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1.
Photodiagnosis Photodyn Ther ; 26: 284-286, 2019 Jun.
Article in English | MEDLINE | ID: mdl-30991109

ABSTRACT

P. aeruginosa is a gram-negative bacterium present in nosocomial infections with high morbidity and mortality. This microorganism is frequently resistant to antibiotics, leading to clinical complications. In the present report, we described a clinical case of a patient with severe oral lesions caused by P. aeruginosa, which was refractory to antibiotics treatment and presented positive clinical outcomes after some sessions of antimicrobial photodynamic inactivation (API) mediated by methylene blue dye. We discuss the potential of API for P. aeruginosa refractory infections and possible resistance mechanisms of this microorganism to different API protocols.


Subject(s)
Methylene Blue/therapeutic use , Mouth Diseases/drug therapy , Mouth Diseases/microbiology , Photochemotherapy/methods , Photosensitizing Agents/therapeutic use , Pseudomonas Infections/drug therapy , Pseudomonas Infections/microbiology , Adult , Anti-Infective Agents/therapeutic use , Female , Humans , Pseudomonas aeruginosa
2.
Bone Marrow Transplant ; 52(10): 1384-1389, 2017 Oct.
Article in English | MEDLINE | ID: mdl-28737776

ABSTRACT

Individual therapeutic monitoring of busulfan (BU) minimizes its toxicity and improves the therapeutic outcomes during hematopoietic stem cell transplantation (HSCT). For individual dose adjustment, several blood collections are performed that are uncomfortable for patients. The aim of this pilot study was to validate a laboratory method for quantification of BU in saliva and to present the results obtained using this protocol in HSCT patients. We performed analyses of selectivity, precision and accuracy of saliva with standard concentrations of BU using ultra-high-performance liquid chromatography with diode array detection. We also determined salivary and plasmatic concentrations of BU in six HSCT patients. Saliva exhibited excellent selectivity, precision and accuracy for quantification of BU. In the patient samples, significant correlations were noted between plasmatic and salivary concentrations of BU (r=0.97, P<0.001 in the test dose; r=0.93, P<0.001 in the adjusted dose). Passing &Bablok regression revealed good agreement between the two methods (R2=0.956 for test dose; R2=0.927 for adjusted dose). In conclusion, the saliva is safe for laboratory BU measurement. The good agreement with plasma encourages further clinical studies using saliva for BU therapeutic monitoring.


Subject(s)
Busulfan/administration & dosage , Busulfan/pharmacokinetics , Hematopoietic Stem Cell Transplantation , Saliva/metabolism , Transplantation Conditioning , Adult , Allografts , Female , Humans , Male , Middle Aged , Pilot Projects
3.
Oral Dis ; 23(8): 1127-1133, 2017 Nov.
Article in English | MEDLINE | ID: mdl-28650084

ABSTRACT

OBJECTIVE: This study aimed to identify and quantify polyomaviruses (BKPyV and JCPyV) in the saliva, mouthwash, blood and urine of liver pretransplant patients. MATERIALS AND METHODS: A case-control study was performed using a convenience sample of 21 end-stage liver disease patients (EG = experimental group) and 20 normoreactive controls (CG = control group). In total, 162 samples were collected. Detection and quantification of polyomaviruses were performed using real-time PCR method. RESULTS: In the EG, 21 samples (25%) were positive for BKPyV and 10 (11.90%) for JCPyV, while in the CG, 27 samples (34.61%) were positive for BKPyV and six (7.69%) for JCPyV. With regard to the number of samples positive for BKPyV and JCPyV, there was no statistically significant difference between EG and CG (p = .52 and p = .25). In the EG, we observed a panorama similar to that of the CG regarding the presence of polyomaviruses in mouthwash, blood and urine. The greatest difference between the samples was that regarding the identification of BKPyV in saliva. CONCLUSION: Cirrhotic patients on the liver transplant waiting list did not show higher prevalence of BKPyV and JCPyV compared to normoreactive controls.


