し、その後、冷却してゲル化させることによって調製することが可能である。
The method for producing the Kampo jelly pharmaceutical composition of the present invention is not particularly limited, but can be produced by using ordinary production equipment.
Moreover, the pharmaceutical composition of Kampo jelly of this invention is prepared by a conventionally well-known method other than mix | blending a base with the said Chinese medicine active ingredient, and making it into a jelly form. For example, carrageenan and agar powder, which are bases for making a jelly form, are dispersed in a dispersion medium at an appropriate temperature, and the above-mentioned Chinese medicine drug substance is dispersed therein while adjusting the temperature, and further a sweetener and a corrigent are mixed. Then, it can be prepared by cooling and gelling.
上記のようにして調製された漢方ゼリー医薬組成物を、一回服用量単位毎にスティック状のアルミラミネート包材に小分け包装することにより、本発明の漢方ゼリー医薬品が構成される。
図1に示すように、上記スティック状のアルミラミネート包材1は、シート材1Aを筒状に丸めたうえで両端部の開口のうち一端部1Bを、超音波接着、熱溶着等の方法で綴じて袋状にすることにより、その内部の空間が上記漢方ゼリー医薬組成物を収容する収容部2とされている。更に、筒状に丸められたシート材1Aの両端部の開口のうち他端部1Cには、前記収容部2を密閉するべく、該他端部1Cを超音波接着、熱溶着等の方法で綴じることにより、閉塞部3が、斜め方向へ伸びるように設けられている。更に該他端部1Cには、切り込み部4が、該閉塞部3と交差する横方向へ伸びるように形成されている。そして、前記アルミラミネート包材1は、該切り込み部4で該閉塞部3の中間部を切断しつつ該他端部1Cを切除することにより、前記収容部2を開放して上記漢方ゼリー医薬組成物を前記収容部2外へ吐出可能とする開封口5(図中に点線で示す)が形成されるようになっている。該開封口5は、上記閉塞部1Cが斜めに設けられ、その中間部が上記切り込み部4によって切断されることにより、上記他端部1Cの切除後も上記閉塞部1Cの一部が残ることで、上記他端部1Cの幅長Lよりも狭められた状態で形成されるように構成されている。そして、前記のように該開封口5は、狭くすることにより、収容部2内での塊状から形が崩れて喉に詰まらない形状となるので、窒息リスクの低減に有効な形状とされる。
The Chinese medicine jelly pharmaceutical composition of the present invention is constituted by subdividing the Chinese medicine jelly pharmaceutical composition prepared as described above into a stick-like aluminum laminate packaging material for each dose unit.
As shown in FIG. 1, the stick-shaped aluminum
本発明の漢方ゼリー医薬組成物の充填量は、特に限定されないが、例えば服用し易いスティックに1包あたり1回あたりの投与量1〜20gを充填し、服用者に正しく服用させることができる。
この漢方ゼリー医薬組成物を、先端を狭めたスティック状のアルミラミネート包材に一回服用量単位毎に1〜20gに小分け包装し漢方ゼリー医薬組成物の完成品を得ることは工業的に生産された充填機を使用することにより可能である。
The filling amount of the Kampo jelly pharmaceutical composition of the present invention is not particularly limited. For example, a dose of 1 to 20 g per pack can be filled in a stick that is easy to take, and the user can take it correctly.
It is industrially produced to obtain a finished Kampo jelly pharmaceutical composition by packing this Kampo jelly pharmaceutical composition into sticky aluminum laminate wrapping material with a narrowed tip into 1-20g per dose unit. This is possible by using an automated filling machine.
次に本発明の試験例をあげて説明するが、本発明はこれらに限定されるものではない。
〔漢方原薬1〕
芍薬甘草湯軟エキスA: シャクヤク 3kg、カンゾウ 3kgを、10倍量の30vol%エタノールを抽出溶媒に用いて50℃で1時間抽出した後、この抽出液をろ過し、得られたろ液を減圧濃縮することで、芍薬甘草湯エキスA 4kgを得た。
芍薬甘草湯軟エキスB: 上記芍薬甘草湯エキスA(4kg)の内の2kgを取り、これを常水5Lに加えて撹拌した後、遠心分離ろ過し、得られたろ液を減圧濃縮することで、芍薬甘草湯エキスB 1.8kgを得た。
Next, although the test example of this invention is given and demonstrated, this invention is not limited to these.
