Pricipales of Dental Toxicology

Iyad Abou Rabii DDS, OMFS, MRes, PhD

QASSIM UNIVERSITY
 Pricipales of Dental Toxicology
Iyad Abou Rabii DDS, OMFS, MRes, PhD

Dental Toxicology
Study of poisons and their effects, particularly on living systems.

And Searching for treatments

Forensic toxicology (the use of toxicology and other disciplines such as analytical
chemistry, pharmacology and clinical chemistry to aid medical or legal
investigation of death)

Mercury
Facts
Mercury is the most toxic substance that people are exposed to.
• Potential health risks associated with mercury amalgams include:
• Mercury inhibits sulfhydryl (-SH) group containing enzymes
• Mercury's links to neurological diseases like Alzheimer's disease and autism
• Harm to unborn babies
• Vulnerability to toxicity, particularly among vulnerable pregnant women
and young children
• Greater exposure to the effects of mercury due to chewing and drinking
beverages
• Interaction with other metals and dental materials that increases risks

Mercury Types
There is three types of Mercury
• Inorganic
• Organic: Especially in fishes leaving Lakes and rivers are also contaminated
when there is a direct discharge of mercury industrial
[‫ | ]اختر التاريخ‬Pricipales of Dental Toxicology
• Mercury vapor.

Pharmacodynamics
Mercury can pass the skin barrier, blood-brain and the placental barrier and
thus cause devastating effects on the functioning and growth of the brain
and the growing foetus.
• The most likely routes of exposure are inhalation of inorganic mercury
vapour after a spill or during a manufacturing process, or ingestion of
methyl mercury from contaminated fish, absorption through skin.
• Ditribution
• According to Mercury type
• Vapor : The most dangerous form absorbed in the lungs and stored in the
CNS

1
 • Oraganic Mercury : Lipophile absorbed in the intestin, most of it excerted
with feces
• Inorganic : Accumulate in the blood, plasma, and kidney (scereted in the
urine)
• Mercury plasmatic half-life is about 60-70 days

Mecury in dentistry
Mercury is a component of the amalgam used for "silver" fillings. The other
major ingredients are silver, tin, copper, and zinc. When mixed, these
elements bond to form a strong, stable substance.
• Mercury vapour from amalgam is the most dangerous form of mercury,
most rapidly crossing the blood-brain barrier and mother’s placenta, and
ensuring adverse developmental effects at lower levels than other forms.
• The mercury-free dentists cite the potential for excess exposure to mercury
when removing amalgam fillings as a serious concern for dental
practitioners, some of whom have devised various strategies for reducing
the amount of mercury exposure for both patients and dental staff during
the removal of mercury fillings.

Arsenic
Arsenic is a poisonous chemical often used in herbicides and pesticides and is classified as a Class
1 carcinogen, meaning it is highly toxic to humans.
“arsenic has been linked to cancer of the bladder, lungs, skin, kidney, nasal passages, liver, and
prostate”. Other side effects of consuming arsenic can include nausea, vomiting, diarrhea, partial
paralysis and blindness.

Medical Use of arsenic

• Arsphenamine as well as Neosalvarsan was indicated for syphilis but has been superseded
by modern antibiotics.
• Arsenic trioxide has been used in a variety of ways over the past 500 years, but most
commonly in the treatment of cancer.
• The US Food and Drug Administration in 2000 approved this compound for the treatment
of patients with acute leukemia
• It was also used as Fowler's solution in psoriasis.[
• Recently new research has been done in locating tumours using arsenic-74 (a positron
emitter).
• Arsenic is used in dentistry as gel in order to produce the necrosis of the pulp before
endodontic therapy, in that case intensive car soul be taken to prevent its leakage
[‫ | ]اختر التاريخ‬Pricipales of Dental Toxicology

Lead
Lead is a toxic element existed in the dental clinic (amalgam fillings, Xray
shields, Xray films), once in the body lead can
• Inhibit heme biosynthesis Heme is the essential structural component of
hemoglobin, myoglobin and cytochromes.
• Binds to sulfhydryl groups (-SH groups) of proteins (including a lot of
important metabolic enzymes)

