Provided herein is a pre-Caesarean method for collecting amniotic fluid from a patient. A needle is inserted into the incision site for the future C-section, which may be under ultrasound guidance, through which the amniotic fluid is drawn under a low level suction and, optionally, gravity to a sterile collection container. The method encompasses filtering and/or irradiating the amniotic fluid to collect biomolecules of interest such as growth factors and/or stem cells. Also provided is the sterile amniotic fluid or filtrates thereof collected by the method described herein.

The invention relates to an artificial womb system for supporting newborns, in particular extremely premature infants between the 21/0 and 28/0 week of pregnancy, comprising the following: a chamber (1) of the artificial womb, said chamber being formed by an at least partially ultrasound-permeable wall (2) and comprising a lumen (14) for maintaining a physiologically intraamnial pressure and for receiving the artificial amniotic fluid (15) and a newborn or a premature infant, at least one access for supplying the premature infant in the artificial womb with nutrients, a dialysis device (9), and an oxygenator (8) and/or a gassing device for supplying oxygen to the newborn or premature infant, wherein means are provided in order to maintain an intraamnial pressure of >0 mBar in the chamber (1) of the artificial womb, said pressure acting on the newborn, in addition to the atmospheric pressure.

Compositions, devices, and methods for treating one or more respiratory disorders in a subject (e.g., a mammal) are provided. In an exemplary embodiment, a breathing system is provided and include a pressure-assisted breathing device, and a composition comprising amniotic fluid, an amnion tissue preparation, or a combination thereof. The pressure-assisted breathing device can be a mechanical ventilator. The breathing system can further include a delivery device selected from a nebulizer, a metered dose inhaler, or a dry powder inhaler operably connected to the breathing system to deliver the composition into the breathing system.

A skin regeneration therapy combining precise bioelectric signals, light, and biologics for skin treatment and regeneration. Precise bioelectric signals give clear instructions to the stimulated cell DNA/RNA to produce specific regenerative proteins on demand. Bioelectric signals give clear instructions to cell membranes on what to let in and what to let out and serve as an equivalent or surrogate of environmental stimuli to cause a cell action in response.

A skin regeneration therapy combining precise bioelectric signals, light, and biologics for skin treatment and regeneration. Precise bioelectric signals give clear instructions to the stimulated cell DNA/RNA to produce specific regenerative proteins on demand. Bioelectric signals give clear instructions to cell membranes on what to let in and what to let out and serve as an equivalent or surrogate of environmental stimuli to cause a cell action in response.

A system for aseptic collection of mammalian amniotic fluid. The system includes a cannula having an attachment end and external end. The attachment end provides a concentric opening to a hollow chamber disposed about a central passage. The hollow chamber has a port disposed adjacent to the external end permitting at least a partial suction to be established within the hollow chamber, the attachment end thereby suctionally attached to a surface when the attachment end is disposed upon the surface. The central passage provides access to a central portion of the surface surrounded by the concentric opening of the hollow chamber. An extraction needle is disposed within the central passage of the cannula and presented to the central portion of the surface. The extraction needle penetrates the central portion of the surface and extracts amniotic fluid there beneath. An associated method of use is also provided.

Disclosed is a method for the collection, processing and reuse of amniotic fluid at a C-section site. The method is conducted coincident with and in the operating room wherein the caesarian section is performed. In the method, amniotic fluid is suctioned from the caesarian section collection site using a vacuum line system which includes a canister positioned along the vacuum line. The canister has a port whereby the amniotic fluid can be removed from the canister. The amniotic fluid can be then be mixed with a coagulant or sealant and applied to the wound site of the cesarean section patient. Placental aspirate may also be collected, processed and used in accordance with the method of the present invention.

An external medical device includes a fluid inlet, an inlet valve in fluid communication with the fluid inlet to control fluid flow through the fluid inlet in response to fluid inlet control signals, a fluid outlet in fluid communication with a fluid reservoir, a fluid pump configured to deliver a therapeutic fluid from the fluid reservoir through the fluid outlet in response to fluid outlet control signals, a fluid sensor configured to monitor the therapeutic fluid between the fluid pump and the fluid outlet and further configured to output sensor data corresponding to a monitored condition of the therapeutic fluid, and a control module configured to receive the sensor data and output, based on the sensor data, the fluid inlet control signals to the inlet valve and the fluid outlet control signals to the fluid pump.

A skin regeneration therapy combining precise bioelectric signals, light, and biologics for skin treatment and regeneration. Precise bioelectric signals give clear instructions to the stimulated cell DNA/RNA to produce specific regenerative proteins on demand. Bioelectric signals give clear instructions to cell membranes on what to let in and what to let out and serve as an equivalent or surrogate of environmental stimuli to cause a cell action in response.

Disclosed are products having animal tissue packed within the lumen of a device such as a needle cannula. The needle cannula or other device can be received in a capsule and/or other container. Methods of use of the products are also described and can include ejecting the animal tissue from the lumen of device using pressurized liquid passed through the lumen, potentially to deliver the animal tissue directly into a patient. Methods of manufacture of the products are also described.