ABSTRACT
Abstract The present study entails the systematic development and validation of a stability-indicating RP-HPLC method for the analysis of sitagliptin and ertugliflozin in a fixed-dose combination. Analytical quality by design (AQbD) concepts were used to define critical method variables, employing Pareto risk assessment and a Placket-Burman screening design, preceded by a Box-Behnken design with response surface analysis to optimise critical method parameters such as % acetonitrile (X1), buffer pH (X2) and column oven temperature (X3). Multiple response optimisation (Derringer's desirability) of variables was accomplished by studying critical analytical attributes, such as resolution, retention time and theoretical plates. The title analytes were separated effectively on a PRONTOSIL C18 column at 37 °C using a mobile phase of acetonitrile:acetate buffer, pH 4.4 (36:64 percent v/v), pumped at a flow rate of 1 mL/min, and UV detection at 225 nm. Linearity was observed over a concentration range of 25-150 µg/mL and 3.75-22.5 µg/mL at retention times of 2.82 and 3.92 min for sitagliptin and ertugliflozin, respectively. The method obeyed all validation parameters of the ICH Q2(R1) guidelines. The proposed robust method allows the study of the selected drugs in pharmaceutical dosage forms as well as in drug stability studies under various stress conditions.
Subject(s)
Drawing , Sitagliptin Phosphate/analysis , Pharmaceutical Preparations/administration & dosage , Chromatography, High Pressure Liquid/methods , Total Quality Management/classification , Hydrogen-Ion Concentration/drug effectsABSTRACT
Presentamos el caso de un varón de72 años intervenido de cistectomía radical laparoscópica con derivación urinaria tipo Bricker en el año2016 por cáncer vesical músculo invasivo. Durantesus revisiones con nuestra estomaterapeuta el paciente empezó a desarrollar granulomas periestomales.Nuestro objetivo es eliminar los granulomas formadosy prevenir la aparición de nuevas lesiones mediante elcontrol del pH urinario a través de la administraciónde Lit Control®. El uso de Lit Control® pH Down ennuestro paciente ha conseguido disminuir el pH urinario, eliminar parte de los granulomas periestomalesy mejorar parámetros urinarios como el olor y el color de la orina. (AU)
We present the case of a 72-year-oldman who underwent laparoscopic radical cystectomywith 8po Bricker urinary diversion in 2016 for muscle-invasive bladder cancer. During his follow-upswith our stomatotherapist, the patient started to develop peristomal granulomas. Our aim is to eliminate the granulomas formed and prevent the appearanceof new lesions by controlling the urinary pH throughthe administration of Lit-Control® pH Down. The useof Lit-Control® pH Down in our patient has succeededin lowering urinary pH, eliminating part of the peristomal granulomas, and improving urinary parameterssuch as urine odour and colour. (AU)
Subject(s)
Humans , Male , Aged , Granuloma/drug therapy , Granuloma/etiology , Hydrogen-Ion Concentration/drug effects , Ostomy/adverse effects , Cystectomy/methods , Urinary Diversion , Urinary Bladder Neoplasms/surgeryABSTRACT
The development and clinical application of 2-methoxyestradiol (2-ME) as a new type of antitumor drug are limited due to its poor solubility, rapid metabolism in vivo, and large oral dosage. 2-ME-loaded pH-sensitive liposomes (2-ME-PSLs) was prepared containing the lipids, Lipoid E-80 (E-80), cholesteryl hemisuccinate (CHEMS), and cholesterol (CHOL) via thin-film ultrasonic dispersion. First, preparation conditions of 2-ME-PSLs were optimized by orthogonal test. Then 2-ME-PSL was characterized, and the release behavior and stability of 2-ME-PSL in vitro were evaluated. The optimal preparation conditions for 2-ME-PSLs were as follows: 2-ME : E-80+CHEMS 1:15; CHOL : E-80+CHEMS 1:5; ultrasonication time 20 minutes. The mean particle size, PDI, zeta potential, and entrapment efficiency (EE) of 2-ME-PSLs were 116 ± 9 nm, 0.161 ± 0.025, −22.4 ± 1.7 mV, and 98.6 ± 0.5%, respectively. As viewed under a transmission electron microscope, 2-ME-PSLs were well dispersed and almost spherical. They exhibited significant pH-sensitive properties and were fairly stable when diluted with a physiological solution. In conclusion, 2-ME-PSLs were successfully prepared and possessed a favorable pH sensitivity and good dissolution stability with a normal solution
