DEVICE FOR DETECTING AN ENZYME IN A SAMPLE
A device for detecting a mammalian host-derived enzyme in a sample of a wound fluid, said device comprising: a housing having an inlet for the sample and side walls defining a fluid flow path extending from said inlet an indicator moiety that is bound to a solid substrate by means of a peptide linker moiety that is cleavable by said host-derived enzyme, said solid substrate being located in a reaction zone of said fluid flow path; and a detector moiety located in a detection zone downstream from the reaction zone in said fluid flow path, wherein the detector moiety interacts with an indicator moiety that has been cleaved from said solid substrate to produce a detectable change in said detection zone. Suitably, the device further comprises a control moiety located in a control zone in said device, wherein the control moiety can interact with a component of the wound fluid sample to improve the accuracy of the device. Also provided are systems comprising a device of the invention and a swab or biopsy punch adapted for use therewith.
1 . A device for detecting a mammalian host-derived or an analyte enzyme in a sample of a wound fluid, said device comprising:
a housing having an inlet for the sample and side walls defining a fluid flow path extending from said inlet
an indicator moiety that is bound to a solid substrate by means of a peptide linker moiety that is cleavable by said host-derived enzyme, said solid substrate being located in a reaction zone of said fluid flow path; and
a detector moiety located in a detection zone downstream from the reaction zone in said fluid flow path, wherein the detector moiety interacts with an indicator moiety that has been cleaved from said solid substrate to produce a detectable change in said detection zone.
2 . The device according to claim 1 , wherein said mammalian host-derived enzyme is selected from the group consisting of neutrophil elastase, matrix metalloproteinases (including the group consisting of MMP-9, MMP-8, MMP-1, MMP-2 and MMP-12), proteinase 3, plasmin, low molecular weight gelatinases and latent or active elastases, interleukin converting enzymes, tumor necrosis factor (TNFα) converting enzymes, and mixtures thereof
3 . The device according to claim 1 , wherein the device further comprises a control moiety located in a control zone in said device, wherein the control moiety can interact with a component of the wound fluid sample to improve the accuracy of the device.
4 . The device according to claim 1 , wherein the device further comprises
a control moiety located in a control zone in said device, wherein the control moiety can interact with a component of the wound fluid sample to improve the accuracy of the device.
5 . The device according to claim 4 , wherein said enzyme is selected from the group consisting of mammalian host-derived enzymes and bacterial enzymes.
6 . The device according to claim 5 , wherein said enzyme comprises a bacterial enzyme selected from the group consisting of bacterial protease enzymes of Pseudomonas Aeruginosa, Enterococcus faecalis, Escherichia Coli, Streptococcus Pyogenes and Staphylococcus Aureus.
7 . (canceled)
8 . The device according to claim 1 , wherein the fluid flow path contains one or more porous carrier materials.
9 . The device according to claim 1 , wherein the fluid flow path comprises a sample application zone in fluid communication with said inlet, and the reaction zone is located downstream from the sample application zone.
10 . The device according to claim 9 , wherein the fluid flow path contains a hydrophilic, porous wicking pad in said sample application zone.
11 . The device according to claim 1 , wherein the fluid flow path contains an absorbent reservoir of a porous hydrophilic material at the downstream end of the fluid flow path.
12 . The device according to claim 1 , wherein the indicator moiety comprises an indicator enzyme, and said detector moiety comprises a substrate for the indicator enzyme.
13 . The device according to claim 1 , wherein the device further comprises at least one filtration element to remove impurities from the sample before the sample contacts the reaction zone.
14 . The device according to claim 1 , wherein the device comprises an end-of-assay indicator to indicate when a predetermined minimum volume of liquid has passed through the reaction zone.
15 . The device according to claim 1 , wherein the device comprises a reference assay element for establishing that the total protease content or the total protein content of the sample is higher than a predetermined minimum.
16 . The device according to claim 1 , wherein the device comprises a buffer zone in the flow path upstream of the detection zone and downstream of the reaction zone, wherein the buffer zone is adapted to bind or inactivate a predetermined minimum amount the detector moiety.
17 . The device according to claim 1 , wherein the device comprises a control zone in the flow path upstream of the reaction zone, wherein the control zone is adapted to bind or inactivate one or more interfering enzymes.
18 . The device according to claim 1 , wherein the device comprises a plurality of different said peptide linkers for detecting a plurality of different analyte enzymes.
19 . The device according to claim 18 , wherein the device comprises a plurality of fluid flow paths each having a different peptide linker group in its respective reaction zone for detecting a different enzyme.
20 . The device according to claim 19 , wherein said plurality of fluid flow paths are radially distributed around a single sample receiving port.
21 . (canceled)
22 . (canceled)