Your browser doesn't support javascript.
loading
: 20 | 50 | 100
1 - 20 de 1.046
1.
Clin Oral Investig ; 28(5): 295, 2024 May 03.
Article En | MEDLINE | ID: mdl-38700548

OBJECTIVE: This randomized controlled trial aimed to evaluate the equivalence in the color change, adverse effects, self-perception (AS) and the impact on oral condition (IO) of participants submitted to different application protocols of in-office dental bleaching. MATERIALS AND METHODS: 165 participants were bleached with a 35% hydrogen peroxide gel (Total Blanc Office One-Step, DFL), according to the following protocols: (1) 2 applications of 20-min each (2 × 20 min); (2) 1 × 40-min and; (3) 1 × 30-min. The color change was evaluated with the Vita Easyshade spectrophotometer, Vita Classical and Vita Bleachedguide scales. The intensity and risk of tooth sensitivity (TS) and gingival irritation (GI) were recorded using a 0-10 visual analogue scale (VAS). AS and IO was assessed before and after the bleaching procedure using the Orofacial Aesthetic Scale and Oral Health Impact Profile-14, respectively. RESULTS: Equivalent color change were observed (p < 0.001), with no significant difference between groups. The group 2 × 20 min presented the highest risk of TS (76%, 95% CI 63 to 85), compared to the 1 × 30 min (p < 0.04). The intensity of TS and GI and the risk of GI was similar between groups (p > 0.31). Irrespectively of the group (p = 0.32), significant improvements were observed for all items of AS and IO after bleaching (p < 0.02). CONCLUSIONS: The 1 × 30 min protocol produced equivalent color change to the other bleaching protocols with reduced risk of TS and shorter application time. CLINICAL RELEVANCE: A more simplified application regimen of a single application of 30 min yields effective bleaching and patient satisfaction while minimizing undesirable side effects and improving patient satisfaction.


Dentin Sensitivity , Hydrogen Peroxide , Tooth Bleaching Agents , Tooth Bleaching , Humans , Tooth Bleaching/methods , Female , Hydrogen Peroxide/administration & dosage , Male , Adult , Single-Blind Method , Dentin Sensitivity/chemically induced , Dentin Sensitivity/prevention & control , Spectrophotometry , Treatment Outcome , Middle Aged , Esthetics, Dental , Adolescent
2.
Knee ; 47: 53-62, 2024 Mar.
Article En | MEDLINE | ID: mdl-38244239

BACKGROUND: Currently, in the field of total joint arthroplasty (TJA), there are no studies that have demonstrated the value of the sequential application of hydrogen peroxide, povidone-iodine, and physiological saline during the surgical procedure in decreasing postoperative infections in total knee arthroplasty (TKA), and in decreasing the incidence of periprosthetic joint infections (PJI) in particular. This study aimed to assess the efficacy of the sequential application of hydrogen peroxide, povidone-iodine, and physiological saline in reducing postoperative infections in TKA. METHODS: The study prospectively included 4743 patients, with Group A (2371, 49.9%) receiving sequential intraoperative application of hydrogen peroxide, povidone-iodine, and physiological saline irrigation of the incision, and Group B (2372, 50.1%) receiving intraoperative application of physiological saline irrigation of the incision only, to collect the patients' baseline data and clinical characteristics, and to statistically assess the incidence of superficial infections and the PJI during the follow up period to evaluate the clinical value of the study. RESULTS: The baseline levels of patients in Groups A and B were comparable. There were 132 (2.8%) lost visits during the study period. The incidence of superficial infections within 30 days after surgery was 0.22% in Group A and 1.17% in Group B, the difference between the two groups was statistically significant (P = 0.007). The incidence of PJI was 0.17% in Group A and 1.26% in Group B, the difference between the two groups was statistically significant (P = 0.0121). CONCLUSION: Sequential application of hydrogen peroxide, povidone-iodine, and physiological saline to irrigate incision in TKA can significantly reduce the incidence of postoperative superficial infections and PJI. The scientific and rational application of this therapy intraoperatively greatly reduces the incidence of PJI and postoperative superficial infections, which is of great benefit to the patient's prognosis.