Subject(s)
In Vitro Techniques/instrumentation , 2-Methoxyestradiol/pharmacokinetics , Liposomes/analysis , Drug Screening Assays, Antitumor/classification , Hydrogen-Ion Concentration/drug effectsABSTRACT
ABSTRACT The aim of the present study was to investigate the effect of donor pH on the transdermal permeability of the model drugs across rat skin and also to determine the major route of transport of the drugs. Weakly acidic drugs (partition coefficient) ibuprofen (3.6), aceclofenac (3.9), glipizide (1.9) and weakly basic drugs olanzapine (3.6), telmisartan (6.0), and sildenafil citrate (1.9) were selected for the study. The ex vivo permeation studies of these drugs at different donor pH (pH - 1.2, 4, 5, 6.8, 7.4, and 8) using Franz diffusion cell (area, 7.54 cm2) has shown a pH-dependent permeability. Among these drugs the weakly acidic drugs has shown higher permeation rates compared to the weakly basic drugs. The permeability coefficient and the distribution coefficient of the weakly basic drugs increased on increasing the pH whereas the weakly acidic drugs showed an inverse relation. The weakly basic drugs also showed an increase in permeation with increase in the fraction of unionized species indicating dominance of transcellular route of permeation. With an exception of sildenafil citrate, a weakly basic salt form of the drug which showed a high permeation value at pH 7.4 where 57% of the drug was unionized, indicating the involvement of both paracellular and transcellular route in its permeation.
Subject(s)
Animals , Male , Rats , Amino Acids, Acidic/analysis , Amino Acid Transport Systems, Basic/analysis , Hydrogen-Ion Concentration/drug effects , Skin , Solubility , Pharmaceutical Preparations/analysisABSTRACT
The addition of chlorhexidine (CHX) to a resinous experimental Mineral Trioxide Aggregate (E-MTA) based root-end filling material is an alternative to boost its antimicrobial activity. However, the influence of chlorhexidine on the properties of this material is unclear. The aim of this study was to evaluate the influence of 2% chlorhexidine on the pH, calcium ion release and setting time of a Bisphenol A Ethoxylate Dimethacrylate/Mineral Trioxide Aggregate (Bis-EMA/MTA) based dual-cure experimental root-end filling material (E-MTA), in comparison with E-MTA without the addition of CHX and with conventional white MTA (W-MTA). The materials were placed in polyethylene tubes, and immersed in deionized water to determine pH (digital pH meter) and calcium ion release (atomic absorption spectrometry technique). The setting time of each material was analyzed using Gilmore needles. The data were statistically analyzed at a significance level of 5%. E-MTA + CHX showed an alkaline pH in the 3 h period of evaluation, the alkalinity of which decreased but remained as such for 15 days. The pH of E-MTA + CHX was higher than the other two materials after 7 days, and lower after 30 days (p < 0.05). All of the materials were found to release calcium ions throughout the 30 days of the study. The addition of CHX increased the calcium ion release of E-MTA to levels statistically similar to W-MTA. E-MTA showed shorter initial and final setting time, compared with W-MTA (p < 0.05). The addition of 2% CHX to MTA prevented setting of the material. The addition of CHX to E-MTA increased its pH and calcium ion release. However, it also prevented setting of the material.
