Cold atmospheric plasma (CAP) as a promising therapeutic option for mild to moderate acne vulgaris: Clinical and non-invasive evaluation of two cases

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Cold atmospheric plasma (CAP) as a promising therapeutic option for mild to moderate acne vulgaris: Clinical and non-invasive evaluation of two cases

ReferencesShowing 10 of 28 papers
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Seasonal changes in epidermal ceramides are linked to impaired barrier function in acne patients.
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The effect of nitrogen plasma on the skin and hair follicles: a possible promising future for the treatment of alopecia.
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CitationsShowing 5 of 5 papers
  • Research Article
  • 10.1134/s0030400x2306005x
Study on the Effect of Low-Temperature Atmospheric Pressure Plasma Jet on the Morphofunctional Properties of Living Tissues (in vivo)
  • Aug 1, 2023
  • Optics and Spectroscopy
  • K M Giraev + 6 more

Study on the Effect of Low-Temperature Atmospheric Pressure Plasma Jet on the Morphofunctional Properties of Living Tissues (in vivo)

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  • Research Article
  • 10.17816/dv640815
Experience of using of low-temperature argon plasma in the treatment of postacne
  • Dec 23, 2024
  • Russian Journal of Skin and Venereal Diseases
  • Anastasia A Kostina + 4 more

BACKGROUND: In recent years, there has been a growing number of scientific literature concerning the correction of the consequences of acne vulgaris, united by the term "post-acne symptom complex". Post-inflammatory pigmentation and postacne scars can be persistent, progress and persist for months to years, significantly reducing patients' quality of life. Moreover, consequences of acne vulgaris require expensive treatment. Thus, the problem of postacne prevention and treatment remains actual for both dermatovenerologists, cosmetologists and patients. AIM: Clinical and morphofunctional assessment of the effectiveness and tolerability of the monotherapy of using of low-temperature argon plasma in patients with postacne. MATERIALS AND METHODS: The study involved 15 patients with postacne (13 women and 2 men) aged 18 to 30 years, 10 of them had mild severity, 5 had moderate-to-severe postacne. All patients received monotherapy using the Plazmoran plasma arc installation. The course of treatment consisted of 10 procedures performed every other day, the observation period was 1 month. Dermatological examination was carried out visually with assessment of the severity of pigmented spots, erythema and scarring using the postacne scar scales by G.J. Goodman et al. In order to assess the morphofunctional parameters of facial skin, all patients underwent a non-invasive digital study using the Capricorn AI Intelligent Imager Bitmoji device, based on 3D visualization. To study the impact of the disease on various aspects of the patient's life and as an effectiveness criterion, the Dermatology Life Quality Index (DLQI) was used. RESULTS: In the majority of patients using Plazmoran monotherapy a reduction in postacne manifestations was observed within the first 2 weeks. Moreover, there was a significant regression of inflammatory elements, the skin texture was improved. As a result of the treatment, significant improvement was achieved in 10 patients and improvement in 5. At the end of the entire observation period, according to the questionnaire, the subjects observed a decrease in DLQI compared with the baseline (15.6±3.4 vs. 8.3±0.9; p 0.05), which indicates an improvement of the quality of life and psychoemotional state of patients and the effectiveness of therapy. CONCLUSION: The Plazmoran plasma arc installation is a highly effective method for correcting and preventing the development of the post-acne symptom complex of mild and moderate severity, which is as confirmed based on the results of a visual examination and the positive dynamics of indicators of superficial and deep analysis of facial skin (sebumetry, corneometry, pigmentation, reactivity and level colonization by Cutibacterium acnes). The procedure is well tolerated by patients with no any adverse events.

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  • Research Article
  • Cite Count Icon 10
  • 10.3390/app13053324
Synergistic Effect of Hydrogen Peroxide and Cold Atmospheric Pressure Plasma-Jet for Microbial Disinfection
  • Mar 6, 2023
  • Applied Sciences
  • Ku Youn Baik + 4 more

The efficiency of simultaneous treatment of the cold atmospheric pressure plasma jet (CAP) and hydrogen peroxide (H2O2) was investigated. A CAP with a thin and long plume was generated with Ar gas and applied to a common oral bacterium, Enterococcus faecalis (E. faecalis). The bactericidal efficiency was evaluated with the electron microscopy and the colony forming unit (CFU) assay. The underlying mechanisms were studied by measuring extracellular chemical changes in the water solution and by measuring biological responses such as the trans-membrane potential, the intracellular oxidative stress, and the membrane permeability. The combination of CAP with H2O2 could provide dramatic synergistic effects in bacterial disinfection through the enhanced membrane transportation of reactive species and the oxidation of intracellular molecules. Since the byproducts of both H2O2 and CAP are not significantly toxic, the synergistic bactericidal effects of their combination could be a good candidate to clinical applications.

