Plasma activated Ringer’s lactate solution

References

• Hori M. Radical-controlled plasma processes. Rev Mod Plasma Phys. 2022;6(1):36.
   Google Scholar
• Laroussi M, Bekeschus S, Keidar M, et al. Low temperature plasma for biology, hygiene, and medicine: perspective and roadmap. IEEE Trans Radiat Plasma Med Sci. 2021;6:127–157.
   Web of Science ®Google Scholar
• Fridman G, Friedman G, Gutsol A, et al. Applied plasma medicine. Plasma Process Polym. 2008;5(6):503–533.
   Web of Science ®Google Scholar
• Von Woedtke T, Schmidt A, Bekeschus S, et al. Plasma medicine: a field of applied redox biology. In Vivo. 2019;33(4):1011–1026.
   PubMed Web of Science ®Google Scholar
• Isbary G, Shimizu T, Li YF, et al. Cold atmospheric plasma devices for medical issues. Expert Rev Med Devices. 2013;10(3):367–377.
   PubMed Web of Science ®Google Scholar
• Kaushik NK, Bekeschus S, Tanaka H, et al. Plasma medicine technologies. Appl Sci. 2021;11(10):4584.
   Google Scholar
• Metelmann HR, Seebauer C, Miller V, et al. Clinical experience with cold plasma in the treatment of locally advanced head and neck cancer. Clin Plasma Med. 2018;9:6–13.
   Web of Science ®Google Scholar
• Toyokuni S, Ikehara Y, Kikkawa F, et al. Plasma medical science. San Diego: Academic Press; 2018.
   Google Scholar
• Tanaka H, Bekeschus S, Yan D, et al. Plasma-treated solutions (PTS) in cancer therapy. Cancers. 2021;13(7):1737.
   PubMed Web of Science ®Google Scholar
• Tanaka H, Mizuno M, Ishikawa K, et al. Molecular mechanisms of non-thermal plasma-induced effects in cancer cells. Biol Chem. 2018;400(1):87–91.
   PubMed Web of Science ®Google Scholar
• Tanaka H, Mizuno M, Ishikawa K, et al. New hopes for plasma-based cancer treatment. Plasma. 2018;1(1):150–155.
   Google Scholar
• Tanaka H, Ishikawa K, Mizuno M, et al. State of the art in medical applications using non-thermal atmospheric pressure plasma. Rev Mod Plasma Phys. 2017;1(1):1–89.
   Google Scholar
• Tanaka H, Mizuno M, Ishikawa K, et al. Plasma medical science for cancer therapy: toward cancer therapy using nonthermal atmospheric pressure plasma. IEEE Trans Plasma Sci. 2014;42(12):3760–3764.
   Web of Science ®Google Scholar
• Tanaka H, Mizuno M, Ishikawa K, et al. Plasma-activated medium selectively kills glioblastoma brain tumor cells by down-regulating a survival signaling molecule, AKT kinase. Plasma Med. 2011;1(3–4):265–277.
   Google Scholar
• Utsumi F, Kajiyama H, Nakamura K, et al. Effect of indirect nonequilibrium atmospheric pressure plasma on anti-proliferative activity against chronic chemo-resistant ovarian cancer cells in vitro and in vivo. PLOS One. 2013;8(12):e81576.
   PubMed Web of Science ®Google Scholar
• Tanaka H, Mizuno M, Ishikawa K, et al. Cell survival and proliferation signaling pathways are downregulated by plasma-activated medium in glioblastoma brain tumor cells. Plasma Med. 2012;2(4):207–220.
   Google Scholar
• Torii K, Yamada S, Nakamura K, et al. Effectiveness of plasma treatment on gastric cancer cells. Gastric Cancer. 2015;18(3):635–643.
   PubMed Web of Science ®Google Scholar
• Hattori N, Yamada S, Torii K, et al. Effectiveness of plasma treatment on pancreatic cancer cells. Int J Oncol. 2015;47(5):1655–1662.