Subject(s)
Aluminum Compounds/chemistry , Calcium Compounds/chemistry , Calcium/chemistry , Chlorhexidine/chemistry , Methacrylates/chemistry , Oxides/chemistry , Root Canal Filling Materials/chemistry , Silicates/chemistry , Analysis of Variance , Drug Combinations , Hydrogen-Ion Concentration/drug effects , Immersion , Materials Testing , Reference Values , Statistics, Nonparametric , Time FactorsABSTRACT
O objetivo deste estudo, in vitro, foi analisar a variação do pH de três pastas à base de Ca(OH)2 e de cada um de seus componentes. Foram formados quatro grupos teste: GI: Ca(OH)2 + propilenoglicol (PG) + Aloe vera; GII: Ca(OH)2 + PG + paramonoclorofenol canforado (PMCC); GIII: Ca(OH)2 + PG + clorexidina 2% e grupo controle (água destilada). As pastas foram depositadas em frascos contendo 15 ml de água destilada e estes armazenados em estufa a 37° C. A mensuração do pH foi realizada em 7 intervalos de tempo. Os grupos testados apresentaram crescimento exponencial dos valores de pH registrados até 24 h e estabilização em 14 dias. Os controles apresentaram valores de pH inferiores em relação aos demais grupos (p<0,05 ANOVA). A partir de t = 24 h, GII e GIII apresentaram maiores valores de pH em relação a GI (p<0,05 Bonferroni). Numa segunda etapa, foram formados cinco grupos com os componentes individuais de cada pasta: GIc clorexidina líquida 2%; GIIc PG; GIIIc PMCC; GIVc hidróxido de cálcio P.A.; GVc Aloe vera. GIVc e GVc apresentaram, respectivamente, os maiores e menores valores de pH registrados até o final do experimento (12,63 e 5,54). Conclui-se que o pH das pastas de Ca(OH)2 pode variar em função da sua composição, porém sempre se mantendo alcalino, mesmo quando associada à Aloe vera, cujo pH ácido foi registrado no presente estudo. No entanto, uma maior alcalinidade foi apresentada pelas pastas contendo clorexidina ou PMCC em sua composição.
The objective of this study, in vitro, was to analyze the variation of the pH of threeCa(OH)2 - based pastes and each of its components. There were four groups test: GI: Ca(OH)2 + propylene glycol (PG) + Aloe vera; GII: Ca(OH)2 + PG + camphorated paramonochlorophenol (CMCP); GIII: Ca(OH)2 + PG + 2% chlorhexidine and control group (distilled water). The pastes were deposited in vials containing 15 ml of distilled water and stored in a 37° C incubator. The measurement of pH was performed in 7 time intervals.The groups tested showed exponential growth of pH values recorded up to 24 h and stabilization in 14 days. The controls showed pH values lower than the other groups (p<0.05 ANOVA). From t = 24 h, GII and GIII had higher levels of pH compared to GI (p<0.05 - Bonferroni). Subsequently, five groups were formed with the individual components of each paste: GIc - 2% chlorhexidine liquid; GIIc - PG; GIIIc - CMCP; GIVc - calcium hydroxide; GVc - Aloe vera. GIVc and GVc showed, respectively, the highest and lowest pH values recorded by the end of the experiment (12.63 and 5.54). It was concluded that the pH of Ca(OH)2 pastes may change depending on their composition, but always remained alkaline, even when associated with Aloe vera, whose acidic pH was recorded in this study. However, a higher alkalinity was presented by pastes containing chlorhexidine or CMCP in its composition.
Subject(s)
Calcium Hydroxide/analysis , Aloe , Hydrogen-Ion Concentration/drug effects , In Vitro Techniques , Endodontics , PhytotherapyABSTRACT
OBJECTIVES: The aim of this work was to evaluate saliva and tongue coating pH in oral healthy patients with morning bad breath before and after use of different oral mouthrinses. MATERIAL AND METHODS: Saliva and tongue coating pH of 50 patients allocated in 5 groups were measured respectively by a digital pHmeter and color pH indicators, before, immediately after and 30 min after rinsing 5 different mouthrinses: cetilpiridine chloride associated with sodium chloride, triclosan, enzymatic solution, essential oil and distilled water. RESULTS: Only triclosan and essential oil increased salivary pH immediately after rising. The enzymatic solution decreased salivary and tongue coating pH immediately after rinsing. CONCLUSIONS: Salivary pH tended to be acidic while tongue coating pH tended to be alkaline, even after rising. Triclosan and essential oil mouthrinses increased salivary pH immediately after rinsing. Enzymatic solution decreased saliva and tongue coating pH immediately after rising.
