Melanin Binding Agents for Targeted Topical Delivery

Patent metadata

Field	Value
Publication number	US-2016235642-A1
Application number	US-201414379795-A
Country	US
Kind code	A1
Filing date	Mar 11, 2014
Priority date	Mar 15, 2013
Publication date	Aug 18, 2016
Grant date	—

Abstract

Compositions and methods are disclosed for targeted delivery of a benefit agent to areas of a human integument having melanin deposits. The compositions comprise a pyridinium compound having affinity for melanin. The compounds may be bound to a benefit agent, such as a pigment and may be topically applied to a human integument.

First claim

1 .- 41 . (canceled)

42 . A method for targeted delivery of a benefit agent to areas of human integument having melanin deposits, comprising topically applying to said integument a composition comprising the reaction product of a benefit agent and compound capable of binding to melanin having the structure of Formula (I):

wherein, L is a divalent C 4-32 hydrocarbon moiety, optionally substituted with heteroatoms selected from Si, O, S, N, and halogen, and optionally substituted with one or more groups R; and is a functional group capable of forming a bond with said benefit agent; for conjugating said compound to a benefit agent, and
R 1 -R 5 are independently selected, at each occurrence, from a group R; wherein R is selected from hydrogen, —F; —Cl; —Br; —I; —OH, —OR*; —NH 2 ; —NHR*; —N(R*) 2 ; —N(R*) 3 + ; —N(R*)—OH; —N(→O)(R*) 2 ; —O—N(R*) 2 ; —N(R*)—O—R*; —N(R*)—N(R*) 2 ; —C═N—R*; —N═C(R*) 2 ; —C═N—N(R*) 2 ; —C(═NR*)—N(R*) 2 ; —SH; —SR*; —C≡N, —NC; —(C═O)—R*; —CHO; —CO 2 H; —CO 2 − ; —CO 2 R*; —C(═O)Cl, —(C═O)—S—R*; —O—(C═O)—H; —O—(C═O)—R*; —S—(C═O)—R*; —(C═O)—NH 2 ; —(C═O)—N(R*) 2 ; —(C═O)—NHNH 2 ; —O—(C═O)—NHNH 2 ; —(C═S)—NH 2 ; —(C═S)—N(R*) 2 ; —N(R*)—CHO; —N(R*)—(C═O)—R*; —(C═NR)—O—R*; —O—(C═NR*)—R*, —SCN; —NCS; —NSO; —SSR*; —N(R*)—C(═O)—N(R*) 2 ; —N(R*)—C(═S)—N(R*) 2 ; —SO 2 —R*; —O—S(═O) 2 —R*; —S(═O) 2 —OR*; —N(R*)—SO 2 —R*; —SO 2 —N(R*) 2 ; —O—SO 3 − ; —O—S(═O) 2 —OR*; —O—S(═O)—OR*; —O—S(═O)—R*; —S(═O)—OR*; —S(═O)—R*; —NO; —NO 2 ; —NO 3 ; —O—NO; —O—NO 2 ; —N 3 ; —N 2 —R*; —N(C 2 H 4 ); —Si(R*) 3 ; —CF 3 ; —O—CF 3 ; —PR* 2 ; —O—P(═O)(OR*) 2 ; —P(═O)(OR*) 2 ; —CH 3 , —CR*═CR* 2 , —C≡CH, —Si(OR*) 3 , —Si(R*) 2 H, C 1 -C 12 perfluoroalkyl; an aliphatic C 1 -C 12 hydrocarbon radical; a C 1 -C 12 aromatic hydrocarbon radical; or a C 1 -C 12 heteroaryl radical;
R* is independently at each occurrence hydrogen or a straight chained, branched, or cyclic C 1 -C 20 hydrocarbon radical, which may be saturated, partially saturated, or aromatic, each of which may be optionally substituted with 1-6 heteroatoms selected from nitrogen, oxygen, sulfur, or halogen, and wherein any two adjacent R* groups may together form a 3-8 membered aromatic, partially unsaturated, or saturated ring.
and topically acceptable salts thereof.

43 . The method according to claim 42 , wherein L is further characterized as having an octanol-water partition coefficient, expressed as Log(K ow ), of the corresponding alcohol HO-L-CH 3 between 1 and about 10.

44 . The method according to claim 42 , wherein L is a C 4-32 alkyl or alkenyl group.

45 . The method according to claim 44 , wherein L is a straight chained C 6-16 alkyl or alkenyl group.

