JP2016216652A - 発泡錠剤及びその製造方法 - Google Patents
発泡錠剤及びその製造方法 Download PDFInfo
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- JP2016216652A JP2016216652A JP2015104872A JP2015104872A JP2016216652A JP 2016216652 A JP2016216652 A JP 2016216652A JP 2015104872 A JP2015104872 A JP 2015104872A JP 2015104872 A JP2015104872 A JP 2015104872A JP 2016216652 A JP2016216652 A JP 2016216652A
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- JP
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- Prior art keywords
- tablet
- fragrance
- component
- effervescent
- effervescent tablet
- Prior art date
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- 238000004519 manufacturing process Methods 0.000 title claims abstract description 38
- 238000005187 foaming Methods 0.000 title abstract description 6
- 239000000203 mixture Substances 0.000 claims abstract description 26
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- 150000007524 organic acids Chemical class 0.000 claims abstract description 10
- 150000007522 mineralic acids Chemical class 0.000 claims abstract description 9
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 claims abstract description 8
- 239000007938 effervescent tablet Substances 0.000 claims description 118
- 239000003826 tablet Substances 0.000 claims description 95
- 239000003205 fragrance Substances 0.000 claims description 89
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- JRKICGRDRMAZLK-UHFFFAOYSA-L peroxydisulfate Chemical compound [O-]S(=O)(=O)OOS([O-])(=O)=O JRKICGRDRMAZLK-UHFFFAOYSA-L 0.000 claims description 12
- 238000000034 method Methods 0.000 claims description 9
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 7
- 239000001257 hydrogen Substances 0.000 claims description 7
- 229910052739 hydrogen Inorganic materials 0.000 claims description 7
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- 230000000052 comparative effect Effects 0.000 description 19
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- 230000000694 effects Effects 0.000 description 16
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- 238000002156 mixing Methods 0.000 description 3
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- 238000003860 storage Methods 0.000 description 3
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- 230000037303 wrinkles Effects 0.000 description 3
- GRWFGVWFFZKLTI-IUCAKERBSA-N (-)-α-pinene Chemical compound CC1=CC[C@@H]2C(C)(C)[C@H]1C2 GRWFGVWFFZKLTI-IUCAKERBSA-N 0.000 description 2
- ZCHHRLHTBGRGOT-SNAWJCMRSA-N (E)-hex-2-en-1-ol Chemical compound CCC\C=C\CO ZCHHRLHTBGRGOT-SNAWJCMRSA-N 0.000 description 2
- BJEPYKJPYRNKOW-REOHCLBHSA-N (S)-malic acid Chemical compound OC(=O)[C@@H](O)CC(O)=O BJEPYKJPYRNKOW-REOHCLBHSA-N 0.000 description 2
- ZPVFWPFBNIEHGJ-UHFFFAOYSA-N 2-octanone Chemical compound CCCCCCC(C)=O ZPVFWPFBNIEHGJ-UHFFFAOYSA-N 0.000 description 2
