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1.
Pakistan Journal of Pharmaceutical Sciences. 2018; 31 (4): 1259-1266
in English | IMEMR | ID: emr-198423

ABSTRACT

The screening of plants for medicinal purposes represents an effort to discover newer, safer, and possibly more effective drugs. Design of the present study was made aiming to the optimization of the antibacterial activity of ethanolic extracts of Eucalyptus tereticornis [leaves] and Nigella sativa [seeds] against bacteria belongings to both Gram-positive [Bacillus subtilis and Staphylococcus aureus] and Gram-negative [Escherichia coli] spectrum by using response surface methodology. 20 g powder of each E. tereticornis [leaf] and N. sativa [seeds] were mixed with 200ml of ethanol at room temperature, and then it was centrifuged at 4000 rpm for 10 min to separate the supernatants, and allowed to dry in order to obtain ethanol free extracts. A fresh bacterial culture of 100microl of test microorganism was inoculated onto media and spread homogeneously. The antimicrobial activity of ethanolic extracts showed that all the concentrations tested were effective against the test microorganisms. The diameters of zones of inhibition exhibited by S. aureus PCSIR-83 were in the range of 0-28mm, E. coli PCSIR-102 [0-28mm] and B. subtilis PCSIR-05 [15-26mm]. The combination of N. sativa [15mg/micro l] and E. tereticornis [20mg/micro l] were found most effective at pH 9.0 and temperature 35°C. Our results clearly indicate that Gram positive bacteria showed more sensitivity than Gram-negative bacteria

2.
Blood Research ; : 274-278, 2016.
Article in English | WPRIM | ID: wpr-167167

ABSTRACT

BACKGROUND: Characterization of the ABO blood group at the phenotype and genotype levels is clinically essential for transfusion, forensics, and population studies. This study elucidated ABO phenotypes and genotypes, and performed an evaluation of their distribution in individuals from the western region of Saudi Arabia. METHODS: One-hundred and seven samples underwent standard serological techniques for ABO blood group phenotype analysis. ABO alleles and genotypes were identified using multiplex polymerase chain reaction, and electrophoretic analysis was performed to evaluate the highly polymorphic ABO locus. RESULTS: A phenotype distribution of 37.4%, 30.8%, 24.3%, and 7.5% was found for blood groups O, A, B, and AB respectively in our study cohort. Genotype analysis identified 10 genotype combinations with the O01/O02 and A102/O02 genotypes being the most frequent with frequencies of 33.6% and 14.95%, respectively. Common genotypes such as A101/A101, A101/A102, A101/B101, B101/B101, and O01/O01 were not detected. Similarly, the rare genotypes, cis-AB01/O02, cis-AB01/O01, and cis-AB01/A102 were not found in our cohort. The most frequently observed allele was O02 (35.98%) followed by the A102 allele (17.76%). Furthermore, our findings are discussed in reference to ABO allele and genotype frequencies found in other ethnic groups. CONCLUSION: The study has a significant implication on the management of blood bank and transfusion services in Saudi Arabian patients.


Subject(s)
Humans , ABO Blood-Group System , Alleles , Blood Banks , Blood Group Antigens , Cohort Studies , Ethnicity , Genotype , Multiplex Polymerase Chain Reaction , Phenotype , Saudi Arabia
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