RISK ANALYSIS OF HEAVY METAL (PB) EXPOSURE THROUGH DERMAL ROUTE ON DNA DAMAGE IN WORKERS IN SOME PAINT INDUSTRY IN INDONESIA
Lead (Pb) as a toxic heavy metal is still used in paint production process in Indonesia as a pigment, dryer or anti-corrosion agent and some paint industries still exceed the standard for Pb content in paints set out in SNI 8011-2014. It has the potential to be a major source of lead exposure to...
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Format: | Theses |
Language: | Indonesia |
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Online Access: | https://digilib.itb.ac.id/gdl/view/75877 |
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Institution: | Institut Teknologi Bandung |
Language: | Indonesia |
Summary: | Lead (Pb) as a toxic heavy metal is still used in paint production process in Indonesia as a
pigment, dryer or anti-corrosion agent and some paint industries still exceed the standard for
Pb content in paints set out in SNI 8011-2014. It has the potential to be a major source of lead
exposure to paint industry workers via the dermal route during the paint production process.
Blood lead levels (PbB) are often used as biomarkers of lead exposure. Lead as an exogenous
factor can cause oxidative stress due to accumulation of Reactive Oxygen Species (ROS) and
can inhibit antioxidant defense enzymes. Imbalance of Reactive Oxygen Species (ROS) and
antioxidant defenses can cause DNA damage which can be used as a biomarker of the effects
of lead. So it is necessary to investigate the genotoxic effects of lead on paint industry workers
in Indonesia. The aims of this study was to analyse the health risks of paint industry workers
of Pb exposure via dermal routes, determine the relationship between Pb exposure and PbB
levels, and determine the relationship between PbB levels and DNA damage using a crosssectional epidemiological study of 52 workers from three paint industries in Indonesia.
Samples of Pb exposure via the dermal route were measured based on NIOSH 7702 issue 1
using a 0.8 µm pore MCE patch filter, Ø=47 mm attached to exposed body parts for 3 hours,
while the Pb content in the air was measured using LVAS (PTFE filter; 45 µm; Ø=47 mm; flow
rate 2.5 LPM) based on SNI 16-7058-2004 as many as 5 sampling points in each industry.
However, the limitations of this study were that each point was measured for 3 hours, which
was then analysed using EDXRF. As many as 6 mL of blood samples were taken to determine
PbB levels which were analyzed using ICP-MS and 3 mL to analyse DNA damage using the
Comet Assay method. Interviews were conducted to determine the characteristics of the
respondents. The Pb content in occupational environment (indoor) is 0.113 ± 0.165 µg/m3
, and
below the standards set by Permenaker RI 5/2018. However, the dose received by workers
through the dermal route is 3.69x10-6 ± 8.13x10-6 mg/kg.day and resulting a non-carcinogenic
risk (HQ>1) from 1 worker in industry C, so it is necessary to carry out risk management,
such as elimination, substitution, engineering control or use of PPE. Meanwhile, the
carcinogenic risk (ELCR) was still within acceptable limits, 4.95x10-8±1.21x10-7 mg/kg.day.
The PbB level was 4.22 ± 1.6 µg/dL, and 17 workers exceeded the safe limit (5 µg/dL), as many
as 1 worker from industry A and B, respectively. While, 15 workers (88.24%) were obtained
from industry C. Pb exposure via the dermal route was significantly positively correlated with
PbB levels (p=0.04; r=0.39). Factors affecting PbB levels were length of work and alcohol
consumption (p<0.05). Meanwhile, PbB levels were negatively correlated with Tail DNA (%)
(r=-0.049) and Tail Length (µm) (r=-0.047), and positively correlated with Tail moment (µm)
(r=0.159), but not significant (p >0.05). The value of Tail DNA (%) for workers was 9.62 ±
0.19%, all workers were classified as having low DNA damage (Class 2). Pb exposure in this
study has not reached a level that can significantly cause DNA damage. However, it is necessary to monitor blood lead levels in workers due to indications of an increase in the Tail
Moment (µm) due to dermal Pb exposure. |
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