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Inhibition zone (IZ) of bacterial growth of selected pathogens in relation to atmospheric pressure plasma jet exposure duration (seconds). The interior circles in the second column represent examples of determined IZ .  

Inhibition zone (IZ) of bacterial growth of selected pathogens in relation to atmospheric pressure plasma jet exposure duration (seconds). The interior circles in the second column represent examples of determined IZ .  

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The Plaz4 electrosurgical generator produces a nonequilibrium atmospheric pressure plasma jet (APPJ) at 26°C. This APPJ was tested for its antibacterial capabilities on common wound-related pathogens. The inhibition zone (IZ) of bacterial growth and surviving colony-forming units (CFUs) within the IZ were determined for 4 common clinical isolates:...

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... show a positive correlation between the duration of plasma exposure and the size of the bacterial growth IZ, as well as a negative correlation between exposure dura- tion and the number of surviving colonies inside the IZ (Figs. ...
Context 2
... time, the diameter of the IZ for all strains increases from a mean of 2.8 cm at 30 seconds - ence between strains until 140 seconds of exposure time, at which point all strains have a substantially equivalent IZ. Post-hoc testing reveals that P. aeruginosa is the sole outlier P. aeru- ginosa and other strains at 30 seconds is shown clearly in Fig. 4; it begins to ...

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Citations

... Joshi et al.(2011) andLiu et al.(2013 suggested thatlonger treatment times and higher plasma voltages are more successful at inhibiting it.Also,cells exposed to direct plasma may experience stress, and the active ions may immediately impact those cells.UV radiation, active ions, charged molecules, reactive oxygen kinds (ROS), and reactive nitrogen types (RNS) are a few examples of reactive types that can be produced.The most significant part of ROS is the inactivation of microbes [16,17]. These results agreed with Sanaei (2015), which suggested that the more extended plasma exposure over 5 min., the higher the bacterial inhibition of pS.aureus strain[12], Kulaga et al.(2016) noticed to other exposure times, expect 2min.Depending on infection injuries and inflammations, they can be adopted as adequate treatment times. The antibacterial peculiarity of APCPJ makes it a powerful tool to curb and demoralize MDR pathogens.The efficacy scope of APCPJ, as antibacterial is affected, depends on the devices' types, operating gas composition and flow rate, variation of source frequency, voltage and power, exposure distance, treatment time, initial concentration of microorganism suspension, and growth media and nature of target microorganisms.Further, the role of various APCPJ agents, i.e., the electric field in the inactivation mechanism, UV radiation, reactive species,and charged particles[10], alsoScholtz et al. (2015) and Bourke et al.(2017) suggested that the effectiveness of bacterial eradication by APCPJ is based on the time of treatment and the kinds of microorganisms and also the concentration or amount of the pathogens [11,15]; there for the results is diverging among previous and recent literature studies. ...
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... Thus, CAP, relying on ROS to take on actions, may reduce the amount and frequency of CAR-T cells infused to the patient to achieve the desired therapeutic efficacy, and thus reduce the probability of causing side effects related to over-activated immune response. On the other hand, CAP is a mild approach with multiple clinical applications, the safety of which has been rigorously examined and clinically validated for years (106)(107)(108)(109)(110)(111). Being a treatment strategy with multi-modality nature, CAP has demonstrated its power in creating synergies with chemotherapies such as Temozolomide (91) and Bortezomib (92), as well as rewiring drug resistant cells to a chemo-sensitive state (112). ...
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... The biofilm composed of complex microorganism community can also be effectively inactivated by CAP treatment (Figure 2c) [32][33][34][35]. These anti-bacterial capacities of CAP may be the foundation to drastically improve wound healing efficacy (Figure 2d) [29,[36][37][38][39]. Over the past decade, CAP has shown impressive potential as a novel anti−cancer tool both in vitro and in vivo. ...
... The biofilm composed of complex microorganism community can also be effectively inactivated by CAP treatment (Figure 2c) [32][33][34][35]. These anti-bacterial capacities of CAP may be the foundation to drastically improve wound healing efficacy ( Figure 2d) [29,[36][37][38][39]. Over the past decade, CAP has shown impressive potential as a novel anti-cancer tool both in vitro and in vivo. ...
... CAP also can inactivate many food-borne pathogens [145,146]. So far, most studies focused to describe the inhibition capacity of CAP on bacteria in vitro [36,147,148]. The direct microscopic observation of such cellular death is rare. ...
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Atmospheric pressure gas plasmas are emerging as a promising treatment in cancer that can supplement the existing set of treatment modalities and, when combined with other therapies, enhance their selectivity and efficacy against resistant cancers. With further optimisation in production and administration of plasma treatment, plasma-enabled therapy has a strong potential to mature as a tool for selectively curing highly resistant solid tumours. Although intense preclinical studies have been conducted to exploit the unique traits of plasma as an oncotherapy, few clinical studies are underway. This review identifies types of cancers and patient groups that most likely benefit from plasma oncotherapy, to introduce clinical practitioners to plasma therapy and accelerate the speed of translating plasma for cancer control in clinics.
Chapter
Cold atmospheric plasma (CAP) operates at temperatures between 36 and 52°C. It is a highly efficient tool in a number of hygiene and biomedical applications. CAP is effective against microorganisms and viruses. Development of microbial resistance has not been observed yet and is not expected. As opposed to some chemical disinfectants and sterilization processes, cold plasmas are suitable for treatment of temperature-sensitive materials without leaving toxic residues. CAP has been used in combination with hydrogen peroxide vapor for sterilization in health care services and industry since 1993. New developments for sterilization are emerging with peracetic acid, N2 or Ar-N2 plasma, microwave-excited plasma, and steam plasma-flow autoclave techniques. Technical solutions for disinfection of medical devices are still being developed.