Determination of antioxidant status of pre-eclamptic and normotensive sub-rural Nigerian pregnant women at the Irrua specialist teaching hospital, Irrua, Edo State

2012 ◽  
Vol 25 (10) ◽  
pp. 2046-2050 ◽  
Author(s):  
M. A. Ikpen ◽  
J. Eigbefoh ◽  
R. A. Eifediyi ◽  
P. A. Isabu ◽  
S Okogbenin ◽  
...  
2014 ◽  
Vol 13 (9) ◽  
pp. 79-82
Author(s):  
Ochei Kingsley Chinedum ◽  
◽  
Obeagu Emmanuel ifeanyi ◽  
Ugwu Getrude Uzoma ◽  
George Christiana Ngozi

1961 ◽  
Vol 38 (4) ◽  
pp. 545-562 ◽  
Author(s):  
L. Kecskés ◽  
F. Mutschler ◽  
I. Glós ◽  
E. Thán ◽  
I. Farkas ◽  
...  

ABSTRACT 1. An indirect paperchromatographic method is described for separating urinary oestrogens; this consists of the following steps: acidic hydrolysis, extraction with ether, dissociation of phenol-fractions with partition between the solvents. Previous purification of phenol fraction with the aid of paperchromatography. The elution of oestrogen containing fractions is followed by acetylation. Oestrogen acetate is isolated by re-chromatography. The chromatogram was developed after hydrolysis of the oestrogens 'in situ' on the paper. The quantity of oestrogens was determined indirectly, by means of an iron-reaction, after the elution of the iron content of the oestrogen spot, which was developed by the Jellinek-reaction. 2. The method described above is satisfactory for determining urinary oestrogen, 17β-oestradiol and oestriol, but could include 16-epioestriol and other oestrogenic metabolites. 3. The sensitivity of the method is 1.3–1.6 μg/24 hours. 4. The quantitative and qualitative determination of urinary oestrogens with the above mentioned method was performed in 50 pregnant and 9 non pregnant women, and also in 2 patients with granulosa cell tumour.


1980 ◽  
Vol 45 (4) ◽  
pp. 1099-1108 ◽  
Author(s):  
Mikuláš Chavko ◽  
Michal Bartík ◽  
Evžen Kasafírek

A polarographic study of the hydrolysis of [8-lysine]vasopressin and some hormonogens of the vasopressin series with the blood serum of women in the last week of pregnancy was studied. The dependence of hydrolysis on pH (pH optimum: 7.4-7.50, substrate concentration (Km 1.2 . 10-5M), pH stability and thermal stability were determined. The rate of hydrolysis of individual vasopressin analogues decreases in the order: [8-lysine]vasopressin > Nα-glycyl-prolyl[8-lysine]-vasopressin > Nα-leucyl-[8-lysine]vasopressin > Nα-alanyl-[8-lysine]vasopressin > Nα-phenyl alanyl-[8-lysine]vasopressin > Nα-diglycyl-[8-lysine]vasopressin > Nα-prolyl-[8-lysine]vasopressin > Nα-triglycyl-[8-lysine]vasopressin > Nα-sarcosyl-glycyl-[8-lysine]vasopressin. The degree of hydrolysis gradually increases to a multiple with the length of the pregnancy in consequence of the presence of oxytocine. However, vasopressin is also hydrolysed to a small extent with the enzymes from the blood sera of non-pregnant women. Under similar analytical conditions oxytocin was not hydrolysed with the sera of non-pregnant women and therefore oxytocin is a more suitable substrate than vasopressin for polarographic determination of serum oxytocinase.


1981 ◽  
Vol 27 (1) ◽  
pp. 149-152 ◽  
Author(s):  
M J Obregon ◽  
A Kurtz ◽  
R Ekins ◽  
G Morreale de Escobar

Abstract We assessed a commercial kit (Corning Medical) for "free" and total thyroxine determination, results being compared to those obtained by the Ekins and Ellis dialysis method (free thyroxine) and the method of Weeke and Orskov (total thyroxine). The kit procedure permits determination of both free and total thyroxine within 4 to 5 h, and the combined results may disclose changes in binding to plasma proteins that would be missed if only free thyroxine were determined. With both free-thyroxine methods, the values distinguished hyperthyroid patients from normal controls and pregnant women with 100% accuracy, but there was some overlap between hypothyroid patients and controls. Absolute values with the kit procedure often exceed those obtained by dialysis, especially for hypothyroid patients and pregnant women. We conclude that the kit may be of as much diagnostic value as the dialysis method if the limitations regarding absolute values are kept in mind and the test is not used as a substitute for thyrotropin determinations in cases of suspected hypothyroidism.


2021 ◽  
Author(s):  
Hamid Talebzadeh ◽  
Hamid Mellali ◽  
hamid solgi

Abstract Background The spread of plasmid-mediated multidrug resistance in Klebsiella pneumonia is a serious threat to the public health. We investigated the clinical characteristics and molecular epidemiology of K. pneumoniae isolated at a teaching hospital in Iran. Methods A total of 50 third-generation cephalosporins resistant K. pneumoniae strains were collected from patients’ clinical cultures. Antibiotic susceptibility testing and determination of MIC values for ceftazidime, cefotaxime and ciprofloxacin were performed. PCR and DNA sequencing were used to assess the presence of ESBL genes (blaCTX−M, blaTEM, blaSHV) and PMQR genes (qnrA, qnrB, qnrS, qepA, oqxA, oqxB and aac(6)-Ib-cr). Multilocus sequence typing (MLST) was performed on the strains to assess homology. Results Our results showed that the rates of resistance to all of antibiotics is high. All 50 K. pneumoniae strains harboured at least one of the ESBL resistance determinants. The blaCTX−M−15 gene was the major ESBLs determinant found in K. pneumoniae (88%; 44/50). PMQR was detected in 96% of the isolates and aac(6′)-Ib-cr was the most common (78% 39/50) followed by oqxA 36 (72%), oqxB 34 (68%), qnrS 20 (40%), qnrB 14 (28%) and qepA 1 (2%). MLST identified seven sequence types (STs), with the most common being ST11 (19/39). There was a strong association between PMQR genes (especially aac(6′)-Ib-cr) and ESBL genes. Conclusion The widespread detection of ESBLs-producing K. pneumoniae that co-carried PMQR determinants has become a threat to the treatment of infections in Isfahan Province of center Iran. Our findings suggest that K. pneumoniae ST11 and ST893 has a clonal distribution in our hospital. Therefore, this study highlighted the crucial need for implementing strict control measures to prevent cross transmission of these endemic clones.


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