Facilitating spiritual intelligence in South African secondary school learners

This article was motivated by concern for the challenges – on a spiritual level –that secondary school learners in South Africa facein the context of moral decay. It therefore aimsto develop educational strategies that Life Orientation teachers in particular can use to facilitate spiritual intelligence (SQ) in learners,especially when religious and cultural diversity inschools is considered. To this end, a programme to develop SQ was designed based ona literature review, andthen implemented within the framework of socio-constructivism. Purposive sampling was employed to select 10 Grade 11 learners in a secondary school in Pretoria. The programme was implemented with the learners in seven contact sessions over a period ofthree months.To evaluate the programme, a qualitative case study design was employed. Continuous evaluation during implementation wasby means of learnerreflective activities, informal conversation interviews, focus groups, semi-structured interviews, observations and a researcher self-reflective journal. The findings of this exploratory study revealed that certain content and educational strategies can facilitate SQ in secondary school learners. Key words: Spiritual intelligence, secondary school, educational strategies, socio-constructivism  Abstrak:Die fasilitering van spirituele intelligensie by Suid-Afrikaanse sekondêreskool-leerdersHierdie artikel is gemotiveer uit kommer oor die uitdagings van ’n spirituele aard en binne die konteks van morele verval, waarvoor sekondêreskool-leerders in Suid-Afrika te staan kom. Die doel was dus om onderrigstrategieë te ontwikkel wat veral Lewensoriëntering-onderwysers kan gebruik om spirituele intelligensie in leerders te fasiliteer, met in agneming van godsdienstige en kulturele diversiteit. Met dié doel voor oë is ’n program om spirituele intelligensie te ontwikkel uit die literatuur ontwerp en geïmplementeer binne die raamwerk van sosio-konstruktivisme. Doelbewuste steekproefneming is gebruik om tien Graad 11-leerders in ’nsekondêre skool in Pretoria te selekteer. Die program is met die leerders geïmplementeer in sewe kontaksessies oor ’nperiodevan drie maande. Om die program te evalueer het die studie ’n kwalitatiewe gevallestudie-ontwerp gebruik. Kontinue evaluering is gedurende hierdie tyd gedoen deur middel van aktiwiteite wat leerder-refleksie stimuleer, asook informeleonderhoude, fokusgroepe, semi-gestruktureerdeonderhoude, observasie en ’n joernaalmet navorser-refleksies. Die bevindinge van hierdie eksploratiewe studie toon aan dat sekereinhoude en opvoedkundige stragtegieë spirituele intelligensie van sekondêreskool-leerders kan fasiliteer.Kernbegrippe: Spirituele intelligensie, sekondêreskool, opvoedkundige strategieë, sosio-konstruktiwismehttps://doi.org/10.19108/KOERS.80.2.222

Evaluation of binder and disintegrant properties of starch derived from Xanthosoma sagittifolium in metronidazole tablets

The aim of the study was to formulate metronidazole tablets using starch from Xanthosoma sagittifolium as binder and disintegrant in metronidazole tablets. Metronidazole tablets were produced by wet granulation method using X. sagittifolium starch as binder at concentrations of 5, 10, 15 and 20% w/w, and as disintegrant (5% w/w). The micromeritic properties of the granules were determined using the direct and indirect methods. The necessary official and non official tests were performed on the tablets to include uniformity of tablets weight, content of active ingredient, disintegration test, hardness, friability tests and in vitro drug release. Also, the phytochemical constituents of the starch were determined. The results show that the granules had a good flow and values obtained were within the specified limits for the production of good quality tablets. Deviations obtained from the tablet weight uniformity test were significantly (p< 0.05) below 5%. Tablets disintegration time ranged from 3.00 ± 0.08 min to 14.00 ± 0.10 min for M1 and M4 tablets formulated with 5 and 20% of X. sagittifolium starch respectively. The tablets hardness ranged from 7.20 ± 1.25 to 8.55 ± 1.17 kgf. In vitro release showed that M1 tablets had T25, T50 and T90 % at 5, 13 and 23 min respectively, while M4 tablets had T25, T50 and T90 % at 8, 18 min and were unable to release 90% of metronidazole at 30 min. Phytochemical analysis showed that the starch contained alkaloids, glycosides, carbohydrate and steroids. Therefore, starch from X. sagittifolium could be used to formulate metronidazole tablets for improved oral bioavailability of metronidazole.Keywords: Xanthosoma sagittifolium starch, tablets binder and disintegrant, metronidazoleAfrican Journal of Biotechnology Vol. 12(20), pp. 3064-307

