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1.
PLoS One ; 11(5): e0155427, 2016.
Article in English | MEDLINE | ID: mdl-27224027

ABSTRACT

Considering the ability of atmospheric-pressure cold plasma (ACP) to disrupt the biofilm matrix and rupture cell structure, it can be an efficient tool against virulent oral biofilms. However, it is fundamental that ACP does not cause damage to oral tissue. So, this study evaluated (1) the antimicrobial effect of ACP on single- and dual-species biofilms of Candida albicans and Staphylococcus aureus as well as (2) the biological safety of ACP on in vitro reconstituted oral epithelium. Standardized cell suspensions of each microorganism were prepared for biofilm culture on acrylic resin discs at 37°C for 48 hours. The biofilms were submitted to ACP treatment at 10 mm of plasma tip-to-sample distance during 60 seconds. Positive controls were penicillin G and fluconazole for S. aureus and C. albicans, respectively. The biofilms were analyzed through counting of viable colonies, confocal laser scanning microscopy, scanning electron microscopy and fluorescence microscopy for detection of reactive oxygen species. The in vitro reconstituted oral epithelium was submitted to similar ACP treatment and analyzed through histology, cytotoxocity test (LDH release), viability test (MTT assay) and imunnohistochemistry (Ki67 expression). All plasma-treated biofilms presented significant log10 CFU/mL reduction, alteration in microorganism/biofilm morphology, and reduced viability in comparison to negative and positive controls. In addition, fluorescence microscopy revealed presence of reactive oxygen species in all plasma-treated biofilms. Low cytotoxicity and high viability were observed in oral epithelium of negative control and plasma group. Histology showed neither sign of necrosis nor significant alteration in plasma-treated epithelium. Ki67-positive cells revealed maintenance of cell proliferation in plasma-treated epithelium. Atmospheric-pressure cold plasma is a promissing approach to eliminate single- and dual-species biofilms of C. albicans and S. aureus without having toxic effects in oral epithelium.


Subject(s)
Argon/pharmacology , Atmospheric Pressure , Biofilms/growth & development , Candida albicans/physiology , Mouth Mucosa/microbiology , Plasma Gases/pharmacology , Staphylococcus aureus/physiology , Epithelial Cells/microbiology , Female , Humans , Male
3.
Arch Med Res ; 44(3): 169-77, 2013 Apr.
Article in English | MEDLINE | ID: mdl-23506720

ABSTRACT

BACKGROUND AND AIMS: The efficacy of a direct application of plasma needle to in vivo wound healing was experimentally studied in mice. This kind of plasma has achieved considerable success in blood coagulation and tissue restoration in mice. In the development of the present study, an argon plasma needle was chosen for coagulation purposes, whereas for healing purposes, a helium plasma needle was used. METHODS: Treatment was applied with a plasma needle produced by argon and helium to a wound induced in laboratory mice. Tissue regeneration was carried out by three argon plasma treatments with 0.5 SLPM flow for 1 min and three treatments of helium with 1.5 SLPM flow. Intervals between each treatment were 5 min and 60 min for argon and helium plasmas, respectively, thus completing a total treatment time of 180 min. Histological sections were performed to corroborate the internal bleeding and tissue regeneration. RESULTS: After three treatments with argon plasma, the blood produced in the wound was coagulated and protein material appeared. By means of treatment with helium plasma, an approach of the wound edges was produced until the conclusion thereof. These results were corroborated histologically. CONCLUSIONS: This type of acceleration during the skin wound healing process can be attributed to the formation of reactive species such as NO, which were increased in the helium plasma needle with respect to the argon plasma needle.


