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WO2013115636A1 - Composition pour le traitement et/ou la prévention de maladie du foie gras - Google Patents

Composition pour le traitement et/ou la prévention de maladie du foie gras Download PDF

Info

Publication number
WO2013115636A1
WO2013115636A1 PCT/MY2013/000018 MY2013000018W WO2013115636A1 WO 2013115636 A1 WO2013115636 A1 WO 2013115636A1 MY 2013000018 W MY2013000018 W MY 2013000018W WO 2013115636 A1 WO2013115636 A1 WO 2013115636A1
Authority
WO
WIPO (PCT)
Prior art keywords
tocotrienol
fld
liver
composition
alcoholic
Prior art date
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.)
Ceased
Application number
PCT/MY2013/000018
Other languages
English (en)
Inventor
Enrico MAGOSSO
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.)
Universiti Sains Malaysia (USM)
Original Assignee
Universiti Sains Malaysia (USM)
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.)
Filing date
Publication date
Application filed by Universiti Sains Malaysia (USM) filed Critical Universiti Sains Malaysia (USM)
Publication of WO2013115636A1 publication Critical patent/WO2013115636A1/fr
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/335Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
    • A61K31/35Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having six-membered rings with one oxygen as the only ring hetero atom
    • A61K31/352Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having six-membered rings with one oxygen as the only ring hetero atom condensed with carbocyclic rings, e.g. methantheline 
    • A61K31/3533,4-Dihydrobenzopyrans, e.g. chroman, catechin
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/16Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics

Definitions

  • drug-induced liver disease is used to describe those instances in which an active agent has caused injury to the liver.
  • Drug-induced liver injury may account for as many as 10 percent of hepatitis cases in adults overall, 40 percent of hepatitis cases in adults over fifty years old, and 25 percent of cases of fulminant liver failure.
  • Certain active agents such as glucocorticoids, synthetic estrogens, amiodarone, tamoxifen and valproic acid, for example, have been associated with fatty liver.
  • the tocotrienol tail has three double bonds.
  • Homologs of tocotrienols may be chemically synthesized. Experimental details are provided on a new tocotrienol synthesis which provides stereochemical ⁇ pure materials.
  • the study is a completely randomised interventional study.
  • Animals (Mus musculus or Swiss albino mice, sourced from the animal facilities of Universiti Sains Malaysia (Penang, Malaysia) were randomised into 3 groups of treatment with the first group (Control) fed a standard diet of commercially sourced P702 pellets (Gold Coin, Port Klang, Malaysia), the second group fed high fat-high fructose (HFF) diet comprising 50% P702, 30% clarified butter and 20% fructose and the third group a high-fat-high fructose plus tocotrienols (HFF- T3) diet comprising 50% P702, 30% clarified butter and 20% fructose plus mixed tocotrienols (Tocomin, Carotech, Ipoh, Malaysia).
  • HFF high fat-high fructose
  • HFF- T3 diet high-fat-high fructose plus tocotrienols
  • the animals assigned to the control group received throughout the study duration a standard diet consisting in P702 pellets (Gold Coin, Port Klang, Malaysia).
  • the HFF diet group received a in-house developed and extruded feed consisting of a mixture of standard P702 pellets powder, dairy fat (Kee Wee, Penang, Malaysia) and fructose (HMBG Chemicals, Hamburg, Germany).
  • the HFF-T3 feed was prepared from the HFF ingredients and enriched with tocotrienols (Tocomin50%, Carotec, Ipoh, Malaysia).
  • the in- house feed was prepared weekly and stored at -20 ⁇ until dispensed. Details of the composition of the developed feed is given in table 2 below
  • tocotrienol was extracted from homogenised liver grafts weighing 250 pg each by addition of 1 ml of ethanol, followed by 4 ml of extraction solvent consisting of hexane:ethyl acetate (95:5 v/v).
  • the prepared samples were first vortexed for 2 min then centrifuged at 3500 rpm for 10 min.
  • a 50 ⁇ aliquot of supernatant was injected into a Waters (Milford, MA, USA) high-performance liquid chromatography (HPLC) system, consisting of autosampler 717 Plus, separation module 600Control and fluorescent detector 2475.
  • the detector excitation wavelength was set 296 nm and the emission wavelength was set 330 nm.

