WO2014135170A1 - Novel formula of iron based nanocomposites for rapid and efficient treatment of iron deficiency anemia - Google Patents

Novel formula of iron based nanocomposites for rapid and efficient treatment of iron deficiency anemia Download PDF

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Publication number
WO2014135170A1
WO2014135170A1 PCT/EG2013/000027 EG2013000027W WO2014135170A1 WO 2014135170 A1 WO2014135170 A1 WO 2014135170A1 EG 2013000027 W EG2013000027 W EG 2013000027W WO 2014135170 A1 WO2014135170 A1 WO 2014135170A1
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WIPO (PCT)
Prior art keywords
iron
nano
composites
vitamin
composite
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Ceased
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PCT/EG2013/000027
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English (en)
French (fr)
Inventor
Mona Bakr Mohamed MAHMOUD
Sherine Hassan Abbas HELMY
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EUROPEAN EGYPTIAN PHARMACEUTICAL INDUSTRIES (EEPI)
NANOTECH FOR PHOTOELECTRONICS RESEARCH
Original Assignee
EUROPEAN EGYPTIAN PHARMACEUTICAL INDUSTRIES (EEPI)
NANOTECH FOR PHOTOELECTRONICS RESEARCH
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Priority to EP13876801.5A priority Critical patent/EP2964205A4/en
Priority to CN201380074286.1A priority patent/CN105101957A/zh
Priority to US14/772,648 priority patent/US20160022733A1/en
Priority to BR112015021212A priority patent/BR112015021212A2/pt
Priority to JP2015560555A priority patent/JP2016511261A/ja
Publication of WO2014135170A1 publication Critical patent/WO2014135170A1/en
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

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Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K33/00Medicinal preparations containing inorganic active ingredients
    • A61K33/24Heavy metals; Compounds thereof
    • A61K33/26Iron; Compounds thereof
    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23LFOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES, NOT OTHERWISE PROVIDED FOR; PREPARATION OR TREATMENT THEREOF
    • A23L33/00Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof
    • A23L33/10Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof using additives
    • A23L33/15Vitamins
    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23LFOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES, NOT OTHERWISE PROVIDED FOR; PREPARATION OR TREATMENT THEREOF
    • A23L33/00Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof
    • A23L33/10Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof using additives
    • A23L33/16Inorganic salts, minerals or trace elements
    • 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
    • A61K31/365Lactones
    • A61K31/375Ascorbic acid, i.e. vitamin C; Salts thereof
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/455Nicotinic acids, e.g. niacin; Derivatives thereof, e.g. esters, amides
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/519Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/0012Galenical forms characterised by the site of application
    • A61K9/0053Mouth and digestive tract, i.e. intraoral and peroral administration
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/48Preparations in capsules, e.g. of gelatin, of chocolate
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/48Preparations in capsules, e.g. of gelatin, of chocolate
    • A61K9/50Microcapsules having a gas, liquid or semi-solid filling; Solid microparticles or pellets surrounded by a distinct coating layer, e.g. coated microspheres, coated drug crystals
    • A61K9/51Nanocapsules; Nanoparticles
    • A61K9/5107Excipients; Inactive ingredients
    • A61K9/5115Inorganic compounds
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P7/00Drugs for disorders of the blood or the extracellular fluid
    • A61P7/06Antianaemics