Anti-Infective Agents, Local , Arthroplasty, Replacement, Knee , Hydrogen Peroxide , Povidone-Iodine , Prosthesis-Related Infections , Saline Solution , Surgical Wound Infection , Humans , Arthroplasty, Replacement, Knee/adverse effects , Povidone-Iodine/administration & dosage , Povidone-Iodine/therapeutic use , Hydrogen Peroxide/administration & dosage , Male , Female , Prospective Studies , Anti-Infective Agents, Local/administration & dosage , Aged , Middle Aged , Surgical Wound Infection/prevention & control , Surgical Wound Infection/epidemiology , Surgical Wound Infection/etiology , Prosthesis-Related Infections/prevention & control , Prosthesis-Related Infections/etiology , Prosthesis-Related Infections/epidemiology , Saline Solution/administration & dosage , Therapeutic Irrigation/methods , Incidence
3.
Laryngoscope ; 134(6): 2954-2957, 2024 Jun.
Article En | MEDLINE | ID: mdl-38149667

We present the case of a child impaled in the face by a meat thermometer who subsequently suffered a significant complication due to the administration of hydrogen peroxide to the wound. The soft tissues of the face rapidly expanded and blanched, the child experienced mental status changes, and imaging revealed massive subcutaneous emphysema, pneumomediastinum, and pneumo-orbit. Herein we review the literature on this rare complication and provide photodocumentation in the hopes that other practitioners, patients, and parents avoid administering hydrogen peroxide into or near any penetrating injury. Laryngoscope, 134:2954-2957, 2024.


Facial Injuries , Hydrogen Peroxide , Subcutaneous Emphysema , Therapeutic Irrigation , Wounds, Penetrating , Humans , Subcutaneous Emphysema/etiology , Subcutaneous Emphysema/chemically induced , Hydrogen Peroxide/adverse effects , Hydrogen Peroxide/administration & dosage , Therapeutic Irrigation/adverse effects , Therapeutic Irrigation/methods , Wounds, Penetrating/etiology , Male
4.
Oper Dent ; 48(2): 146-154, 2023 Mar 01.
Article En | MEDLINE | ID: mdl-36786759

PURPOSE: The objective of this study was to evaluate if the application method (tip with brush or tip without brush) and hydrogen peroxide (HP) concentration (6% or 35% self-mixing) of in-office bleaching gel influences the penetration of HP into the pulp chamber, color change, and the amount of bleaching gel used. METHODS: Forty healthy premolars were randomly divided into the following five groups (n=8): no treatment; HP6% using a tip with a brush, HP6% using a tip without a brush, HP35% using a tip with a brush, and HP35% using a tip without a brush. After treatments, the HP concentration (µg/mL) within the pulp chamber was determined using UV-Vis spectrophotometry. The color change (ΔEab, ΔE00, and ΔWID) was evaluated using a digital spectrophotometer. The amount of gel used (g) in each group was measured using a precision analytical balance. Data from each test were submitted to parametric tests (α=0.05). RESULTS: The tip with a brush resulted in a lower amount of HP inside the pulp chamber and less gel used when compared with the tip without a brush, regardless of HP concentration (p<0.05). However, regarding the tip used, although no significant difference was observed when HP35% was used (p>0.05), a higher whitening effect was observed when the 6% HP was applied without a brush as opposed to with a tip brush (p<0.05). CONCLUSIONS: The use of a tip with a brush, regardless of the in-office bleaching gel concentration (6% or 35% self-mixing), presented a lower penetration and lower volume of spent gel when compared to a tip without brush. However, the whitening effect depended on the concentration of HP used.


