Polymer glucan ether derivatives, their manufacturing as well as their use
First Claim
1. A method of treating skin for prophylaxis and/or therapy of diseases and/or irritations induced by oxidative stress in the skin, comprising topically applying a composition to the skin, said composition containing as an active ingredient a therapeutically effective amount of at least one glucan ether derivative, said at least one glucan ether derivative comprising respective monomer units of a formula I and a formula II:
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wherein the monomer units of the formula I are connected with the monomer units of the formula II by a 1,3-beta-glycosidic bond; and
in the monomer units of formula II, X is selected from the group consisting of —
CH2—
COO—
Y, —
CH2—
CH2—
COO—
Y, CH(CH3)—
COO—
Y, —
CH2—
CH2—
SO3—
Y, and mixtures thereof, and Y is selected from the group consisting of hydrogen, an alkali-metal, an alkaline-earth metal and mixtures thereof; and
wherein said at least one glucan ether derivative comprises a combination of monomer units of formula I and formula II so that there is an average degree of substitution of 0.75±
0.1.
1 Assignment
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Accused Products
Abstract
A method for treatment of skin includes topical application of a composition containing a therapeutically effective amount of a 1,3-beta-glucan ether derivative. Such application effectively provides treatment and/or prophylaxis of various skin-related problems, such as neurodermatitis and psoriasis, and reduces the evidence of aging by minimizing wrinkles. In an advantageous embodiment, the glucan ether derivative is present in the composition in a range of concentration of about 0.002% to about 8% by weight. In another embodiment the glucan ether derivative is advantageously carboxymethyl glucan sodium salt.
26 Citations
11 Claims
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1. A method of treating skin for prophylaxis and/or therapy of diseases and/or irritations induced by oxidative stress in the skin, comprising topically applying a composition to the skin, said composition containing as an active ingredient a therapeutically effective amount of at least one glucan ether derivative, said at least one glucan ether derivative comprising respective monomer units of a formula I and a formula II:
-
wherein the monomer units of the formula I are connected with the monomer units of the formula II by a 1,3-beta-glycosidic bond; and
in the monomer units of formula II, X is selected from the group consisting of —
CH2—
COO—
Y, —
CH2—
CH2—
COO—
Y, CH(CH3)—
COO—
Y, —
CH2—
CH2—
SO3—
Y, and mixtures thereof, and Y is selected from the group consisting of hydrogen, an alkali-metal, an alkaline-earth metal and mixtures thereof; and
wherein said at least one glucan ether derivative comprises a combination of monomer units of formula I and formula II so that there is an average degree of substitution of 0.75±
0.1.- View Dependent Claims (2, 3, 4, 5, 6, 7, 8, 9, 10, 11)
an alcohol in a range of about 0% to about 3% by weight;
an alkylenglycol in a range of about 0.5% to about 15% by weight;
a paraffin in a range of about 1% to about 3% by weight;
other additives in a range of about 5.5% to about 9.5% by weight; and
water in a range of about 75% to about 92.988% by weight.
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6. A method according to claim 5, wherein said concentration is about 0.04% by weight.
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7. A method according to claim 5, wherein said at least one glucan ether derivative is carboxymethyl glucan sodium salt, and said concentration is about 0.04% by weight.
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8. A method according to claim 1, wherein said therapeutically effective amount is a concentration in a range of about 0.002% to about 1% by weight, said composition having a cream-like consistency and further comprising:
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panthenol in a range of about 1% to about 3% by weight;
a fatty additive in a range of about 15% to about 28% by weight;
other additives in a range of about 0.05% to about 7% by weight; and
water in a range of about 61% to about 83.948% by weight.
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9. A method according to claim 1, wherein said composition further comprises at least one phospholipid, at least one oil and water.
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10. A method according to claim 1, wherein said composition is a nanoemulsion of at least one phospholipid and at least one oil, and of said at least one glucan ether derivative.
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11. A method according to claim 1, wherein said therapeutically effective amount is a concentration in a range of about 0.05% to about 1% by weight, said composition further comprising:
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an oil in a range of about 15% to about 25% by weight;
a phospholipid in a range of about 1% to about 5% by weight;
an alcohol in a range of about 0% to about 8% by weight other additives in a range of about 8% to about 15% by weight; and
water in a range of about 46% to about 75.9% by weight.
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Specification