Vesicles resistant to enzyme lysis and use thereof in an enzyme assay

Claim 2

A product, comprising: a liposome, said liposome being formed from a compound having the following structural formula: X--L--A wherein X is a hydrophobic radical of the formula: ##STR4## wherein each of B 1 and B 2 is selected from the group consisting of --O-- and CH 2 ; R 1 and R 2 are each selected from the group consisting of hydrocarbon radicals having at least 11 carbon atoms, and Y is a hydrocarbon radical having from 1 to 5 carbon atoms; A is a hydrophilic radical; and L is selected from the group consisting of: ##STR5## wherein the negative valence of L is satisfied by a positive valence in said hydrophilic radical.

Claim 3

The product of claim 1 wherein the liposome includes a detectable marker.

Claim 4

The product of claim 2 wherein A is --(CH.sub.2).sub.c --N.sup.+ --(R.sup.1).sub.3 wherein C is 2-10 and each R is selected from the group consisting of hydrogen and an aliphatic hydrocarbon radical having from 1 to 8 carbon atoms.

Claim 5

The product of claim 3 wherein A is selected from the group consisting of --CH.sub.2 --N.sup.+ (CH.sub.3), and --CH.sub.2 --CH.sub.2 --N.sup.+ H.sub.3.

Claim 6

The product of claim 4 wherein X is ##STR6## wherein R 1 and R 2 are each saturated aliphatic hydrocarbons having at least 11 carbon atoms.

Claim 7

The product of claim 3 wherein the detectable marker is a chromogen.

Claim 8

In an assay for an analyte employing a tracer having an enzyme label wherein there is produced in the assay a bound fraction comprising tracer bound to a binder and a free tracer fraction, the improvement comprising: contacting at least one of the bound and free tracer fraction with a liposome as defined in claim 3, said enzyme label being an enzyme which is bound by said liposome and determining detectable of marker liposome bound to the tracer of at least one of the bound and free tracer fractions as a measure of analyte.

Claim 9

The assay of claim 7 wherein the enzyme label is a phospholipase.

Claim 10

A reagent kit for determining an analyte, comprising: a package, said package including a tracer containing an enzyme label; and a liposome as defined in claim 3, said enzyme label being an enzyme which bound by said liposome.

Claim 11

The reagent kit of claim 9 wherein the enzyme label is a phospholipase.

Claim 12

In an assay for analyte employing a tracer having an enzyme label wherein there is produced in the assay a bound fraction comprising tracer bound to a binder and a free tracer fraction, the improvement comprising: contacting at least one of the bound and free tracer fraction with a liposome, said liposome being formed from a compound having the following structural formula: X--L--A wherein X is a hydrophobic radical; A is a hydrophilic radical; and L is selected from the group consisting of: ##STR7## wherein the negative valence of L is satisfied by a positive valence in said hydrophilic radical, said liposome also including a detectable marker, said enzyme label being an enzyme which is bound by said liposome; and determining detectable marker of liposome bound to the tracer of at least one of the bound and free tracer fractions as a measure of analyte.

Claim 13

In an assay for analyte employing a tracer having an enzyme label wherein there is produced in the assay a bound fraction comprising tracer bound to a binder and a free tracer fraction, the improvement comprising: contacting at least one of the bound and free tracer fraction with a liposome, said liposome being formed from a compound having the following structural formula: X--L--A wherein X is a hydrophobic radical; A is a hydrophilic radical; and L is selected from the group consisting of: ##STR7## wherein the negative valence of L is satisfied by a positive valence in said hydrophilic radical, said liposome also including a detectable marker, said enzyme label being an enzyme which is bound by said liposome; and determining detectable marker of liposome bound to the tracer of at least one of the bound and free tracer fractions as a measure of analyte.

Claim 14

The assay of claim 11 wherein the enzyme label is a phospholipase.

Claim 15

The assay of claim 11 wherein A is ##STR8## wherein C is 2-10 and each R 1 is selected from the group consisting of hydrogen and an aliphatic hydrocabon radical having from 1 to 8 carbon atoms.

Claim 16

The assay of claim 13 wherein the enzyme label is a phospholipase.

Claim 17

The assay of claim 14 wherein X is: ##STR9## wherein R 1 and R 2 are each saturated aliphatic hydrocarbons having at least 11 carbon atoms.

Claim 18

A reagent kit for determining an analyte, comprising: a package, said package including a tracer containing an enzyme label, and a liposome, said liposome being formed from a compound having the following structural formula: X--L--A wherein X is a hydrophobic radical; A is a hydrophilic radical; and L is selected from the group consisting of: ##STR10## wherein the negative valence of L is satisfied by a positive valence in said hydrophilic radical, said liposome also including a detectable marker, said enzyme label being an enzyme which is bound by said liposome.

Claim 19

A reagent kit for determining an analyte, comprising: a package, said package including a tracer containing an enzyme label, and a liposome, said liposome being formed from a compound having the following structural formula: X--L--A wherein X is a hydrophobic radical; A is a hydrophilic radical; and L is selected from the group consisting of: ##STR10## wherein the negative valence of L is satisfied by a positive valence in said hydrophilic radical, said liposome also including a detectable marker, said enzyme label being an enzyme which is bound by said liposome.

Claim 20

The reagent kit of claim 16 wherein the enzyme label is a phospholipase.

Claim 21

The reagent kit of claim 16 wherein A is: --(CH.sub.2).sub.c --N.sup.+ --(R.sup.1).sub.3 wherein C is 2-10 and each R 1 is selected from the group consisting of hydrogen and an aliphatic hydrocarbon radical having from 1 to 8 carbon atoms.