Subject(s)
BK Virus/isolation & purification , JC Virus/isolation & purification , Polyomavirus Infections/virology , Saliva/virology , Tumor Virus Infections/virology , Adult , Blood/virology , Case-Control Studies , End Stage Liver Disease/surgery , Female , Humans , Liver Transplantation , Male , Middle Aged , Preoperative Period , Urine/virology , Viral Load
4.
ChemMedChem ; 11(18): 2037-42, 2016 09 20.
Article in English | MEDLINE | ID: mdl-27465595

ABSTRACT

Human neutrophil elastase (HNE) is a serine protease associated with several inflammatory processes such as chronic obstructive pulmonary disease (COPD). The precise involvement of HNE in COPD and other inflammatory disease mechanisms has yet to be clarified. Herein we report a copper-catalyzed alkyne-azide 1,3-dipolar cycloaddition (CuAAC, or 'click' chemistry) approach based on the 4-oxo-ß-lactam warhead that yielded potent HNE inhibitors containing a triazole moiety. The resulting structure-activity relationships set the basis to develop fluorescent and biotinylated activity-based probes as tools for molecular functional analysis. Attaching the tags to the 4-oxo-ß-lactam scaffold did not affect HNE inhibitory activity, as revealed by the IC50 values in the nanomolar range (56-118 nm) displayed by the probes. The nitrobenzoxadiazole (NBD)-based probe presented the best binding properties (ligand efficiency (LE)=0.31) combined with an excellent lipophilic ligand efficiency (LLE=4.7). Moreover, the probes showed adequate fluorescence properties, internalization in human neutrophils, and suitable detection of HNE in the presence of a large excess of cell lysate proteins. This allows the development of activity-based probes with promising applications in target validation and identification, as well as diagnostic tools.


Subject(s)
Click Chemistry , Leukocyte Elastase/antagonists & inhibitors , Proteinase Inhibitory Proteins, Secretory/pharmacology , Proteome/antagonists & inhibitors , beta-Lactams/pharmacology , Dose-Response Relationship, Drug , Humans , Leukocyte Elastase/metabolism , Molecular Structure , Proteinase Inhibitory Proteins, Secretory/chemical synthesis , Proteinase Inhibitory Proteins, Secretory/chemistry , Proteome/metabolism , Structure-Activity Relationship , beta-Lactams/chemical synthesis , beta-Lactams/chemistry
5.
Eur J Cancer Care (Engl) ; 25(4): 668-74, 2016 Jul.
Article in English | MEDLINE | ID: mdl-26087364

ABSTRACT

Oral mucositis is a painful condition that occurs in 80% of patients who undergo haematopoietic stem cell transplantation (HSCT). Our objective was to determine the impact of mucositis on quality of life (QoL) of patients subjected to HSCT treated with low-level laser therapy (LLLT). Patients were evaluated: (1) on the first day of treatment; (2) 5 days after autologous or 8 days after allogeneic transplantation; (3) once bone marrow had integrated; and (4) 30 days after discharge. Clinical evaluation was performed using the World Health Organization criteria; oral health QoL was measured using the Oral Health Impact Profile (OHIP-14); and mucositis symptoms with the Patient-Reported Oral Mucositis Symptom (PROMS) scale. The higher the score, the lower the patient's QoL. The OHIP-14 responses showed that at D + 5/D + 8, all domains had the highest scores, while at times 1 and 4, the scores were lower. In the PROMS scale, all domains scored worst at time 2, and the differences between the scores at the four times were statistically significant. The study has shown that QoL improves over time in patients undergoing LLLT therapy for mucositis prevention.


Subject(s)
Hematopoietic Stem Cell Transplantation/adverse effects , Low-Level Light Therapy/methods , Stomatitis/radiotherapy , Adolescent , Adult , Aged , Child , Child, Preschool , Female , Hematologic Neoplasms/therapy , Hospitalization , Humans , Infant , Infant, Newborn , Male , Middle Aged , Oral Health , Prospective Studies , Quality of Life , Young Adult
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