Subject(s)
Humans , Halitosis/drug therapy , Mouthwashes/pharmacology , Saliva/chemistry , Tongue/chemistry , Analysis of Variance , Anti-Infective Agents, Local/pharmacology , Case-Control Studies , Chlorine Compounds/pharmacology , Dental Disinfectants/pharmacology , Hydrogen-Ion Concentration/drug effects , Oxides/pharmacology , Saliva/drug effects , Sodium Chloride/pharmacology , Time Factors , Tongue/drug effects , Triclosan/pharmacologyABSTRACT
Both epidural and general anesthesia can impair thermoregulatory mechanisms during surgery. However, there is lack of information about the effects of different methods of anesthesia on newborn temperature. The purpose of this study was to determine whether there are differences in newborn rectal temperature related to type of anesthesia. Sixty-three pregnant women were randomly assigned to receive general or epidural anesthesia. Maternal core temperature was measured three times with a rectal probe just before anesthesia, at the beginning of surgery and at delivery. In addition, umbilical vein blood was sampled for pH. The rectal temperatures of the babies were recorded immediately after delivery, and Apgar scores were determined 1, 5, and 10 min after birth. The duration of anesthesia and the volume of intravenous fluid given during the procedure (833 ± 144 vs 420 ± 215 mL) were significantly higher in the epidural group than in the general anesthesia group (P < 0.0001). Maternal rectal temperatures were not different in both groups at all measurements. In contrast, newborn rectal temperatures were lower in the epidural anesthesia group than in the general anesthesia group (37.4 ± 0.3 vs 37.6 ± 0.3°C; P < 0.05) immediately after birth. Furthermore, the umbilical vein pH value (7.31 ± 0.05 vs 7.33 ± 0.01; P < 0.05) and Apgar scores at the 1st-min measurement (8.0 ± 0.9 vs 8.5 ± 0.7; P < 0.05) were lower in the epidural anesthesia group than in the general anesthesia group. Since epidural anesthesia requires more iv fluid infusion and a longer time for cesarean section, it involves a risk of a mild temperature reduction for the baby which, however, did not reach the limits of hypothermia.
Subject(s)
Adult , Female , Humans , Infant, Newborn , Pregnancy , Anesthesia, Epidural , Anesthesia, General , Anesthesia, Obstetrical/methods , Body Temperature/drug effects , Cesarean Section , Apgar Score , Fetal Blood/chemistry , Hydrogen-Ion Concentration/drug effects , Rectum/physiologyABSTRACT
Two-year trials (20062007) suggested that the use of calcium oxide (CaO) on acid soils increased soil pH and yields in strawberry cultivars Marmolada, Selena and Senga Sengana, under the environmental conditions of Cacak (Western Serbia). The highest yield was obtained when CaO was applied at 750 kg ha-1 rate. Further increase in rate up to 1,500 kg ha-1 did not show corresponding increase in yield; the result was a slight yield drop compared to the peak yield shown at 750 kg ha¹ rate. Overall, yields at rates above 750 kg ha¹ were still higher than control and in the treatment employing lowest CaO application rate of 250 kg ha-1.
Dois anos de ensaios (2006-2007) sugeriram que o uso deóxido cálcio (CaO) em solos ácidos aumentou o pH do soloe o rendimento das cultivares de morango, Marmolada, Selena e Senga Sengana, sob as condições ambientais de Cacak (oeste da Sérvia). O rendimento mais elevado foi obtido quando CaO foi aplicado na quantidade de 750 kg ha-1. O aumento da quantidade para nível até 1500 kg ha-1 não mostrouaumento correspondente do rendimento; o resultado foi umaligeira queda em comparação com o rendimento máximo obtidoa 750 kg ha¹. Globalmente, os resultados a taxas superiores a 750 kg ha¹ foram ainda mais elevados do que no controle e no tratamento empregando quantidade mais baixa de 250 kg ha-1 de CaO.
