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1.
Crit Care ; 19: 30, 2015 Feb 02.
Artigo em Inglês | MEDLINE | ID: mdl-25641219

RESUMO

INTRODUCTION: The primary objective of this study was to determine the efficiency of hydrogen peroxide (H2O2) techniques in disinfection of ICU rooms contaminated with multidrug-resistant organisms (MDRO) after patient discharge. Secondary objectives included comparison of the efficiency of a vaporizator (HPV, Bioquell) and an aerosolizer using H2O2, and peracetic acid (aHPP, Anios) in MDRO environmental disinfection, and assessment of toxicity of these techniques. METHODS: This prospective cross-over study was conducted in five medical and surgical ICUs located in one University hospital, during a 12-week period. Routine terminal cleaning was followed by H2O2 disinfection. A total of 24 environmental bacteriological samplings were collected per room, from eight frequently touched surfaces, at three time-points: after patient discharge (T0), after terminal cleaning (T1) and after H2O2 disinfection (T2). RESULTS: In total 182 rooms were studied, including 89 (49%) disinfected with aHPP and 93 (51%) with HPV. At T0, 15/182 (8%) rooms were contaminated with at least 1 MDRO (extended spectrum ß-lactamase-producing Gram-negative bacilli 50%, imipenem resistant Acinetobacter baumannii 29%, methicillin-resistant Staphylococcus aureus 17%, and Pseudomonas aeruginosa resistant to ceftazidime or imipenem 4%). Routine terminal cleaning reduced environmental bacterial load (P <0.001) without efficiency on MDRO (15/182 (8%) rooms at T0 versus 11/182 (6%) at T1; P = 0.371). H2O2 technologies were efficient for environmental MDRO decontamination (6% of rooms contaminated with MDRO at T1 versus 0.5% at T2, P = 0.004). Patient characteristics were similar in aHPP and HPV groups. No significant difference was found between aHPP and HPV regarding the rate of rooms contaminated with MDRO at T2 (P = 0.313). 42% of room occupants were MDRO carriers. The highest rate of rooms contaminated with MDRO was found in rooms where patients stayed for a longer period of time, and where a patient with MDRO was hospitalized. The residual concentration of H2O2 appears to be higher using aHPP, compared with HPV. CONCLUSIONS: H2O2 treatment is efficient in reducing MDRO contaminated rooms in the ICU. No significant difference was found between aHPP and HPV regarding their disinfection efficiency.


Assuntos
Infecção Hospitalar/prevenção & controle , Desinfetantes/farmacologia , Desinfecção/instrumentação , Eficiência , Peróxido de Hidrogênio/farmacologia , Unidades de Terapia Intensiva/normas , Volatilização , Estudos Cross-Over , Desinfetantes/uso terapêutico , Desinfecção/métodos , Farmacorresistência Bacteriana Múltipla/efeitos dos fármacos , Peróxido de Hidrogênio/uso terapêutico , Quartos de Pacientes/normas , Ácido Peracético/farmacologia , Ácido Peracético/uso terapêutico , Estudos Prospectivos
2.
J Med Chem ; 48(9): 3379-88, 2005 May 05.
Artigo em Inglês | MEDLINE | ID: mdl-15857144

RESUMO

We designed and synthesized new photoactivatable linear vasopressin analogues containing benzophenone photophores. All compounds were monitored and purified using RP-HPLC and characterized by mass spectrometry. Affinity and selectivity were determined in CHO cells expressing either human V(1a), V(1b) or V(2) receptor subtypes. Within the series, compounds 6 (PhCH(2)CO-lBpa-Phe-Gln-Asn-Arg-Pro-Arg-Tyr(3I)-NH(2)) and 9 (PhCH(2)CO-dBpa-Phe-Gln-Asn-Arg-Pro-Arg-Tyr(3I)-NH(2)), containing a benzoylphenylalanine residue (Bpa), were selected and their antagonistic properties determined (K(inact) = 1.87 and 0.35 nM, respectively). The dissociation constant of the most potent candidate (compound 9) was further calculated from saturation experiments using the (125)I derivative (K(d) = 0.07 +/- 0.01 nM). Photolabeling experiments using radioactive compound 9 as a probe were specific and UV-dependent and allowed the identification of two bands at molecular masses around 85-90 kDa and 46 kDa, respectively, as previously described by Phalipou et al., using two photoreactive linear azidopeptide antagonists. The results suggest therefore that compound 9 is a potent new tool for the accurate mapping of the human V(1a) receptor antagonist binding site.


Assuntos
Antagonistas dos Receptores de Hormônios Antidiuréticos , Benzofenonas/síntese química , Oligopeptídeos/síntese química , Marcadores de Fotoafinidade/síntese química , Animais , Benzofenonas/química , Benzofenonas/farmacologia , Sítios de Ligação , Células CHO , Cricetinae , Cricetulus , Humanos , Radioisótopos do Iodo , Cinética , Luz , Oligopeptídeos/química , Oligopeptídeos/farmacologia , Marcadores de Fotoafinidade/química , Marcadores de Fotoafinidade/farmacologia , Ensaio Radioligante , Receptores de Vasopressinas/metabolismo , Relação Estrutura-Atividade
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