Hydrogen Peroxide , Tooth Bleaching Agents , Tooth Bleaching , Color , Dental Pulp Cavity , Hydrogen Peroxide/administration & dosage , Spectrophotometry/methods , Tooth Bleaching/methods , Tooth Bleaching Agents/administration & dosage , Bicuspid , Humans
5.
Neural Plast ; 2022: 5567174, 2022.
Article En | MEDLINE | ID: mdl-35096052

Sensorineural hearing loss (SNHL) is one of the most common causes of disability worldwide. Previous evidence suggests that reactive oxygen species (ROS) may play an important role in the occurrence and development of SNHL, while its mechanism remains unclear. We cultured dissected organs of Corti in medium containing different concentrations (0, 0.25, 0.5, 0.75, 1, and 1.25 mM) of hydrogen peroxide (H2O2) and established a four-concentration model of 0, 0.5, 0.75, and 1 mM to study different degrees of damage. We examined ROS-induced mitochondrial damage and the role of sirtuin 3 (SIRT3). Our results revealed that the number of ribbon synapses and hair cells appeared significantly concentration-dependent decrease with exposure to H2O2. Outer hair cells (OHCs) and inner hair cells (IHCs) began to be lost, and activation of apoptosis of hair cells (HCs) was observed at 0.75 mM and 1 mM H2O2, respectively. In contrast with the control group, the accumulation of ROS was significantly higher, and the mitochondrial membrane potential (MMP) was lower in the H2O2-treated groups. Furthermore, the expression of SIRT3, FOXO3A, and SOD2 proteins declined, except for an initial elevation of SIRT3 between 0 and 0.75 mM H2O2. Administration of the selective SIRT3 inhibitor 3-(1H-1,2,3-triazol-4-yl) pyridine resulted in increased damage to the cochlea, including loss of ribbon synapses and hair cells, apoptosis of hair cells, more production of ROS, and reduced mitochondrial membrane potential. Thoroughly, our results highlight that ROS-induced mitochondrial oxidative damage drives hair cell degeneration and apoptosis. Furthermore, SIRT3 is crucial for preserving mitochondrial function and protecting the cochlea from oxidative damage and may represent a possible therapeutic target for SNHL.


Cochlea/drug effects , Hydrogen Peroxide/administration & dosage , Mitochondria/drug effects , Oxidative Stress/drug effects , Reactive Oxygen Species/administration & dosage , Sirtuin 3/metabolism , Animals , Apoptosis/drug effects , Cells, Cultured , Cochlea/cytology , Cochlea/metabolism , Mice , Mitochondria/metabolism , Superoxide Dismutase/metabolism
6.
Biomed Res Int ; 2021: 6960143, 2021.
Article En | MEDLINE | ID: mdl-34796235

OBJECTIVE: To evaluate the effect of the combination of calcium hydroxide (Ca(OH)2) and a novel electrolyzed superoxidized solution at neutral pH, known as OxOral® on Enterococcus faecalis growth in root canals. METHODS: Sixty human teeth were used, from which root canals were infected and randomly divided into the following treatment groups: saline solution, saline solution plus Ca(OH)2, OxOral®, and OxOral® plus Ca(OH)2. RESULTS: A permanent reduction in bacterial growth was observed at days 1, 6, 12, and 18 after OxOral® plus Ca(OH)2 treatment from 4.4 ± 0.074 log10 CFU/mL to 0.0 ± 0.001 log10 CFU/mL. In addition, alkaline conditions maintenance was observed from application time (pH = 12.2 ± 0.033) to 18 d posttreatment (pH = 12.6 ± 0.083). CONCLUSION: The combination of OxOral® and Ca(OH)2 provides an alkaline pH and inhibits E. faecalis growth into the root canals. Our study opens the possibility for further research on the use of OxOral® in endodontic therapy.


Anti-Infective Agents/administration & dosage , Calcium Hydroxide/administration & dosage , Dental Pulp Cavity/drug effects , Dental Pulp Cavity/microbiology , Enterococcus faecalis/drug effects , Hydrogen Peroxide/administration & dosage , Enterococcus faecalis/growth & development , Humans , Hydrogen Peroxide/chemistry , Hydrogen-Ion Concentration , In Vitro Techniques , Root Canal Irrigants/administration & dosage , Root Canal Irrigants/chemistry , Root Canal Therapy/methods , Solutions
7.
BMC Microbiol ; 21(1): 302, 2021 11 03.
Article En | MEDLINE | ID: mdl-34732139

