PubMed HealthSearch

SEARCH · PubMed Health

Results for “Particle Accelerators”

Explore indexed PubMed citations for clinical trials, systematic reviews and public health research. Read source abstracts and follow each citation to its original PubMed record.

Quote a phrase for an exact phrase match. Source license links do not imply unrestricted reuse.

At least 37 records · Page 2Linked to original sources

Accelerated heavy particles and the lens. V. Theoretical basis of cataract enhancement by dose fractionation.

That accelerated heavy ions are highly cataractogenic is indisputable. The basis of heavy particle effectiveness and the augmentation by fractionation, as recently demonstrated, remains less clear. There is no question, however, that these are tied to the 'track structure' and densely ionizing nature of the radiation. The unique energy deposition characteristics relating to charge and track structure are now being explored to begin to dissect the cellular response of the lens epithelium to radiation exposure. The elucidation of the basis of the cataractogenic effect of accelerated heavy ions is important not only to risk assessment, but also in the consideration of theories of radiation action and the mechanism of cortical opacification arising from a myriad of cataractotoxic agents.

Animals

Therapeutic radionuclides: production and decay property considerations.

The development of effective therapeutic radiopharmaceuticals requires careful consideration in the selection of the radionuclide. The in vivo targeting and clearance properties of the carrier molecule must be balanced with the decay properties of the attached radionuclide. Radionuclides for therapeutic applications fall into three general categories: beta-particle emitters, alpha-particle emitters, and Auger and Coster-Kronig-electron emitters following electron capture. Alpha particles and Auger electrons deposit their energy over short distances with a high LET that limits the ability of cells to repair damage to DNA. Despite their high levels of cytotoxicity, the relatively short range of alpha particles requires binding of the carrier molecule to most cancer cells within a tumor in order to be effective. Because of the extremely short range of Auger electrons, the radionuclide must be carried directly into the nucleus to elicit high radiotoxicity, making it necessary to deliver the radionuclide to every cell within a tumor cell population. These characteristics impose rigid restrictions on the nature of the carrier molecules for these types of particle emitters but successful targeting of these types of radionuclides could result in high therapeutic ratios. Most beta-emitting radionuclides are produced in nuclear rectors via neutron capture reactions; however, a few are produced in charged-particle accelerators. For radionuclides produced by direct neutron activation, the quantities and specific activities that can be produced are determined in large part by the cross-section of the target isotope and the flux of the reactor. Many applications (e.g., therapeutic bone agents, radiolabeled microspheres, radiocolloids) do not require high-specific activities and can therefore utilize the wide range of radionuclides that can be produced in sufficient quantity by direct neutron activation. Other applications (e.g., MAb labeling) require high-specific activity radionuclides in order to deliver a sufficient number of radionuclide atoms to the target site without saturating the target or compromising the integrity of the carrier molecule. Most radionuclides, produced at NCA levels in reactors, are produced via indirect reactions. High-specific activity beta emitters can also be obtained from radionuclide generator systems where the longer-lived parent radionuclide may be obtained from direct neutron activation, as a fission product, or from charged-particle accelerators. It is essential that the half-life of a radionuclide used in RNT be compatible with the rates of localization in target tissues and clearance of the carrier molecule from normal tissues. This consideration is especially important for the various MAbs and their fragments that are currently under investigation as carrier molecules to RIT.(ABSTRACT TRUNCATED AT 400 WORDS)

Half-Life

Detection of infrasound by the Atlantic cod.

Below about 50 kHz the level of ambient noise in the sea increases continuously towards lower frequencies. In the infrasound range the spectral slope is particularly steep. This low-frequency noise may propagate long distances with little attenuation, causing a directional pattern of infrasound in the sea. Using a standing-wave acoustic tube, we have studied the sensitivity of cod to infrasound down to 0.1 Hz by means of the cardiac conditioning technique. The threshold values, measured as particle acceleration, showed a steady decline towards lower frequencies below 10 Hz, reaching a value close to 10(-5)ms-2 at 0.1 Hz. The spectrum level at 0.1 Hz in the sea ranges between 120 and 180 dB (re 1 microPa), with corresponding particle accelerations from less than 10(-6) to more than 10(-4)ms-2. The sensitivity of cod is thus sufficient to detect the highest levels of ambient infrasound, and we put forward the hypothesis that fish may utilize information about the infrasound pattern in the sea for orientation during migration, probably in addition to an array of other sensory inputs.

Acoustic Stimulation

[Biophysical foundations of the effect of cosmic radiation and accelerator radiation].