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  • Research Article
  • Cite Count Icon 3
  • 10.3390/app112311181
A Prospective, Randomised, Controlled, Split-Face Clinical Trial to Assess the Safety and the Efficacy of Cold Atmospheric Plasma in the Treatment of Acne Vulgaris
  • Nov 25, 2021
  • Applied Sciences
  • Sigrid Karrer + 4 more

The increase in antibiotic resistance requires effective non-antibiotic therapies for acne. Cold atmospheric plasma (CAP) inactivates bacteria and improves wound healing, but its effect on acne has not been investigated. The objective of this controlled split-face study was to assess safety and efficacy of CAP in moderate acne. One side of the face received 8–10 treatments with cold helium plasma within 4–6 weeks; follow-up was two and four weeks thereafter. Acne lesions were counted, followed by global acne severity ratings. Of the 34 patients included, 29 completed the study. No serious adverse events occurred. The two facial sides did not significantly differ in the number of inflammatory and non-inflammatory lesions. An interaction effect of number and type of treatment was found for inflammatory lesions. Lesion reduction after 10 treatments was significantly higher on the treated than on the untreated side. Percentage of patients reporting improved aesthetics was higher for the treated than for the untreated side after treatment completion (79% vs. 45%) and at the two- (72% vs. 45%) and four-week follow-up (79% vs. 52%). In conclusion, CAP was safe with excellent tolerability, showed moderate reduction in acne lesions and led to higher patient-based ratings of aesthetics than non-treatment.

  • Research Article
  • 10.1155/dth/4228323
Therapeutic Use of Cold Atmospheric Plasma for the Treatment of Mild Acne Papulopustulosa—A Randomized, Controlled, Double‐Blind Pilot Study
  • Jan 1, 2025
  • Dermatologic Therapy
  • Melvin Bae + 4 more

Acne is a common disease worldwide, predominantly occurring in teenagers. Commonly prescribed therapies often cause adverse effects and in case of antibiotics bare the risk of developing resistances. Cold atmospheric plasma (CAP) is a well‐tolerable, physical treatment method, which is well established in the treatment of chronic wounds since it provides bactericidal and wound healing properties. Our aim was to evaluate the efficacy and safety of CAP as a potential add‐on therapy for mild acne papulopustulosa in a randomized controlled, double‐blind pilot study. Forty participants were randomized into two arms of 20 each. Both groups self‐applied 0.1% of adapalene cream daily and received weekly skin‐cleansing by a physician combined with either CAP verum‐device treatments or placebo‐device applications instead. The endpoint of the treatment segment was at 6, and follow‐up was at 10 weeks. The co‐primary endpoints total inflammatory lesion count (TILC) and acne‐specific Investigator Global Assessment (IGA) score as well as secondary endpoints sebumetry, total porphyrin count (TPC) reflecting Cutibacterium acnes colonization, and occurrence of adverse events (AEs) were measured from baseline until follow‐up, while the Acne‐specific Quality of Life (AQOL) questionnaire was assessed at baseline and endpoint. TILC decreased greater in the verum versus control group from baseline (45.8 vs. 49.4) toward endpoint (22.1 vs. 38.6; p = 0.07) to follow‐up (16.5 vs. 28.7; p = 0.48), matched by the IGA score with similarly greater improvement in the verum versus control group from baseline (2.3 vs. 2.6) to endpoint (1.3 vs. 2.3; p < 0.001) until follow‐up (1.0 vs. 1.9; p = 0.006). Sebumetry, TPC, and AQOL scores decreased more during treatment and in the verum group. AE occurred less frequently in the verum group without serious AE reported overall (all p < 0.05). Conclusively, CAP proved to be an efficient and well‐tolerable add‐on therapy for the treatment of mild acne papulopustulosa.Trial Registration: German Registry of Clinical Trials: DRKS00032416

