A falloposcope is described, and a method of screening a patient for fallopian tube and/or ovarian cancer with the falloposcope. The falloposcope can perform optical imaging, including fluorescence imaging and/or optical coherence tomography (OCT), and optionally include a channel for a sampling wire, within a diameter of about 0.7 millimeter. The method includes inserting the falloposcope through a lumen of vagina, cervix, uterus, and fallopian tube so a tip of the falloposcope is in proximity to a first fallopian tube or ovary of the patient; providing fluorescence stimulus wavelength through an illumination fiber of the falloposcope while imaging light at fluorescence emission wavelength through a coherent fiber bundle to form fluorescence emissions images; and determining suspect tissue. Then the sampling wire is used to collect cells from the suspect tissue for karyotype and other analysis.

A device comprises a cannula having a first end, a second end, and a channel between the first end and the second end; an imaging probe couplable to the first end of the cannula, where the imaging probe includes: a transducer, and a reflective surface; and a biopsy device coupled to the cannula, where the biopsy device is configured to collect a tissue sample from an organ of a patient.

The present disclosure provides a female reproductive system sample collector, including a sampling device and an elution preservation device, where the elution preservation device is filled with an elution preservation solution, after sampling is completed, the sampling device is submerged in the elution preservation solution of the elution preservation device and sealed for preservation; the sampling device includes a sampling rod and a sheath; the sampling rod includes an operating rod, a straight rod brush and a ball head brush, an opening and closing cover corresponding to the ball head is disposed at a front end of the sheath, and the opening and closing cover includes four oscillating rods that are hinged with a front port of the sheath and the oscillating rods are connected through thin films. The present disclosure can collect cells or nucleic acids of uterus and ovaries in a uterine cavity, a sampling rod can deform in a shape along an outline of the uterine cavity. The sampling rod can avoid sample falling when finishing sampling and recovering; an elution preservation device can prevent liquid from overflowing and leaking or polluting a sealing cap. The present disclosure provides a quick, convenient, widely applicable and less discomfort sample collection channel and a sample protection method for early detection of the ovarian cancer, the endometrial cancer and the cervical cancer.

The current invention concerns a sample vial for receiving a liquid cell sample, to be used in conjunction with a digital holographic microscope (DHM), said sample vial comprises at least two compartments in fluid connection with one another, said compartments comprising at least one pair of screening surfaces, said screening surfaces are essentially flat; and characterized in that the distance between the pair of screening surfaces of the second compartment is smaller than the distance between the pair of screening surfaces of the first compartment. In a second and third aspect, the current invention pertains to a method and system for analyzing a liquid cell sample by DHM, employing the sample vial of the current invention.

A protective guide for protecting a cell extraction device used during a Pap smear. An access tunnel receives the cell extraction device and allows for access and movement of the cell extraction device. A protective chamber covers and protects the head of the cell extraction device as the cell extraction device is being removed and inserted from the patient's vagina. A protective guide connector attaches the protective guide to an imaging transducer. After inserted into the patient's vagina, the location of the patient's cervix is determined by utilization of the imaging transducer. Once the cervix is located the cell extraction device is pushed outward from the protective chamber so that the cell extraction device head contacts the cervix and then removes cells from the cervix. The cell extraction device head is then pulled back into the protective chamber and the protective guide is removed from the patient's vagina.

According to exemplary embodiments of the present disclosure, a system for collection and analysis of cells from a body lumen of a patient may include a diagnostics device including a tube having a distal end and a proximal end and a balloon having a first end coupled to the distal end of the tube. The balloon may be disposed in the tube in a first, inverted position and movable to a second, everted position. A push wire may have a distal end coupled to a second end of the balloon. The balloon may be movable from the first inverted position to the second everted position by actuation of the push wire. One or more receptacles may be included for processing a balloon sample. The system may further include at least one of a sample preparation fluid, a sample preservation liquid, or both. The sample may be preparable for cytological analysis.

A sampling probe, having a housing, with a flange at housing's proximal end, and an internal step ring including a protruding follower tab toward housing's distal end. The sampling probe further includes a shaft inside the housing, with a brush at shaft's distal end and a handle at shaft's proximal end. The shaft includes a solid proximal section, and a spirally grooved distal section, engaging the housing's follower tab. A retracting compression spring is positioned on the spirally grooved distal section of the shaft inside the housing. With the sampling probe distally inserted in a vagina canal for a Pap smear, pushing the shaft handle distally, the brush at the end of the shaft protrudes out of the housing rotationally, taking a cell sample, followed by the retracting compression spring retracting the brush back into the housing when the shaft handle is released, completing the Pap smear.

A system and a method for a medical diagnostic device are described herein. The medical diagnostic device can include an outer sleeve having a hollow interior and open distal and proximal ends, the outer sleeve being defined by a substantially tubular configuration including a proximal section having a substantially conical shape. A core is configured to be inserted axially within the outer sleeve. The core includes an axial inner cavity. The core is further defined by a proximal section having a conical shape substantially conforming to the proximal section of the outer sleeve. The core retains a diagnostic assembly, that can include at least one of a sample collecting assembly and an imaging assembly, that can be integrally or interchangeably attached and wherein the device can be utilized for self-patient or single patient use.

An exemplary device for collecting cervicovaginal cells includes a proximal end portion configured for gripping by a user, a distal end portion configured for contacting an ectocervical region and obtaining a sampling of cells therefrom, an elongated body portion extending between and connecting the proximal end portion and the distal end portion, and an elongated slot sized and shaped to receive a bristled portion of a brush having disposed thereon endocervical cells.

The present invention comprises methods and devices comprising a cutting element used to contact circumferentially and longitudinally the surface walls of the endocervical canal to provide for broad and complete contact of the intended surface with the device, resulting in attainment of a sufficient volume and comprehensive tissue sample for analysis as an endocervical curettage or screening pap smear. The device may provide for a reservoir for the obtained sample to be contained when removing from the cervical canal and vagina. The device may be comprised of a detachable means or be of a material that allows the user to cut the sampling head of the device for placement in collection means to maximize the amount of tissue or cells being sent to the laboratory for analysis.