Definitions

  • Iron is a component of proteins required for crucial cellular processes. Iron-containing proteins have essential roles in oxygen transport, ATP production, DNA synthesis and other physiological processes [1-3].
  • Low consumption of foods rich in bioavailable iron (Fe) such as red meat or hemorrhage are the main causes of iron deficiency Anemia.
  • the symptoms of iron deficiency anemia include dyspnea, headaches, light-headedness, short breath, fatigue, be forgetful, feel grouchy, lose appetite and weight and have trouble concentrating. All of these symptoms appear as a result of the reduction in the oxygen-carrying capacity of red blood cells. Therefore, anemia has been associated with reduced health-related quality of life and its treatment is essential to improve our health and performance.
  • iron is extremely important, the iron overload and significant increase in iron stores can be toxic to the body.
  • the process of lipid peroxidation is initiated by reactive oxygen species, such as hydroxyl radicals, and stimulated by excess iron ions.
  • reactive oxygen species such as hydroxyl radicals
  • iron-deficient rats rapidly accumulate copper eightfold higher than those in normal rats, and consequently, excess copper can also catalyze lipid peroxidation as iron.
  • iron overload may influence the development of cancer. It has been suggested that excess iron may alter immune status and act as a co-carcinogen as well a catalyst for hydroxyl radical production and lipid peroxidation. Reactive oxygen species are considered to be carcinogenic because of their ability to produce DNA adducts, DNA strand breaks, and to modulate gene expression. High dietary iron levels could also enhance oxidative stress by interfering with absorption of other minerals as copper and manganese (Mn), in which their depletion may result in decreased antioxidant enzyme activity, particularly that of copper-zinc (Cu, Zn) and manganese superoxide dismutase (SOD).
  • Cu, Zn copper-zinc
  • SOD manganese superoxide dismutase
  • iron supplements should be prescribed especially for children and pregnant women, but under recommendation. Because iron is difficultly excreted outside the body, a lot of care should be taken in order to avoid cellular iron accumulation and generation of lipid peroxidation, oxidative stress and cancer.
  • These challenges raise the need for a new form/preparation that can I)- secure the iron availability in the body through its high absorption rate 2)- has the ability to treat the iron-deficiency anemia in short time-course 3)- has the high efficacy to overcome the life-threatening situation due to significantly low-Hb levels.
  • Vitamin B9 folic acid
  • vitamin B3 Nicotinic acid
  • Vitamin C antioxidant
  • Immature nucleated erythrocytes respire and presumably, must utilize the pyridine nucleotides in this respiration.
  • Boosting iron stores is an advantage, particularly for patients receiving Erythropoiesis Stimulating Agents (ESAs) [8].
  • iron gluconate iron gluconate
  • iron saccharate iron saccharate
  • low molecular weight iron dextran The best gives rise in the HP level after one week, and it comes back to the normal level after a month of treatment through twice weekly intravenous administration does.
  • iron oxides nano-composites capped with Folic acid (vitamin B9), Nicotinic acid (vitamin B3), and/ or Ascorbic acid (vitamin C) can be used as new formula or food supplementary for Anemia treatment and it rise the RBCs and correct the HP level to their normal values within less than a week.
  • the aim of this study is to test the ability of single doses Nano-sized iron oxide (Magnetite) particles capped with vitamin mixture (folic, nicotinic and ascorbic acids) to treat life-threatening iron deficiency anemic rats within one week.
  • the results were compared with Ferric Chloride treated group (The parent iron source) in order to measure and differentiate between the efficacies of Nano- and Micro-sized iron supplements.
  • Ferric Chloride treated group The parent iron source
  • ICP Inductivity Coupled Plasma
  • Rats of groups 1-5 were exposed daily to blood withdrawal from inner canthus of eyes.
  • the hemoglobin concentration of collected blood samples in heparinized tubes was measured by colorimetric method using commercially available kit (Drabkin's solution).
  • the blood withdrawal was stopped when rat lives were threatened and hemoglobin reached the range of 4 - 5 g/dL in all lab animals. Rats of control group were not exposed to any blood withdrawal.
  • Groups 1 - 3 were administered 1.0 ml/rat of Nano-sized iron (Magnetite) of different concentrations (2.57, 5.14, and 10.28 mg Kg " 1 respectively rat body weight, which equivalent to 25, 50, 100 mg dose in human, respectively), while group 4 was administered 10.28 mg Kg " ' of Ferric chloride (1 ml/Rat; the parent material of magnetite).
  • Magnetite Nano-sized iron
  • Rats of different groups were left for 3 days after oral administration of different treatments, fed ad libitum on balanced diet containing iron and clean tap water. Blood samples were collected on 4 th and 7 th day after dosing and Hb concentration was measured using colorimetric method.
  • Table 3 Hemoglobin concentration of rat groups at 1 day before, 4 and 7 days after all treatments
  • D. el raise from 4.4 up to 14.6 g/dl within seven days and stabilized at 13.6 for more than 80 days after administration.
  • Administration of Ferric Chloride to anemic rats corrected the Hb. concentration but achieved neither the levels in Nano-sized magnetite groups nor the level in control non- anemic rats.
  • Administration of vitamins mixture (Ascorbic, Folic and Nicotinic acids) to anemic rats was able to increase the absorption of iron significantly and elevated the concentration of hemoglobin but it didn't reach or exceed the same levels of any other group.
  • the single dose of 2.57 mg/kg rat body which equal to 25 mg in human of nano-sized iron oxide nanoparticles capped with a mixture of vitamins (B3, B9 and C) regained the anemia due to iron deficiency in less than 4 days.
  • the used dose is apparently safe as it is 554 times less than the LD50 of Magnitite nanoparticles in human.
  • magnetite nanoparticles has been already FDA approved (10)
  • Figure 2 TEM images of nano-sized iron oxide nanoparticles capped with a vitamins mixture (B3, B9 & C).
  • Figure 3 graphical illustration of anemia induction in all groups except the control
  • Figure 4 HB level after anemia induction, then single dose treatment with 25 mg iron nano- composite with vitamins.
  • Figure 5 Bone-marrow section of the anemic rat (left) and after introducing single dose of nano-sized iron-Vitamins composite (right), Vitamin mixtures (B3, B9 and C) used as stabilizer and capping for iron nanoparticles.