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- GNKZMNRKLCTJAY-UHFFFAOYSA-N 4'-Methylacetophenone Chemical compound CC(=O)C1=CC=C(C)C=C1 GNKZMNRKLCTJAY-UHFFFAOYSA-N 0.000 description 2
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- WEEGYLXZBRQIMU-UHFFFAOYSA-N Eucalyptol Chemical compound C1CC2CCC1(C)OC2(C)C WEEGYLXZBRQIMU-UHFFFAOYSA-N 0.000 description 2
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- 239000002736 nonionic surfactant Substances 0.000 description 1
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- 239000012188 paraffin wax Substances 0.000 description 1
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- 239000010452 phosphate Substances 0.000 description 1
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- WRMXOVHLRUVREB-UHFFFAOYSA-N phosphono phosphate;tributylazanium Chemical compound OP(O)(=O)OP([O-])([O-])=O.CCCC[NH+](CCCC)CCCC.CCCC[NH+](CCCC)CCCC WRMXOVHLRUVREB-UHFFFAOYSA-N 0.000 description 1
- 239000001738 pogostemon cablin oil Substances 0.000 description 1
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- XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 description 1
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- TYJJADVDDVDEDZ-UHFFFAOYSA-M potassium hydrogencarbonate Chemical compound [K+].OC([O-])=O TYJJADVDDVDEDZ-UHFFFAOYSA-M 0.000 description 1
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- 238000003825 pressing Methods 0.000 description 1
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- 102000004169 proteins and genes Human genes 0.000 description 1
- GRWFGVWFFZKLTI-UHFFFAOYSA-N rac-alpha-Pinene Natural products CC1=CCC2C(C)(C)C1C2 GRWFGVWFFZKLTI-UHFFFAOYSA-N 0.000 description 1
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- RYYKJJJTJZKILX-UHFFFAOYSA-M sodium octadecanoate Chemical compound [Na+].CCCCCCCCCCCCCCCCCC([O-])=O RYYKJJJTJZKILX-UHFFFAOYSA-M 0.000 description 1
- 239000012418 sodium perborate tetrahydrate Substances 0.000 description 1
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- CHQMHPLRPQMAMX-UHFFFAOYSA-L sodium persulfate Substances [Na+].[Na+].[O-]S(=O)(=O)OOS([O-])(=O)=O CHQMHPLRPQMAMX-UHFFFAOYSA-L 0.000 description 1
- 229910000031 sodium sesquicarbonate Inorganic materials 0.000 description 1
- 235000018341 sodium sesquicarbonate Nutrition 0.000 description 1
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- 239000002562 thickening agent Substances 0.000 description 1
- BSVBQGMMJUBVOD-UHFFFAOYSA-N trisodium borate Chemical class [Na+].[Na+].[Na+].[O-]B([O-])[O-] BSVBQGMMJUBVOD-UHFFFAOYSA-N 0.000 description 1
- WCTAGTRAWPDFQO-UHFFFAOYSA-K trisodium;hydrogen carbonate;carbonate Chemical compound [Na+].[Na+].[Na+].OC([O-])=O.[O-]C([O-])=O WCTAGTRAWPDFQO-UHFFFAOYSA-K 0.000 description 1