This book summaries the results of numerous studies, mainly by Soviet investigators, of the characteristics of radiation effects of high energy cosmic rays and of their simulation by heavy charged particle accelerators, and also of their biological effects. It contains the first systematic presentation of data on specific hadron effects. Facts are given showing the ability of these particles to cause profound local damage in tissues and organs. There is evidence that these particles should be considered one of the main factors limiting the duration of space flights. In the book a generalized kinetic model of radiation-induced cellular damage also is presented. This model allows an explanations of the observed changes in dose related survival with increasing LET and dose-rate, based on microdosimetric conceptions.

Animals

Cyclotrons and positron emission tomography radiopharmaceuticals for clinical imaging.

Positron emission tomography (PET) requires positron-emitting radionuclides that emit 511-keV photons detectable by PET imagers. Positron-emitting radionuclides are commonly produced in charged particle accelerators, eg, linear accelerators or cyclotrons. The most widely available radiopharmaceuticals for PET imaging are carbon-11-, nitrogen-13-, and oxygen-15-labeled compounds, many of which, either in their normal state or incorporated in other compounds, serve as physiological tracers. Other useful PET radiopharmaceuticals include fluorine-18-, bromine-75-, gallium-68 (68Ga)-, rubidium-82 (82Rb)-, and copper-62 (62Cu)-labeled compounds. Many positron emitters have short half-lives and thus require on-site cyclotrons for application, and others (68Ga, 82Rb, and 62Cu) are available from radionuclides generators using relatively long-lived parent radionuclides. This review is divided into two sections: cyclotrons and PET radiopharmaceuticals for clinical imaging. In the cyclotron section, the principle of operation of the cyclotron, types of cyclotrons, medical cyclotrons, and production of radionuclides are discussed. In the section on PET radiopharmaceuticals, the synthesis and clinical use of PET radiopharmaceuticals are described.

Brain

Plasma clearance of emulsified triolein in conscious rats: effects of phosphatidylcholine species, cholesterol content and emulsion surface physical state.

In vivo clearance of an emulsified triglyceride from rat plasma is strongly influenced by the phosphatidylcholine molecular species and the cholesterol content of the emulsion. Chylomicron-sized, glycerol-tri[9,10-3H]oleate (triolein)-sonicated emulsions containing 2-3 or 9-14 mol% unesterified cholesterol and specific phosphatidylcholines (egg, dimyristoyl, dipalmitoyl, distearoyl) were prepared above the phospholipid gel----liquid crystalline transition temperatures and injected intravenously into awake, non-fasting rats in bolus doses of 1-3 mg lipid. The emulsified triolein was cleared from plasma both by lipolysis during circulation and by uptake of emulsion particles or their remnants into tissues. Increasing the cholesterol content greatly accelerated particle clearance from plasma when emulsions were made with mixed-chain (egg) phosphatidylcholine, but prolonged their circulation time when the emulsions contained saturated phosphatidylcholines. The relative amounts cleared by reticuloendothelial versus liver parenchymal cells were influenced both by the cholesterol content and the phosphatidylcholine species of the emulsions. Significant triolein lipolysis in plasma occurred only with egg or dimyristoyl phosphatidylcholine emulsions containing 2-3% cholesterol and this lipolysis was blocked by increasing the cholesterol content. No lipolysis occurred when emulsions contained dipalmitoyl or distearoyl phosphatidylcholine, irrespective of cholesterol content.

Animals

Visual sensations induced by relativistic nitrogen nuclei.

The ability of the human eye to detect nitrogen nuclei that enter the retina at speeds just above the Cerenkov threshold has been confirmed in an experiment at the Princeton Particle Accelerator. A system for beam transport and subject alignment delivered individual nitrogen nuclei onto a spot 3 millimeters in diameter on the retina at a visual angle of 7 degrees on the temporal side of the fovea. The beam particles entered the retina within 25 degrees of normal and induced visual sensations that had the appearance of streaks for three out of four subjects.

Dark Adaptation

Expression of inducible angiosperm promoters in a gymnosperm, Picea glauca (white spruce).