IN VITRO PROPERTIES OF SOLID LIPID MICROPARTICLES (SLMS) LOADED WITH METHANOLIC EXTRACT OF GARCINIA KOLA (HECKEL) SEED

Objective: The decline in the use of herbal medicine especially in the Western world may be due to lack of readily available market brand formulations and the fact that most herbal remedies are taken as tea, decoctions and infusions. The taste of some of these herbal drugs is not palatable, and some have unpleasant odour and colour hence, the need to formulate these drugs in form of encapsulated dosage forms. The objective of the work was to formulate solid lipid microparticles (SLMs) loaded with the methanolic extract of Garcinia kola seed. Methods: The SLMs containing 1 and 3 % of Garcinia kola seed extract were formulated using fat from Capra hircus and Phospholipon® 90H (3:1). The particle morphology and size, encapsulation efficiency (EE%), pH, in vitro release and the inhibition zone diameter (IZD) of the SLMs were determined. Results: The results showed that the extract was very bitter while, the encapsulated G. kola had slight bitter taste. The pH remained in the acidic region from 1 to 30 days. Particle size of 28.65 ± 1.13 and 29.49 ± 1.24 µm were obtained for SLMs loaded with 1 and 3 % of the extract respectively. SLMs had high EE% of 94 % and also exhibited good release of the extract in simulated intestinal fluid (SIF, pH 7.2). Garcinia kola-loaded SLMs had good activity against Staphylococcus aureus and no action against Escherichia coli. Conclusion: Therefore, Garcinia kola seed extract could be formulated as SLMs in order to mask its bitter taste and improve compliance. Â

Energy Consumption in Wireless Sensor Network

Energy is a limited resource in wireless sensor networks. In fact, the reduction of power consumption is crucial to increase the lifetime of low power sensor networks. Wireless sensor networks consist of small, autonomous devices with wireless networking capabilities. In order to further increase the applicability in real world applications, minimizing power consumption is one of the most critical issues. Therefore, accurate power model is required for the evaluation of wireless sensor networks. To estimate the lifetime of sensor node, the energy characteristics of sensor node are measured. Research in this area has been growing in the past few years given the wide range of applications that can benefit from such a technology. Based on the proposed model, the estimated lifetime of a battery powered sensor node can be increased significantly. Keywords—Sensor, Wireless Sensor Network, Energy Consumptio

FORMULATION AND EVALUATION OF ETHANOLIC EXTRACT OF CRYPTOLEPIS SANGUINOLENTA ROOT TABLETS

Objectives: To study were to formulate the ethanolic extract of Cryptolepis sanguinolenta root into tablets and to evaluate the effect of different binders and binder concentration on the properties of tablets. Materials and method: The phytochemistry of ethanolic extract of Cryptolepis sanguinolenta was evaluated. The tablets were formulated by wet granulation using gelatin and sodium carboxymethyl cellulose (SCMC) as binders at concentrations of 2 %, 4 %, 6 % and 8 %w/w. The tablets were evaluated using the necessary official and unofficial tests. Results: Phytochemical analysis revealed the presence of alkaloids, terpenoids, steroids, proteins, carbohydrate, resins, reducing sugars and glycosides. Tannins, saponins, flavonoids and acidic compounds were absent.  The tablets passed the uniformity of weight test and deviations obtained complied with BP specifications. Tablets disintegration time ranged from 8.00 ± 0.10 to 13.50 ± 0.21 min for tablets formulated with 2 and 4 % gelatin and 10.00 ± 0.17 to 31.00 ± 0.27 min for tablets formulated with 2 and 8 % SCMC. C. sanguinolenta tablets formulated gelatin significantly showed higher hardness values than SCMC (p < 0.05). Tablets showed friability of approximately ≤ 1 %. Conclusion: Therefore, gelatin showed good properties for formulating Cryptolepis sanguinolenta normal release tablets than SCMC.Â

Distinct and shared gene expression for human innate versus adaptive helper lymphoid cells