Landscapes

  • Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Engineering & Computer Science (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Organic Chemistry (AREA)
  • Gastroenterology & Hepatology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
PCT/MY2013/000018 2012-02-02 2013-01-31 Composition pour le traitement et/ou la prévention de maladie du foie gras Ceased WO2013115636A1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
MYPI2012000461 2012-02-02
MYPI2012000461 2012-02-02

Publications (1)

Publication Number Publication Date
WO2013115636A1 true WO2013115636A1 (fr) 2013-08-08

Family

ID=48905587

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/MY2013/000018 Ceased WO2013115636A1 (fr) 2012-02-02 2013-01-31 Composition pour le traitement et/ou la prévention de maladie du foie gras

Country Status (1)

Country Link
WO (1) WO2013115636A1 (fr)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20240058300A1 (en) * 2021-01-06 2024-02-22 The Trustees Of Indiana University Tocotrienol compositions and methods to treat non-alcoholic steatohepatitis

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20030007961A1 (en) * 2001-06-22 2003-01-09 Wilburn Michael D. Orthomolecular vitamin E derivatives
WO2004096137A2 (fr) * 2003-04-08 2004-11-11 Barrie Tan Compositions d'extrait de rocou contenant des geranylgeraniols et modes d'utilisation
WO2005009135A1 (fr) * 2003-04-10 2005-02-03 Barrie Tan Compositions d'extrait de rocou comprenant des tocotrienols et des tocopherols et procedes d'utilisation
WO2011027344A2 (fr) * 2009-09-01 2011-03-10 Hadasit Medical Research Services And Development Ltd. Combinaison de vitamine e et de bêta-glycosphingolipides dans des compositions, méthodes de prévention et de traitement des troubles hépatiques
WO2011097273A1 (fr) * 2010-02-02 2011-08-11 Martek Biosciences Corporation Méthodes et compositions permettant le traitement de la stéatose hépatique non alcoolique au moyen d'acide docosahexaénoïque et de n-acétyl-l-cystéine

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20030007961A1 (en) * 2001-06-22 2003-01-09 Wilburn Michael D. Orthomolecular vitamin E derivatives
WO2004096137A2 (fr) * 2003-04-08 2004-11-11 Barrie Tan Compositions d'extrait de rocou contenant des geranylgeraniols et modes d'utilisation
WO2005009135A1 (fr) * 2003-04-10 2005-02-03 Barrie Tan Compositions d'extrait de rocou comprenant des tocotrienols et des tocopherols et procedes d'utilisation
WO2011027344A2 (fr) * 2009-09-01 2011-03-10 Hadasit Medical Research Services And Development Ltd. Combinaison de vitamine e et de bêta-glycosphingolipides dans des compositions, méthodes de prévention et de traitement des troubles hépatiques
WO2011097273A1 (fr) * 2010-02-02 2011-08-11 Martek Biosciences Corporation Méthodes et compositions permettant le traitement de la stéatose hépatique non alcoolique au moyen d'acide docosahexaénoïque et de n-acétyl-l-cystéine

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
YACHI, R. ET AL.: "Protective Effects of Vitamin E Analogs against Carbon Tetrachloride-Induced Fatty Liver in Rats", J. CLIN. BIOCHEM. NUTR., vol. 47, September 2010 (2010-09-01), pages 148 - 154, XP055078787 *

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20240058300A1 (en) * 2021-01-06 2024-02-22 The Trustees Of Indiana University Tocotrienol compositions and methods to treat non-alcoholic steatohepatitis
EP4274566A4 (fr) * 2021-01-06 2024-10-30 The Trustees of Indiana University Compositions de tocotriénol et procédés de traitement de la stéatohépatite non alcoolique

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