BACKGROUND: Antimicrobial agents are considered valuable adjuncts to mechanical methods of plaque control. However, their long-term use can be limited because of side effects. Therefore, using physiological substances is promising due to no risk of development, for example, of microbial resistances, allergies or DNA damaging. The lactoperoxidase-thiocyanate-hydrogen peroxide system (LPO-system) is a highly effective antimicrobial system. This study aimed to evaluate in a randomized study with a four-replicate cross-over design the effectiveness of two oral hygiene lozenges containing LPO-system in oral hygiene. RESULTS: After using the mouth rinse as positive control (A) and allocated test lozenges (B) (0.083% H2O2) & (C) (0.04% H2O2) for 4 days instead of the normal oral hygiene procedures (tooth brushing etc.), Listerine rinse (A) was statistically significantly more effective than the LPO-system-lozenge with 0.083% H2O2, the LPO-system-lozenge with 0.04% H2O2, and the placebo lozenge (D) in inhibiting plaque. Lozenges B and C were statistically significantly more effective than the placebo lozenge, but no statistically significant differences could be observed between them. The LPO-system-lozenge (B) reduced statistically significantly more S. mutans than the LPO-system-lozenge with (C) and the placebo lozenge (D). The LPO-system-lozenge (C) reduced statistically significantly more Lactobacilli than Listerine (A), the LPO-system-lozenge (B) and the placebo lozenge (D). There were no statistically significant differences in the total CFUs between Listerine rinse, the LPO-system-lozenge with 0.083% H2O2 (B), the LPO-system-lozenge with 0.04% H2O2 (C), and the placebo lozenge (D). On day 5 there were no differences of the OSCN--values between all A, B, C, and D. However, the SCN--values increased over the days in both LPO-system-lozenges (B/C). The statistically significant differences between B/C and A/D on day 5 were as followed: A to B p = 0.0268; A to C p = 0.0035; B to D p = 0.0051; C to D p = 0.0007. Only in the group of Listerine (A) increased the NO3-/NO2--quotient over the test time, which indicates a reduction of nitrate-reducing bacteria. On Day 5 the statistically significant difference between A and B was p = 0.0123. CONCLUSIONS: The results indicate that lozenges containing a complete LPO-system, inhibiting plaque regrowth and reducing cariogenic bacteria, may be used in the daily oral hygiene.


Anti-Bacterial Agents/administration & dosage , Dental Plaque/drug therapy , Hydrogen Peroxide/administration & dosage , Lactoperoxidase/administration & dosage , Mouthwashes/administration & dosage , Bacteria/drug effects , Bacteria/growth & development , Dental Plaque/microbiology , Humans , Mouth/microbiology , Saliva/microbiology
8.
Arch Toxicol ; 95(12): 3803-3813, 2021 12.
Article En | MEDLINE | ID: mdl-34609522

The comet assay is widely used in basic research, genotoxicity testing, and human biomonitoring. However, interpretation of the comet assay data might benefit from a better understanding of the future fate of a cell with DNA damage. DNA damage is in principle repairable, or if extensive, can lead to cell death. Here, we have correlated the maximally induced DNA damage with three test substances in TK6 cells with the survival of the cells. For this, we selected hydrogen peroxide (H2O2) as an oxidizing agent, methyl methanesulfonate (MMS) as an alkylating agent and etoposide as a topoisomerase II inhibitor. We measured cell viability, cell proliferation, apoptosis, and micronucleus frequency on the following day, in the same cell culture, which had been analyzed in the comet assay. After treatment, a concentration dependent increase in DNA damage and in the percentage of non-vital and apoptotic cells was found for each substance. Values greater than 20-30% DNA in tail caused the death of more than 50% of the cells, with etoposide causing slightly more cell death than H2O2 or MMS. Despite that, cells seemed to repair of at least some DNA damage within few hours after substance removal. Overall, the reduction of DNA damage over time is due to both DNA repair and death of heavily damaged cells. We recommend that in experiments with induction of DNA damage of more than 20% DNA in tail, survival data for the cells are provided.