   PubMed Web of Science ®Google Scholar
• Takeda S, Yamada S, Hattori N, et al. Intraperitoneal administration of plasma-activated medium: proposal of a novel treatment option for peritoneal metastasis from gastric cancer. Ann Surg Oncol. 2017;24(5):1188–1194.
   PubMed Web of Science ®Google Scholar
• Nakamura K, Peng Y, Utsumi F, et al. Novel intraperitoneal treatment with non-thermal plasma-activated medium inhibits metastatic potential of ovarian cancer cells. Sci Rep. 2017;7(1):6085.
   PubMedGoogle Scholar
• Bruggeman P, Leys C. Non-thermal plasmas in and in contact with liquids. J Phys D Appl Phys. 2009;42(5):053001.
   Web of Science ®Google Scholar
• Lukes P, Dolezalova E, Sisrova I, et al. Aqueous-phase chemistry and bactericidal effects from an air discharge plasma in contact with water: evidence for the formation of peroxynitrite through a pseudo-second-order post-discharge reaction of H2O2 and HNO2. Plasma Sources Sci Technol. 2014;23:015019.
   Web of Science ®Google Scholar
• Bruggeman PJ, Kushner MJ, Locke BR, et al. Plasma–liquid interactions: a review and roadmap. Plasma Sources Sci Technol. 2016;25(5):053002.
   Web of Science ®Google Scholar
• von Woedtke T, Metelmann HR. Focus issue: "plasma–liquid interactions: key role in plasma medical research and new fields of application". Clin Plasma Med. 2015;3(2):41.
   Google Scholar
• Jablonowski H, Schmidt-Bleker A, Weltmann KD, et al. Non-touching plasma–liquid interaction – where is aqueous nitric oxide generated? Phys Chem Chem Phys. 2018;20(39):25387–25398.
   PubMed Web of Science ®Google Scholar
• Takeda K, Ishikawa K, Tanaka H, et al. Spatial distributions of O, N, NO, OH and vacuum ultraviolet light along gas flow direction in an AC-excited atmospheric pressure Ar plasma jet generated in open air. J Phys D Appl Phys. 2017;50(19):195202.
   Web of Science ®Google Scholar
• Kurake N, Tanaka H, Ishikawa K, et al. Cell survival of glioblastoma grown in medium containing hydrogen peroxide and/or nitrite, or in plasma-activated medium. Arch Biochem Biophys. 2016;605:102–108.
   PubMed Web of Science ®Google Scholar
• Bauer G. The synergistic effect between hydrogen peroxide and nitrite, two long-lived molecular species from cold atmospheric plasma, triggers tumor cells to induce their own cell death. Redox Biol. 2019;26:101291.
   PubMed Web of Science ®Google Scholar
• Takai E, Kitamura T, Kuwabara J, et al. Chemical modification of amino acids by atmospheric-pressure cold plasma in aqueous solution. J Phys D Appl Phys. 2014;47:28.
   Web of Science ®Google Scholar
• Uchida G, Mino Y, Suzuki T, et al. Decomposition and oxidation of methionine and tryptophan following irradiation with a nonequilibrium plasma jet and applications for killing cancer cells. Sci Rep. 2019;9(1):6625.
   PubMedGoogle Scholar
• Takahashi Y, Taki Y, Takeda K, et al. Reduced HeLa cell viability in methionine-containing cell culture medium irradiated with microwave-excited atmospheric-pressure plasma. Plasma Process Polym. 2018;15:1–9.
   Web of Science ®Google Scholar
• Tanaka H, Nakamura K, Mizuno M, et al. Non-thermal atmospheric pressure plasma activates lactate in Ringer’s solution for anti-tumor effects. Sci Rep. 2016;6:36282.
   PubMed Web of Science ®Google Scholar
• Nakamura K, Yoshikawa N, Yoshihara M, et al. Adjusted multiple gases in the plasma flow induce differential antitumor potentials of plasma-activated solutions. Plasma Process Polym. 2020;17(10):e1900259.
   Web of Science ®Google Scholar
• Tanaka H, Hosoi Y, Ishikawa K, et al. Low temperature plasma irradiation products of sodium lactate solution that induce cell death on U251SP glioblastoma cells were identified. Sci Rep. 2021;11(1):18488.