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  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Veterinary Medicine (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Epidemiology (AREA)
  • Engineering & Computer Science (AREA)
  • Inorganic Chemistry (AREA)
  • Nutrition Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Polymers & Plastics (AREA)
  • Mycology (AREA)
  • Food Science & Technology (AREA)
  • Physiology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Physics & Mathematics (AREA)
  • Biomedical Technology (AREA)
  • Nanotechnology (AREA)
  • Optics & Photonics (AREA)
  • Organic Chemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Hematology (AREA)
  • Diabetes (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Medicinal Preparation (AREA)
PCT/EG2013/000027 2013-03-06 2013-10-29 Novel formula of iron based nanocomposites for rapid and efficient treatment of iron deficiency anemia Ceased WO2014135170A1 (en)

Priority Applications (5)

Application Number Priority Date Filing Date Title
EP13876801.5A EP2964205A4 (en) 2013-03-06 2013-10-29 NOVEL IRON-BASED NANOCOMPOSITE FORMULA FOR RAPID AND EFFICIENT TREATMENT OF ANEMIA RELATED TO IRON FAILURE
CN201380074286.1A CN105101957A (zh) 2013-03-06 2013-10-29 快速有效治疗缺铁性贫血的铁基纳米复合物新配方
US14/772,648 US20160022733A1 (en) 2013-03-06 2013-10-29 Novel formula of iron based nanocomposites for rapid and efficient treatment of iron deficiency anemia
BR112015021212A BR112015021212A2 (pt) 2013-03-06 2013-10-29 fórmula de nanocompósitos com base de ferro para tratamento rápido e eficiente de anemia ferropriva
JP2015560555A JP2016511261A (ja) 2013-03-06 2013-10-29 鉄欠乏性貧血の迅速かつ効果的な治療のための鉄系ナノ複合材料の新規な製剤

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EG2013030371 2013-03-06
EG2013030371 2013-03-06

Publications (1)

Publication Number Publication Date
WO2014135170A1 true WO2014135170A1 (en) 2014-09-12

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PCT/EG2013/000027 Ceased WO2014135170A1 (en) 2013-03-06 2013-10-29 Novel formula of iron based nanocomposites for rapid and efficient treatment of iron deficiency anemia

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US (1) US20160022733A1 (https=)
EP (1) EP2964205A4 (https=)
JP (1) JP2016511261A (https=)
CN (1) CN105101957A (https=)
BR (1) BR112015021212A2 (https=)
WO (1) WO2014135170A1 (https=)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR102085115B1 (ko) * 2017-07-21 2020-03-05 스노우화이트팩토리(주) 마그헤마이트-사포닌 나노결합체를 유효성분으로 함유하는 조혈기능 장애 질환 예방 또는 치료용 약학조성물
CN109602914B (zh) * 2019-01-08 2022-05-17 扬州大学 维生素b2修饰的铁基纳米酶及其制备方法和应用
WO2024100213A1 (fr) 2022-11-10 2024-05-16 Université De Lorraine Nanoclusters de fer, leurs procédés d'obtention et leurs utilisations pour lutter contre les carences en fer

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20070065521A1 (en) * 2005-09-19 2007-03-22 Bala Venkataraman Composition and method for treating iron deficiency anemia
WO2009120702A2 (en) * 2008-03-25 2009-10-01 Emory University Elemental iron nanoparticles
WO2010034319A1 (en) * 2008-09-29 2010-04-01 Innovative Research And Development Co. (Inrad) Magnetite nanoparticles as a single dose treatment for iron deficiency anemia
WO2012092305A2 (en) * 2010-12-27 2012-07-05 Incube Labs, Llc Nanonized iron compositions and methods of use thereof

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
TWI321133B (en) * 2006-08-01 2010-03-01 Univ Kaohsiung Medical Folate-receptor-targeting iron oxide nanoparticles coated with poly(ethylene glycol)
JP4793202B2 (ja) * 2006-09-27 2011-10-12 大日本印刷株式会社 壁紙
CN102730767B (zh) * 2012-06-13 2014-05-21 湖北工业大学 一种纳米α-氧化铁粉体的快速制备方法

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20070065521A1 (en) * 2005-09-19 2007-03-22 Bala Venkataraman Composition and method for treating iron deficiency anemia
WO2009120702A2 (en) * 2008-03-25 2009-10-01 Emory University Elemental iron nanoparticles
WO2010034319A1 (en) * 2008-09-29 2010-04-01 Innovative Research And Development Co. (Inrad) Magnetite nanoparticles as a single dose treatment for iron deficiency anemia
WO2012092305A2 (en) * 2010-12-27 2012-07-05 Incube Labs, Llc Nanonized iron compositions and methods of use thereof

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See also references of EP2964205A4 *

Also Published As

Publication number Publication date
BR112015021212A2 (pt) 2017-07-18
EP2964205A1 (en) 2016-01-13
US20160022733A1 (en) 2016-01-28
CN105101957A (zh) 2015-11-25
JP2016511261A (ja) 2016-04-14
EP2964205A4 (en) 2016-07-27

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