Apoptosis/drug effects , Cell Survival/drug effects , Comet Assay , DNA Damage/drug effects , Antineoplastic Agents, Alkylating/administration & dosage , Antineoplastic Agents, Alkylating/toxicity , Cell Line , Cell Proliferation/drug effects , DNA Repair/drug effects , Dose-Response Relationship, Drug , Etoposide/administration & dosage , Etoposide/toxicity , Humans , Hydrogen Peroxide/administration & dosage , Hydrogen Peroxide/toxicity , Methyl Methanesulfonate/administration & dosage , Methyl Methanesulfonate/toxicity , Oxidants/administration & dosage , Oxidants/toxicity , Time Factors , Topoisomerase II Inhibitors/administration & dosage , Topoisomerase II Inhibitors/toxicity
9.
Sci Rep ; 11(1): 13177, 2021 06 23.
Article En | MEDLINE | ID: mdl-34162984

This systematic review assessed the effectiveness of ozone (O3) in the color change of in-office tooth bleaching in vital teeth (TB) and the sensitivity control. Only randomized controlled clinical trials were included. Seven databases were used as primary search sources, and three additional sources were searched to capture the "grey literature" partially. The JBI tool was used to assess the risk of bias. TB was assessed using the ΔELab color change metric comparing tooth color pre- and post-bleaching. We meta-analyzed the ΔELab estimates per method and calculated the absolute standardized mean difference using random-effect models. The GRADE approach assessed the certainty of the evidence. The ΔELab estimates ranged from 1.28 when the O3 was used alone to 6.93 when combined with hydrogen peroxide (HP). Two studies compared O3 and HP alone, but their TB was similar (SMD = - 0.02; 95%CI: - 0.54; 0.49). The bleaching effectiveness for the combination of O3 + HP compared to HP was similar (SMD = 0.38; 95%CI: - 0.04; 0.81). Thus, based on the available literature, our findings suggest that O3 is not superior to the conventional technique using HP on the change of tooth color. The O3 did not present sensitivity when used alone. When O3 was used in combination with HP, patients reported hypersensitivity only when O3 was applied before HP, i.e., no sensitivity was perceived when O3 was applied after HP.


Dentin Sensitivity/chemically induced , Ozone/pharmacology , Tooth Bleaching Agents/pharmacology , Tooth Bleaching/methods , Colorimetry , Drug Interactions , Humans , Hydrogen Peroxide/administration & dosage , Hydrogen Peroxide/adverse effects , Hydrogen Peroxide/pharmacology , Ozone/administration & dosage , Ozone/adverse effects , Randomized Controlled Trials as Topic/statistics & numerical data , Tooth Bleaching/adverse effects , Tooth Bleaching Agents/administration & dosage , Tooth Bleaching Agents/adverse effects
10.
Epidemiol Health ; 43: e2021032, 2021.
Article En | MEDLINE | ID: mdl-33957025

OBJECTIVES: To evaluate the effectiveness of hydrogen peroxide (H2O2) in the form of mouthwash and nasal spray as an auxiliary treatment for coronavirus disease 2019 (COVID-19). METHODS: Forty hospitalized patients who tested positive for severe acute respiratory syndrome coronavirus 2 using a reverse-transcription polymerase chain reaction test were evaluated. They were randomly divided into an experimental group (n= 20; gargling with 1.0% H2O2 and nasal wash with 0.5% H2O2) or a control group (n= 20). The solutions were used for 7 days and the patients were monitored every 2 days, for a total of 8 days. At check-ups, patients were asked about their symptoms and possible adverse effects of the solutions. The presence and severity (mild, moderate, or severe) of symptoms were recorded. Data were compared using the Student test and the Fisher exact test (α= 0.05). RESULTS: There was no significant difference between the 2 groups in the length of hospital stay (p= 0.65). The most frequent symptom on day 0 was coughing (72.0% in the experimental group and 76.5% in the control group), which abated over time. There was no significant difference between the groups in the evaluated symptoms. Most (75.0%) of the patients in the experimental group presented a reduction in dyspnea between days 0 and 2. Few patients reported adverse effects from the use of the solutions. CONCLUSIONS: H2O2 as a mouthwash and nasal spray is safe to use. There is insufficient evidence to demonstrate that H2O2 is effective as an auxiliary treatment for hospitalized COVID-19 patients.


