A highly reactive form of the oxygen molecule (O2) formed during PDT that helps to destroy cancer cells by attacking their cell membranes.
| Medical Glossary: Singlet oxygen |
A highly reactive form of the oxygen molecule (O2) formed during PDT that helps to destroy cancer cells by attacking their cell membranes.
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| Wikipedia: Singlet oxygen |
Singlet oxygen is the common name used for the diamagnetic form of molecular oxygen (O2), which is less stable than the normal triplet oxygen. Because of its unusual properties, singlet oxygen can persist for over an hour at room temperature, depending on the environment. Because of the differences in their electron shells, singlet and triplet oxygen differ in their chemical properties. The damaging effects of sunlight on many organic materials (polymers, etc.) are often attributed to the effects of singlet oxygen.
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The chemistry of singlet oxygen is different from that of ground state oxygen. For example, singlet oxygen can participate in Diels-Alder reactions and ene reactions. It can be generated in a photosensitized process by energy transfer from dye molecules such as rose bengal, methylene blue or porphyrins, or by chemical processes such as spontaneous decomposition of hydrogen trioxide in water or the reaction of hydrogen peroxide with hypochlorite.[1] Singlet oxygen reacts with an alkene -C=C-CH- by abstraction of the allylic proton in an ene reaction type reaction to the allyl hydroperoxide HO-O-R (R = alkyl), which can then be reduced to the allyl alcohol.[2] An example is an oxygenation of citronellol:[3][4]
With some substrates dioxetanes are formed and cyclic dienes such as 1,3-cyclohexadiene form [4+2]cycloaddition adducts.[5]
In photosynthesis, singlet oxygen can be produced from the light-harvesting chlorophyll molecules. One of the roles of carotenoids in photosynthetic systems is to prevent damage caused by produced singlet oxygen by either removing excess light energy from chlorophyll molecules or quenching the singlet oxygen molecules directly.
In mammalian biology, singlet oxygen is one of the reactive oxygen species, which is linked to oxidation of LDL cholesterol and resultant cardiovascular effects. Polyphenol antioxidants can scavenge and reduce concentrations of reactive oxygen species and may prevent such deleterious oxidative effects.[6]
Ingestion of pigments capable of producing singlet oxygen with activation by light can produce severe photosensitivity of skin. This is especially a concern in herbivorous animals (see Photosensitivity in animals).
Singlet oxygen is the active species in photodynamic therapy.
Molecular orbital theory predicts two low-lying excited singlet states O2(a¹Δg) and O2(b¹Σg+) (for nomenclature see article on Molecular term symbol). These electronic states differ only in the spin and the occupancy of oxygen's two degenerate antibonding πg-orbitals (see degenerate energy level). The O2(b¹Σg+)-state is very short lived and relaxes quickly to the lowest lying excited state, O2(a¹Δg). Thus, the O2(a¹Δg)-state is commonly referred to as singlet oxygen. The energy difference between the lowest energy of O2 in the singlet state and the lowest energy in the triplet state is about 11340 kelvin (Te (a¹Δg <- X³Σg-) = 7882 cm−1, 94.3 kJ/mol.)[1] Molecular oxygen differs from most molecules in having an open-shell triplet ground state, O2(X³Σg-).
The energy difference between ground state and singlet oxygen is 94.3 kJ/mol and corresponds to a transition in the near-infrared at ~1270 nm. In the isolated molecule, the transition is strictly forbidden by spin, symmetry and parity selection rules, making it one of nature's most forbidden transitions. In other words, direct excitation of ground state oxygen by light to form singlet oxygen is very improbable. As a consequence, singlet oxygen in the gas phase is extremely long lived (72 minutes). Interaction with solvents, however, reduces the lifetime to microseconds or even nanoseconds.[7]
Direct detection of singlet oxygen is possible through its extremely weak phosphorescence at 1270 nm, which is not visible to the eye. However, at high singlet oxygen concentrations, the fluorescence of the so-called singlet oxygen dimol (simultaneous emission from two singlet oxygen molecules upon collision) can be observed as a red glow at 634 nm.[8]
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