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"LD50" redirects here. For other uses, see LD50 (disambiguation).

In toxicology, the median lethal dose, LD50 (abbreviation for “lethal dose, 50%”), LC50 (lethal concentration, 50%) or LCt50 (lethal concentration & time) of a toxin, radiation, or pathogen is the dose required to kill half the members of a tested population after a specified test duration. LD50 figures are frequently used as a general indicator of a substance's acute toxicity. The test was created by J.W. Trevan in 1927.[1] The term semilethal dose is occasionally used with the same meaning, in particular in translations from non-English-language texts, but can also refer to a sublethal dose; because of this ambiguity, it is usually avoided. LD50 is usually determined by tests on animals such as laboratory mice. In 2011 the U.S. Food and Drug Administration approved alternative methods to LD50 for testing the cosmetic drug BOTOX.[2][3]


The LD50 is usually expressed as the mass of substance administered per unit mass of test subject, typically as milligrams of substance per kilogram of body mass, but stated as nanograms (suitable for botulinum), micrograms, milligrams, or grams (suitable for paracetamol) per kilogram as toxicity decreases. Stating it this way allows the relative toxicity of different substances to be compared, and normalizes for the variation in the size of the animals exposed (although toxicity does not always scale simply with body mass).

The choice of 50% lethality as a benchmark avoids the potential for ambiguity of making measurements in the extremes and reduces the amount of testing required. However, this also means that LD50 is not the lethal dose for all subjects; some may be killed by much less, while others survive doses far higher than the LD50. Measures such as "LD1" and "LD99" (dosage required to kill 1% or 99%, respectively, of the test population) are occasionally used for specific purposes.[4]

Lethal dosage often varies depending on the method of administration; for instance, many substances are less toxic when administered orally than when intravenously administered. For this reason, LD50 figures are often qualified with the mode of administration, e.g., "LD50 i.v."

The related quantities LD50/30 or LD50/60 are used to refer to a dose that without treatment will be lethal to 50% of the population within (respectively) 30 or 60 days. These measures are used more commonly within Radiation Health Physics, as survival beyond 60 days usually results in recovery.

A comparable measurement is LCt50, which relates to lethal dosage from exposure, where C is concentration and t is time. It is often expressed in terms of mg-min/m³. LCt50 is the dose that will cause incapacitation rather than death. These measures are commonly used to indicate the comparative efficacy of chemical warfare agents, and dosages are typically qualified by rates of breathing (e.g., resting = 10 l/min) for inhalation, or degree of clothing for skin penetration. The concept of Ct was first proposed by Fritz Haber and is sometimes referred to as Haber's Law, which assumes that exposure to 1 minute of 100 mg/m³ is equivalent to 10 minutes of 10 mg/m³ (1 × 100 = 100, as does 10 × 10 = 100).

Some chemicals, such as hydrogen cyanide, are rapidly detoxified by the human body, and do not follow Haber's Law. So, in these cases, the lethal concentration may be given simply as LC50 and qualified by a duration of exposure (e.g., 10 minutes). The Material Safety Data Sheets for toxic substances frequently use this form of the term even if the substance does follow Haber's Law.

For disease-causing organisms, there is also a measure known as the median infective dose and dosage. The median infective dose (ID50) is the number of organisms received by a person or test animal qualified by the route of administration (e.g., 1,200 org/man per oral). Because of the difficulties in counting actual organisms in a dose, infective doses may be expressed in terms of biological assay, such as the number of LD50's to some test animal. In biological warfare infective dosage is the number of infective doses per minute for a cubic meter (e.g., ICt50 is 100 medium doses - min/m³).


As a measure of toxicity, LD50 is somewhat unreliable and results may vary greatly between testing facilities due to factors such as the genetic characteristics of the sample population, animal species tested, environmental factors and mode of administration.[5]

There can be wide variability between species as well; what is relatively safe for rats may very well be extremely toxic for humans, and vice versa. For example, chocolate, harmless to humans, is known to be toxic to many animals. When used to test venom from venomous creatures, such as snakes, LD50 results may be misleading due to the physiological differences between mice, rats, and humans. Many venomous snakes are specialized predators on mice, and their venom may be adapted specifically to incapacitate mice; and mongooses may be exceptionally resistant. While most mammals have a very similar physiology, LD50 results may or may not be directly relevant to humans.

A low LD50 in animals may still be a cause for concern for humans, and a high animal value does not guarantee that a substance is similarly harmful to humans.


NOTE: Comparing substances (especially drugs) to each other by LD50 can be misleading in many cases due (in part) to differences in effective dose (ED50). Therefore, it is more useful to compare such substances by therapeutic index, which is simply the ratio of LD50 to ED50.

The following examples are listed in reference to LD50 values, in descending order, and accompanied by LC50 values, {bracketed}, when appropriate.