[Chinese drug substance 1]
Shakuyakukanzo-to soft extract A: Extracted 3 kg of peony and 3 kg of licorice at 50 ° C. for 1 hour using 10 times the amount of 30 vol% ethanol as an extraction solvent, filtered this extract, and concentrated the resulting filtrate under reduced pressure As a result, 4 kg of glaze licorice extract A was obtained.
Shakuyakukanzoto soft extract B: Take 2 kg of the above-mentioned Shakuyakukanzoto extract A (4 kg), add it to 5 L of normal water, stir, centrifuge and filter, and concentrate the resulting filtrate under reduced pressure. Thus, 1.8 kg of glaze licorice extract B was obtained.
〔試料作製1〕
カンテン末を予め熱湯に溶解させたうえで、上記芍薬甘草湯エキスBを用いるとともに、常法に従って表1に示す組成でゼリー剤を調製し、実施例1,2及び比較例1〜3の試料を得た。
[Sample preparation 1]
Kanteng powder was dissolved in hot water in advance, and the above-mentioned Shakuyakukanzoto extract B was used, and jelly preparations were prepared with the compositions shown in Table 1 according to conventional methods. Samples of Examples 1 and 2 and Comparative Examples 1 to 3 Got.
〔性状比較試験1〕
上記実施例1,2及び比較例1〜3の試料をそれぞれアルミラミネート包材に10gずつ封入し、その性状を比較した。性状比較試験の項目及び結果を表2に示す。
試験の結果、実施例1,2は比較例1〜3に比べ、離水が少なく、服用感、使用性および粘弾性に優れていた。
[Property comparison test 1]
10 g of each of the samples of Examples 1 and 2 and Comparative Examples 1 to 3 were sealed in an aluminum laminate packaging material, and the properties were compared. Table 2 shows the items and results of the property comparison test.
As a result of the test, Examples 1 and 2 had less water separation than Comparative Examples 1 to 3, and were excellent in feeling of use, usability and viscoelasticity.
〔漢方原薬2〕
上記〔漢方原薬1〕と同様にして、抑肝散料エキス10.7gを創製した。
〔試料作製2〕
上記抑肝散料エキスを用い、上記〔試料作製1〕と同様にして表3に示す組成でゼリー剤を調製し、実施例3,4及び比較例4,5の試料を得た。
[Chinese drug substance 2]
In the same manner as [Chinese drug substance 1], 10.7 g of yokukansan extract was created.
[Sample preparation 2]
Using the yokukan powder extract, a jelly agent was prepared with the composition shown in Table 3 in the same manner as in [Sample Preparation 1], and samples of Examples 3 and 4 and Comparative Examples 4 and 5 were obtained.
〔性状比較試験2〕
上記実施例3,4及び比較例4,5の試料をそれぞれアルミラミネート包材に15gずつ封入し、その性状を比較した。性状比較試験の項目及び結果を表4に示す。
試験の結果、実施例3,4は比較例4,5に比べ、服用感、使用性および粘弾性に優れていた。
[Property comparison test 2]
15 g of each of the samples of Examples 3 and 4 and Comparative Examples 4 and 5 were sealed in an aluminum laminate packaging material, and their properties were compared. Table 4 shows the items and results of the property comparison test.
As a result of the test, Examples 3 and 4 were superior to Comparative Examples 4 and 5 in taking feeling, usability and viscoelasticity.
本発明によって、予め創製した芍薬甘草湯エキス、あるいは抑肝散料エキスから選択される漢方原薬を含み、また基剤としてカラギーナン、カンテン末を含み、さらに甘味料、及び矯味剤を混和して生成される組成物を、一回服用量単位毎に先端を狭めたスティック状のアルミラミネート包材に1〜20gに小分け包装することを特徴とする漢方ゼリー医薬品を製造することが可能となる。 According to the present invention, it contains a traditional Chinese medicine active ingredient selected from a shakuyakukanzoto extract or a yokukansan extract, which contains carrageenan and agar powder as a base, and further contains a sweetener and a corrigent. It becomes possible to produce a Chinese medicine jelly medicine characterized in that the composition to be produced is subdivided into 1 to 20 g in a stick-like aluminum laminate packaging material having a narrowed tip for each dose unit.
