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  <title>DSpace Communidade:</title>
  <link rel="alternate" href="http://repositorio.ufc.br/handle/riufc/15288" />
  <subtitle />
  <id>http://repositorio.ufc.br/handle/riufc/15288</id>
  <updated>2026-09-12T07:42:22Z</updated>
  <dc:date>2026-09-12T07:42:22Z</dc:date>
  <entry>
    <title>Avaliação dos efeitos da ozonioterapia na dor, trismo e consumo medicamentoso após cirurgia de terceiro molar: ensaio clínico randomizado e triplo cego</title>
    <link rel="alternate" href="http://repositorio.ufc.br/handle/riufc/87540" />
    <author>
      <name>Paiva, Calebe Lamonier De Oliveira Costa</name>
    </author>
    <id>http://repositorio.ufc.br/handle/riufc/87540</id>
    <updated>2026-08-18T15:52:25Z</updated>
    <published>2026-01-01T00:00:00Z</published>
    <summary type="text">Título: Avaliação dos efeitos da ozonioterapia na dor, trismo e consumo medicamentoso após cirurgia de terceiro molar: ensaio clínico randomizado e triplo cego
Autor(es): Paiva, Calebe Lamonier De Oliveira Costa
Abstract: Third molar extraction is a common surgical procedure, often associated with postoperative complications such as pain, swelling and trismus. Ozone therapy has been proposed as a promising adjunctive approach to modulate the inflammatory response and accelerate healing. The aim of the&#xD;
present study was to evaluate the efficacy and safety of ozone therapy as an adjunct in the postoperative management of third molar extractions, compared with the conventional surgical technique. This was a randomized, triple-blind, split-mouth clinical trial conducted in 20 patients undergoing bilateral mandibular third molar extraction. One side was treated with ozone therapy&#xD;
in various forms (ozone gas, ozonated water and ozonated oil—Ozone Group), while the contralateral side received placebo interventions (Placebo Group). Outcomes assessed included self-reported pain intensity (visual analog scale, VAS), maximal interincisal opening and the quantity of analgesic medication consumed at 24 h, 72 h and 7 days postoperatively. Data were&#xD;
analyzed using Wilcoxon and Friedman/Dunn tests (p &lt; 0.05). There was no statistically significant difference in surgical time between groups (p = 0.407). The Ozone Group reported lower pain perception at all time points (p = 0.037) and reduced analgesic consumption (7.75 ± 10.79 tablets) compared with the Placebo Group (10.40 ± 10.52 tablets) (p = 0.001). Maximal interincisal&#xD;
opening was significantly greater in the Ozone Group (51.75 ± 6.88 mm) versus the Placebo Group (50.00 ± 6.23 mm) on postoperative day 7 (p = 0.049). No complications such as infection or alveolitis were observed in either group. Ozone therapy proved to be an effective and safe adjunctive approach for reducing postoperative pain, decreasing analgesic consumption and&#xD;
improving mouth opening after third molar extractions. Although the sample size was limited, the results indicate a potential clinical benefit of ozone therapy.
Tipo: Dissertação</summary>
    <dc:date>2026-01-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Atividades biológicas dos derivados semissintéticos do triterpeno cl-1 isolado do combretum leprosum mart. em modelos experimentais: uma revisão de escopo.</title>
    <link rel="alternate" href="http://repositorio.ufc.br/handle/riufc/87539" />
    <author>
      <name>Leão, Rebeca Moita</name>
    </author>
    <id>http://repositorio.ufc.br/handle/riufc/87539</id>
    <updated>2026-08-18T15:48:09Z</updated>
    <published>2026-01-01T00:00:00Z</published>
    <summary type="text">Título: Atividades biológicas dos derivados semissintéticos do triterpeno cl-1 isolado do combretum leprosum mart. em modelos experimentais: uma revisão de escopo.