Anti-Infective Agents, Local/administration & dosage , COVID-19 Drug Treatment , Hydrogen Peroxide/administration & dosage , SARS-CoV-2 , Adult , Brazil , COVID-19/virology , Double-Blind Method , Female , Hospitalization , Humans , Male , Middle Aged , Mouthwashes/administration & dosage , Nasal Sprays , Severity of Illness Index , Treatment Outcome
11.
Med Oncol ; 38(6): 59, 2021 Apr 21.
Article En | MEDLINE | ID: mdl-33880669

Cancer is one of the diseases that threatens human health and is a leading cause of mortality worldwide. High levels of reactive oxygen species (ROS) have been observed in cancer tissues compared with normal tissues in vivo, and it is not yet known how this influences chemotherapeutic drug action. Cationic porphyrin 5,10,15,20-tetra-(N-methyl-4-pyridyl) porphyrin (TMPyP4) is a photosensitizer used in photodynamic therapy (PDT) and a telomerase inhibitor used in the treatment of telomerase-positive cancer. Here, we investigated the anticancer activity of TMPyP4 in A549 and PANC cells cultured in H2O2. The results showed that compared to TMPyP4 alone, the combination of TMPyP4 and H2O2 exhibited sensitization effects on cell viability and colony formation inhibition and apoptosis in A549 and PANC cells, but had no effect in human normal MIHA cells. Mechanistically, the combination of TMPyP4 and H2O2 activates high ROS and mitochondrial membrane potential in A549 and PANC cells, resulting in intense DNA damage and DNA damage responses. Consequently, compared to TMPyP4 alone, TMPyP4 and H2O2 combined treatment upregulates the expression of BAX, cleaved caspase 3, and p-JNK and downregulates the expression of Bcl-2 in A549 and PANC cells. Taken together, these data suggested that H2O2 enhanced the anticancer activity of TMPyP4-mediated ROS-dependent DNA damage and related apoptotic protein regulation, revealing that the high ROS tumor microenvironment plays an important role in chemotherapeutic drug action.


Antineoplastic Combined Chemotherapy Protocols/pharmacology , Mitochondria/drug effects , Pancreatic Neoplasms/drug therapy , Reactive Oxygen Species/metabolism , A549 Cells , Cell Line, Tumor , Comet Assay , DNA Damage , Hepatocytes/drug effects , Humans , Hydrogen Peroxide/administration & dosage , Membrane Potential, Mitochondrial/drug effects , Mitochondria/genetics , Mitochondria/metabolism , Pancreatic Neoplasms/metabolism , Pancreatic Neoplasms/pathology , Porphyrins/administration & dosage , Tumor Microenvironment/drug effects
13.
Medicine (Baltimore) ; 100(3): e23175, 2021 Jan 22.
Article En | MEDLINE | ID: mdl-33545925

ABSTRACT: Hydrogen peroxide is a liquid that functions in mechanical removal of the necrotic tissue via the elimination of tissue debris.In this study, we aimed to evaluate the effectiveness of the use of hydrogen peroxide in necrosectomy treatment of walled-off pancreatic necrosis.Records of 24 patients who were diagnosed with pancreatic necrosis or walled-off pancreatic necrosis and underwent endoscopic necrosectomy (EN) were retrospectively assessed. Patients were divided into 2 groups; hydrogen peroxide used for treatment or not used, and these 2 groups were compared.A total of 24 patients underwent endoscopic intervention for walled-off pancreatic necrosis. Procedural success was comparable between the 2 groups. During the post-procedural follow-up, the duration of the hospital stay, recurrence, and complication rates were found to be similar in both groups. The mean number of the endoscopic interventions was significantly lower in the hydrogen peroxide group (4.2 ±â€Š1.4 vs 6.1 ±â€Š4.2; P = .01).The use of hydrogen peroxide for EN in walled-off pancreatic necrosis patients seems to have similar efficiency and safety. However, it can be said that the use of hydrogen peroxide could reduce the number of endoscopic procedures.


