CA1257131A - Compose pour nutrition parenterale et enterale totale - Google Patents

Compose pour nutrition parenterale et enterale totale

Info

Publication number: CA1257131A
Authority: CA; Canada
Prior art keywords: acid; peptide; emulsion; emulsion according; group
Prior art date: 1984-07-27
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.): Expired

Application number

CA000487133A

Other languages

English (en)

Inventor

John Y. Park

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Individual

Original Assignee

Individual

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1984-07-27

Filing date

1985-07-19

Publication date

1989-07-11

1985-07-19 Application filed by Individual filed Critical Individual

1989-07-11 Application granted granted Critical

1989-07-11 Publication of CA1257131A publication Critical patent/CA1257131A/fr

Status Expired legal-status Critical Current

Links

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239000000787 lecithin Substances 0.000 description 2
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229940035034 maltodextrin Drugs 0.000 description 2
229920000642 polymer Polymers 0.000 description 2
238000002360 preparation method Methods 0.000 description 2
230000008569 process Effects 0.000 description 2
LXNHXLLTXMVWPM-UHFFFAOYSA-N pyridoxine Chemical compound CC1=NC=C(CO)C(CO)=C1O LXNHXLLTXMVWPM-UHFFFAOYSA-N 0.000 description 2
JPJALAQPGMAKDF-UHFFFAOYSA-N selenium dioxide Chemical compound O=[Se]=O JPJALAQPGMAKDF-UHFFFAOYSA-N 0.000 description 2
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238000003786 synthesis reaction Methods 0.000 description 2
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FPIPGXGPPPQFEQ-UHFFFAOYSA-N 13-cis retinol Natural products OCC=C(C)C=CC=C(C)C=CC1=C(C)CCCC1(C)C FPIPGXGPPPQFEQ-UHFFFAOYSA-N 0.000 description 1
SXQWVGXLKTZECH-UHFFFAOYSA-N 2,2-diaminopentanoic acid Chemical compound CCCC(N)(N)C(O)=O SXQWVGXLKTZECH-UHFFFAOYSA-N 0.000 description 1
LRDIEHDJWYRVPT-UHFFFAOYSA-N 4-amino-5-hydroxynaphthalene-1-sulfonic acid Chemical compound C1=CC(O)=C2C(N)=CC=C(S(O)(=O)=O)C2=C1 LRDIEHDJWYRVPT-UHFFFAOYSA-N 0.000 description 1
241001192665 Anous Species 0.000 description 1
OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
GHOKWGTUZJEAQD-UHFFFAOYSA-N Chick antidermatitis factor Natural products OCC(C)(C)C(O)C(=O)NCCC(O)=O GHOKWGTUZJEAQD-UHFFFAOYSA-N 0.000 description 1
229910021555 Chromium Chloride Inorganic materials 0.000 description 1
OCUCCJIRFHNWBP-IYEMJOQQSA-L Copper gluconate Chemical compound [Cu+2].OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C([O-])=O.OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C([O-])=O OCUCCJIRFHNWBP-IYEMJOQQSA-L 0.000 description 1
AUNGANRZJHBGPY-UHFFFAOYSA-N D-Lyxoflavin Natural products OCC(O)C(O)C(O)CN1C=2C=C(C)C(C)=CC=2N=C2C1=NC(=O)NC2=O AUNGANRZJHBGPY-UHFFFAOYSA-N 0.000 description 1
ZZZCUOFIHGPKAK-UHFFFAOYSA-N D-erythro-ascorbic acid Natural products OCC1OC(=O)C(O)=C1O ZZZCUOFIHGPKAK-UHFFFAOYSA-N 0.000 description 1
AHLPHDHHMVZTML-BYPYZUCNSA-N L-Ornithine Chemical compound NCCC[C@H](N)C(O)=O AHLPHDHHMVZTML-BYPYZUCNSA-N 0.000 description 1
IFQSXNOEEPCSLW-DKWTVANSSA-N L-cysteine hydrochloride Chemical compound Cl.SC[C@H](N)C(O)=O IFQSXNOEEPCSLW-DKWTVANSSA-N 0.000 description 1
229930182844 L-isoleucine Natural products 0.000 description 1
229930182821 L-proline Natural products 0.000 description 1
241000124008 Mammalia Species 0.000 description 1
241001465754 Metazoa Species 0.000 description 1
OVBPIULPVIDEAO-UHFFFAOYSA-N N-Pteroyl-L-glutaminsaeure Natural products C=1N=C2NC(N)=NC(=O)C2=NC=1CNC1=CC=C(C(=O)NC(CCC(O)=O)C(O)=O)C=C1 OVBPIULPVIDEAO-UHFFFAOYSA-N 0.000 description 1
DFPAKSUCGFBDDF-UHFFFAOYSA-N Nicotinamide Chemical compound NC(=O)C1=CC=CN=C1 DFPAKSUCGFBDDF-UHFFFAOYSA-N 0.000 description 1
AHLPHDHHMVZTML-UHFFFAOYSA-N Orn-delta-NH2 Natural products NCCCC(N)C(O)=O AHLPHDHHMVZTML-UHFFFAOYSA-N 0.000 description 1
UTJLXEIPEHZYQJ-UHFFFAOYSA-N Ornithine Natural products OC(=O)C(C)CCCN UTJLXEIPEHZYQJ-UHFFFAOYSA-N 0.000 description 1
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