46 . The method according to claim 42 , wherein L is a divalent C 4-32 hydrocarbon moiety of the form —X 1 —(CR* 2 ) n —X 2 —(CR* 2 ) m —X 3 —, where X 1 is selected from the group consisting of a bond, —CH 2 —, —CR* 2 —, —CR*═CR*—, —C≡C—, —(C═O)—, —(C═O)—O—, —(C═O)—NR*—, —Si(R*) 2 —, —(CR* 2 ) i —Si(R*) 2 —, —(CR* 2 ) i —(Si(R*) 2 ) j —(O—Si(R*) 2 ) k — (where “i” is an integer from 0-10, “j” is zero or one and “k” is an integer from 1-10); and X 2 , and X 3 are independently at each occurrence a bond, —O—, —NR*—, —S—, —CH 2 —, —CR* 2 —, —CR*═CR*—, —C≡C—, —(C═O)—, —(C═O)—O—, —(C═O)—NR*—, —(OCH 2 CH 2 ) y —, or —(CH 2 CH 2 O) z — (wherein “y” and “z” are independently an integer from 1 to 12), —Si(R*) 2 —, —(Si(R*) 2 ) j —(O—Si(R*) 2 ) k — (where “j” is zero or one and “k” is an integer from 1-10), and “n” and “m” are independently an integer from 0 to 30

47 . The method according to claim 46 , wherein “n” and “m” are independently integers from 6 to 24, with the proviso that at least one of “m” and “n” is not zero.

48 . The method according to claim 46 , wherein L has the form —(CH 3 ) z — (where “z” is an integer from 6-18), —R a —O—R b —, —R a —S—R b —, —R a —Si(CH 3 ) 2 —R b —, —R a —Si(CH 3 ) 2 —O—Si(CH 3 ) 2 —R b —, or —R a —Si(CH 3 ) 2 —(O—Si(CH 3 ) 2 ) k —R b —, where R a and R b are independently C 1-12 straight chain alkyl groups, and “k” is an integer from 1-12.

49 . The method according to claim 42 , wherein R 1 , R 2 , R 4 , and R 5 are hydrogen.

50 . The method according to claim 42 , wherein Ω is selected from chloro, bromo, iodo, mesyl, tosyl, —OH, —SH, —NH 2 ; —NHR*, —(C—NR* 2 )═R*, —CR*═CR* 2 , —C≡CH, —CR*(O)CR* (epoxide), —Si(OR*) 3 , —Si(R*) 2 H, —(Si(R*) 2 ) j —(O—Si(R*) 2 ) k —Si(OR*) 3 , —(Si(R*) 2 ) j —(O—Si(R*) 2 ) k —Si(R*) 2 H, —CO 2 H; —CO 2 R*; —C(═O)Cl, —CH 2 O(C═O)CH 2 (C═O)CH 3 , —C(O)—O—(N(—(C═O)—R*) 2 ), —SO 2 Cl, —NCS, —NCO, —N 3 , —N 2 + Cl; or a group R.

51 . The method according to claim 42 , wherein Ω is a trialkoxysilane of the form —Si(OR*) 3 where R* is independently selected at each occurence from C 1-6 hydrocarbons.

52 . The reaction product of an inorganic oxide particle and a compound of Formula (I):

where L has the form —(CH 3 ) z —, where “z” is an integer from 6-18;
Ω is a trialkoxysilane of the form —Si(OR*) 3 , where R* is independently selected at each occurence from C 1-6 hydrocarbons; and
R 1 , R 2 , R 4 , and R 5 are hydrogen, R 3 is hydrogen, —CH 3 , —OCH 3 , —OH, —SH, or —NH 2 .

53 . The method according to claim 52 , wherein said inorganic oxide is selected from the group consisting of iron oxides, titanium dioxide, zinc oxide, alumina, and silica.

54 . A surface-functionalized pigment, wherein said pigment has covalently attached to the surface thereof, a plurality lipophilic pyridinium compounds.

55 . A compound of Formula (II):

Assignees

• Avon Prod Inc

Inventors

• Howell Ashley L
• Bansal Amitabh
• Ebanks Jody P

Classifications

• A61Q19/02

  for chemically bleaching or whitening the skin · CPC title

• C07F7/28

  Titanium compounds · CPC title

• A61K33/24

  Heavy metals; Compounds thereof · CPC title

• C09C1/24

  Oxides of iron · CPC title

• A61K9/0014

  Skin, i.e. galenical aspects of topical compositions (non-active ingredients are additionally classified in A61K47/00; A61K9/0009, A61K9/0021, A61K9/7015, A61K9/7023 take precedence; cosmetic preparations A61K8/00, A61Q; preparations for wound dressings or bandages A61L26/00) · CPC title