Subject(s)
Calcium Compounds/pharmacology , Fragaria/growth & development , Oxides/pharmacology , Soil/analysis , Hydrogen-Ion Concentration/drug effects , SerbiaABSTRACT
Limited evidence is available regarding antiretroviral (ARV) safety for uninfected infants exposed to these drugs in utero. Our objective was to determine if ARV administered to pregnant women is associated with decreasing umbilical arterial pH and base excess in uninfected infants. A prospective study was conducted on 57 neonates divided into three groups: ZDV group, born to mothers taking zidovudine (N = 20), triple therapy (TT) group, born to mothers taking zidovudine + lamivudine + nelfinavir (N = 25), and control group (N = 12), born to uninfected mothers. Umbilical cord blood was used to determine umbilical artery gases. A test was performed to calculate the sample by comparing means by the unpaired one-tailed t-test, with a = 0.05 and ß = 20 percent, indicating the need for a sample of 18 newborn infants for the study groups to detect differences higher than 20 percent. The control and ARV groups were similar in gestational age, birth weight, and Apgar scores. Values of pH, pCO2, bicarbonate, and base excess in cord arterial blood obtained at delivery from the newborns exposed to TT were 7.23, 43.2 mmHg, 19.5 mEq/L, and -8.5 nmol/L, respectively, with no significant difference compared to the control and ZDV groups. We conclude that intrauterine exposure to ARV is not associated with a pathological decrease in umbilical arterial pH or base excess. While our data are reassuring, follow-up is still limited and needs to be continued into adulthood because of the possible potential for adverse effects of triple antiretroviral agents.
Subject(s)
Adult , Female , Humans , Infant, Newborn , Pregnancy , Acid-Base Equilibrium/drug effects , Anti-HIV Agents/therapeutic use , Fetal Blood/chemistry , HIV Infections/drug therapy , Anti-HIV Agents/adverse effects , Case-Control Studies , Drug Therapy, Combination , HIV Infections/blood , Hydrogen-Ion Concentration/drug effects , Infectious Disease Transmission, Vertical , Lamivudine/adverse effects , Lamivudine/therapeutic use , Nelfinavir/adverse effects , Nelfinavir/therapeutic use , Pregnancy Outcome , Prospective Studies , Zidovudine/adverse effects , Zidovudine/therapeutic useABSTRACT
INTRODUÇÃO: A Doença do Refluxo Gastroesofágico (DRGE) é a doença digestiva mais prevalente da atualidade e, recentemente, tem sido implicada em uma gama de alterações do seguimento laringofaríngeo (RLF). No entanto, pouco se sabe dos mecanismos fisiopatológicos destas manifestações supraesofágicas da DRGE. Os achados clínicos contraditórios e recentes pesquisas sugerem haver deficiências na capacidade de defesa deste seguimento. Uma das principais responsáveis pela homeostase da mucosa oral e do trato digestivo é a saliva com seu conteúdo orgânico e inorgânico. Tanto alterações do pH quanto do volume salivar já foram correlacionados com os sintomas e sinais sugestivos da DRGE e RLF. Estudo recente de nossa autoria demonstra diminuição estatisticamente significante do pH salivar de indivíduos com RLF quando comparado a controles sem a doença. Outro estudo constatou correlação entre a redução do volume X pH da saliva em indivíduos com DRGE, estando esta redução diretamente relacionada aos níveis de pH esofágico constatados durante pH-metria esofágica de 24 horas. OBJETIVOS: Avaliar como se comportam o pH e volume da saliva em um mesmo indivíduo com DRGE e RLF antes e após o tratamento clínico. MATERIAL E MÉTODO: Vinte e três pacientes com RLF tiveram o pH e volume da saliva total testados antes e após receberem tratamento com droga bloqueadora de bomba de prótons durante 12 semanas. RESULTADOS: Houve uma diferença estatisticamente significante (p<0,001) entre o pH da saliva antes e após o tratamento, estando este maior após o controle clínico da doença. O volume de saliva no paciente tratado foi significativamente maior do que no paciente pré-tratamento (p=0.009). DISCUSSÃO: Os achados sugerem que o pH salivar é influenciado pela presença de refluxo gastroduodenal à região laringofaríngea. Caso estudos futuros com populações maiores realmente comprovem esta correlação, poderemos cogitar a possibilidade de usar a mensuração do pH salivar, que é feita de forma rápida e não invasiva, como um meio de diagnosticar e avaliar o comportamento e controle do Refluxo Laringofaríngeo.
