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1.
Article | IMSEAR | ID: sea-220262

ABSTRACT

Background: Rheumatic fever principally influences kids in developing states, particularly where deficiency is common. Atrial fibrosis is a mutual characteristic of clinical atrial fibrillation (AF) and is accompanying with AF in a diversity of experiment sittings, Aim and Objectives: The current work aimed to assess whether there are any clinical or echo-cardiographic parameters that expect the existence of AF among cases with rheumatic mitral valve disorder (RMVD), Subjects and Methods: The current study was a comparative cross-sectional was conducted on 100 RMVD cases at cardio-vascular medicine department Tanta university hospitals within 6-mths starting from September 2019. Cases have been allocated into 2 groups: Group-I: 50 cases with sinus rhythm. Group-II: 50 cases with AF, Results: A significant change was found among study groups regarding Fibrosis characteristics, There is a highly significant difference between the three different types regarding mitral valve area (MVA), LA-diameter, LA volume, LA-diameter/BSA and LA volume index, Age, area of mitral valve, LA-diameter and LA volume were found to be significant predictors for AF, Conclusion: Echo-cardiography factors could recognize cases at higher danger of advancing AF among RMVD cases who may benefit from preventive measures.

2.
Int J Pharm Pharm Sci ; 2020 Jan; 12(1): 59-65
Article | IMSEAR | ID: sea-205999

ABSTRACT

Objective: This study was undertaken to formulate a floating drug delivery system of theophylline hydrochloride using different concentrations of a chosen polymer and then investigate how polymer concentration affects buoyancy and drug release properties of the tablets. Methods: Hydroxypropyl methylcellulose (HPMC) at different concentration levels of 15% (F1), 20% (F2) and 30% (F3) was used to form the three formulation batches of floating tablets. Wet granulation method was used for the granule preparation while Sodium bicarbonate and citric acid were used as the gas generating agent. The physical properties of the granules and the floating tablets were evaluated. Also determined were the physicomechanical properties, buoyancy and swelling characteristics of the tablets. The in vitro drug release study was carried out according to the USP I (basket method) for 8h in 900 ml 0.1N HCl at 50 rpm. Samples withdrawn at the regular predetermined time were analyzed spectrophotometrically at a wavelength of 271 nm and data obtained statistically analyzed by one-way analysis of variance (ANOVA). The differences between means were considered significant at P<0.05. Results: The result showed that polymer (HPMC) concentration significantly (p>0.05) increased swelling index and improved floating lag time, it had no significant effect on the total floating time. Percentage drug release at the end of 8 h was 100%, 98.2% and 96.13% for formulation F1, F2 and F3, respectively. All three formulations followed the Higuchi drug release kinetics model and the mechanism of drug release was the non Fickian diffusion with exponents of 0.46, 0.51 and 0.56 for the respective batch. Conclusion: Batch F3 gave a better-controlled drug release and floating properties in comparison to batch F1 and F2 thus Polymer concentration influenced the onset of floating and controlled the release of Theophylline.

3.
Journal of the Egyptian Society of Parasitology. 2004; 34 (1): 131-42
in English | IMEMR | ID: emr-66715

ABSTRACT

The antischistosomal activity of praziquantel [PZQ], its alkaline hydrolysis product [HP] and its sun decomposed [SD] products was investigated in S. Mansoni experimentally infected mice. The evaluation depended on the degree of the clinicopathological changes. The obtained results revealed that, PZQ, HP and SD induced a partial suppression of worm fecundity as judged by the significant reduction in eggs per gram of feces in comparison with the infected untreated control. The effect on tissue egg deposition in the treated groups was comparable with the infection of the untreated control. Worm recovery showed a great reduction in the number of worms for SD [47.6%] and HP [28.6%] compared with PZQ [16.6%] treated groups. So, the former two compounds have the superior antischistosomal activities. Glutamate pyruvate transaminase [GPT] and glutamate oxaloacetate transaminase [GOT] concentrations were measured. The GOT values for all treated groups were significantly higher than those for the healthy control group. The SD group enzyme concentration was even higher than the infected untreated control. The GPT values of all groups were greater than the uninfected control and the difference was significant for the infected untreated, PZQ and the SD treated groups


Subject(s)
Animals, Laboratory , Schistosomicides , Models, Anatomic , Drug Stability , Schistosomiasis mansoni , Drug Stability , Aspartate Aminotransferases , Alanine Transaminase , Mice
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