1.Occupational Heat Stress Impacts on Health and Productivity in a Steel Industry in Southern India.
Manikandan KRISHNAMURTHY ; Paramesh RAMALINGAM ; Kumaravel PERUMAL ; Latha Perumal KAMALAKANNAN ; Jeremiah CHINNADURAI ; Rekha SHANMUGAM ; Krishnan SRINIVASAN ; Vidhya VENUGOPAL
Safety and Health at Work 2017;8(1):99-104
BACKGROUND: Workers laboring in steel industries in tropical settings with high ambient temperatures are subjected to thermally stressful environments that can create well-known risks of heat-related illnesses and limit workers’ productivity. METHODS: A cross-sectional study undertaken in a steel industry in a city nicknamed “Steel City” in Southern India assessed thermal stress by wet bulb globe temperature (WBGT) and level of dehydration from urine color and urine specific gravity. A structured questionnaire captured self-reported heat-related health symptoms of workers. RESULTS: Some 90% WBGT measurements were higher than recommended threshold limit values (27.2–41.7°C) for heavy and moderate workloads and radiational heat from processes were very high in blooming-mill/coke-oven (67.6°C globe temperature). Widespread heat-related health concerns were prevalent among workers, including excessive sweating, fatigue, and tiredness reported by 50% workers. Productivity loss was significantly reported high in workers with direct heat exposures compared to those with indirect heat exposures (χ2 = 26.1258, degrees of freedom = 1, p < 0.001). Change in urine color was 7.4 times higher among workers exposed to WBGTs above threshold limit values (TLVs). CONCLUSION: Preliminary evidence shows that high heat exposures and heavy workload adversely affect the workers’ health and reduce their work capacities. Health and productivity risks in developing tropical country work settings can be further aggravated by the predicted temperature rise due to climate change, without appropriate interventions. Apart from industries enhancing welfare facilities and designing control interventions, further physiological studies with a seasonal approach and interventional studies are needed to strengthen evidence for developing comprehensive policies to protect workers employed in high heat industries.
Climate Change
;
Cross-Sectional Studies
;
Dehydration
;
Efficiency*
;
Fatigue
;
Hot Temperature*
;
India*
;
Seasons
;
Specific Gravity
;
Steel*
;
Sweat
;
Sweating
;
Threshold Limit Values
2.Zanamivir Oral Delivery: Enhanced Plasma and Lung Bioavailability in Rats.
Srinivasan SHANMUGAM ; Ho Taek IM ; Young Taek SOHN ; Kyung Soo KIM ; Yong Il KIM ; Chul Soon YONG ; Jong Oh KIM ; Han Gon CHOI ; Jong Soo WOO
Biomolecules & Therapeutics 2013;21(2):161-169
The objective of this study was to enhance the oral bioavailability (BA) of zanamivir (ZMR) by increasing its intestinal permeability using permeation enhancers (PE). Four different classes of PEs (Labrasol(R), sodium cholate, sodium caprate, hydroxypropyl beta-cyclodextrin) were investigated for their ability to enhance the permeation of ZMR across Caco-2 cell monolayers. The flux and Papp of ZMR in the presence of sodium caprate (SC) was significantly higher than other PEs in comparison to control, and was selected for further investigation. All concentrations of SC (10-200 mM) demonstrated enhanced flux of ZMR in comparison to control. The highest flux (13 folds higher than control) was achieved for the formulation with highest SC concentration (200 mM). The relative BA of ZMR formulation containing SC (PO-SC) in plasma at a dose of 10 mg/kg following oral administration in rats was 317.65% in comparison to control formulation (PO-C). Besides, the AUC0-24 h of ZMR in the lungs following oral administration of PO-SC was 125.22 +/- 27.25 ng hr ml(-1) with a Cmax of 156.00 +/- 24.00 ng/ml reached at 0.50+/-0.00 h. But, there was no ZMR detected in the lungs following administration of control formulation (PO-C). The findings of this study indicated that the oral formulation PO-SC containing ZMR and SC was able to enhance the BA of ZMR in plasma to an appropriate amount that would make ZMR available in lungs at a concentration higher (>10 ng/ml) than the IC50 concentration of influenza virus (0.64-7.9 ng/ml) to exert its therapeutic effect.
Administration, Oral
;
Animals
;
Biological Availability*
;
Caco-2 Cells
;
Humans
;
Influenza, Human
;
Inhibitory Concentration 50
;
Lung*
;
Orthomyxoviridae
;
Permeability
;
Plasma*
;
Rats*
;
Sodium
;
Sodium Cholate
;
Zanamivir*