Claims
- 1. An amphiphilic compound of the formula: ##STR7## wherein R is NH(CH.sub.2 CH.sub.2 O).sub.n R.sub.1, wherein n is an integer from 1 to 50; and wherein R.sub.1 is hydrogen, --NH2, or a lower alkyl of C.sub.1-6, or a pharmaceutical salt thereof.
- 2. An amphiphilic compound of the formula: ##STR8## wherein R is NH(CH.sub.2 CH.sub.2 O).sub.n R.sub.1, wherein n is an integer from 1 to 50; and wherein R.sub.1 is hydrogen or a lower alkyl of C.sub.1-6, or a pharmaceutical salt thereof.
- 3. An amphiphilic compound according to claim 1 wherein R.sub.1 is hydrogen, or a lower alkyl of C.sub.1-6.
- 4. An amphiphilic compound according to claim 2 wherein n is from 1 to about 20.
- 5. An amphiphilic compound according to claim 4 wherein n is from 1 to about 17.
- 6. An amphiphilic compound according to claim 5 wherein n is from about 3 to about 15.
- 7. An amphiphilic compound according to claim 2 wherein R.sub.1 is a lower alkyl of from 1 to 6 carbon atoms.
- 8. An amphiphilic compound according to claim 7 wherein R.sub.1 is a lower alkyl of from 1 to 3 carbon atoms.
- 9. An amphiphilic compound according to claim 8 wherein R.sub.1 is methyl.
- 10. An amphiphilic compound according to claim 2 wherein n is 3 to 15, and R.sub.1 is methyl.
- 11. The compound according to claim 10 wherein n is 3.
- 12. The compound according to claim 10 wherein n is 6.
- 13. The compound according to claim 10 wherein n is 15.
- 14. A method for improving the antibiotic property of an analogue of Amphotericin B having a --COOH moiety, said analogue having a first critical micelle concentration and that functions by disrupting the cellular membrane of the organism to which it is targeted, said improvement being achieved by altering the chemical structure of said analogue by the substitution of an oligo(ethylene glycol) conjugate in lieu of the OH portion of said --COOH moiety, thereby raising the critical micelle concentration from said first to a second critical micelle concentration.
Government Interests
Partial funding for the making of the invention described herein was provided by the federal government. Accordingly, the United States retains certain statutory rights in the present invention under 35 USC 200 et seq.
US Referenced Citations (1)
Number |
Name |
Date |
Kind |
5204330 |
Driver et al. |
Apr 1993 |
|
Non-Patent Literature Citations (1)
Entry |
Chemical Abstracts, vol. 123 (1995) No. 25196q. Yamashita et al "Micell/Monomer Control over . . . ". |