Pharmacodynamique
Absorbtion
• Skin: alkyl lead compounds, because of lipid solubility (methyl and
tetraethyl lead)

2
 • Inhalation: up to 90% depending upon particle size
• GI: adults 5 to 10%, children 40%
Distribution
Initially carried in red cells and distributed to soft tissues (kidney and liver);
redistributed to bone, teeth and hair mostly as a phosphate salt. Rates of
absorption and distribution are greatly influenced by dietary intake and
body stores of phosphate, calcium and iron relative to lead
• high PO4, Pb storage in bone
• high Vitamin D, Pb storage in soft tissue
• low PO4, Pb sequestered in soft tissue
• high Ca++, Pb sequestered in soft tissue
• Half life in blood 30-60 days, bone 20-30 years

Source of exposure
# GI - paint, pottery,amalgam
# Inhalation - metal fumes, amalgam dust
# Skin -tetraethyl lead in gasoline

Fluoride as Toxic material

Fuorosis
Fluorosis occurs when teeth are developing.
• The most critical ages are from 0 to 6 years. After 8 years, risk of fluorosis is
essentially past.
• During the critical ages F intake in excess of 0.1mg/kg body weight/day can
lead to fluorosis.
• This is roughly 1mg/day for a 1 to 2 year old or 1.5 to 2 mg for a 5 year old.
•
• Remember that all forms of F intake comprise the daily consumption.
• This includes
• water intake (up to 1.5mg/day)
• Foods (0.3 to 1.0mg) and especially significant in young children
• Swallowed toothpaste. Children under 2 years swallow 50% of toothpaste
during tooth brushing and at 5years, 25%, both of which may amount to
1mg F/day. [‫ | ]اختر التاريخ‬Pricipales of Dental Toxicology

Probable toxic dose (PTD)

PTD is 5 mg F/kg body weight.
For a 20 kg 5 to 6 year old this would be 100 mg
for a 10 kg 2 year old, 50 mg.
F content of dental products or treatments may exceed these values for young
children. For example,
a gel tray containing 5 ml of APF contains 61.5mg F (F is absorbed more
quickly when in acidic form.),
100ml of 0.2 or 0.4% F mouth rinse contains 91 or 97mg F and a
tube of fluoridated toothpaste contains as much as 230mg F.

Best Practice of luoride administration

3
 Current clinical recommendations for preventive F measures are
1) to determine total F intake per day from all sources in order to assess over or
under F exposure
2) determine caries risk
3) institute a regimen commensurate with individual caries risk status which
emphasizes bioavailability of post-eruptive topical F (e.g. regular use of F
dentifrice and other home products if indicated)
4) administer professional topical F treatments, the timing of which should also
be gauged to caries risk (This may not be needed in low risk individuals) and
5) administer systemic topical F if indicated. (The latter is currently under review.
Present Academy of Pediatric Dentistry recommendations are presented below.

Toxicological management in dentistry

Prevention
1. Consider all sources of exposure
2. Best practice
3. Management of Dental wastes

Dignosis
1. History of exposure
2. Biological fluids analysis (blood mercury, whole blood lead level, arsenic
blood and urinary levels)

Treatment
Remove from exposure
• Chelating agents
• 1.Lead: Calcium disodium EDTA (IV). 2, 3-dimercaptosuccinic acid (Succimer)
(Oral). 2, 3-dimercaptoproponol (BAL, Dimercaprol) (IM). Penicillamine
(Oral)
•
• Mercury: 2, 3-dimercaptosuccinic acid (Succimer) (Oral). 2, 3-
dimercaptoproponol (BAL, Dimercaprol) (IM). Penicillamine (Oral). N-acetyl-
penicillamine (Oral)
• Arsenic: N-acetyl-penicillamine (Oral). Penicillamine (Oral)
[‫ | ]اختر التاريخ‬Pricipales of Dental Toxicology

• Fuoride : milk and calcium containing products

•
•
• CHELATING AGENTS
• Chelation is the formation of a metal ion complex in which the metal ion is
associated with a charged or uncharged electron donor referred to as a ligand.