229920002472 Starch Polymers 0.000 description 1
229930006000 Sucrose Natural products 0.000 description 1
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 description 1
QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
JZRWCGZRTZMZEH-UHFFFAOYSA-N Thiamine Natural products CC1=C(CCO)SC=[N+]1CC1=CN=C(C)N=C1N JZRWCGZRTZMZEH-UHFFFAOYSA-N 0.000 description 1
FPIPGXGPPPQFEQ-BOOMUCAASA-N Vitamin A Natural products OC/C=C(/C)\C=C\C=C(\C)/C=C/C1=C(C)CCCC1(C)C FPIPGXGPPPQFEQ-BOOMUCAASA-N 0.000 description 1
229930003268 Vitamin C Natural products 0.000 description 1
QYSXJUFSXHHAJI-XFEUOLMDSA-N Vitamin D3 Natural products C1(/[C@@H]2CC[C@@H]([C@]2(CCC1)C)[C@H](C)CCCC(C)C)=C/C=C1\C[C@@H](O)CCC1=C QYSXJUFSXHHAJI-XFEUOLMDSA-N 0.000 description 1
229930003427 Vitamin E Natural products 0.000 description 1
238000013019 agitation Methods 0.000 description 1
FPIPGXGPPPQFEQ-OVSJKPMPSA-N all-trans-retinol Chemical compound OC\C=C(/C)\C=C\C=C(/C)\C=C\C1=C(C)CCCC1(C)C FPIPGXGPPPQFEQ-OVSJKPMPSA-N 0.000 description 1
239000007864 aqueous solution Substances 0.000 description 1
230000008827 biological function Effects 0.000 description 1
229960002685 biotin Drugs 0.000 description 1
235000020958 biotin Nutrition 0.000 description 1
239000011616 biotin Substances 0.000 description 1
239000000679 carrageenan Substances 0.000 description 1
235000010418 carrageenan Nutrition 0.000 description 1
229920001525 carrageenan Polymers 0.000 description 1
229940113118 carrageenan Drugs 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
QSWDMMVNRMROPK-UHFFFAOYSA-K chromium(3+) trichloride Chemical compound [Cl-].[Cl-].[Cl-].[Cr+3] QSWDMMVNRMROPK-UHFFFAOYSA-K 0.000 description 1
150000001875 compounds Chemical class 0.000 description 1
238000011109 contamination Methods 0.000 description 1
238000007796 conventional method Methods 0.000 description 1
238000001816 cooling Methods 0.000 description 1
229940108925 copper gluconate Drugs 0.000 description 1
230000000368 destabilizing effect Effects 0.000 description 1
238000011161 development Methods 0.000 description 1
238000007865 diluting Methods 0.000 description 1
238000010790 dilution Methods 0.000 description 1
239000012895 dilution Substances 0.000 description 1
230000001804 emulsifying effect Effects 0.000 description 1
230000007717 exclusion Effects 0.000 description 1
239000004222 ferrous gluconate Substances 0.000 description 1
235000013924 ferrous gluconate Nutrition 0.000 description 1
229960001645 ferrous gluconate Drugs 0.000 description 1
229960000304 folic acid Drugs 0.000 description 1
235000019152 folic acid Nutrition 0.000 description 1
239000011724 folic acid Substances 0.000 description 1
235000013305 food Nutrition 0.000 description 1
238000009472 formulation Methods 0.000 description 1
WIGCFUFOHFEKBI-UHFFFAOYSA-N gamma-tocopherol Natural products CC(C)CCCC(C)CCCC(C)CCCC1CCC2C(C)C(O)C(C)C(C)C2O1 WIGCFUFOHFEKBI-UHFFFAOYSA-N 0.000 description 1
KWIUHFFTVRNATP-UHFFFAOYSA-N glycine betaine Chemical compound C[N+](C)(C)CC([O-])=O KWIUHFFTVRNATP-UHFFFAOYSA-N 0.000 description 1
230000002949 hemolytic effect Effects 0.000 description 1
238000001802 infusion Methods 0.000 description 1
238000002347 injection Methods 0.000 description 1
239000007924 injection Substances 0.000 description 1
230000003993 interaction Effects 0.000 description 1
VRIVJOXICYMTAG-IYEMJOQQSA-L iron(ii) gluconate Chemical compound [Fe+2].OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C([O-])=O.OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C([O-])=O VRIVJOXICYMTAG-IYEMJOQQSA-L 0.000 description 1
238000009533 lab test Methods 0.000 description 1
239000000463 material Substances 0.000 description 1
229940057917 medium chain triglycerides Drugs 0.000 description 1
230000000813 microbial effect Effects 0.000 description 1
238000002156 mixing Methods 0.000 description 1
230000001338 necrotic effect Effects 0.000 description 1
229960003966 nicotinamide Drugs 0.000 description 1
235000005152 nicotinamide Nutrition 0.000 description 1
239000011570 nicotinamide Substances 0.000 description 1
235000015097 nutrients Nutrition 0.000 description 1
