Detection of amniotic fluid in vaginal secretions of pregnant women due to premature rupture of fetal membranes
View Patent ↗A method is taught for the accurate determination of the premature rupture of membranes (PROM), defined as spontaneous rupture of membranes before the onset of uterine contractions. More specifically, a lateral flow assay strip tests for at least two antigens to greatly limit or eliminate the possibility of false negatives. A built-in timer in the cassette holding the lateral flow assay further increases the accuracy of the test. A collection buffer vial with self-contained shipping and dropper caps and built-in stand is also taught.
1. A method for the detection of biomarkers in vaginal secretions of pregnant women indicative of premature rupture of fetal membranes, the method comprising:
a) obtaining a fluid sample by placing a sterile swab in a vaginal vault of a pregnant woman;
b) removing the swab from the vaginal vault after a period of time from about fifteen seconds to about three minutes, and placing the swab in a vial containing a buffer solution;
c) allowing time for the fluids from the swab to be released into the buffer solution;
d) adding a few drops of the buffer solution that has been exposed to the fluids from the swab to a chromatographic specific binding assay strip device, the device created by including the following components:
i) a non-permeable platform strip;
ii) a permeable membrane testing strip positioned on top of the non-permeable platform strip, the permeable membrane testing strip further comprising a test site for the detection of the premature rupture of fetal membranes, the site comprising a blend, the blend comprising at least:
1) a first set of polyclonal antibodies for the detection of a first biomarker, the first biomarker indicating the premature rupture of fetal membranes, the first biomarker being alpha-fetoprotein;
2) a second set of polyclonal antibodies for the detection of a second biomarker, the second biomarker being indicative of the premature rupture of fetal membranes, the second biomarker being placental protein 12;
3) a first set of monoclonal antibodies for the detection of the first biomarker being indicative of the premature rupture of fetal membranes, the first set of monoclonal antibodies being specific for alpha-fetoprotein; and
4) a second set of monoclonal antibodies for the detection of a second biomarker, the second biomarker being indicative of the premature rupture of fetal membrane the second set of monoclonal antibodies being specific for placental protein 12;
wherein the ratio of polyclonal antibodies blended together are about 75% placental protein 12 to about 25% alpha-fetoprotein antibodies;
iii) a sample receiving pad positioned on top of and at a proximal end of the non-permeable platform strip while in contact with a proximal end of the permeable membrane testing strip;
iv) a reservoir pad positioned on top of and at a distal end of the non-permeable membrane testing strip while in contact with a distal end of the permeable membrane test strip; and
v) a conjugate pad positioned on top of or below the sample receiving pad, the conjugate pad comprising a permeable membrane containing a conjugate, the conjugate comprising a colorant attached to antibodies that can attach to analytes in the sample, wherein the conjugate of the sample binds to the analytes forming conjugate tagged analytes;
e) allowing time for the conjugate tagged analytes to migrate along the length of the permeable membrane strip to the test site; and
f) detecting binding between the biomarkers and their respective the monoclonal antibodies and the polyclonal antibodies by the presence of an indicator line at the test site.
2. The method according to claim 1 , wherein the first set of monoclonal antibodies and the second set of monoclonal antibodies are fixed to the colorant on the conjugate pad.
3. The method according to claim 2 , wherein the first set of polyclonal antibodies and the second set of polyclonal antibodies are positioned at the test site in the shape of a plus sign.
4. The method according to claim 1 , wherein the first set of polyclonal antibodies and the second set of polyclonal antibodies are intermingled with the first set of monoclonal antibodies and the second set of monoclonal antibodies.
5. The method according to claim 4 , wherein the first set of polyclonal antibodies and the second set of polyclonal antibodies intermingled with the first set of monoclonal antibodies and the second set of monoclonal antibodies are positioned at the test site in the shape of a plus sign.
6. The method according to claim 1 , further comprising the detection of additional biomarkers, the additional biomarkers selected from the group consisting of: BETA-IG-H3, prolactin, hCG, and fetal fibronectin.
7. The method according to claim 6 , wherein the alpha-fetoprotein biomarkers and prolactin biomarkers are tested in combination with the placental protein 12 biomarker to detect the fetal membrane rupture.
8. The method according to claim 1 , wherein the chromatographic specific binding assay strip device further comprises a semi-permeable membrane, wherein the semi-permeable membrane is positioned between the sample receiving pad, and the conjugate pad residing on top of the semi-permeable membrane.
9. The method according to claim 1 , wherein the chromatographic specific binding assay strip device further comprises a semi-permeable membrane, wherein the semi-permeable membrane is positioned over the conjugate pad, the conjugate pad being positioned over the sample receiving pad.
10. A method for detecting biomarkers in vaginal secretions, the method comprising:
a) obtaining a fluid sample by placing a sterile swab in a vaginal vault of a pregnant woman;
b) removing the swab from the vaginal vault after a period of time from about fifteen seconds to about three minutes;
c) afterwards placing the swab in a vial containing a buffer solution;
d) allowing time for fluid from the swab to release into the buffer solution in the vial;
e) adding buffer solution that has been contacted with the swab to a chromatographic specific binding assay strip device comprising:
i) a non-permeable platform strip;
ii) a permeable membrane testing strip positioned on top of the non-permeable platform strip, the permeable membrane testing strip comprising a test site for detecting the premature rupture of fetal membranes, the test site comprising a blend, wherein the blend comprises at least:
1) a first set of polyclonal antibodies for detecting alpha-fetoprotein;
2) a second set of polyclonal antibodies for detecting placental protein 12;
3) a first set of monoclonal antibodies specific for detecting alpha-fetoprotein; and
4) a second set of monoclonal antibodies specific for detecting placental protein 12;
wherein the ratio of polyclonal antibodies blended together are about 75% placental protein 12 to about 25% alpha-fetoprotein antibodies;
iii) a sample receiving pad positioned on top of and at a proximal end of the non-permeable platform strip while in contact with a proximal end of the permeable membrane testing strip;
iv) a reservoir pad positioned on top of and at a distal end of the non-permeable membrane testing strip while in contact with a distal end of the permeable membrane test strip; and
v) a conjugate pad positioned on top of or below the sample receiving pad, the conjugate pad comprising a permeable membrane containing a conjugate, the conjugate comprising a colorant attached to antibodies that bind with analytes in the sample, wherein the conjugate of the sample binds to the analytes to form conjugate tagged analytes;
f) allowing time for conjugate tagged analytes to migrate along the length of the permeable membrane strip to the test site; and
g) detecting binding between alpha-fetoprotein, placental protein 12, and their respective monoclonal and polyclonal antibodies at the test site.