1 アルミラミネート包材
1A シート材
1B 一端部
1C 他端部
2 収容部
3 閉塞部
4 切り込み部
5 開封口
DESCRIPTION OF
Claims (6)
ことを特徴とする漢方ゼリー医薬品。 Chinese medicine jelly pharmaceutical composition containing Chinese herbal medicine and carrageenan and Kanten powder as a base, and further mixed with sweetener and corrigent, stick-shaped aluminum laminate packaging material for each dose unit Chinese medicine jelly medicine characterized by being divided into small packages.
請求項1に記載の漢方ゼリー医薬品。 The traditional Chinese medicine jelly pharmaceutical according to claim 1, wherein the Chinese herbal medicine is Shakuyakukanzoto extract and / or Yokukansan extract.
請求項1又は請求項2に記載の漢方ゼリー医薬品。 In the said Kampo jelly pharmaceutical composition, each compounding quantity of the said carrageenan which is the said base and Kanten powder is set to 0.1 to 1.0 weight%, respectively, The Kampo of Claim 1 or Claim 2 set Jelly medicines.
上記矯味剤は、キシリトール、エリスリトール、トレハロース水和物、無水クエン酸、クエン酸ナトリウム水和物からなる群から選択される少なくとも1種である
請求項1から請求項3のうち何れか一項に記載の漢方ゼリー医薬品。 The sweetener is at least one selected from the group consisting of powdered reduced maltose starch syrup, acesulfame potassium, and aspartame,
The said flavoring agent is at least 1 sort (s) selected from the group which consists of a xylitol, an erythritol, a trehalose hydrate, an anhydrous citric acid, and a sodium citrate hydrate. The described Kampo jelly medicine.
請求項1から請求項4のうちいずれか一項に記載の漢方ゼリー医薬品。 The Chinese medicine jelly according to any one of claims 1 to 4, wherein 1 to 20 g of the Chinese medicine jelly pharmaceutical composition is packaged in the stick-shaped aluminum laminate packaging material as a single dose unit. Pharmaceuticals.
請求項1から請求項5のうちいずれか一項に記載の漢方ゼリー医薬品。
The stick-shaped aluminum laminate packaging material is formed by rounding a sheet material into a cylindrical shape, binding one end of the opening at both ends into a bag shape, so that the space inside the above-mentioned Kampo jelly pharmaceutical composition Further, a closing portion and a cut portion for sealing the storage portion are provided at the other end of the openings at both ends, and the closing portion is cut by the cut portion so as to cut the closing portion. 2. An opening for allowing the Chinese medicine jelly pharmaceutical composition to be discharged out of the housing part by opening the medicine is formed in a state narrower than the width of the other end part. The Chinese medicine jelly pharmaceutical according to any one of claims 1 to 5.
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JP2017137246A (en) * | 2016-02-01 | 2017-08-10 | 松浦薬業株式会社 | Chinese medicine jelly pharmaceutical composition |
CN109091504A (en) * | 2018-08-24 | 2018-12-28 | 江西滕王阁药业有限公司 | A kind of Chinese medicine maintenance process |
CN114585267A (en) * | 2019-10-25 | 2022-06-03 | 住友化学株式会社 | Food composition |
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JP2004059503A (en) * | 2002-07-29 | 2004-02-26 | Teikoku Kanpo Seiyaku Kk | Chinese medicine-based jellylike pharmaceutical composition |
JP2004256495A (en) * | 2003-02-27 | 2004-09-16 | Taisho Pharmaceut Co Ltd | Jelling agent |
JP2007238561A (en) * | 2006-03-10 | 2007-09-20 | Taiho Yakuhin Kogyo Kk | Paeoniflorin-containing jelly preparation |
JP2012051621A (en) * | 2010-09-01 | 2012-03-15 | Kagayaki:Kk | Packaging bag |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
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JP2017137246A (en) * | 2016-02-01 | 2017-08-10 | 松浦薬業株式会社 | Chinese medicine jelly pharmaceutical composition |
CN109091504A (en) * | 2018-08-24 | 2018-12-28 | 江西滕王阁药业有限公司 | A kind of Chinese medicine maintenance process |
CN114585267A (en) * | 2019-10-25 | 2022-06-03 | 住友化学株式会社 | Food composition |
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