Treating conditions associated with increased eotaxin with 25-hydroxyvitamin d3

a technology of eotaxin and eotaxin, which is applied in the direction of antiparasitic agents, drug compositions, immunological disorders, etc., can solve the problems of toxicity, rickets in children, osteomalacia in adults, etc., and achieve the effect of reducing the symptoms of conditions, and reducing the level of eotaxin
US20130252927A1Inactive Publication Date: 2013-09-26DSM IP ASSETS BV

Patent Information

Authority / Receiving Office
US · United States
Patent Type
Applications(United States)
Current Assignee / Owner
DSM IP ASSETS BV
Publication Date
2013-09-26
Estimated Expiration
Not applicable · inactive patent
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Abstract

The present invention relates to treating / preventing conditions associated with an increased level of eotaxin in a human with 25-hydroxyvitamin D3 (calcifediol). Optionally, vitamin D3 may be used together with 25-hydroxyvitamin D3.
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Description

FIELD OF THE INVENTION

[0001] The present invention relates to treating / preventing conditions associated with an increased level of eotaxin in a human with 25-hydroxyvitamin D3 (calcifediol). Optionally, vitamin D3 may be used together with 25-hydroxyvitamin D3.BACKGROUND OF THE INVENTION

[0002] Vitamin D (e.g., ergocalciferol and cholecalciferol) is a group of fat-soluble compounds defined by their biological activity. A deficiency of vitamin D causes rickets in children and osteomalacia in adults. But toxicity can occur after chronic intake of more than 100 times the recommended daily allowance (i.e., 5-15 μg or 200-600 IU vitamin D) for several months. For vitamin D, “The threshold for toxicity is 500 to 600 mcg / kg body weight per day. In general, adults should not consume more than three times the RDA for extended period of time” (Garrison & Somer, The Nutrition Desk Reference, Third Ed., McGraw-Hill, pg. 82, 1997). Hypercalcemia may occur at a blood concentration of 25-hydroxyvitam...

Claims

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