Subject(s)
Argon/pharmacology , Helium/pharmacology , Needles , Plasma Gases/administration & dosage , Plasma Gases/therapeutic use , Skin/drug effects , Wound Healing/drug effects , Acute Disease/therapy , Animals , Argon/administration & dosage , Argon/therapeutic use , Helium/administration & dosage , Helium/therapeutic use , Mice , Nitric Oxide/metabolism , Plasma Gases/pharmacology , Skin Diseases/therapy , Time Factors , Wound Healing/physiology
4.
J Biomed Mater Res A ; 101(1): 98-103, 2013 Jan.
Article in English | MEDLINE | ID: mdl-22826209

ABSTRACT

This study investigated the effect of an Argon-based nonthermal plasma (NTP) surface treatment-operated chairside at atmospheric pressure conditions applied immediately prior to dental implant placement in a canine model. Surfaces investigated comprised: Calcium-Phosphate (CaP) and CaP + NTP (CaP-Plasma). Surface energy was characterized by the Owens-Wendt-Rabel-Kaelble method and chemistry by X-ray photoelectron spectroscopy (XPS). Six adult beagles dogs received 2 plateau-root form implants (n = 1 each surface) in each radii, providing implants that remained 1 and 3 weeks in vivo. Histometric parameters assessed were bone-to-implant contact (BIC) and bone area fraction occupancy (BAFO). Statistical analysis was performed by Kruskall-Wallis (95% level of significance) and Dunn's post-hoc test. The XPS analysis showed peaks of Ca, C, O, and P for the CaP and CaP-Plasma surfaces. Both surfaces presented carbon primarily as hydrocarbon (C-C, C-H) with lower levels of oxidized carbon forms. The CaP surface presented atomic percent values of 38, 42, 11, and 7 for C, O, Ca, and P, respectively, and the CaP-Plasma presented increases in O, Ca, and P atomic percent levels at 53, 12, and 13, respectively, in addition to a decrease in C content at 18 atomic percent. At 1 week no difference was found in histometric parameters between groups. At 3 weeks significantly higher BIC and BAFO were observed for CaP-Plasma treated surfaces. Surface elemental chemistry was modified by the Ar-based NTP. Ar-based NTP improved bone formation around plateau-root form implants at 3 weeks compared with CaP treatment alone.


Subject(s)
Argon/pharmacology , Calcium Phosphates/pharmacology , Coated Materials, Biocompatible/pharmacology , Dental Implants , Implants, Experimental , Osseointegration/drug effects , Plasma Gases/pharmacology , Animals , Dogs , Male , Microscopy, Electron, Scanning , Osteogenesis/drug effects
5.
Genet Mol Res ; 9(2): 785-96, 2010 Apr 27.
Article in English | MEDLINE | ID: mdl-20449812

ABSTRACT

The relationship between pollen germination and the dynamic organization of the actin cytoskeleton during pollen germination is a central theme in plant reproductive biology research. Maize (Zea mays) pollen grains were implanted with 30 keV argon ion (Ar(+)) beams at doses ranging from 0.78 x 10(15) to 13 x 10(15) ions/cm(2). The effects of low-energy ion implantation on pollen germination viability and the dynamic organization of the actin cytoskeleton during pollen germination were studied using confocal laser scanning microscopy. Maize pollen germination rate increased remarkably with Ar(+) dose, in the range from 3.9 x 10(15) to 6.5 x 10(15) ions/cm(2); the germination rate peaked at an Ar(+) dose of 5.2 x 10(15) ions/cm(2). When the implantation dose exceeded 7.8 x 10(15) ions/cm(2), the rate of pollen germination decreased sharply. The actin filaments assembled in pollen grains implanted with 5.2 x 10(15) ions/cm(2) Ar(+) much earlier than in controls. The actin filaments organized as longer parallel bundles and extended into the emerging pollen tube in treated pollen grains, while they formed random and loose fine bundles and were gathered at the pollen aperture in the control. The reorganization of actin cytoskeleton in the pollen implanted with 9.1 x 10(15) ions/cm(2) Ar(+) was slower than in controls. There was a positive correlation between pollen germination and the dynamic organization of the actin cytoskeleton during pollen germination. Ion implantation into pollen did not cause changes in the polarization of actin filaments and organelle dynamics in the pollen tubes. The effects of Ar(+) implantation on pollen germination could be mediated by changes in the polymerization and rearrangement of actin polymers.