210000000056 organ Anatomy 0.000 description 1
229960003104 ornithine Drugs 0.000 description 1
229940055726 pantothenic acid Drugs 0.000 description 1
235000019161 pantothenic acid Nutrition 0.000 description 1
239000011713 pantothenic acid Substances 0.000 description 1
239000003182 parenteral nutrition solution Substances 0.000 description 1
230000002093 peripheral effect Effects 0.000 description 1
150000003904 phospholipids Chemical class 0.000 description 1
239000000244 polyoxyethylene sorbitan monooleate Substances 0.000 description 1
235000010482 polyoxyethylene sorbitan monooleate Nutrition 0.000 description 1
229920000053 polysorbate 80 Polymers 0.000 description 1
229940068968 polysorbate 80 Drugs 0.000 description 1
229960003975 potassium Drugs 0.000 description 1
229910052700 potassium Inorganic materials 0.000 description 1
239000011591 potassium Substances 0.000 description 1
239000001103 potassium chloride Substances 0.000 description 1
235000011164 potassium chloride Nutrition 0.000 description 1
239000001508 potassium citrate Substances 0.000 description 1
229960002635 potassium citrate Drugs 0.000 description 1
QEEAPRPFLLJWCF-UHFFFAOYSA-K potassium citrate (anhydrous) Chemical compound [K+].[K+].[K+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O QEEAPRPFLLJWCF-UHFFFAOYSA-K 0.000 description 1
235000011082 potassium citrates Nutrition 0.000 description 1
208000037920 primary disease Diseases 0.000 description 1
238000012545 processing Methods 0.000 description 1
238000001243 protein synthesis Methods 0.000 description 1
238000010926 purge Methods 0.000 description 1
RADKZDMFGJYCBB-UHFFFAOYSA-N pyridoxal hydrochloride Natural products CC1=NC=C(CO)C(C=O)=C1O RADKZDMFGJYCBB-UHFFFAOYSA-N 0.000 description 1
238000011084 recovery Methods 0.000 description 1
235000019192 riboflavin Nutrition 0.000 description 1
229960002477 riboflavin Drugs 0.000 description 1
239000002151 riboflavin Substances 0.000 description 1
239000011780 sodium chloride Substances 0.000 description 1
239000011684 sodium molybdate Substances 0.000 description 1
235000015393 sodium molybdate Nutrition 0.000 description 1
TVXXNOYZHKPKGW-UHFFFAOYSA-N sodium molybdate (anhydrous) Chemical compound [Na+].[Na+].[O-][Mo]([O-])(=O)=O TVXXNOYZHKPKGW-UHFFFAOYSA-N 0.000 description 1
241000894007 species Species 0.000 description 1
230000006641 stabilisation Effects 0.000 description 1
238000011105 stabilization Methods 0.000 description 1
235000019698 starch Nutrition 0.000 description 1
238000003756 stirring Methods 0.000 description 1
239000000126 substance Substances 0.000 description 1
239000005720 sucrose Substances 0.000 description 1
230000000153 supplemental effect Effects 0.000 description 1
235000019157 thiamine Nutrition 0.000 description 1
KYMBYSLLVAOCFI-UHFFFAOYSA-N thiamine Chemical compound CC1=C(CCO)SCN1CC1=CN=C(C)N=C1N KYMBYSLLVAOCFI-UHFFFAOYSA-N 0.000 description 1
229960003495 thiamine Drugs 0.000 description 1
239000011721 thiamine Substances 0.000 description 1
230000014616 translation Effects 0.000 description 1
210000003462 vein Anatomy 0.000 description 1
235000019155 vitamin A Nutrition 0.000 description 1
239000011719 vitamin A Substances 0.000 description 1
235000019158 vitamin B6 Nutrition 0.000 description 1
239000011726 vitamin B6 Substances 0.000 description 1
235000019154 vitamin C Nutrition 0.000 description 1
239000011718 vitamin C Substances 0.000 description 1
QYSXJUFSXHHAJI-YRZJJWOYSA-N vitamin D3 Chemical compound C1(/[C@@H]2CC[C@@H]([C@]2(CCC1)C)[C@H](C)CCCC(C)C)=C\C=C1\C[C@@H](O)CCC1=C QYSXJUFSXHHAJI-YRZJJWOYSA-N 0.000 description 1
235000005282 vitamin D3 Nutrition 0.000 description 1
239000011647 vitamin D3 Substances 0.000 description 1
235000019165 vitamin E Nutrition 0.000 description 1
229940046009 vitamin E Drugs 0.000 description 1
239000011709 vitamin E Substances 0.000 description 1
229940045997 vitamin a Drugs 0.000 description 1
229940011671 vitamin b6 Drugs 0.000 description 1
229940021056 vitamin d3 Drugs 0.000 description 1
239000011787 zinc oxide Substances 0.000 description 1
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 description 1