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Transdermal delivery of topical lidocaine in a mouse model is enhanced by treatment with cold atmospheric plasma.
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Topical anesthetics are widely used in dermatology and cosmetology to alleviate the pain from nonsurgical cosmetic procedures, while the transdermal drug delivery is limited by the skin barrier. Cold atmospheric plasma (CAP) is a potential approach used for skin pretreatment to enhance transdermal delivery of topical medications. To assess the efficacy of CAP as a pretreatment to improve the transdermal delivery of topical anesthetic. First, we conducted ex vivo permeation studies on 30 mice with a Franz cell diffusion experiment. CAP irradiations of different intensity and duration were pretreated on the epidermal layer of mice before topical lidocaine applied, with the control group received no pretreatment. The amount of drug penetrated through the skin and drug flux were determined by high-performance liquid chromatography. Then, we treated 3 living mice with CAP followed by application of methylene blue cream (MB) and used skin biopsies to measure penetration depth by microscope. Last, we measured the transepidermal water loss (TEWL) of mouse skin in vivo before and after CAP treatment to observe its effect on the skin barrier function. In the permeation study, the transdermal flux of lidocaine was enhanced to 1.97 times of the control samples by CAP pretreatment. We also observed that the accumulative amount of lidocaine varied with the duration of the CAP treatment in a biphasic manner. In the MB penetration study, significant amount of MB deposition was observed under the epidermis and deeper parts of the skin after CAP pretreatment compared with the control sample. A sharp increase in TEWL value was observed directly after the CAP treatment, but 30minutes later, it began to decrease and recovered to baseline in the next 3hours, indicating that the skin barrier property had been changed reversibly. Our studies suggested that the transdermal absorption of topical lidocaine can be efficiently and safely enhanced by pretreatment of the skin with CAP. We believe that CAP could be used as an assistance to improve analgesia in dermatology.

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PO-030 Cold atmospheric plasma treatment in breast cancer
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Plasma is the fourth state of matter, and it is species of partially ionized gas generated under an electric field that contains photons, free electrons, ions, free radicals, and reactive oxygen/nitrogen species. Plasma can be produced at atmospheric pressure or under a vacuum in two ways; thermal and non-thermal. Furthermore, they can be classified into natural and artificial plasmas. Non-thermal atmospheric plasma, also known as cold atmospheric plasma (CAP), is produced in a cold form under a high electrical field at atmospheric pressure. CAP is primarily produced using two methods which are the dielectric barrier discharge (DBD) and plasma jet. The electrical discharge between two electrodes separated by an insulating dielectric barrier is known as DBD. This method is quite widely used in many studies in the literature and has an important place in the field of plasma medicine. In the DBD method, the electrode configuration, shape, material, and substance from which the dielectric barrier is made are important. There are many studies conducted with different electrode configurations in the literature. Besides the electrode configuration and shape, the barrier and electrode materials can also affect the reactivity of the discharge by changing the discharge electrical power. It is thought that plasma discharge at different times will vary in CAP applications due to the change in conductivity of the conductive material used depending on the capacitive resistance. In this study, deionized water (DIW) activated with CAP treatment using different electrode materials (copper, stainless steel, and aluminum) to compare the physical quantities that can change such as pH and conductivity. The aim of this study is to observe the effect of using different electrode materials (copper, stainless steel, and aluminum) on the biological outcome of CAP treatment and compare the antimicrobial activities of different materials.

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Cold atmospheric plasma (CAP) has shown good clinical efficacy in treating chronic wounds, but its superiority over conventional treatment is still under debate. This meta-analysis systematically analyzed the clinical efficacy of CAP compared to control therapy. Relevant literature was obtained online according to PRISMA guidelines. Randomized controlled trials (RCTs) were selected based on reduced bacterial load and wound size or area in chronic wounds as observation outcomes. The data were pooled and analyzed using REVMAN 5.2. Twelve studies were included in the meta-analysis, comprising two on wound bacterial load, four on wound size or area, and six on both wound bacterial load and size. For the reduction in wound size or area, CAP showed a significant superior effect compared to the control group. Out of the five RCTs that evaluated wound size, CAP showed a higher number of wounds reduced (CAP vs. control: OR = 1.75; 95% CI = 1.11 - 2.77; p = 0.02). The percentage of relative reduced wound area was evaluated by five RCTs (CAP vs. control: MD = 43.24%; 95% CI = 24.95% - 61.54%; p < 0.00001). For reduced bacterial load, CAP also showed significantly better efficacy than control, as evaluated in eight RCTs (CAP vs. control: OR = 2.06; 95% CI = 1.16 - 3.68; p = 0.01). A total of 448 patients with chronic wounds were included in all 12 meta-analysis studies, indicating that CAP has better clinical efficacy in treating chronic wounds. These findings provide a valuable reference for the clinical application of CAP.

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  • Cite Count Icon 19
  • 10.1016/j.cpme.2020.100101
Dose-dependent effect of plasma-chemical NO-containing gas flow on wound healing. An experimental study
  • Jun 3, 2020
  • Clinical Plasma Medicine
  • Anatoly B Shekhter + 8 more

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