INTRODUCTION: Gastroesophageal Reflux Disease (GERD) is the most prevalent digestive disease of the modern society and has been associated with abnormalities in the larynx and pharynx (LPR). Nonetheless, little is known about the mechanisms involved in this atypical form of the disease. Contradictory clinical data suggest a defense deficit at this segment. Saliva with its organic and inorganic components is responsible for the homeostasis of the oral mucosa and the digestive tract. Salivary pH and volume abnormalities have been linked to laryngopharyngeal symptoms of GERD and LPR. In a recent study we demonstrated significant salivary pH reduction in patients with LPR. Another study found correlation between reduced salivary pH and volume directly related to esophageal pH-metry results. AIM: To evaluate salivary pH and volume before and after clinical treatment of LPR. MATERIAL AND METHOD: Twenty-three adults with LPR had total fasting saliva tested before and after a 12-week course of oral proton pump inhibitor. RESULTS: A statistically significant difference was found in salivary pH before and after treatment with increase of pH values after control of the disease (p<0.001). Salivary volumes of treated patients were also significantly higher than in pre-treated patients (p=0.009). DISCUSSION: These findings suggest that salivary pH and volume are influenced by the presence of gastroesophageal contents and that salivary pH monitoring can potentially become a cost-effective method for diagnosing and controlling LPR.
Subject(s)
Humans , Male , Female , Adult , Middle Aged , Proton Pumps/antagonists & inhibitors , Pharyngitis/diagnosis , Laryngitis/diagnosis , Omeprazole/therapeutic use , Saliva/chemistry , Proton Pumps/pharmacology , Chronic Disease , Hydrogen-Ion Concentration/drug effects , Pharyngitis/drug therapy , Pharyngitis/etiology , Laryngitis/drug therapy , Laryngitis/etiology , Manometry , Monitoring, Physiologic , Omeprazole/pharmacology , Gastroesophageal Reflux/complications , Gastroesophageal Reflux/drug therapy , Saliva/drug effects , SalivaABSTRACT
We studied the relationship between alpha- and beta-adrenergic agonists and the activity of carbonic anhydrase I and II in erythrocyte, clinical and vessel studies. Kinetic studies were performed. Adrenergic agonists increased erythrocyte carbonic anhydrase as follows: adrenaline by 75 percent, noradrenaline by 68 percent, isoprenaline by 55 percent, and orciprenaline by 62 percent. The kinetic data indicated a non-competitive mechanism of action. In clinical studies carbonic anhydrase I from erythrocytes increased by 87 percent after noradrenaline administration, by 71 percent after orciprenaline and by 82 percent after isoprenaline. The increase in carbonic anhydrase I paralleled the increase in blood pressure. Similar results were obtained in vessel studies on piglet vascular smooth muscle. We believe that adrenergic agonists may have a dual mechanism of action: the first one consists of a catecholamine action on its receptor with the formation of a stimulus-receptor complex. The second mechanism proposed completes the first one. By this second component of the mechanism, the same stimulus directly acts on the carbonic anhydrase I isozyme (that might be functionally coupled with adrenergic receptors), so that its activation ensures an adequate pH for stimulus-receptor coupling for signal transduction into the cell, resulting in vasoconstriction
Subject(s)
Humans , Male , Adult , Middle Aged , Animals , Adrenergic alpha-Agonists/pharmacology , Adrenergic beta-Agonists/pharmacology , Carbonic Anhydrases/metabolism , Catecholamines/pharmacology , Vasoconstriction/drug effects , Analysis of Variance , Carbonic Anhydrases/isolation & purification , Epinephrine/pharmacology , Erythrocytes/drug effects , Erythrocytes/enzymology , Hydrogen-Ion Concentration/drug effects , Isoenzymes/metabolism , Isoproterenol/pharmacology , Metaproterenol/pharmacology , Muscle, Smooth, Vascular/drug effects , Norepinephrine/pharmacology , Signal TransductionABSTRACT