Classifications

- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/10—Dispersions; Emulsions
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/0012—Galenical forms characterised by the site of application
- A61K9/0019—Injectable compositions; Intramuscular, intravenous, arterial, subcutaneous administration; Compositions to be administered through the skin in an invasive manner
- A61K9/0029—Parenteral nutrition; Parenteral nutrition compositions as drug carriers
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
- A61K38/01—Hydrolysed proteins; Derivatives thereof

Landscapes

Health & Medical Sciences (AREA)
Life Sciences & Earth Sciences (AREA)
Chemical & Material Sciences (AREA)
Animal Behavior & Ethology (AREA)
Veterinary Medicine (AREA)
Public Health (AREA)
Medicinal Chemistry (AREA)
Pharmacology & Pharmacy (AREA)
General Health & Medical Sciences (AREA)
Epidemiology (AREA)
Bioinformatics & Cheminformatics (AREA)
Engineering & Computer Science (AREA)
Proteomics, Peptides & Aminoacids (AREA)
Immunology (AREA)
Nutrition Science (AREA)
Dermatology (AREA)
Dispersion Chemistry (AREA)
Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Medicinal Preparation (AREA)

CA000487133A 1984-07-27 1985-07-19 Compose pour nutrition parenterale et enterale totale Expired CA1257131A (fr)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
US63508984A	1984-07-27	1984-07-27
US635,089		1984-07-27

Publications (1)

Publication Number	Publication Date
CA1257131A true CA1257131A (fr)	1989-07-11

Family

ID=24546409

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CA000487133A Expired CA1257131A (fr)	1984-07-27	1985-07-19	Compose pour nutrition parenterale et enterale totale

Country Status (6)

Country	Link
EP (1)	EP0188602A1 (fr)
JP (1)	JPS61502822A (fr)
KR (1)	KR860000862A (fr)
CA (1)	CA1257131A (fr)
WO (1)	WO1986000810A1 (fr)
ZA (1)	ZA855604B (fr)

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
SE8505047L (sv) *	1985-10-25	1987-04-26	Nutritional Int Res Inst	Fettemulsion
US5514720A (en) *	1986-07-09	1996-05-07	Hemagen/Pfc	Stable emulsions of highly fluorinated organic compounds
US5684050A (en) *	1986-01-24	1997-11-04	Hemagen/Pfc	Stable emulsions of highly fluorinated organic compounds
GB8719988D0 (en) *	1987-08-25	1987-09-30	Efamol Ltd	Chemical compounds
US5171755A (en) *	1988-04-29	1992-12-15	Hemagen/Pfc	Emulsions of highly fluorinated organic compounds
US5403575A (en) *	1991-12-12	1995-04-04	Hemagen/Pfc	Highly fluorinated, chloro-substituted organic compound-containing emulsions and methods of using them
JP2005515156A (ja) *	2001-05-25	2005-05-26	セレメディックス，インク．	反応性酸素種およびフリーラジカルの効力を中和するための単一アミノ酸に基づく化合物
KR200453914Y1 (ko) *	2009-09-03	2011-06-03	권영철	천정재 인쇄용 지지장치
US20110240050A1 (en) *	2010-04-01	2011-10-06	L'oreal S.A.	Cosmetic compositions containing a fatty acid, arginine, and a co-emulsifier

