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Screening test and procedure using apocrine sweat

a technology of sweat collection and test, applied in the field of screening test and procedure using apocrine sweat, can solve the problems of not being able to quickly test for the presence of drugs using presently available sweat collection patches and procedures, and not being able to recognize the unique diagnostic function

Inactive Publication Date: 2003-10-23
HERMETIC DIAGNOSTICS
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, he fails to recognize the unique diagnostic function of apocrine sweat glands and proceeds to collect eccrine sweat from the chest because large quantities of sweat can be collected.
However, the percentage of false negative results with the patches indicates that weekly sweat testing may be less sensitive than thrice weekly urine testing in detecting opiate use.
This is most likely because those skilled in the art selected an inappropriate source of sweat (eccrine sweat), not recognizing the unique diagnostic capacity of apocrine sweat.
Further, because of the extended wear requirement (up to 14 days), the ability to rapidly test for the presence of drugs using presently available sweat collection patches and procedures is not possible.
The requirement for such a procedure results in a major deficiency for diagnostic test strips as it is often desirable to be able to read the test strip on the patient or immediately upon removal of the test strip without performing a further analytical procedure.

Method used

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Examples

Experimental program
Comparison scheme
Effect test

example 1

[0022] The superior and unexpected diagnostic utility of apocrine sweat collection and analysis in cancer detection is demonstrated by the analysis for PSA in apocrine sweat when compared to eccrine sweat or blood. Approximately 0.5 cc of eccrine sweat, apocrine sweat, and blood of two individuals was tested for PSA. One individual had normal PSA blood levels while the other had significantly elevated blood PSA. Values for PSA in blood, eccrine sweat and apocrine sweat are as follows:

1 PSA level (ng / ml) eccrine sweat apocrine sweat blood RK 0.34 10.3 3.91 SB 0.08 0.16 0.92

[0023] RK has an abnormally high blood PSA level. This was reflected in a significantly greater quantity of PSA in apocrine sweat and a 29.4 to 1 ratio of PSA in apocrine compared to eccrine sweat. Still further, PSA is elevated in apocrine sweat when compared to blood with a 2.6 magnification of PSA in apocrine sweat. This means that there is an active process taking place in the apocrine gland to increase the con...

example 2

[0028]

2 Blood Serum Eccrine Apocrine Normal Sodium (mEq / l) 138 (N) 119 (VL) 127 (L) 135-149 Potassium (mEq / l) 4.2 (N) 65.0 (VH) 69.2 (VH) 3.5-5.2 Chloride (mEq / l) 99 (N) 80 (L) 96 (N) 98-108 CO.sub.2 (mEq / l) 25 (N) 2 (VL) 21 (N) 22-32 Glucose (mg / dl) 121 (H) 52 (L) 22 (VL) 61-114 BUN (mg / dl) 60 (H) 437 (VH) 401 (VH) 6-25 Creatinine 2.4 (H) 2.2 (H) 2.2 (H) 0.6-1.5 (VL = Very low; L = Low; N = Normal; H = High; VH = Very High)

[0029] Standard analysis indicates that both eccrine sweat, apocrine sweat and blood have about the same values for the various analytes with the exception of BUN that the body must excrete, and glucose which the body must conserve. However, apocrine BUN levels can be readily used to signal an abnormally high concentration. Apparently a marker for diabetes was not identified or, because glucose was near normal, no marker was magnified in apocrine sweat. The conclusion that can be reached from this data is that a proper marker has not been identified. It can not b...

example 3

[0031] Samples of apocrine and eccrine sweat were collected prior to oral consumption of a THC containing product. No THC was detected in either sample. The test individual then orally consumed (smoked) a quantity of a THC containing product. Small quantities (0.5 cc) of apocrine and eccrine sweat was separately collected over a period of 30 minutes under ambient conditions to induce sweating. When the collected samples were tested using standard laboratory tests for THC metabolites no detectable levels were found in either sample. However, samples tested for THC (rather than metabolites) using standard laboratory tests showed the following significant differences between eccrine and apocrine sweat, compared with THC concentrations in blood and urine.

3 Blood eccrine apocrine urine Delta 9 THC (nanograms / ml) 21 4 107 undetect-able

[0032] The quantity of THC in apocrine sweat was significantly greater than in eccrine sweat (26.75 times) and blood (5.1 times).

[0033] The unique diagnosti...

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PUM

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Abstract

Marker compounds indicative of variations in physiological conditions, genetic defects or disease states have been found to be present in apocrine sweat and, in many conditions, these markers are present in apocrine sweat in elevated levels when compared to blood. These markers are collected and / or detected in apocrine sweat and used as an indicator that a disease state or particular physiological condition exists. A skin patch, wipe or other collection means is used to collect apocrine sweat. The apocrine sweat is then used to indicate the existence of a disease state or changing physiological condition by the presence of specific marker compounds. Apocrine sweat can also be collected from individuals known to have a specific disease or physiological condition and, by comparison with apocrine sweat from normal individuals, used to identify new markers indicative of the specific disease state or physiological condition.

Description

[0001] This is a Continuation-in-Part of U.S. application Ser. No. 09 / 994, 535, filed Nov. 26, 2001, now U.S. Pat. No. ______ issued ______, which claims benefit of Provisional Application 60 / 250, 206 filed Nov. 29, 2000.[0002] The present invention relates primarily to a test for diagnosing the existence of certain disease states or physiological conditions in mammals based on the collection and analysis of apocrine sweat.[0003] It is known that certain disease states or variations from normal physiological conditions can be detected or monitored by analyzing body fluids for variations in constituents of those body fluids. Blood is a highly complex suspension with many elements, which can be measured and analyzed to measure normal homeostasis and variations from normality. Blood is frequently analyzed for variations of various constituents (cholesterol, glucose, etc.), as well as its cellular constituents, as indicators of possible abnormal health conditions. In a like manner, a ur...

Claims

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Application Information

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Patent Type & Authority Applications(United States)
IPC IPC(8): G01N33/52G01N33/574
CPCG01N33/57434G01N33/528
Inventor BERLIN, STUART M.
Owner HERMETIC DIAGNOSTICS
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