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1.
Reprod Toxicol ; 65: 359-364, 2016 10.
Article in English | MEDLINE | ID: mdl-27629360

ABSTRACT

This study evaluated the effects of thiamine pyrophosphate (PPT) on the biochemical profiles of full-term rabbit foetuses that were subjected to experimental ischemia followed by 24h reperfusion. A total of 16 gestating rabbit dams were divided into two groups, one of which was treated by administering PPT and subjected to a process ischemia. During this interval, fetal blood samples were drawn from each dam (in the ischemia group) at 0, 15 and 45min. Ischemia for 15 and 45min was not associated with changes in lactate levels of the Ischemia group foetuses. However, in the foetuses in the reperfusion groups without PPT lactate levels were significantly higher after 15 and 45min of arterial occlusion compared to time zero. These results demonstrate that PTT alters some acute and some longer-term biochemical outcomes of uterine ischemia perhaps important in preserving energy metabolism under hypoxic conditions.


Subject(s)
Fetus/drug effects , Ischemia/metabolism , Protective Agents/pharmacology , Thiamine Pyrophosphate/pharmacology , Uterus/blood supply , Animals , Blood Glucose/analysis , Calcium/metabolism , Female , Fetus/metabolism , Hydrogen-Ion Concentration , Hypoxia/metabolism , Lactic Acid/blood , Rabbits
2.
J Laryngol Otol ; 128(7): 630-40, 2014 Jul.
Article in English | MEDLINE | ID: mdl-25075948

ABSTRACT

BACKGROUND: Collagen-covered prostheses can be used as a non-circumferential segmental tracheal replacement. However, the applicability of these implants in young subjects has not yet been reported. METHODS: In this experimental, longitudinal study, dogs aged 29-32 days underwent limited segmental tracheal replacement with a polyester prosthesis or were allocated to a control, untreated group. The dogs were evaluated clinically, endoscopically and tomographically for up to one year. RESULTS: Although there was evidence of tracheal growth in the experimental group, tomographic measurements were significantly smaller in this group than in the control group throughout the observation period. At the end of the study, there was no evidence of implant rejection, stenosis or collapse. Normal respiratory epithelium had grown across the implanted membrane in the experimental group. CONCLUSION: The homologous collagen mersylene membrane allowed for limited structural tracheal growth and was functionally integrated into the segmented tracheal wall in growing dogs.


Subject(s)
Coated Materials, Biocompatible , Plastic Surgery Procedures/methods , Prostheses and Implants , Trachea/surgery , Tracheal Diseases/surgery , Animals , Disease Models, Animal , Dogs , Female , Laryngoscopy , Male , Multidetector Computed Tomography , Prosthesis Design , Trachea/diagnostic imaging , Trachea/pathology , Tracheal Diseases/diagnostic imaging , Tracheal Diseases/pathology
3.
Int J Pharm ; 282(1-2): 87-94, 2004 Sep 10.
Article in English | MEDLINE | ID: mdl-15336384

ABSTRACT

As part of the development of a new series of antibacterial agents derived from coupling a beta-lactamic precursor with a fluoroquinolone and named cephalones, the pharmacokinetics of one derivate: CQ-M-EPCA in rats after intravenous, intragastric and intraduodenal routes, was carried out. After the IV injection of 20 mg/kg or 40 mg/kg of this cephalone, plasma concentrations at the time zero (Cp0) were 3.1 and 11.26 microg/ml, respectively. Plasma concentrations decreased rapidly to almost disappear in both instances. Forty-five minutes later, a surge in concentrations, in the 40 mg/kg group, with a maximal plasma concentration (Cpmax) of 2.97 microg/ml was observed. An elimination half-life (T1/2el) of 2.36 +/- 0.33 h. was calculated. The drug was undetected by the ninth hour. Intragastric administration of the drug resulted in Cpmax of 3.78 +/- 0.26 microg/ml with a time to reach Cpmax (Tmax) of 25 min and T1/2el = 3.22 h. Same variables after intraduodenal administration were Cpmax 4.71 microg/ml; Tmax 1h, and T1/2el 3.41 h. Outstandingly high bioavailabilities after intragastric and intraduodenal administration (169 and 246%, respectively), together with the shape of the concentration versus time profiles after IV administration suggest that the drug undergoes a complex redistribution phenomenon, while showing high tissue diffusion with an apparent volume of distribution of 3.33 l/kg.


Subject(s)
Anti-Bacterial Agents/pharmacokinetics , Fluoroquinolones/pharmacokinetics , Administration, Oral , Animals , Anti-Bacterial Agents/administration & dosage , Area Under Curve , Chromatography, High Pressure Liquid , Duodenum/metabolism , Fluoroquinolones/administration & dosage , Half-Life , Injections, Intravenous , Intubation, Gastrointestinal , Male , Rats , Rats, Wistar
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