En este trabajo, se utilizaron conductos radicularesartificiales divididos en tres grupos y obturados de la siguiente forma: Grupo 1: con una pasta de Ca(OH2); Grupo 2: con cono unico de gutapercha que contiene Ca(OH2) en su formulacion; Grupo 3: impresionando el tercio apical con el mismo tipo de cono, habiendo sumergido previamente sus 4 mm apicales en agua destilada cuya temperatura era de 80ºC. Los especimenes se conservaron a 37 ºC en recipientes individuales con agua destilada, y las modificaciones de pH del medio que rodeaba los mismos se determinaron luego de 3, 24 y 48 horas de inmersion. Los resultados demostraron que los incrementos de
Subject(s)
In Vitro Techniques , Hydrogen-Ion Concentration/drug effects , Gutta-Percha/diagnosis , Gutta-Percha/therapeutic use , Calcium Hydroxide/diagnosis , Calcium Hydroxide/therapeutic use , Root Canal Obturation , Tooth Root/drug effectsABSTRACT
Urinary parameters related to acid base homeostasis were studied in adrenalectomized rats (ADX) as well as in ADX treated with physiological doses of corticosterone (B), aldosterone (aldo) or 18-Hydroxycorticosterone (l8HOB) during 1,3 or 5 days, under basal conditions and after gravage with 200 mM HCI. The results showed: a) a persistent effect of B and l8HOB increasing titratable acidity principally in response to acidosis; b) an increased phosphate elimination in acidotic B treated ADX on the first day, and in 18 HOB treated ADX on days 3 and 5; c) pronounced increases in blood pH and blood bicarbonate levels provoked by the three steroids on day 1; d) increments of ammonium elimination in response to acidosis by aldo treatmets on the first day, while B and l8HOB increase ammonium elimination under almost all conditions during the whole experiment; e) the effects of B and 18 HOB would be independent of an increase in sodium retention as well as glomerular filtration rate.
Subject(s)
Rats , Animals , Male , Aldosterone/pharmacology , Corticosterone/analogs & derivatives , Corticosterone/pharmacology , Homeostasis/drug effects , Kidney/drug effects , Hydrogen-Ion Concentration/drug effects , Rats, Sprague-Dawley , UrinalysisABSTRACT
Urinary parameters related to acid base homeostasis were studied in adrenalectomized rats (ADX) as well as in ADX treated with physiological doses of corticosterone (B), aldosterone (aldo) or 18-Hydroxycorticosterone (l8HOB) during 1,3 or 5 days, under basal conditions and after gravage with 200 mM HCI. The results showed: a) a persistent effect of B and l8HOB increasing titratable acidity principally in response to acidosis; b) an increased phosphate elimination in acidotic B treated ADX on the first day, and in 18 HOB treated ADX on days 3 and 5; c) pronounced increases in blood pH and blood bicarbonate levels provoked by the three steroids on day 1; d) increments of ammonium elimination in response to acidosis by aldo treatmets on the first day, while B and l8HOB increase ammonium elimination under almost all conditions during the whole experiment; e) the effects of B and 18 HOB would be independent of an increase in sodium retention as well as glomerular filtration rate. (AU)
Subject(s)
Rats , Animals , Male , RESEARCH SUPPORT, NON-U.S. GOVT , Aldosterone/pharmacology , Corticosterone/pharmacology , Corticosterone/analogs & derivatives , Homeostasis/drug effects , Kidney/drug effects , Urinalysis , Hydrogen-Ion Concentration/drug effects , Rats, Sprague-DawleyABSTRACT
En la presente comunicación se analiza la relación existente entre el estado de la microperfusión esplánica y la incidencia de fallas orgánicas, sepsis y mortalidad, en el postoperatorio de pacientes quirúrgicos críticos. El flujo esplánico fue evaluado directamente a través de la medición del pH intracelular de la mucosa gástrica (pHi). Se estudiaron en forma prospectiva 125 pacientes críticos, operados por patología abdominal. El pHi se midió durante las primeras 24 horas del postoperatorio mediante un tonómetro ubicado en la cavidad gástrica. Se diferenciaron dos grupos de enfermos, Grupo I: con todas las mediciones de pHi superiores a 7.40 y Grupo II: con una o más determinaciones iguales o inferiores a 7.40. La sumatoria de puntos Apache II y el promedio de falls orgánicas fueron significativamente inferiores en el Grupo I (12.6 y 0.4 respectivamente vs. 16.1 y 1.1 respectivamente en el Grupo II) con una p<0.01. Fallecieron 39 pacientes (31.2//). El pHi fue significativamente superior en los sobrevivientes, a partir de las 6 horas del postoperatorio. Otros parámetros habitualmente utilizados para evaluar la gravedad, no mostraron diferencias significativas en ese momento de la evolución. La incidencia de fallas orgánicas y sepsis fue mayor en los fallecidos. La medición del pHi en las primeras 24 horas del postoperatorio fue útil para predecir la evolución de los pacientes