Hydrogen Peroxide/administration & dosage , Oxidants/administration & dosage , Pancreatitis, Acute Necrotizing/surgery , Endosonography , Female , Humans , Male , Middle Aged , Pancreatitis, Acute Necrotizing/diagnostic imaging , Retrospective Studies , Treatment Outcome , Ultrasonography, Interventional
14.
J Clin Pharm Ther ; 46(5): 1473-1475, 2021 Oct.
Article En | MEDLINE | ID: mdl-33626185

WHAT IS KNOWN AND OBJECTIVE: Formation of methaemoglobinaemia (MetHb) decreases oxygen capacity in the blood, leading to tissue hypoxia. This condition may be acquired following exposure to certain drugs. CASE SUMMARY: A critically ill patient with necrotizing fasciitis unexpectedly developed marked and unexplained MetHb (6.7%). Her digital medication list did not reveal the causative factor. However, deeper exploration showed the use of other compounds (acetone, hydrogen peroxide) not routinely visible on the medication list. WHAT IS NEW AND CONCLUSION: Elevated MetHb likely resulted from high-volume hydrogen peroxide 3% exposure. Clinicians should be cautious rinsing large open wounds with hydrogen peroxide. When MetHb is diagnosed, less familiar compounds, usually not on the medication list, should be considered in the differential diagnosis and extensive hetero-anamnesis is mandatory.


Critical Illness , Fasciitis, Necrotizing/drug therapy , Hydrogen Peroxide/administration & dosage , Hydrogen Peroxide/adverse effects , Methemoglobinemia/chemically induced , Female , Humans , Middle Aged
15.
J Food Sci ; 86(3): 881-891, 2021 Mar.
Article En | MEDLINE | ID: mdl-33598951

The combined effect of ascorbic acid (AsA) and hydrogen peroxide (H2 O2 ) on gel-forming ability and structural changes of lizardfish (LZ) and threadfin bream (TB) surimi were investigated. Addition of 0.15% AsA and 0.1% H2 O2 greatly increased breaking force and distance of LZ surimi by 300% and 55%, respectively. Combination of 0.2% AsA and 0.15% H2 O2 resulted in the maximum TB surimi gel improvement with 150% and 90% increase in breaking force and distance, respectively. Browning reaction obviously occurred when combined AsA and H2 O2 was added, due to ascorbic acid oxidation. Polymerization of myosin heavy chain via disulfide bonds was promoted, and the formation of disulfide bonds was involved through oxidation of sulfhydryl groups with increasing AsA and H2 O2 . Fourier-transform infrared (FT-IR) spectroscopy revealed a decrease in α-helix and an increase in ß-sheet content as AsA and H2 O2 increased in both species. A decrease of band area of aliphatic (2,800 to 3,000 and 1,450 cm-1 ), aromatic (1,208, 757, and ratio 850/830 cm-1 ), and change of disulfide bonds (525 and 540 cm-1 ) suggested an increase in hydrophobic interactions and disulfide bonds with addition of these additives. Based on principal component analysis (PCA), textural characteristics were positively correlated with ß-sheet content. Our study suggested that combination of AsA and H2 O2 greatly enhanced gelation of LZ and TB by increasing not only disulfide bonds but also hydrophobic interactions. PRACTICAL APPLICATION: The combined ascorbic acid and hydrogen peroxide can be used to improve gelation of two important tropical surimi species, namely threadfin bream and lizardfish surimi, without requirement of setting. The optimum concentration of each additive varied with fish species.


Ascorbic Acid/administration & dosage , Fish Proteins/chemistry , Gels/chemistry , Hydrogen Peroxide/administration & dosage , Animals , Colloids , Fish Products/analysis , Food Handling/methods , Hydrophobic and Hydrophilic Interactions , Mechanical Phenomena , Myosin Heavy Chains/chemistry , Sea Bream , Spectroscopy, Fourier Transform Infrared , Vibration
18.
Nutr Neurosci ; 24(2): 90-101, 2021 Feb.
Article En | MEDLINE | ID: mdl-30929586

