General requirements for plasma sources for the generation of cold atmospheric pressure plasma (CAP) for medical applications
Abstract
This topic has been submitted as a request for the development of a DIN SPEC according to the PAS procedure. DIN SPECs in accordance with the PAS procedure are developed within DIN SPEC (PAS)-consortiums set up on a temporary basis. In the attached business plan you will find detailed information on the planned project as well as concrete time limits for commenting on the business plan (four-week commentary period) and for registering for the kick-off. This document will be developed and approved by the authors named in the business plan. This DIN SPEC is intended to establish requirements for the characterization of basic performance parameters of cold atmospheric pressure plasma sources intended for biomedical applications as well as for further development into medically applicable plasma sources. The test methods include physical-technical criteria (temperature, thermal power, radiation emission, UV irradiance, gas emission, electric current flow) for plasma sources for biomedical applications, as well as basic criteria for the characterization of biological plasma effects (effects on microorganisms in vitro, vitality of cultured cells or tissues, detection of chemical species in liquids and of the pH value).
Begin
2023-06-29
Planned document number
DIN SPEC 91315
Project number
17600001
previous edition(s)
General requirements for plasma sources in medicine
2014-06
