IMPROVED SOPHOROLIPID DERIVATIVES WITH THERAPEUTIC AGENT CARGOS AND THEIR USE
The present invention provides modified sophorolipids of formula (I) incorporating therapeutic molecules as therapeutic agent cargos to improve the bioavailability and/or delivery of such agents. The modified sophorolipids of the present invention are capable of efficiently delivering the therapeutic agent cargos to the target site and enhancing the efficacy of the therapeutic agent cargos and/or the sophorolipids. Additionally, the present invention provides methods of treating skin conditions or ailments as well as of maintaining or restoring gut health in a subject.
1 . A compound of formula (I) or a salt thereof:
wherein:
Y is hydrogen or methyl;
R 1 is a first therapeutic agent cargo linked via an ester linkage with X═O or an amide linkage with X═NR 0 , wherein R 0 is hydrogen or a substituent; or R 1 is hydrogen and X is O;
R 2 and R 3 are each independently hydrogen, acetyl, or a second therapeutic agent cargo linked via an ester linkage; and
n is an integer from 4 to 16, and the chain defined by n has 0-3 unsaturation,
wherein at least one of R 1 , R 2 , and R 3 is a therapeutic agent cargo.
2 . The compound according to claim 1 , wherein Y is methyl, n is 12, and the chain defined by n has at least 1 unsaturation that is a double bond.
3 . The compound according to claim 1 , wherein:
the first therapeutic agent cargo is salicylic acid, β-hydroxybutyric acid, amino acid, or succinic acid; and
the second therapeutic agent cargo is salicylic acid, butyric acid, β-hydroxybutyric acid, amino acid, succinic acid, or phosphoric acid,
wherein the first and second therapeutic agent cargos may be same or different.
4 . The compound according to claim 1 , as a salt wherein X is O − and R 1 is lithium (Li + ), sodium (Na + ), or potassium (K + ).
5 . The compound according to claim 1 , wherein the efficacy of the first and/or second therapeutic agent cargo is enhanced.
6 . The compound according to claim 1 , wherein:
R 1 is a first therapeutic agent cargo linked via an ester linkage with X═O or an amide linkage with X═NR 0 , wherein R 0 is hydrogen, lower alkyl, aryl, or a combination thereof; and
R 2 and R 3 are each independently hydrogen or acetyl.
7 . The compound according to claim 6 , wherein:
the first therapeutic agent cargo is salicylic acid, β-hydroxybutyric acid, amino acid, or succinic acid.
8 . The compound according to claim 6 , wherein the efficacy of the first therapeutic agent cargos is enhanced.
9 . The compound according to claim 1 , wherein:
R 1 is a first therapeutic agent cargo linked via an ester linkage with X═O or an amide linkage with X═NR 0 , wherein R 0 is hydrogen, lower alkyl, aryl, or a combination thereof;
R 2 and R 3 are each independently hydrogen, acetyl, or a second therapeutic agent cargo linked to the sophorolipid structure via an ester linkage, provided that at least one of R 2 and R 3 is the second therapeutic agent cargo; and
wherein the first and second therapeutic agent cargos may be same or different.
10 . The compound according to claim 9 , wherein:
the first therapeutic agent cargo is salicylic acid, β-hydroxybutyric acid, amino acid, or succinic acid; and
the second therapeutic agent cargo is salicylic acid, butyric acid, β-hydroxybutyric acid, amino acid, succinic acid, or phosphoric acid,
wherein the first and second therapeutic agent cargos may be same or different.
11 . The compound according to claim 9 , wherein the efficacy of the first and/or second therapeutic agent cargos is enhanced.
12 . The compound according to claim 1 , wherein:
R 1 is hydrogen and X is O; and
R 2 and R 3 are each independently hydrogen, acetyl, or a second therapeutic agent cargo linked to the sophorolipid structure-via an ester linkage, provided that at least one of R 2 and R 3 is the second therapeutic agent cargo.
13 . The compound according to claim 12 , wherein:
the second therapeutic agent cargo is salicylic acid, butyric acid, β-hydroxybutyric acid, amino acid, succinic acid, or phosphoric acid.
14 . The compound according to claim 12 , wherein the efficacy of the second therapeutic agent cargos is enhanced.
15 . A method of improving the bioavailability and/or dermal penetrability of an active ingredient in a subject comprising administering to the subject an effective amount of the compound according to claim 1 , wherein said active ingredient is the first therapeutic agent cargo and/or the second therapeutic agent cargo.
16 . A method of treating a skin condition or ailment of a subject by administering to the subject an effective amount of the compound according to claim 1 , wherein the first therapeutic agent cargo and the second therapeutic agent cargo are each independently salicylic acid or succinic acid.
17 . The method according to claim 16 , wherein the skin condition or ailment is acne.
18 . A method of maintaining or restoring gut health in a subject comprising administering to the subject an effective amount of the compound according to claim 1 , wherein the first therapeutic agent cargo and the second therapeutic agent cargo are each independently amino acid, butyric acid, β-hydroxybutyric acid, or phosphoric acid.
19 . A method of reducing pathogenic gram-negative bacteria in the microbiome of a subject comprising administering to the subject an effective amount of the compound according to claim 1 , wherein the first therapeutic agent cargo and the second therapeutic agent cargo are each independently amino acid, butyric acid, β-hydroxybutyric acid, or phosphoric acid.
20 . A method of improving weight gain of a subject comprising administering to the subject an effective amount of the compound according to claim 1 , wherein the first therapeutic agent cargo and the second therapeutic agent cargo are each independently amino acid, butyric acid, β-hydroxybutyric acid, or phosphoric acid.