Electrical discharge particle acceleration was used to test the transient expression of numerous inducible angiosperm promoters in a gymnosperm Picea glauca (white spruce). Promoter expression was assayed in three different tissues capable of in vitro regeneration, zygotic embryos, seedlings and embryogenic callus. The promoters tested include the light-inducible Arabidopsis and soybean ribulose-1,5-bisphosphate small subunit promoters and a maize phosphoenolpyruvate carboxylase promoter; a soybean heat-shock-inducible promoter, a soybean auxin inducible promoter and a maize alcohol dehydrogenase promoter. Promoters were cloned into a promoter-less expression vector to form a promoter-beta-glucuronidase-nopaline synthase 3' fusion. A similar construct was made using the cauliflower mosaic virus 35S (CaMV 35S) promoter as a control. All promoters were expressed in white spruce embryos, yet at levels lower than CaMV 35S. In addition, in the embryos the heat-shock and the alcohol dehydrogenase promoters showed inducible expression when given the proper induction stimulus. In seedlings, expression of all promoters was lower than in the embryos and expression was only inducible with the heat-shock promoter in the cotyledons. Of the tissues tested, the expression level of all promoters was lowest in embryogenic callus. Interestingly, the expression of the beta-glucuronidase gene in embryogenic callus was restricted to the proembryonal head cells regardless of the promoter used. These results clearly demonstrate the use of particle bombardment to test the transient expression of heterologous promoters in organized tissue and the expression of angiosperm promoters in a gymnosperm.

Cloning, Molecular

Iodination-deiodination. A radiochemical method for detection of structure and changes in structure in RNA.

Bound iodine is released from radioiodinated nucleotides in polymers exposed to sodium bisulfite. The rate of bisulfite-catalyzed deiodination of pyrimidines can be controlled both by change of temperature of pH and is also dependent on the molecular association of the nucleotide. The rate of release of iodine from iodocytidine in polycytidylate is greater than the rate of elimination from RNA. Experiments testing the influence of base-pairing of the iodopyrimidines in synthetic polynucleotides showed that pairing of the substituted nucleotide protected the iodine bond. The rates of bisulfite-catalyzed deiodination of several radioiodinated RNAs were measured. The action of bisulfite on all single stranded RNAs tested was multiphasic consisting of a rapid early deiodination reaction supplanted by a slower phase which was followed by reacceleration of release. The release of iodine from double stranded RNA and DNA-RNA duplexes was retarded in comparison with the release from ribosomal and messenger RNA fractions. The deiodination profiles of single and double stranded RNA suggested that the intermediate stage iodine release is governed by melting of paired zones of low stability. Late release may result from destablization of the molecule through the addition of bisulfite to the pyrimidine ring or deamination. The effect of several substances expected to complex with polynucleotides was tested. Acridine orange and ethidium bromide increased loss of iodine from ribosomal RNA but slightly decreased elimination from double stranded viral RNA. A basic protein fraction isolated from ribosomal particles accelerated the deiodination of ribosomal RNA. While the destabilization caused by this protein fraction was greater than that caused by an equal amount of albumin, as tested the effect was non-specific. The results show that a change in sensitivity to chemical deiodination may folow the interaction of small amounts of protein with polynucleotides.

Animals

Measurement of absorbed dose from radionuclide solutions mixed intimately with the FBX dosimeter.

Chemical dosimeters are used widely for accurate measurement of large radiation doses due to external beam irradiation from radionuclide sources and from particle accelerators. Their use for measurement of absorbed doses from radioactive solutions mixed in the dosimeter solution was reported as early as 1952, but the large activities needed to produce suitable absorbance values in the relatively insensitive dosimeters of that time discouraged further work. This manuscript reports the results of an investigation into the suitability of the ferrous sulfate-benzoic acid-xylenol orange (FBX) dosimeter for measurement of small absorbed doses caused by radionuclide solutions mixed with the dosimeter solution. The FBX dosimeter exhibited a linear dose response as a function of activity for two common radiopharmaceuticals, 99mTc sodium pertechnetate and 131I sodium iodide. Conditions under which the FBX dosimeter may be used with radionuclide solutions were studied and were found to be amenable to routine use by laboratories possessing relatively unsophisticated instrumentation. That any radionuclide could be studied using this dosimeter appears likely.

Benzoates

Spatial distribution of biological effect n a 3.9-Gev nitrogen ion beam.

A beam of nitrogen ions obtained with the Princeton Particle Accelerator was used for the irradiation of Chinese hamster (M3-1) cells in monolayer culture. The 3.9-billion-electron-volt (Gev) beam passed along the monolayer, so that ions were stopped in the culture. A sharply defined zone of extensive cell destruction occurred in the last centimeter of the beam path.

Animals

[Radiation safety in space flights in the Intercosmos program].

This paper reviews the basic stages in the development of radiation safety of space flights within the framework of the Intercosmos program, including ground-based experiments on charged particle accelerators and gamma-emitters and actual flight studies onboard biosatellites and orbital stations. The paper also discusses norms and standards of radiation safety as related to flights of varying duration. It emphasizes the contribution made by Intercosmos cooperative projects into the development of space flight radiation safety parameters adopted as standards by the USSR Standardization Committee.

Humans