Innate lymphoid cells (ILCs) are the latest identified innate immune cell family. Given their similarity in transcription factor expression and cytokine secretion profiles, ILCs have been considered as the innate phenocopy of CD4 Th cells. Here, we explored the transcriptome of circulating human ILC subsets as opposed to CD4 Th cell subsets. We describe transcriptomic differences between total ILCs and total CD4 Th cells, as well as between paired innate and adaptive cell subsets (ILC1 vs. Th1; ILC2 vs. Th2; and ILC3 vs. Th17 cells). In particular, we observed differences in expression of genes involved in cell trafficking such as CCR1, CCR6 and CXCR3, innate activation and inhibitory functions, including CD119, 2B4, TIGIT, and CTLA-4, and neuropeptide receptors, such as VIPR2. Moreover, we report for the first time on distinct expression of long noncoding RNAs (lncRNAs) in innate vs. adaptive cells, arguing for a potential role of lncRNA in shaping human ILC biology. Altogether, our results point for unique, rather than redundant gene organization in ILCs compared to CD4 Th cells, in regard to kinetics, fine-tuning and spatial organization of the immune response

SUSTAINED RELEASE ARTEMETHER-LOADED SOLID LIPID MICROPARTICLES, BASED ON SOLIDIFIED REVERSE MICELLAR SOLUTION (SRMS)

Objectives: To prepare and evaluate sustained release artemether-loaded SLMs based on SRMS Material and methods: SRMS, consisting of mixtures of Phospholipon® 90H (P90H) and Softisan® 154 (1:1, 2:1 and 1:2) were formulated and characterized using differential scanning calorimetry (DSC). The SRMS were used to formulate artemether-loaded SLMs by melt homogenization. The SLMs were characterized based on particle size and morphology, pH stability, encapsulation efficiency (EE%) and loading capacity. In vitro release was carried out in simulated intestinal fluid (SIF, pH 7.5). Results: Thermograms of the SRMS (1:1, 2:1 and 1:2) showed sharp endothermic peaks at 65.5, 64.4 and 62.3 oC respectively. Maximum EE% of 70.00 ± 1.50 % was obtained for SLMs formulated with SRMS 1:1 and 1 % artemether. Loading capacity ranged from 5.67 to 17.90 g drug/100 g lipid. In vitro release showed about 80 to 84 % drug release at 7 h. Particle size of artemether-loaded SLMs ranged from 18.60 ± 0.09 to 34.80 ± 0.30 µm. The pH decreased significantly at 60 days from 6 to 4.8 for batch A2 formulated with SRMS 2:1 and 3 % artemether (p < 0.05). Conclusion: artemether-loaded SLMs based on SRMS had good sustained release properties and could be used once daily in order to enhance patient's compliance.   Key words: Malaria, artemether, SRMS, lipids, sustained release SLMs Â

Low haemoglobin predicts early mortality among adults starting antiretroviral therapy in an HIV care programme in South Africa: a cohort study

BACKGROUND: Antiretroviral therapy (ART) has dramatically reduced morbidity and mortality among people with HIV infection; however, mortality after the start of ART is high in resource-limited settings. We investigated risk factors for mortality among adults starting ART in a multi-clinic community programme in South Africa. METHODS: Cohort of adults starting ART at 27 clinics between February 2005 and June 2006, followed to 31st March 2007. Kaplan-Meier survival estimates were used to describe overall mortality. Shared frailty Cox regression was used to identify baseline risk factors for early mortality. RESULTS: Among 1350 participants (median age 35.5 years, 60% female, median CD4 count 83/microL [interquartile range (27-147)], median follow-up 13.4 months), there were 185 deaths, overall mortality rate 13/100 pyrs; for 0-3, 3-9 and >9 months from ART start mortality rates were 24, 13 and 6/100 pyrs respectively. 43% of the deaths were in the first 3 months of treatment. Risk factors for mortality in univariable analysis were baseline CD4 count, viral load, haemoglobin and body mass index, in multivariable analysis adjusting for age and gender, only CD4 count and haemoglobin remained independently associated with proportional hazards not being satisfied for haemoglobin. Adjusted hazard ratios (aHR) for participants with haemoglobin 11.9(f)/12.9 (m) g/mL were 4.99, 3.05 and 0.12 respectively comparing to 10-11.9 (f)/12.9 (m)g/mL in the first 3 months of ART. aHRs for CD4 counts were 0.40, 0.38 and 0.34 for 50-99, 100-200 and >200/microL comparing to <50/microL. CONCLUSIONS: The high mortality rate in the first 3 months underlines the need for earlier HIV diagnosis so that ART can be initiated earlier. Low haemoglobin and low CD4 count are both strong predictors of mortality, and could be used to identify individuals at high risk who might benefit from intensive case management