Subject(s)
Comparative Study , Humans , Male , Female , Microcirculation/physiopathology , Critical Care/methods , Postoperative Period , Hydrogen-Ion Concentration/drug effects , Multiple Organ Failure/physiopathology , Multiple Organ Failure/diagnosis , Multiple Organ Failure/etiology , Intubation, Gastrointestinal/instrumentation , Cell Hypoxia/physiology , Postoperative Complications/diagnosis , Postoperative Complications/mortality , Postoperative Complications/prevention & control , Peritonitis/complicationsABSTRACT
En la presente comunicación se analiza la relación existente entre el estado de la microperfusión esplánica y la incidencia de fallas orgánicas, sepsis y mortalidad, en el postoperatorio de pacientes quirúrgicos críticos. El flujo esplánico fue evaluado directamente a través de la medición del pH intracelular de la mucosa gástrica (pHi). Se estudiaron en forma prospectiva 125 pacientes críticos, operados por patología abdominal. El pHi se midió durante las primeras 24 horas del postoperatorio mediante un tonómetro ubicado en la cavidad gástrica. Se diferenciaron dos grupos de enfermos, Grupo I: con todas las mediciones de pHi superiores a 7.40 y Grupo II: con una o más determinaciones iguales o inferiores a 7.40. La sumatoria de puntos Apache II y el promedio de falls orgánicas fueron significativamente inferiores en el Grupo I (12.6 y 0.4 respectivamente vs. 16.1 y 1.1 respectivamente en el Grupo II) con una p<0.01. Fallecieron 39 pacientes (31.2//). El pHi fue significativamente superior en los sobrevivientes, a partir de las 6 horas del postoperatorio. Otros parámetros habitualmente utilizados para evaluar la gravedad, no mostraron diferencias significativas en ese momento de la evolución. La incidencia de fallas orgánicas y sepsis fue mayor en los fallecidos. La medición del pHi en las primeras 24 horas del postoperatorio fue útil para predecir la evolución de los pacientes
Subject(s)
Humans , Male , Female , Critical Care/methods , Hydrogen-Ion Concentration/drug effects , Microcirculation/physiopathology , Multiple Organ Failure/physiopathology , Postoperative Period , Cell Hypoxia/physiology , Intubation, Gastrointestinal/instrumentation , Multiple Organ Failure/diagnosis , Multiple Organ Failure/etiology , Peritonitis/complications , Postoperative Complications/diagnosis , Postoperative Complications/mortality , Postoperative Complications/prevention & controlABSTRACT
Os autores realizaram um estudo duplo-cego para determinar uma possível entre potássio sérico e efeitos colaterais, que aparecem nos primeiros 5 dias de tratamento com acetazolamida 500 mg, via oral. Em todos aqueles que usaram a droga produziu-se efeitos colaterais, sendo o mais comum parestesias. Näo houve diferença significativa entre os níveis de postássio sérico antes e após o tratamento
Subject(s)
Humans , Acetazolamide/pharmacology , Hydrogen-Ion Concentration/drug effects , Potassium/pharmacology , Potassium/adverse effectsABSTRACT
Estudio prospectivo, aleatorio y en doble ciego. Noventa pacientes sometidos a cirugía abdominal recibieron preoperatoriamente 20 mg de famotidina intravenosa o un placebo. Se midió el pH y volumen gástrico postintubación traqueal (T1), al momento del vaciamiento total del estómago (T2) y antes de la extubación (T3). El pH gástrico fue significativamente superior en el grupo de pacientes que recibió famotidina en los tres tiempos de medición. El volumen gástrico fue significativamente inferior en el grupo con famotidina en el tiempo 1, no habiendo diferencia entre los dos grupos en los tiempos 2 y 3. La población "en riesgo" (pH < 3 y volumen > 25 ml) fue significativamente inferior en el grupo que recibió famotidina en los tres tiempos de medición