Autor(es): Leão, Rebeca Moita
Abstract: Natural products represent an important source for the identification of bioactive molecules, particularly when combined with structural modification strategies such as semisynthesis. In this  context,  the  triterpene CL-1,  isolated from Combretum leprosum Mart., has  attracted considerable interest due to the pharmacological potential of its semisynthetic derivatives. This scoping review aimed to analyze the available evidence regarding the biological activities of CL-1  semisynthetic  derivatives  in  experimental  models.  The  review  was  conducted  in accordance with the recommendations of the Joanna Briggs Institute and the PRISMA-ScR &#xD;
guidelines.  The research question was structured using the Population–Concept–Context framework, in which the population consisted of CL-1 semisynthetic derivatives, the concept encompassed biological activities and pharmacological outcomes, and the context included  in vitro, in vivo,  and/or  in silico experimental models.  The search covered all publications available  up  to  February  14,  2026,  without  language  restrictions.  Following  the  selection process,  seven  studies  were  included  in  the  final  sample.  The  results  revealed  a  variety  of biological  activities  attributed  to  CL-1  semisynthetic  derivatives,  including  antiparasitic, antiplasmodial,  cytotoxic,  antinociceptive,  osteogenic,  osteoprotective,  and  antiresorptive &#xD;
effects. The findings demonstrated that structural modifications of the parent molecule were capable of modulating its biological behavior, enhancing, reducing, or redirecting its activity depending  on  the  derivative  evaluated  and  the  experimental  model  employed.  Among  the investigated &#xD;
compounds,  CL-P2  and  CL-P2A  stood  out  due  to  their  recurrence  in  the  most recent  studies  and  their  favorable  results  related  to  biological  safety,  inflammatory pain modulation,  and  bone  metabolism.  Evidence  regarding  bone  formation,  mineralization,  the RANKL/OPG axis, and the reduction of experimental bone loss highlights a promising field for future investigations, particularly in conditions associated with impaired bone remodeling.  However, the available studies remain predominantly preclinical and exhibit methodological  heterogeneity  regarding  experimental  models,  doses,  routes  of  administration,  and  assessed outcomes. It can be concluded that CL-1 semisynthetic derivatives possess relevant biological &#xD;
potential, especially concerning bone metabolism, but additional studies are still required to elucidate  their  mechanisms  of  action,  assess  selectivity,  determine  long-term  safety,  and validate their effects in more robust experimental models.
Tipo: Dissertação</summary>
    <dc:date>2026-01-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Desenvolvimento de um gel contendo trans-cinamaldeído e avaliação da atividade antibacteriana sobre Enterococcus faecalis: um estudo in vitro e ex vivo</title>
    <link rel="alternate" href="http://repositorio.ufc.br/handle/riufc/87525" />
    <author>
      <name>Maia Júnior, Virgílio Mendes</name>
    </author>
    <id>http://repositorio.ufc.br/handle/riufc/87525</id>
    <updated>2026-08-17T18:53:20Z</updated>
    <published>2026-08-01T00:00:00Z</published>
    <summary type="text">Título: Desenvolvimento de um gel contendo trans-cinamaldeído e avaliação da atividade antibacteriana sobre Enterococcus faecalis: um estudo in vitro e ex vivo
Autor(es): Maia Júnior, Virgílio Mendes
Abstract: Eliminating microorganisms from the root canal system (RCS) is a fundamental step for the success of any endodontic procedure. Chemomechanical preparation and the administration of intracanal  medication  (IM)  significantly  reduce  the  microbial  load  and  its  metabolic byproducts.  The  aim  of  this  study  was  to  develop  an  IM  containing  trans-cinnamaldehyde &#xD;
(GelTC-Paste), evaluate, in vitro and  ex vivo, its antibacterial effect on &#xD;
Enterococcus faecalis(ATCC  29212),  and  assess  the  cytotoxicity  of  trans-cinnamaldehyde  (TC)  in  L-929 fibroblasts (ATCC CCL-1). In the in vitro study, concentrations of 0.1%, 0.5%, 1.0%, 2.5%, and 5.0% of GelTC-Paste were tested. For the  ex vivo  experiment, 64 single-rooted human permanent teeth were used. The specimens were decoronated, instrumented, and contaminated &#xD;
with  E. faecalis  for 21 days at 37  ºC, except for the control group. They were then flooded with saline solution, and absorbent paper points were inserted for 1 minute and immersed in Eppendorf  tubes  containing  1  ml  of  saline  solution.  Aliquots  of  100  μl  were  streaked  onto brain heart infusion (BHI) plates and incubated for 24 hours at 37  ºC. The specimens were randomly  divided  into  four  groups:  Saline  (n  =  6),  5%  GelTC-Paste  (n  =  10), &#xD;
Calcium Hydroxide  Paste  (n  =  10),  and Control Group (n  =  6). After 7 and 14 days,  the IMs were removed,  and  bacterial  growth  was  measured  by  counting  colony-forming  units  (CFU/ml). For statistical analysis, analysis of variance (ANOVA) and Tukey's post-hoc test were used. The  GelTC-Paste  demonstrated  structural  stability  under  stress  and  maintenance  of  its &#xD;
physicochemical characteristics. The inhibition halo measurements showed an average of 12.2 (0.1%),  14.5  (0.5%),  18.25  (1%),  24.85  (2.5%),  and  27.2  (5%)  for  each  GelTC-Paste concentration.  The  gel  base  did  not  demonstrate  activity,  and  pure  TC  showed  the  largest inhibition halo (average of 36.9 mm). In the MTT assay, TC maintained cell viability equal to the control group up to a concentration of 15.6 μg/mL.  In the  ex vivo  study, the 5%  GelTCPaste  eliminated  41.9% of the intracanal biofilm of E. faecalis after 7 days, compared to 14% for the calcium hydroxide paste. After 14 days, there was a 34.9% reduction in biofilm in the 5%  GelTC-Paste  group, surpassing the 19.6% reduction achieved by Ca(OH)2. The findings of  this  study  indicate  that  the  5% GelTC-Paste has an antibacterial effect on E. faecalis biofilms when compared to calcium hydroxide,  suggesting  potential  for application as an IM &#xD;
in cases of resistant infections.