Background: An imbalance of free radicals and antioxidant defense systems in physiological processes can result in protein/DNA damage, inflammation, and cellular apoptosis leading to neurodegenerative disorders such as Alzheimer's disease (AD), Parkinson's disease (PD), and Huntington's disease (HD). Sesamin and sesamol, compounds derived from sesame seeds and oil, have been reported to exert various pharmacological effects, especially antioxidant activity. However, their molecular mechanisms against the oxidative stress induced by exogenous hydrogen peroxide (H2O2) remain to be elucidated. Aim: In this study, neuroprotective effects of sesamin and sesamol on H2O2-induced human neuroblastoma (SH-SY5Y) cell death and possible signaling pathways in the cells were explored. Methods: MTT assay and flow cytometry were conducted to determine cell viability and apoptotic profiles of neuronal cells treated with sesamin and sesamol. Carboxy-DCFDA assay was used to measure reactive oxygen species (ROS). Moreover, Western blot analysis was performed to investigate protein profiles associated with neuroprotection. Results: Pretreatment of the cells with 1 µM of sesamin and sesamol remarkably reduced the SH-SY5Y cell death induced by 400 µM H2O2 as well as the intracellular ROS production. Moreover, the molecular mechanisms underlying neuroprotection of the compounds were associated with activating SIRT1-SIRT3-FOXO3a expression, inhibiting BAX (proapoptotic protein), and upregulating BCL-2 (anti-apoptotic protein). Conclusion: The findings suggest that sesamin and sesamol are compounds that potentially protect neuronal cells against oxidative stress similar to that of the resveratrol, the reference compound. These antioxidants are thus of interest for further investigation in in vivo models of neuroprotection.


Benzodioxoles/administration & dosage , Dioxoles/administration & dosage , Hydrogen Peroxide/metabolism , Lignans/administration & dosage , Neurons/drug effects , Neurons/metabolism , Neuroprotective Agents/administration & dosage , Oxidative Stress/drug effects , Phenols/administration & dosage , Cell Line, Tumor , Forkhead Box Protein O3/metabolism , Humans , Hydrogen Peroxide/administration & dosage , Signal Transduction/drug effects , Sirtuin 1/metabolism , Sirtuin 3/metabolism
19.
Ann Pharmacother ; 55(2): 216-221, 2021 02.
Article En | MEDLINE | ID: mdl-32646224

OBJECTIVE: Hydrogen peroxide 40% (HP40) was approved by the US Food and Drug Administration for topical treatment of seborrheic keratosis (SK) in December 2017. This article will review phase II and III clinical trials to assess the drug's efficacy, safety, and clinical application. DATA SOURCES: A systematic literature review was performed using the terms "Eskata AND seborrheic keratosis," and "hydrogen peroxide AND seborrheic keratosis" in the OVID MEDLINE, PubMed, Cochrane Library, EMBASE, and Web of Science databases. ClinicalTrials.gov was searched to identify ongoing or nonpublished studies. STUDY SELECTION AND DATA ABSTRACTION: Articles written in English between January 2000 and mid-June 2020 discussing phase II and phase III clinical trials were evaluated. DATA SYNTHESIS: In 2 phase III clinical trials, 4% and 8% of patients treated with HP40 had a Physician Lesion Assessment score of zero for all 4 SKs, respectively, compared with 0% in both vehicle groups at the primary end point of day 106 (P < 0.01; P < 0.0001). RELEVANCE TO PATIENT CARE AND CLINICAL PRACTICE: HP40, although less effective, has a better safety profile than other treatment options. It should be especially considered for treatment of facial SKs, where it is most efficacious and where other treatment modalities, such as cryotherapy, are more challenging. CONCLUSIONS: HP40 is a new, safe alternative treatment for SKs, although it is expensive and only modestly effective, both of which somewhat limit its overall utility. HP40 is a promising topical alternative, particularly for cosmetically sensitive locations, such as the face.


Hydrogen Peroxide/therapeutic use , Keratosis, Seborrheic/drug therapy , Oxidants/therapeutic use , Administration, Topical , Clinical Trials, Phase II as Topic , Clinical Trials, Phase III as Topic , Female , Humans , Hydrogen Peroxide/administration & dosage , Hydrogen Peroxide/adverse effects , Keratosis, Seborrheic/pathology , Oxidants/administration & dosage , Oxidants/adverse effects , Randomized Controlled Trials as Topic , Treatment Outcome , United States , United States Food and Drug Administration
...