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
GB1256162A (en) *	1968-08-16	1971-12-08	Braun Fa B	Improvements in and relating to liquid products for intravenous administration
JPS537492B2 (fr) *	1973-02-12	1978-03-18
JPS51115909A (en) *	1975-04-01	1976-10-13	Otsuka Pharmaceut Factory Inc	A process for preparing amino acid parenteral injection mixed with a r educing sugar
US4126628A (en) *	1977-03-28	1978-11-21	Canadian Patents And Development Limited	Acylation of amino acids
JPS6030652B2 (ja) *	1979-05-07	1985-07-17	株式会社ミドリ十字	静脈注射用脂肪乳剤

1985
- 1985-07-19 CA CA000487133A patent/CA1257131A/fr not_active Expired
- 1985-07-24 EP EP85903930A patent/EP0188602A1/fr not_active Withdrawn
- 1985-07-24 JP JP60503477A patent/JPS61502822A/ja active Pending
- 1985-07-24 WO PCT/US1985/001415 patent/WO1986000810A1/fr not_active Ceased
- 1985-07-25 ZA ZA855604A patent/ZA855604B/xx unknown
- 1985-07-25 KR KR1019850005341A patent/KR860000862A/ko not_active Withdrawn

Also Published As

Publication number	Publication date
JPS61502822A (ja)	1986-12-04
ZA855604B (en)	1986-08-27
WO1986000810A1 (fr)	1986-02-13
KR860000862A (ko)	1986-02-20
EP0188602A1 (fr)	1986-07-30

Legal Events

Date	Code	Title	Description
2006-07-11	MKEX	Expiry

Publication	Publication Date	Title
DE2556100C2 (fr)	1987-06-19
EP0312612B1 (fr)	1993-03-24	Emulsion nutritive
DE68905387T2 (de)	1993-10-21	Aminosäure-Nahrungsmittelzusammensetzungen.
US3873720A (en)	1975-03-25	Nutrient fat emulsion
EP0220153B1 (fr)	1991-07-24	Emulsion nutritive capable de transporter de l'oxygène et son procédé de préparation
JP2728134B2 (ja)	1998-03-18	非経口栄養サポート用アミノ酸組成物
EP0176094B1 (fr)	1988-06-29	Solution parentérale alimentaire
DE69033521T2 (de)	2000-08-31	Verwendung von arginin als immunstimulator
WO2007121807A1 (fr)	2007-11-01	Solution d'acides aminés pour la nutrition parentérale pédiatrique
CA1257131A (fr)	1989-07-11	Compose pour nutrition parenterale et enterale totale
US5206220A (en)	1993-04-27	Soluble and stable sources of tyrosine, cysteine and glutamine for total parenteral nutrition
CA1217725A (fr)	1987-02-10	Emulsion huileuse renfermant des acides amines
CA1039190A (fr)	1978-09-26	Solute pour alimentation par voie parenterale
JPH06312923A (ja)	1994-11-08	末梢静脈投与用栄養輸液
JP3182564B2 (ja)	2001-07-03	栄養組成物
JPH05506644A (ja)	1993-09-30	構造化脂質を用いる癌治療方法
EP0146474A2 (fr)	1985-06-26	Composition nutritive contenant de l'acide alpha-cétoisocaproique ou un de ses sels
JP3132085B2 (ja)	2001-02-05	脂肪乳剤
JPH07330583A (ja)	1995-12-19	遊離型グルタミン酸を含有する液状製剤
JP3914585B2 (ja)	2007-05-16	マクロファージ一酸化窒素産生亢進剤
JP3097196B2 (ja)	2000-10-10	脂肪乳剤の安定化法
US4567045A (en)	1986-01-28	Isotonic glycerol free intravenous fat emulsion
FR2561522A1 (fr)	1985-09-27	Solution injectable, notamment pour le traitement de la cetose et son procede de preparation
EP0608217A1 (fr)	1994-08-03	Sources stables et solubles de tyrosine, de cysteine et de glutamine pour une alimentation parenterale totale
JPH05148149A (ja)	1993-06-15	輸液製剤