Tipo: Dissertação</summary>
    <dc:date>2026-08-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Atividade antifúngica do trans-cinamaldeído contra biofilme de candida albicans formado em resina acrílica termopolimerizável</title>
    <link rel="alternate" href="http://repositorio.ufc.br/handle/riufc/87477" />
    <author>
      <name>Cunha, Abrahão Lincoln Alves</name>
    </author>
    <id>http://repositorio.ufc.br/handle/riufc/87477</id>
    <updated>2026-08-12T19:21:08Z</updated>
    <published>2026-01-01T00:00:00Z</published>
    <summary type="text">Título: Atividade antifúngica do trans-cinamaldeído contra biofilme de candida albicans formado em resina acrílica termopolimerizável
Autor(es): Cunha, Abrahão Lincoln Alves
Abstract: Dental prosthesis stomatitis (DPS) is a multifactorial inflammatory condition frequently found in patients who wear removable full dentures, with the microbial biofilm that develops on the acrylic resin being a key factor in its onset. Biofilms are complex communities that can consist  of  different  species  of  bacteria  and  fungi,  with  Candida  albicans  being  the  primary &#xD;
microorganism responsible for the development of DPS. Cleaning agents are recommended to minimize  biofilm  formation;  however,  they  can  cause  adverse  effects,  such  as  mucosal irritation,  alter  the  physical  properties  of  the  resin,  and  promote  resistance  among microorganisms. Compounds derived from medicinal plants are a promising alternative for the formulation of new drugs; trans-cinnamaldehyde stands out as the major compound present in the bark of  Cinnamomum zeylanicum, an option due to its broad antimicrobial activity. The objective  of  this  study  was  to  evaluate  the  antifungal  and  antibiofilm  activity  of  transcinnamaldehyde  against  Candida  albicans  biofilm  induced  on  the  surface of thermopolymerizable acrylic resins. The concentration of interest was selected based on the minimum  inhibitory  concentration  (MIC).  Antimicrobial  activity  was  also  evaluated  by quantifying the biofilm and assessing the viability of fungal cells present in the biofilm using the 3-[4,5-dimethylthiazol-2-yl]-2,5-diphenyl tetrazolium bromide (MTT) colorimetric assay. For qualitative analysis of the biofilm present on the surfaces of the acrylic resin, samples o f the  biofilm  formed—treated  and  untreated  with  trans-cinnamaldehyde—had  their  surfaces &#xD;
photographed using atomic force microscopy (AFM). The minimum inhibitory concentration was 0.078 mg/mL, and the minimum fungicidal concentration was 0.156 mg/mL. In biofilm inhibition assays, the compound significantly reduced biofilm viability, achieving inhibition rates exceeding 90% at concentrations of 4xMIC, 8xMIC, and 16xMIC. In acrylic resin test specimens,  a  progressive  decrease  in  biofilm  formation  was  observed  as  concentration  and exposure time increased. Atomic force microscopy analyses revealed morphological changes in  C.  albicans  hyphae,  especially  at  the  highest  concentrations  tested.  Furthermore,  transcinnamaldehyde exhibited low cytotoxicity in L929 fibroblasts, maintaining cell viability at concentrations  below  250  µg/mL,  demonstrating  promising  potential  as  a  therapeutic &#xD;
alternative  for  the  management  of  prosthetic  stomatitis  associated  with  fungal  biofilms composed of C. albicans.
Tipo: Dissertação</summary>
    <dc:date>2026-01-01T00:00:00Z</dc:date>
  </entry>
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