US 5,087,618 A · Redox carriers for brain-specific drug delivery

Abstract

The invention provides compounds of the formula D--DHC].sub.n (I) and the nontoxic pharmaceutically acceptable salt thereof, wherein D is the residue of a centrally acting drug containing at least one reactive functional group selected from the group consisting of amino, hydroxyl, mercapto, carboxyl, amide and imide, said residue being characterized by the absence of a hydrogen atom from at least one of said reactive functional groups in said drug; n is a positive integer equal to the number of said functional groups from which a hydrogen atom is absent; and [DHC] is the reduced, biooxidizable, bloodbrain barrier penetrating lipoidal form of a dihydropyridine.revreaction.pyridinium salt redox carrier, said carrier comprising a bivalent radical of the formula ##STR1## wherein the alkylene group can be straight or branched and can contain 1 to 3 carbon atoms; R.sub.o is a radical identical to the corresponding portion of a natural amino acid; and p is 1 or 2, provided that, when p is 2, then the alkylene groups can be the same or different and the R.sub.0 radicals can be the same or different; said bivalent radical being so positioned that the terminal carbonyl function of the bivalent radical is linked to the drug residue while the terminal amino function of the bivalent radical is linked to the remaining portion of the carrier moiety. The subject compounds are adapted for the site-specific/sustained delivery of centrally acting drugs to the brain. The corresponding pyridinium salt type drug/carrier entities D--QC.sup.+ ].sub.n qY.sup.-t are also disclosed.

Claims50

Dependent claims

A compound having the structural formula

D-- DHC].sub.n
or a nontoxic pharmaceutically acceptable salt thereof, wherein D is the residue of a centrally acting drug containing at least one reactive hydroxyl functional group, said drug being a nucleaside-type antiviral, anticancer or antitumor agent, said residue being characterized by the absence of a hydrogen atom from at least one of said reactive hydroxyl functional groups in said drug;
n is a positive integer equal to the number of said functional groups from which a hydrogen atom is absent;
and is a radical of the formula ##STR1196## wherein the alkylene group can be straight or branched and can contain 1 to 3 carbon atoms;
R.sub.o is hydrogen, methyl, --CH(CH.sub.3).sub.2, --CH.sub.2 --CH(CH.sub.3).sub.2, ##STR1197## --CH.sub.2 OH, --CH(OH)CH.sub.3, --(CH.sub.2).sub.2 --SCH.sub.3, --CH.sub.2 --CONH.sub.2, --CH.sub.2 CH.sub.2 --CONH.sub.2, ##STR1198## --CH.sub.2 COOH or --CH.sub.2 CH.sub.2 COOH;
p is 1 or 2, provided that, when p is 2, then the alkylene groups can be the same or different and the R.sub.o radicals can be the same or different;
the dotted line in formula (a') indicates the presence of a double bond in either the 4 or 5 position of the dihydropyridine ring;
the dotted line in formula (d') indicates the presence of a double bond in either the 2 or 3 position of the dihydroquinoline ring;
R.sub.1 is C.sub.1 -C.sub.7 alkyl, C.sub.1 -C.sub.7 haloalkyl or C.sub.7 -C.sub.10 aralkyl;
the carbonyl-containing grouping in formula (a') can be attached at the 2, 3 or 4 position of the dihydropyridine ring;
the carbonyl-containing grouping in formula (d') can be attached at the 2, 3 or 4 position of the dihydroquinoline ring;
and the carbonyl-containing grouping in formula (g') can be attached at the 1, 3 or 4 position of the dihydroisoquinoline ring.

9 more elements

A quaternary salt having the structural formula

D-- QC.sup.+].sub.n qY.sup.-t
wherein D is the residue of a centrally acting drug containing at least one reactive hydroxyl functional group, said drug being an antiviral, anticancer or antitumor agent, said residue being characterized by the absence of a hydrogen atom from at least one of said reactive hydroxyl functional groups in said drug;
n is a positive integer equal to the number of said functional groups from which a hydrogen atom is absent;
is a radical of the formula ##STR1200## wherein the alkylene group can be straight or branched and can contain 1 to 3 carbon atoms;
R.sub.o is hydrogen, methyl, --CH(CH.sub.3).sub.2, --CH.sub.2 --CH(CH.sub.3).sub.2, ##STR1201## --CH.sub.2 OH, --CH(OH)CH.sub.3, --(CH.sub.2).sub.2 --SCH.sub.3, --CH.sub.2 --CONH.sub.2, --CH.sub.2 CH.sub.2 --CONH.sub.2, ##STR1202## --CH.sub.2 SH, --CH.sub.2 COOH or --CH.sub.2 CH.sub.2 COOH;
p is 1 or 2, provided that, when p is 2, then the alkylene groups can be the same or different and the R.sub.o radicals can be the same or different;
R.sub.1 is C.sub.1 -C.sub.7 alkyl, C.sub.1 -C.sub.7 haloalkyl or C.sub.1 -C.sub.10 aralkyl;
the carbonylcontaining grouping in formula (a) can be attached at the 2, 3 or 4 position of the pyridinium ring;
the carbonyl-containing grouping in formula (d) can be attached at the 2, 3 or 4 position of the quinolinium ring;
the carbonylcontaining grouping in formula (g) can be attached at the 1, 3 or 4 position of the isoquinolinium ring;
Y.sup.- is the anion of a pharmaceutically acceptable organic or inorganic acid;
t is the valence of the acid anion;
and q is the number which when multiplied by t is equal to n.

10 more elements