JP2007291135A - 不快を緩和するための医薬組成物 - Google Patents
不快を緩和するための医薬組成物 Download PDFInfo
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- JP2007291135A JP2007291135A JP2007187280A JP2007187280A JP2007291135A JP 2007291135 A JP2007291135 A JP 2007291135A JP 2007187280 A JP2007187280 A JP 2007187280A JP 2007187280 A JP2007187280 A JP 2007187280A JP 2007291135 A JP2007291135 A JP 2007291135A
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Abstract
【解決手段】この発明は、乳児、あるいは、障害のあるあるいは高齢者の完全栄養のための製品に関する。この製品は、葉酸、ビタミンB6、及びビタミンB12あるいはこれらの機能的等価物の増量されたレベルによって特徴付けられる。これらの製品は、乳児、特に、若年齢の乳児の幸福感を改善し、セロトニン及びメラトニン代謝障害に関連する疾患の治療及び予防に有用である。
【選択図】なし
Description
本発明は、幸福感、未熟の代償、および代謝能力における問題を改善するため、乳児用組成物を含めた医薬および/または栄養組成物に関する。栄養製品は、乳児、疾病に罹った者および高齢者に完全栄養を提供し、そしてそれらの組成物は、増加された補助因子の量によって特徴づけられる。栄養製品は、補助因子、およびさらなる所望の食品成分の一部のみを提供する栄養補助食品の形態でもありうる。
現時点で、工業国における赤ん坊の人口の大部分は、特化された乳児用組成物で保育される。これらの組成物の消費は、胃腸障害の頻度が増大されること、および免疫状態が減少されることのようないくつかの医療上の問題に関連していることが報告されている。このような問題は、若年で生じうるが、しかしヒトの母乳で独占的に育てられる乳児がこれらのパラメーターでよい評価を得るので、おそらく後年にも起こりうる。これらの人工的組成物で独占的に育てられる乳児が、ヒトの母乳で育てられる乳児に比較してより長く泣くことも報告された。これは、おそらく、空腹感、痛みまたはさらには医療上の問題による全般的な不快感を示唆する。これらの問題は、子供の発達を遅延し、そして親に懸念および実際の問題を生じさせうる。
本発明による組成物の特徴は、請求項および以下においてさらに詳細に記述される。最適な効果のためには、毎日投与量当たりに少なくとも200μgの葉酸、少なくとも1.9μgのビタミンB12および少なくとも0.3mgのビタミンB6がが必要であり、葉酸、ビタミンB12及びビタミンB6のぞれぞれにつき、少なくとも300μg、少なくとも4.8μgおよび少なくとも3.0mgであることが好ましい。
表1
成分 製品100kcal当たりの量
範囲 好ましい範囲
消化性炭水化物 4-25 6-22 g
葉酸 44-4000 50-2000 (g
ビタミンB12 0.8-2000 1-1000* (g
ビタミンB6 50-10000 60-2000 (g
リボフラビン 0.08-20 0.14-6 mg
チアミン 55-8000 70-4000 (g
ナイアシン 0.55-60 1.4-25 mgナイアシン等価物
ビタミンK >8 30-90 (g
タウリン 5-100 7-50 mg
ベタイン 50-4000 30-600 mg
マグネシウム 5-400 8-200 mg
亜鉛 0.8-100 1-30 mg
Mg+Zn/Ca >0.08 >0.10 m/m
Mg+Zn/P >0.20 >0.26 m/m
メラトニン 30-3000 60-800 mg
トリプトファン 0.05-8 0.2-2* g
アデノシン 1-1000 50-500 mg
メチオニン 50-1000 100-500 mg
注*:高い用量は、少ない用量の数倍として付与されることが好ましい。
エネルギー密度:製品のエネルギー密度は、先行技術の製品のものに類似し、62〜73kcal/100mlの範囲内にある液体または還元製品である。好ましくは、エネルギー密度は、64〜71kcal/mlの範囲内にある。
乳児による幸福感を改善すること、
通常の食事および睡眠パターンを支持すること、
特に、若年の乳児で、代謝系の不十分な能力を補償する助けになること、
これらの組成物の消費は、従来の組成物の消費に比較して、ヒトの母乳で専有的に育てられる乳児のものにより類似したアミノ酸の血漿中濃度を生じる。
乳児に対する負の副作用を与えない。
したがって、健康および免疫状況を改善し、そして高品質の成長を支持する。
素晴らしい風味を示し、そして許容しうるコストで生産されうる。
表2に表されるとおりの組成を有する液体乳児用組成物が調製された。
表2:液体乳児用組成物の組成
値は、異なって示される場合を除いて100ml当たりのmgで示される。
タンパク質(60%甘味乳清、40%カゼイン) 1400
添加Trp 10
添加Arg 10
ラクトース 7500
表2(続き)
マルトデキストリン(10〜15DE) 1600
脂肪(EP−231904) 3100
Na 18-25
K 60-100
Cl 40-60
Ca 50-85
P 20-50
Mg 4.5-6
Fe 0.5-0.9
Zn 0.6-1.3
Cu 40-60(g
Mn 5-20(g
Se 1.5-2.2(g
I 5-15(g
ビタミンA 80-90 RE
β−カロテン 0-40(g
ビタミンD 1-1.6(g
ビタミンE 0.8-1.4mgTE
ビタミンK 4-20(g
チアミン 35-45(g
リボフラビン 110-150(g
ナイアシン 0.7-1.0mgNE
パントテネート 0.25-0.35