Substance Animal, Route LD50
LD50 : g/kg
{LC50 : g/L}
Water rat, oral >Template:Number table sorting/Qyes/090,000 mg/kg >90 [6]
Sucrose (table sugar) rat, oral Template:Number table sorting/Qyes/029,700 mg/kg 29.7 [7]
Monosodium glutamate (MSG) rat, oral Template:Number table sorting/Qyes/016,600 mg/kg 16.6 [8]
Vitamin C (ascorbic acid) rat, oral Template:Number table sorting/Qyes/011,900 mg/kg 11.9 [9]
Cyanuric acid rat, oral Template:Number table sorting/Qyes/07,700 mg/kg 7.7 [10]
cadmium sulfide rat, oral Template:Number table sorting/Qyes/07,080 mg/kg 7.08 [11]
Grain alcohol (ethanol) rat, oral Template:Number table sorting/Qyes/07,060 mg/kg 7.06 [12]
sodium isopropyl methylphosphonic acid (IMPA, metabolite of sarin) rat, oral Template:Number table sorting/Qyes/06,860 mg/kg 6.86 [13]
Melamine rat, oral Template:Number table sorting/Qyes/06,000 mg/kg 6 [10]
Melamine cyanurate rat, oral Template:Number table sorting/Qyes/04,100 mg/kg 4.1 [10]
Sodium molybdate rat, oral 4,000 mg/kg 4 [14]
Table Salt rat, oral 3,000 mg/kg 3 [15]
Paracetamol (acetaminophen) rat, oral 1,944 mg/kg 1.944 [16]
Delta-9-tetrahydrocannabinol (THC) rat, oral 1,270 mg/kg 1.270 [17]
Metallic Arsenic rat, oral 763 mg/kg 0.763 [18]
Alkyl dimethyl benzalkonium chloride (ADBAC) rat, oral
fish, immersion
aq. invertebrates, imm.
304.5 mg/kg
{0.28 mg/L}
{0.059 mg/L}
Coumarin (benzopyrone, from Cinnamomum aromaticum and other plants) rat, oral 293 mg/kg 0.293 [20]
Aspirin (acetylsalicylic acid) rat, oral 200 mg/kg 0.2 [21]
Caffeine rat, oral 192 mg/kg 0.192 [22]
Arsenic trisulfide rat, oral 185–6,400 mg/kg 0.185 [23]
Sodium nitrite rat, oral 180 mg/kg 0.18 [24]
Bisoprolol mouse, oral 100 mg/kg 0.1 [25]
Cobalt(II) chloride rat, oral 80 mg/kg 0.08 [26]
Cadmium oxide rat, oral 72 mg/kg 0.072 [27]
Sodium fluoride rat, oral 52 mg/kg 0.052 [28]
Nicotine rat, oral
mice, oral
50 mg/kg
3.3 mg/kg
Pentaborane human, oral <50 mg/kg <0.05 [31]
Capsaicin mouse, oral 47.2 mg/kg 0.0472 [32]
Mercury(II) chloride rat, dermal 41 mg/kg 0.041 [33]
Lysergic acid diethylamide (LSD) rat, intravenous 16.5 mg/kg 0.0165 [34]
Arsenic trioxide rat, oral 14 mg/kg 0.014 [35]
Metallic Arsenic rat, intraperitoneal 13 mg/kg 0.013 [36]
Sodium cyanide rat, oral 6.4 mg/kg 0.0064 [37]
White phosphorus rat, oral 3.03 mg/kg 0.00303 [38]
Strychnine human, oral 1–2 mg/kg(estimated) 0.001 [39]
Cantharidin human, oral 0.5 mg/kg 0.0005
Aflatoxin B1 (from Aspergillus flavus) rat, oral 0.48 mg/kg 0.00048 [40]
Venom of the Inland Taipan (Australian snake) rat, subcutaneous Template:Number table sorting/Qyes/025 µg/kg 0.000025 [41]
Ricin rat, intraperitoneal
rat, oral
Template:Number table sorting/Qyes/022 μg/kg
20–30 mg/kg
Dioxin (TCDD) rat, oral Template:Number table sorting/Qyes/020 µg/kg 0.00002 [43]
Sarin mouse, subcutaneous injection Template:Number table sorting/Qyes/017.23 µg/kg (estimated) 0.0000172 [44]
VX human, oral, inhalation, absorption through skin/eyes Template:Number table sorting/Qyes/02.3 µg/kg (estimated) 0.0000023 [45]
Batrachotoxin (from poison dart frog) human, sub-cutaneous injection Template:Number table sorting/Qyes/02-7 µg/kg (estimated) 0.000002 [46]
Maitotoxin mouse, intraperitoneal Template:Number table sorting/Qyes/00.13 µg/kg 0.00000013 [47]
Polonium-210 human, inhalation Template:Number table sorting/Qyes/010 ng/kg (estimated) 0.00000001 [48]
Botulinum toxin (Botox) human, oral, injection, inhalation Template:Number table sorting/Qyes/01 ng/kg (estimated) 0.000000001 [49]
Ionizing radiation human, irradiation 3-6 Gy

Animal rights concerns

Animal-rights and animal-welfare groups, such as Animal Rights International,[50] have campaigned against LD50 testing on animals in particular as, in the case of some substances, causing the animals to die slow, painful deaths. Several countries, including the UK, have taken steps to ban the oral LD50, and the Organization for Economic Co-operation and Development (OECD) abolished the requirement for the oral test in 2001 (see Test Guideline 401, Trends in Pharmacological Sciences Vol 22, February 22, 2001).

See also

Other measures of toxicity

Related measures

  • TCID50 Tissue Culture Infective Dosage
  • EID50 Egg Infective Dosage
  • ELD50 Egg Lethal Dosage
  • Plaque forming units (pfu)


External links

  • Canadian Centre for Occupational Health and Safety

pl:LD 50 ru:LD50

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