- KYWIYKKSMDLRDC-UHFFFAOYSA-N undecan-2-one Chemical compound CCCCCCCCCC(C)=O KYWIYKKSMDLRDC-UHFFFAOYSA-N 0.000 description 1
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Landscapes
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Abstract
Description
項1.下記(A)成分及び下記(B)成分を含有する混合物を打錠して錠剤を形成する第1工程と、該工程により得られた錠剤に下記(C)成分を担持させる第2工程を含む、下記(A)〜(C)成分を含有する発泡錠剤の製造方法:
(A)炭酸塩及び/又は炭酸水素塩、
(B)有機酸及び/又は無機酸、
(C)香料。
項2.前記発泡錠剤中の香料の含有量が0.1〜10重量%である、項1に記載の製造方法。
項3.前記発泡錠剤が更に下記(D)及び/又は下記(E)成分を含有し、前記第1工程が、前記(A)成分及び(B)成分ならびに該(D)及び/又は(E)成分を含有する混合物を打錠して錠剤を形成する工程である、項1または2に記載の製造方法:
(D)過硫酸塩及び/又は過硫酸水素塩、
(E)過ホウ酸塩。
項4.前記第1工程により得られた錠剤がその一部に凹部が形成されているものである、項1〜3のいずれかに記載の製造方法。
項5.項1〜4のいずれかに記載の製造方法により得られる発泡錠剤。
(A)炭酸塩及び/又は炭酸水素塩、
(B)有機酸及び/又は無機酸、
(C)香料。
発泡錠剤
本発明の発泡錠剤は下記(A)〜(C)成分を含有する。
(A)炭酸塩及び/又は炭酸水素塩として、従来公知の炭酸塩及び/又は炭酸水素塩が挙げられ、本分野において発泡剤の一成分として従来使用されてきた炭酸塩及び/又は炭酸水素塩が好ましく挙げられる。
(B)有機酸及び/又は無機酸として、従来公知の有機酸及び/又は無機酸が挙げられ、本分野において発泡剤の一成分として従来使用されてきた有機酸及び/又は無機酸が好ましく挙げられる。
(C)香料は、用途や趣向性に応じて適宜決定すればよく制限されない。香料として、精油等の天然香料を単独もしくは組み合わせて用いてもよく、合成の単品香料を単独もしくは組み合わせて用いてもよく、また、天然香料と合成香料を任意に組み合わせて調合香料として用いてもよい。
本発明の発泡錠剤には、本発明の効果を妨げない範囲で、必要に応じて任意の成分を更に含有してもよい。
本発明は、下記(A)成分及び下記(B)成分を含有する混合物を打錠して錠剤を形成する第1工程と、該工程により得られた錠剤に下記(C)成分を担持させる第2工程を含む、下記(A)〜(C)成分を含有する発泡錠剤の製造方法を提供する。
(A)炭酸塩及び/又は炭酸水素塩
(B)有機酸及び/又は無機酸
(C)香料
該第1工程は、該(A)及び(B)成分を含有する混合物を打錠して錠剤を形成できる限り制限されない。該(A)及び(B)成分は前述の通りであり、第1工程で形成される錠剤は、前述の発泡錠剤中の含有量が充足される範囲において該(A)及び(B)成分を含有する。また、第1工程で形成される錠剤は、必要に応じて前述の任意の成分、また、スティッキングが生じないことを限度として前記(C)成分の一部、すなわち香料の一部を更に含有してもよい。任意の成分や香料も前述と同様に説明され、前述の発泡錠剤中の各成分の含有量が前記説明の通り充足される範囲において該錠剤に含有される。
1.発泡錠剤の製造
表1に従い、発泡錠剤(実施例1)、比較発泡錠剤(比較例1)、参考発泡錠剤(参考例1)を製造した。
各発泡錠剤におけるスティッキング評価は、前述の油圧ポンプによる打錠後、上下の杵への粉体の付着具合と製造された錠剤の表面の状態とを、目視で観察することにより行った。スティッキングが認められたものをスティッキング「あり」、認められなかったものを「なし」とした。
結果を表1に示す。
膨張率(%)={(保存後の体積)−(密封直後の体積)}÷(密封直後の体積)×100
1.発泡錠剤の製造、評価
実施例1において香料の種類及び含有量を代えた以外は、表2に従って前述と同様にして、発泡錠剤(実施例4〜7)を製造、評価した。
結果を表2に示す。
1.発泡錠剤の製造、評価
表3に従い、比較発泡錠剤(比較例2)、参考発泡錠剤(参考例2)を製造した。該比較発泡錠剤は、従来通り、賦形剤に香料をあらかじめ含浸させて、これを他の成分と混合して製造した発泡錠剤である。一方、該参考発泡錠剤は、香料を用いていない以外は比較例2の比較発泡錠剤と同様にして製造した発泡錠剤であり、賦形剤を他の成分と混合したものである。
結果を表3に示す。
Claims (5)
- 下記(A)成分及び下記(B)成分を含有する混合物を打錠して錠剤を形成する第1工程と、該工程により得られた錠剤に下記(C)成分を担持させる第2工程を含む、下記(A)〜(C)成分を含有する発泡錠剤の製造方法:
(A)炭酸塩及び/又は炭酸水素塩、
(B)有機酸及び/又は無機酸、
(C)香料。 - 前記発泡錠剤中の香料の含有量が0.1〜10重量%である、請求項1に記載の製造方法。
- 前記発泡錠剤が更に下記(D)及び/又は下記(E)成分を含有し、前記第1工程が、前記(A)成分及び(B)成分ならびに該(D)及び/又は(E)成分を含有する混合物を打錠して錠剤を形成する工程である、請求項1または2に記載の製造方法:
(D)過硫酸塩及び/又は過硫酸水素塩、
(E)過ホウ酸塩。 - 前記第1工程により得られた錠剤がその一部に凹部が形成されているものである、請求項1〜3のいずれかに記載の製造方法。
- 請求項1〜4のいずれかに記載の製造方法により得られる発泡錠剤。
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JP2020111719A (ja) * | 2019-01-10 | 2020-07-27 | シーバイエス株式会社 | 加熱調理機器用固形洗浄剤組成物およびそれを用いた洗浄方法 |
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JP7246091B2 (ja) | 2019-12-05 | 2023-03-27 | 株式会社ヘルスカンパニー | 洗浄剤セット |
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