OAR@½ñÈÕºÚÁÏ Collection:/library/oar/handle/123456789/84262026-08-14T11:42:50Z2026-08-14T11:42:50ZAntimicrobial efficacy of a novel assisted ultrasound technology/library/oar/handle/123456789/89312018-04-03T12:18:59Z2015-01-01T00:00:00ZTitle: Antimicrobial efficacy of a novel assisted ultrasound technology
Abstract: Two
different essential oils (oregano and thyme essential oils) were
tested with the continuous and pulse 2s on/ 8s off mode . The
concentrations of oregano essential oil tested were : 0 .0 10%,
0. 01 4%, 0. 0 18%, 0. 02 2% an d 0 .0 25% v /v , while with thyme
essential oil the same concen t r a t io ns p lu s 0 .0 4% v/ v were tested.
Application of both
oregano and thyme essential oils at the mentioned concentrations
further reduced the levels of bacteria from the surface.
Significant
differences were found at concentrations of 0 .0 18%, 0 .0 2 2% and
0 0 25% v/v of oregano essential oil with both continuous and pulsed
modes when compared to the samples treated with US alone , while
for thyme essential oil significant reductions were observed with
0.01 8% v/ v and higher concentrations for continuous mode, and
0 . 01 4% v/ v an d higher concentrations for pulsed mode.
Only the
highest concentration of thyme essential oil (0.04% v/ v) using both
continuous and pulsed mode reduced the levels of Salmonella in
water below the limit of detection. The effectiveness of the
assisted ultrasound process was dependent on the processing times
rather than the configuration of the ultrasound used (continuous
versus pulsed mode) .
When the antimicrobial efficacy of oregano
and thyme essential oil were compared, it was evident that oregano
essential oil was more effective at detaching the bacteria from the
surface of the lettuce, while thyme essential oil was more effective
at inactivating the bacteria from the wash water . The use of both
oregano and thyme essential oils proved to show synergistic effects
in enhancing the removal and inactivation of the bacteria from the
surface of the lettuce. The energy applied to the ultrasound system
was also optimized , to obtain maximum reduction in bacterial
levels with minimum energy being utilised.
Description: B.SC.(HONS)BIOMED.SCI.2015-01-01T00:00:00ZValidation of a PCR technique for kidd blood group genotyping/library/oar/handle/123456789/88642016-09-28T08:54:04Z2015-01-01T00:00:00ZTitle: Validation of a PCR technique for kidd blood group genotyping
Abstract: The Kidd blood group antigens, Jka and Jkb, are two of the main surface
markers which are found on the red blood cells’ membrane. The determination of
whether a donor or a recipient has the Jka and/or the Jkb antigens is crucially
important in order to have a successful transfusion without the development of
adverse incompatibility-related reactions. In Malta, routine serological-based tests
are applied with the purpose of differentiating between homozygous and
heterozygous states for the Jk antigens respectively. Although these tests are
highly specific and sensitive, there are particular clinical scenarios where
haemagglutination assays are not suitable for determining the individual’s Kidd
blood group status. Additionally, the alternative genotyping procedure has never
been applied in Malta within the context of molecular transfusion. Thus, this study
was performed to determine whether Polymerase Chain Reaction - Restriction
Fragment Length Polymorphism (PCR-RFLP) is suitable for distinguishing
amongst the three different Kidd phenotypes. After extracting 50 DNA from
blood samples obtained from serologically-tested healthy donors who expressed at
least one of the Kidd antigens, PCR-RFLP analyses were carried out and the
results of the latter were compared with the ones previously obtained with
haemagglutination. Since the results of both tests were a complete match with one
another, the PCR-RFLP method was confirmed as a suitable laboratory technique
that can be used to determine the Kidd blood group of donors and recipients.
Description: B.SC.(HONS)BIOMED.SCI.2015-01-01T00:00:00ZInterleukin 6, white blood cell count and risk of myocardial infarction/library/oar/handle/123456789/88622016-09-28T08:54:29Z2015-01-01T00:00:00ZTitle: Interleukin 6, white blood cell count and risk of myocardial infarction
Abstract: Interleukin 6 (IL-6) is pro-inflammatory cytokine which is reported to have a positive association
with total and differential white blood cell (WBC) levels. Elevated white blood cell levels have
been implicated as an independent risk factor of cardiovascular disease and myocardial infarction
(MI). Single nucleotide polymorphisms (SNP) located within the promoter region of the IL6 gene
have been associated with elevated serum IL-6 levels. The aim of this study is to determine whether
the IL-6 -597 G→A promoter polymorphism influences white blood cell count and therefore the
risk of MI. The results of this study indicate that there is no increased risk of myocardial infarction
(MI) associated with the IL-6 -597 G→A polymorphism when including all cases and controls
[1.0 (95% CI 0.4 – 2.2) in homozygous mutants and 1.0 (95% CI 0.7 – 1.3) in heterozygotes], after
adjusting for age and gender. The polymorphism shows no interaction with smoking, a wellestablished
risk factor of MI. No significant differences are observed in the blood cell levels of
men and women carrying the IL-6 -597A allele when compared to their wildtype counterparts.
These results remain generally unaltered in males after excluding smokers and quitters from blood
cell analysis and observing levels in non-smokers. Female smokers who lack the IL-6 -597A allele
have significantly higher WBC levels than carriers while female non-smokers carrying the allele
have higher WBC levels than homozygous wildtypes, suggesting a possible antagonistic
interaction between the genotype and smoking. The IL-6 -597A allele is associated with lower
BMI in both men and women, indicating a possible protective effect against adiposity and obesity.
Description: B.SC.(HONS)BIOMED.SCI.2015-01-01T00:00:00ZLysophosphatidic acid receptor 1, monocyte count and risk of myocardial infarction/library/oar/handle/123456789/86322016-09-28T08:57:17Z2015-01-01T00:00:00ZTitle: Lysophosphatidic acid receptor 1, monocyte count and risk of myocardial infarction
Abstract: Environmental risk factors for myocardial infarction (MI) have been widely studied, yet
the genetic risks associated with its development, although known to be present, are still
not clearly defined. An association between atherosclerosis, MI and different blood
parameter counts is known to exist. In this case-control study the influence of the rs551517
single nucleotide polymorphism (SNP) on blood parameter counts and incidence of MI was
tested. Blood samples of cases with MI and age- and gender-matched controls from the
Maltese population were used to measure blood parameter counts and for genotyping of the
SNP. The rs551517 polymorphism was not associated with a risk of MI since OR for the
homozygous mutant genotype was 0.9 (95% CI 0.5-1.4) and that for the heterozygous
genotype was 1.2 (95% CI 0.9-1.6) when adjusting for age and gender. A risk for MI
however was observed in smokers where the heterozygous genotype may have a 2-fold risk
of MI, a risk not observed in non-smokers. When measuring the effect of the SNP on blood
parameter counts, variations between genotypes were observed for white blood cells
(WBC), platelet, eosinophil, reticulocyte and lymphocyte count. No effect of the rs551517
SNP on monocyte count was observed. This led to the conclusion that the rs551517
polymorphism is unlikely to have an effect on incidence of MI without the risk factor of
smoking while an effect on a number of blood cell and platelet counts was observed.
Description: B.SC.(HONS)BIOMED.SCI.2015-01-01T00:00:00Z