Forensic toxicology

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Forensic toxicology is the use of toxicology to aid medicolegal investigation of death, poisoning, and drug use. Many toxic substances do not produce characteristic lesions, so if a toxic reaction is suspected, visual investigation may not suffice.

A forensic toxicologist must consider the context of an investigation, in particular any physical symptoms recorded, and any evidence collected at a crime scene that may narrow the search, such as pill bottles, powders, trace residue, and any available chemicals. Provided with this information and samples with which to work, the forensic toxicologist must determine which toxic substances are present, in what concentrations, and the probable effect of those chemicals on the person.

Determining the substance ingested is often complicated by the body's natural processes, as it is rare for a chemical to remain in its original form once in the body. For example: heroin is almost immediately metabolised into morphine, making detailed investigation into factors such as injection marks and chemical purity necessary to confirm diagnosis. The substance may also have been diluted by its dispersal through the body; while a pill or other regulated dose of a drug may have grams or milligrams of the active constituent, an individual sample under investigation may only contain micrograms or nanograms.

Contents

[edit] Samples

[edit] Urine

A urine sample is quick and easy for a live subject, and is common among drug testing for employees and athletes. Urine samples do not necessarily reflect the toxic substance(s) the subject was influenced by at the time of the sample collection. An example of this is THC from cannabinoid (for example, marijuana) use, which in heavy users can be detected in urine for up to 10 days following use. Note also that it can take as long as 8 hours until a given substance can be detected.

[edit] Blood

A blood sample of approximately 10 cm³ is usually sufficient to screen and confirm most common toxic substances. A blood sample provides the toxicologist with a profile of the substance that the subject was influenced by at the time of collection; for this reason, it is the sample of choice for measuring blood alcohol content in drunk driving cases.

[edit] Hair sample

Hair is capable of recording medium to long-term or high dosage substance abuse. Chemicals in the bloodstream may be transferred to the growing hair and stored in the follicle, providing a rough timeline of drug intake events. Head hair grows at rate of approximately 1 to 1.5 cm a month, and so cross sections from different sections of the follicle can give estimates as to when a substance was ingested. Testing for drugs in hair is not standard throughout the population. The darker and coarser the hair the more drug that will be found in the hair. If two people consumed the same amount of drugs, the person with the darker and coarser hair will have more drug in their hair than the lighter haired person when tested.

[edit] Other organisms

Bacteria, maggots and other organisms that may have ingested some of the subject matter may have also ingested any toxic substance within it.

[edit] Other

Other bodily fluids and organs may provide samples, particularly samples collected during an autopsy. A common autopsy sample is the gastric contents of the deceased, which can be useful for detecting undigested pills or liquids that were ingested prior to death. In highly decomposed bodies, traditional samples may no longer be available. The vitreous humour from the eye may be used, as the fibrous layer of the eyeball and the eye socket of the skull protects the sample from trauma and adulteration. Other common organs used for toxicology are the brain, liver, spleen and stomach contents

The inspection of the contents of the stomach must be part of every postmortem examination because it may provide qualitative information concerning the nature of the last meal and the presence of abnormal constituents. Using it as a guide to the time of death, however, is theoretically unsound and presents many practical difficulties, although it may have limited applicability in some exceptional instances. Generally, using stomach contents as a guide to time of death involves an unacceptable degree of imprecision and is thus liable to mislead the investigator and the court. Characteristic cell types from food plants can be used to identify a victim's last meal; knowledge about which can be useful in determining the victim's whereabouts or actions prior to death (Bock and Norris, 1997). Some of these cell types include (Dickison, 2000):

  • sclereids (pears)
  • starch grains (potatoes and other tubers)
  • raphide crystals (pineapple)
  • druse crystals (citrus, beets, spinach)
  • silica bodies (cereal grasses and bamboos)

In a case where a young woman had been stabbed to death, witnesses reported that she had eaten her last meal at a particular fast food restaurant. However, her stomach contents did not match the limited menu of the restaurant, leading investigators to conclude that she had eaten at some point after being seen in the restaurant. The investigation led to the apprehension of a man whom the victim knew, and with whom she had shared her actual final meal (Dickison, 2000). Time since death can be approximated by the state of digestion of the stomach contents. It normally takes at least a couple of hours for food to pass from the stomach to the small intestine; a meal still largely in the stomach implies death shortly after eating, while an empty or nearly-empty stomach suggests a longer time period between eating and death (Batten, 1995). However, there are numerous mitigating factors to take into account: the extent to which the food had been chewed, the amount of fat and protein present, physical activity undertaken by the victim prior to death, mood of the victim, physiological variation from person to person. All these factors affect the rate at which food passes through the digestive tract. Pathologists are generally hesitant to base a precise time of death on the evidence of stomach contents alone.

[edit] Detection and Classification

[edit] Gas chromatography

Gas-liquid chromatography is of particular use in examining gases, or substances that can be heated to produce a gas. Volatile organic compounds fall into this category.

[edit] Detection of Metals

The compounds suspected of containing a metal is traditionally separated by the destruction of the organic matrix by chemical or thermal oxidation. This leaves the metal to be identified and quantified in the inorganic residue, and it can be detected using such methods as the Reinsch test, emission spectroscopy or X-ray diffraction. Unfortunately, while this identifies the metals present it removes the original compound, and so hinders efforts to determine what may have been ingested. The toxic effects of various metallic compounds can vary considerably.

[edit] Nonvolatile organic substances

Drugs, both prescribed and illegal, pesticides, natural products, pollutants and industrial compounds are some of the most common compounds encountered. Screening methods include thin-layer chromatography, gas-liquid chromatography. For complete legal identification, a second confirmatory test is usually also required. This is usually a spot test (see Pill testing), typically the Marquis Reagent, Mecke Reagent, and Froehde's Reagent for opiates, Marquis Reagent and Simon's reagent for amphetamine, methamphetamine and other analogs, like MDMA, the Scott's test for cocaine, and the modified Duquinois reagent for marijuana and other cannabinoids. For compounds that don't have a common spot test, like benzodiazepines, another test may be used, typically mass spectroscopy, or spectrophotometry.

[edit] Miscellaneous

Venoms and other toxic mixtures of proteins or uncharacterised constituents are difficult to detect. Immunoassay may be the most practical means of detecting and measuring these highly potent and difficult to isolate substances, if antibodies can be grown against the active constituent. Most frequently, specific analytic procedures must be developed for each analyte of this type.

[edit] External Links

[edit] See also

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