Subject(s)
Actins/metabolism , Argon/pharmacology , Cytoskeleton/drug effects , Cytoskeleton/metabolism , Germination/drug effects , Pollen/physiology , Zea mays/physiology , Actin Cytoskeleton/drug effects , Actin Cytoskeleton/metabolism , Ions , Microscopy, Confocal , Pollen/cytology , Pollen/drug effects , Pollen Tube/cytology , Pollen Tube/drug effects , Pollen Tube/growth & development , Zea mays/cytology , Zea mays/drug effects
6.
Arq. gastroenterol ; Arq. gastroenterol;43(3): 191-195, jul.-set. 2006. ilus, tab
Article in English, Portuguese | LILACS | ID: lil-439780

ABSTRACT

BACKGROUND: Gastric antral vascular ectasia is a disorder whose pathogenetic mechanism is unknown. The endoscopic treatment with argon plasma coagulation has been considered one of the best endoscopic therapeutic options. AIM: To analyze the endoscopic and clinical features of gastric antral vascular ectasia and its response to the argon plasma coagulation treatment. PATIENTS AND METHODS: Eighteen patients were studied and classified into two groups: group 1 - whose endoscopic aspect was striped (watermelon) or of the diffuse confluent type; group 2 - diffuse spotty nonconfluent endoscopic aspect. RESULTS: Group 1 with eight patients, all having autoimmune antibodies, but one, whose antibodies were not searched for. Three were cirrhotic and three had hypothyroidism. All had gastric mucosa atrophy. In group 2, with 10 patients, all had non-immune liver disease, with platelet levels below 90.000. Ten patients were submitted to argon plasma coagulation treatment, with 2 to 36 months of follow-up. Lesions recurred in all patients who remained in the follow-up program and one did not respond to treatment for acute bleeding control. CONCLUSION: There seem to be two distinct groups of patients with gastric antral vascular ectasia: one related to immunologic disorders and other to non-immune chronic liver disease and low platelets. The endoscopic treatment using argon plasma coagulation had a high recurrence in the long-term evaluation.


RACIONAL: "Watermelon stomach" ou ectasia vascular do antro gástrico é uma doença de etiopatogenia desconhecida. O tratamento endoscópico através da coagulação com plasma de argônio é considerado uma das melhores opções terapêuticas. OBJETIVO: Analisar os aspectos clínicos e endoscópicos da ectasia vascular do antro gástrico e a resposta ao tratamento com coagulação com plasma de argônio. PACIENTES E MÉTODOS: Dezoito pacientes foram estudados e classificados em dois grupos: grupo I - oito pacientes que exibiam ectasia vascular do antro gástrico de aspecto difuso confluente ou estriado. Grupo II - 10 pacientes que apresentavam aspecto difuso pontilhado não-confluente. RESULTADOS: Todos os pacientes do grupo I apresentavam auto-anticorpos, exceto um paciente no qual não foi pesquisado. Três eram cirróticos, três tinham hipotireoidismo e todos apresentavam gastrite atrófica. No grupo II, todos tinham doença hepática não-autoimune, com plaquetas menores que 90.000. Dez pacientes foram submetidos a tratamento com coagulação com plasma de argônio, com 2 a 36 meses de seguimento. A ectasia vascular do antro gástrico recorreu em todos os pacientes que continuaram em acompanhamento e um paciente não respondeu ao tratamento para controle de sangramento agudo. CONCLUSÃO: Observou-se a existência de dois grupos distintos de pacientes com ectasia vascular do antro gástrico: um grupo associado a distúrbios imunológicos e outro com doença hepática não auto-imune e plaquetopenia. O tratamento com coagulação com plasma de argônio apresentou alta recurrência das ectasias vasculares.


Subject(s)
Humans , Male , Female , Adult , Middle Aged , Argon/pharmacology , Blood Coagulation/drug effects , Electrocoagulation/methods , Gastric Antral Vascular Ectasia/therapy , Gastrointestinal Hemorrhage/therapy , Hemostasis, Endoscopic/methods , Age Distribution , Autoantibodies/analysis , Follow-Up Studies , Gastric Antral Vascular Ectasia/immunology , Gastrointestinal Hemorrhage/immunology , Sex Distribution , Sex Factors , Treatment Outcome
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