ビオチン 1.5-1.7(g
アスコルビン酸 5-10
タウリン 4-7
葉酸(モノグルタミン酸塩として添加される) 25-32(g
ビタミンB12(ヒドロキシコバラミンとして添加される) 0.4-0.7(g
ビタミンB6(ピリドキシンとして添加される) 50-65(g
この製品は、若年乳児の睡眠行動を改善するために使用できる。
就寝時の飲み物として高齢者およびよちよち歩きの幼児に使用すべき製品:
窒素下で缶に詰められた粉末栄養補助食品;就寝する前の果物ジュースまたはミルクに還元される10g。
8kgマルトデキストリンDE19に、
2.0kg α−ラクトアルブミン
50mg メラトニン
100mg 葉酸モノグルタミン酸塩
25mg シアノコバラミン
100mg ピリドキサール
100mg リボフラビン
60mg チアミンHCl
30g 塩化亜鉛.12H2O
を加える。
適当な分量が、例えば、400gの缶に充填される。
ADHD乳児またはアルツハイマーの患者に使用されるべき製品。
10gサッシェに詰められた粉末製品。サッシェは、朝食シリアルの一部と混合させ、そしてミルクで還元される。
粉末は、
9.5kg マルトデキストリン
100mg 葉酸
25mg ビタミンB12
100mg B6
100mg B2
60mg B1
1.0g ナイアシン
100g ベタイン
300g 塩化マグネシウム
30g 塩化亜鉛
50g アデノシン
100mg ビタミンK
を混合することによって得られる。
Claims (15)
- 幸福感の改善、痛みの感覚の制御、および気分、睡眠行動の改善、または他のセロトニンまたはメラトニン媒介性障害の治療または予防のための、医薬組成物を製造する上での、葉酸、ビタミンB6およびB12またはそれらの機能的類似体の使用。
- 前記組成物が、完全栄養のための組成物である請求項1に記載の使用。
- 前記組成物が、乳児の完全栄養のための組成物である請求項2に記載の使用。
- 前記組成物が、疾患のある者または高齢者の完全栄養のための組成物である請求項2に記載の使用。
- 前記組成物が、100kcal当たり44μgより多くの葉酸および0.8μgより多くのビタミンB12および50μgより多くのビタミンB6を含有する請求項1〜4のいずれか1項に記載の使用。
- 前記組成物が、さらに、100kcal当たり少なくとも0.55mgのナイアシン等価物および/または少なくとも0.08mgのリボフラビンおよび/または少なくとも55μgのチアミンを含有する請求項1〜5のいずれか1項に記載の使用。
- 前記組成物が、さらに、100kcal当たり50mgより多くのコリンまたはベタインまたはその総量、および/または少なくとも5mgのタウリン、および/または少なくとも50mgのメチオニンを含有する請求項1−6のいずれか1項に記載の使用。
- 前記組成物が、さらに、100kcal当たり0.05〜8gのトリプトファンおよび/または30〜3000mgのメラトニンおよび/または50〜1000mgのアデノシンを含有する請求項1〜7のいずれか1項に記載の使用。
- 前記組成物が、さらに、100kcal当たり5〜400mgのマグネシウムおよび/または0.7−100mgの亜鉛を含有し、カルシウムに対するマグネシウム及び亜鉛の重量比が、0.08より高い請求項1〜8のいずれか1項に記載の使用。
- 前記組成物が、100kcal当たり9〜15gの炭水化物を含有する請求項1〜9のいずれか1項に記載の使用。
- 前記組成物が、疾患のある者および高齢者についての栄養補助食品である請求項1の記載の使用。
- 前記組成物が、日投与量で、少なくとも200μgの葉酸、少なくとも1.9μgのビタミンB12および少なくとも0.3mgのビタミンB6を含有する請求項1〜11のいずれか1項に記載の使用。
- 前記組成物が、さらに、日投与量当たり、少なくとも0.5mgのリボフラビン、および/または少なくとも1.0mgのチアミン、および/または少なくとも2mgのナイアシン等価物、および/または少なくとも0.3gのトリプトファン、少なくとも0.5gのメラトニン、少なくとも50mgのアデノシン、少なくとも50mgのコリンおよび/またはベタイン、および/または少なくとも100mgのメチオニン、および/または少なくとも0.03mgのビタミンK、および少なくとも5gの消化性炭水化物を含有する請求項12に記載の使用。
- 幸福感の改善、痛みの感覚の制御、および気分、睡眠行動の改善、または他のセロトニンまたはメラトニン媒介性障害の治療または予防のための、医薬組成物であって、
100kcal当たり44μgより多くの葉酸、0.8μgより多くのビタミンB12および50μgより多くのビタミンB6を含有することを特徴とする、組成物。 - 幸福感の改善、痛みの感覚の制御、および気分、睡眠行動の改善、または他のセロトニンまたはメラトニン媒介性障害の治療または予防のための処置方法であって、
そのような処理の必要な者に、毎日の投与量当たり少なくとも200μgの葉酸、少なくとも2μgのビタミンB12および少なくとも2mgのビタミンB6の量を投与することを特徴とする、方法。
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EP99201359A EP0951842B1 (en) | 1999-01-20 | 1999-04-29 | Infant formula |
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EP (2) | EP0951842B1 (ja) |
JP (2) | JP2002535277A (ja) |
AT (2) | ATE228779T1 (ja) |
AU (2) | AU2466500A (ja) |
CA (2) | CA2627837C (ja) |
DE (2) | DE69904257T2 (ja) |
DK (1) | DK0951842T3 (ja) |
ES (2) | ES2187115T3 (ja) |