   PubMed Web of Science ®Google Scholar
• Sato Y, Yamada S, Takeda S, et al. Effect of plasma-activated lactated Ringer’s solution on pancreatic cancer cells in vitro and in vivo. Ann Surg Oncol. 2018;25(1):299–307.
   PubMed Web of Science ®Google Scholar
• Nakamura K, Yoshikawa N, Mizuno Y, et al. Preclinical verification of the efficacy and safety of aqueous plasma for ovarian cancer therapy. Cancers. 2021;13(5):1141.
   PubMed Web of Science ®Google Scholar
• Toyokuni S, Yanatori I, Kong YY, et al. Ferroptosis at the crossroads of infection, aging and cancer. Cancer Sci. 2020;111(8):2665–2671.
   PubMed Web of Science ®Google Scholar
• Yan DY, Xiao HJ, Zhu W, et al. The role of aquaporins in the anti-glioblastoma capacity of the cold plasma-stimulated medium. J Phys D Appl Phys. 2017;50:055401.
   Web of Science ®Google Scholar
• Chang JW, Kang SU, Shin YS, et al. Non-thermal atmospheric pressure plasma induces apoptosis in oral cavity squamous cell carcinoma: involvement of DNA-damage-triggering Sub-G(1) arrest via the ATM/p53 pathway. Arch Biochem Biophys. 2014;545:133–140.
   PubMed Web of Science ®Google Scholar
• Ma Y, Ha CS, Hwang SW, et al. Non-thermal atmospheric pressure plasma preferentially induces apoptosis in p53-mutated cancer cells by activating ROS stress-response pathways. PLOS One. 2014;9(4):e91947.
   PubMed Web of Science ®Google Scholar
• Tanaka H, Mizuno M, Katsumata Y, et al. Oxidative stress-dependent and -independent death of glioblastoma cells induced by non-thermal plasma-exposed solutions. Sci Rep. 2019;9(1):13657.
   PubMedGoogle Scholar
• Jack GD, Cabrera MC, Manning ML, et al. Activated stress response pathways within multicellular aggregates utilize an autocrine component. Cell Signal. 2007;19(4):772–781.
   PubMed Web of Science ®Google Scholar
• Liebermann DA, Hoffman B. Gadd45 in stress signaling. J Mol Signal. 2008;3:15.
   PubMedGoogle Scholar
• Moskalev AA, Smit-McBride Z, Shaposhnikov MV, et al. Gadd45 proteins: relevance to aging, longevity and age-related pathologies. Ageing Res Rev. 2012;11(1):51–66.
   PubMed Web of Science ®Google Scholar
• Zhu QS, Ren W, Korchin B, et al. Soft tissue sarcoma cells are highly sensitive to AKT blockade: a role for p53-independent up-regulation of GADD45 alpha. Cancer Res. 2008;68(8):2895–2903.
   PubMed Web of Science ®Google Scholar
• Ishikawa K, Hosoi Y, Tanaka H, et al. Non-thermal plasma-activated lactate solution kills U251SP glioblastoma cells in an innate reductive manner with altered metabolism. Arch Biochem Biophys. 2020;688:108414.
   PubMed Web of Science ®Google Scholar
• Tanaka H, Maeda S, Nakamura K, et al. Plasma-activated Ringer’s lactate solution inhibits the cellular respiratory system in HeLa cells. Plasma Process Polym. 2021;18(10):e2100056.
   Web of Science ®Google Scholar
• Jiang L, Zheng H, Lyu Q, et al. Lysosomal nitric oxide determines transition from autophagy to ferroptosis after exposure to plasma-activated Ringer’s lactate. Redox Biol. 2021;43:101989.
   PubMed Web of Science ®Google Scholar
• Ichimura Y, Waguri S, Sou Y-S, et al. Phosphorylation of p62 activates the Keap1–Nrf2 pathway during selective autophagy. Mol Cell. 2013;51(5):618–631.
   PubMed Web of Science ®Google Scholar