Disclosed is a menses cell capture device having at least one endometrial cell filter having a filter substrate defining a plurality of pores sized and arrayed so as to be effective in capturing endometrial cells, and a collection platform, such as a sanitary napkin or tampon, supporting said endometrial cell filters at least partially in the path of a menstrual flow in a configuration effective in collecting endometrial cells discharged in the menstrual flow.

Also disclosed is a method of screening for endometrial disorders in a subject by providing an endometrial cell filter at least partially positioned in a menstrual flow of said subject, recovering and identifying endometrial cells collected in the endometrial cell filter, and determining whether any of said endometrial cells present with an endometrial disorder, such as inter alia atypical hyperplasia and adenocarcinoma.

Described herein are a wearable apparatus and methods for detecting the presence of a targeted substance in a liquid. For example, the wearable apparatus can be a fingernail that detects illicit drugs in a beverage. The wearable apparatus comprises a detection layer comprising an indicator that is configured to display a signal upon the detection of an interaction with the targeted substance. In some examples, the wearable apparatus can include a lateral flow assay.

Described herein are apparatus and methods for detecting substances of abuse or other analytes in liquids. For example, the apparatus and methods described herein can be used for real-time detection of analytes, such as substances of abuse. The methods comprise providing a detection area comprising a chromatographic membrane capable of receiving the liquid and allowing for migration of the liquid, the chromatographic membrane comprising an anti-analyte antibody-particle conjugate, an analyte-conjugate protein at a test line; exposing at least the first location of the apparatus to the liquid; and determining whether an interaction between the analyte-conjugate protein and the liquid occurs to detect the presence of the analyte. The chromatographic membrane may further comprise an anti-species antibody at a control line. Specific buffers are disclosed, and these buffers may be used in the preparation of the apparatus to overcome challenges associated with miniaturization and challenges associated with exposure to beverages.

A personal hygiene product with a digital element is described. In one embodiment, a conductive sensor assembly is disposed within the personal hygiene product that includes one or more moisture sensors that generate a resistive signal indicative of saturation of the personal hygiene product when in wetting contact with menstrual fluid.

An incontinence detection system includes an incontinence detection pad underneath a patient's pelvic area for detecting an incontinence event. The incontinence detection system further includes a moisture detection sensor, a gas detection sensor, and a reader. The moisture detection sensor is embedded in the incontinence detection pad for detecting a presence of moisture in incontinence detection pad. The gas detection sensor is positioned near the incontinence detection pad for detecting a presence of targeted gas, such as methane. The reader is communicatively coupled to the moisture detection sensor and the gas detection sensor to receive moisture data and gas data, respectively. The reader is configured to determine a type of the incontinence event based on the received moisture data and the gas data and transmit a signal indicative of the type of incontinence event to a server.

A disposable diaper product useful for collecting a urine sample from an infant is disclosed. In one example the product may have a liquid control structure overlying a liquid impermeable backsheet, with a plan surface area defining a volume coextensive therewith, wherein a portion of the volume defined by at least 50 percent of the plan surface area contains no more than 50 percent by weight absorbent material. In another example the product may have a liquid control structure overlying a liquid impermeable backsheet, and have an average Liquid Release Ratio of at least 3 percent. A method for collecting a urine sample from an infant is also disclosed, in which a diaper is used for collection.

The present invention protects a system for monitoring the vital signs of a user of a disposable absorbent article that comprises a sensor device, a bi-dimensional code and a receiver, such that the sensor device is placed in contact with the user and the system is triggered by the reading of the bi-dimensional code through the receiver, such that the bi-dimensional code is place inside the packaging or the disposable absorbent article.

A system for collecting a physiological sample from a subject includes a lancet configured to draw a physiological sample and a cartridge configured to be affixed to the subject's skin. The cartridge includes a physiological sample well, a sloped physiological sample channel in open communication with the physiological sample well and a sample collection pad in in open communication with the sloped physiological channel and configured to absorb the drawn physiological sample. The physiological sample well is configured to retain the drawn physiological sample and the sloped physiological channel is configured to carry the drawn physiological sample from the physiological sample to the sample collection pad.

A disposable, wearable article can be used for collecting a sample and performing urinalysis. The article incorporates a test port feature to simplify this function. The test port has a resealable cover that can be used to selectively expose an aperture through the backsheet of the disposable article. The test port is used to position test devices, such as urine test strips to urine collected in the disposable article.

A system for monitoring at least one characteristic of biological material of an individual includes a wearable product. The wearable product includes an outer surface and a skin contact surface defining an internal area. An analysis portal is disposed in the internal area, and includes a sensing portion and an investigation portion. The sensing portion has at least one sensor, and the investigation portion that includes a computing device having a health screener. The sensing portion of the analysis portal comes into contact with a biological material of the individual, and the health screener is configured to determine at least one characteristic of the biological material. The computing device is communicatively coupled to the sensors and the display.