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1999
- 1999-04-29 EP EP99201359A patent/EP0951842B1/en not_active Expired - Lifetime
- 1999-04-29 AT AT99201359T patent/ATE228779T1/de active
- 1999-04-29 DK DK99201359T patent/DK0951842T3/da active
- 1999-04-29 DE DE69904257T patent/DE69904257T2/de not_active Expired - Lifetime
- 1999-04-29 ES ES99201359T patent/ES2187115T3/es not_active Expired - Lifetime
- 1999-04-29 PT PT99201359T patent/PT951842E/pt unknown
-
2000
- 2000-01-20 AU AU24665/00A patent/AU2466500A/en not_active Abandoned
- 2000-01-20 AU AU24666/00A patent/AU2466600A/en not_active Abandoned
- 2000-01-20 WO PCT/NL2000/000043 patent/WO2000042868A1/en active Application Filing
- 2000-01-20 US US09/889,691 patent/US6613367B1/en not_active Expired - Lifetime
- 2000-01-20 DE DE60019722T patent/DE60019722T2/de not_active Expired - Lifetime
- 2000-01-20 EP EP00903030A patent/EP1143974B1/en not_active Revoked
- 2000-01-20 US US09/889,793 patent/US6900180B1/en not_active Expired - Lifetime
- 2000-01-20 ES ES00903030T patent/ES2240060T3/es not_active Expired - Lifetime
- 2000-01-20 AT AT00903030T patent/ATE293974T1/de active
- 2000-01-20 JP JP2000594467A patent/JP2002535277A/ja active Pending
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- 2000-01-20 WO PCT/NL2000/000042 patent/WO2000043013A1/en active IP Right Grant
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2007
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2008
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Also Published As
Publication number | Publication date |
---|---|
DE60019722D1 (de) | 2005-06-02 |
DE69904257T2 (de) | 2003-04-17 |
CA2359592C (en) | 2008-07-29 |
DE60019722T2 (de) | 2005-11-17 |
DE69904257D1 (de) | 2003-01-16 |
JP2002535277A (ja) | 2002-10-22 |
AU2466500A (en) | 2000-08-07 |
AU2466600A (en) | 2000-08-07 |
DK0951842T3 (da) | 2003-01-06 |
EP1143974B1 (en) | 2005-04-27 |
EP0951842B1 (en) | 2002-12-04 |
US8124585B2 (en) | 2012-02-28 |
WO2000042868A1 (en) | 2000-07-27 |
PT951842E (pt) | 2003-04-30 |
ES2187115T3 (es) | 2003-05-16 |
EP0951842A3 (en) | 1999-12-22 |
CA2627837A1 (en) | 2000-07-27 |
WO2000043013A1 (en) | 2000-07-27 |
CA2359592A1 (en) | 2000-07-27 |
ES2240060T3 (es) | 2005-10-16 |
ATE228779T1 (de) | 2002-12-15 |
US20080145451A1 (en) | 2008-06-19 |
EP1143974A1 (en) | 2001-10-17 |
US20050256031A1 (en) | 2005-11-17 |
CA2627837C (en) | 2013-09-10 |
EP0951842A2 (en) | 1999-10-27 |
US6900180B1 (en) | 2005-05-31 |
US6613367B1 (en) | 2003-09-02 |
US8450347B2 (en) | 2013-05-28 |
ATE293974T1 (de) | 2005-05-15 |
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