PubMed Health⌕ Search

SEARCH · PubMed Health

Results for “Radiation, Nonionizing”

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 703 records · Page 39Linked to original sources

Assessment of bone density using ultrasonic backscatter.

The goal of this project was to investigate the utility of ultrasonic backscatter for the assessment of bone status. Ultrasound offers a low-cost, portable, nonionizing alternative or complement to common X-ray- or radioisotope (gamma ray)-based methods of bone densitometry. Ultrasonic backscatter may provide useful information not revealed by ultrasonic attenuation and sound-speed densitometers. Backscatter is sensitive to microstructural variations in acoustic impedance and should therefore provide information regarding architecture (which is related to fracture risk), as well as density. Ultrasonic backscatter at 2.25 MHz and CT bone densitometric data have been acquired from 10 healthy human volunteers. The degree of correlation between CT and ultrasonic backscatter is high (r = 0.87, p < 0.001). The envelope signal-to-noise ratio was 1.81 +/- 0.08 (mean +/- standard deviation). This suggests that the number of scatterers per resolution cell is large, the radiofrequency signal approximately obeys circular Gaussian statistics, and the envelope obeys Rayleigh statistics. These results indicate promise for ultrasonic backscatter as a substitute for or an adjunct to other ultrasonic measurements (attenuation and sound speed) and X-ray measurements for the assessment of bone status.

Adult↗

Coil-globule transition of DNA molecules induced by cationic surfactants: a dynamic light scattering study.

The compaction and aggregation of DNA induced by cationic surfactants was studied by dynamic light scattering (DLS). Furthermore, the effect on surfactant-compacted DNA of the addition of nonionic amphiphiles and salt was studied. When using sufficiently low amounts of DNA and cetyltrimethylammonium bromide (CTAB), compacted DNA molecules could be monitored by the appearance of a band characterized by lower hydrodynamic radius and by the decrease in the intensity of the peak corresponding to extended DNA molecules. Notably, we observed a region where compacted molecules coexist with extended ones; these two populations were found to be stable with time. For higher concentrations of CTAB, only compacted molecules were observed and the size of the particles increased with time indicating aggregation. The number of globules present in the coexistence region increased linearly with the surfactant concentrations, as given by the area of the band corresponding to this population, which indicates a double-cooperativity of the binding. The DLS experiments were in good agreement with previous fluorescence microscopy studies, with certain advantages over this technique since there is no need to add fluorescence dyes and antioxidants. Furthermore, it allows the study of molecules which are too small to be visualized by fluorescence microscopy.

Cations↗

Effect of the hydrophilic size on the structural phases of aqueous nonionic gemini surfactant solutions.

Aggregate structures of aqueous nonionic Gemini surfactant solutions, alpha,alpha'-[2,4,7,9-tetramethyl-5-decyne-4,7-diyl]bis[omega-hydroxyl-polyoxyethylene] with three different length polyoxyethylenes (i.e., 10, 20, and 30 ethylene oxide monomers, denoted from now on as S-10, S-20, and S-30, respectively), are investigated using small angle neutron scattering, dynamic light scattering, and fluorescence spectroscopy. For S-10 at low surfactant concentrations (Cs < 0.9 wt %), large "clusters", with an average hydrodynamic radius (RH) > 40 nm, are found to coexist with monomers. At intermediate Cs (0.9 < Cs < 2 wt %), some clusters break down forming micelles, with an (RH) approximately 2-3 nm, while the remaining clusters coexist with micelles. Increasing Cs further (>2 wt %) results in a pure micellar phase with little or no clusters present. S-20 and S-30 mixtures, on the other hand, differ from S-10 in that irrespective of surfactant concentration, large clusters and small monomers/dimers are found to coexist, while there is no direct evidence for the presence of micelles.

Light↗

A stability test of liposome preparations using steady-state fluorescent measurements.

The stability of liposome preparations under the action of the nonionic detergent Triton X-100 was measured using the fluorescent molecular probe octadecylrhodamine B (R18). The probe inserted in the lipid bilayer shows a self-quenched fluorescence and the degree of quenching depends both on the probe concentration and the phase state of the lipid membrane. The addition of detergent to the liposomes produces a steep decrease in self-quenching caused by dilution of the probe in the bilayer. The curves of steady-state fluorescence intensity show an abrupt change in slope that corresponds to the point at which liposomes break down into lipid-detergent mixed entities that are different from the earlier liposome-monodisperse population. The lytic process was followed in parallel by dynamic light scattering (DLS), and the analysis of the DLS results agree with the interpretation of the fluorescence measurements. The probe R18 therefore is a useful marker to test the stability of liposome preparations. The advantages of the present method are discussed by comparison with other techniques.

1,2-Dipalmitoylphosphatidylcholine↗

Functional imaging in computed tomography. The use of contrast-enhanced computed tomography for the study of renal function and physiology.

RATIONALE AND OBJECTIVES: Computed tomography (CT) numbers may provide the raw material for calculations of important physiologic parameters, such as organ regional perfusion and glomerular filtration rate. Because, except in cases of severe renal dysfunction, iodinated intravascular contrast agents are excreted primarily by passive glomerular filtration, the decline in their concentration in blood or tissues will reflect renal function. The time evolution of contrast agent distribution within the kidney, from blood to tubules, can also be seen as a measure of renal function. The authors illustrate how CT numbers may be employed to obtain useful data regarding renal function. METHODS: Two CT methods were used to yield information on renal function. Delayed CT: 2 hours after administration of 200 mL of a contrast agent (iohexol) for a routine CT, a patient with normal renal function was brought back to the scanner, and a single fixed section through the abdomen, including the psoas muscles, was imaged; the scan was repeated at 2, 3, and 4 hours. Large regions of interest were selected in soft tissue, and six measurements of CT numbers were taken and averaged for each time; after taking logs, these were plotted against time. Dynamic CT: A rapid bolus of 40 mL nonionic contrast agent was injected into an antecubital vein at 5 mL/sec. At a fixed level, images were taken through the center of the kidneys at 5-second intervals for 2 minutes after injection. The patient was allowed to breathe gently throughout the examination. Regions of interest were selected over the kidney and the aorta, and curves of CT numbers against time were generated; a Patlak plot was performed using the parameters measured. Using the renal CT numbers collected during the first 2 minutes after injection, it was possible to analyze the handling of the contrast agent and to obtain a measure of the glomerular filtration rate. RESULTS: Delayed CT: Data yielded good values for glomerular filtration rate; the typical patient illustrated had a glomerular filtration rate per unit extracellular fluid volume of 0.005 min-1. Dynamic CT: The correlation coefficient for the line fit was 0.97, a value typically found in these studies, indicating the efficacy and ruggedness of this method in spite of the patient's shallow breathing throughout the examination. CONCLUSIONS: Computed tomography offers the potential for quantitative and physiologic measurement that has not been widely explored. The problem with the delayed CT technique is that since measurements are made at 2 hours and onward, it is applicable only to patients who have received larger doses of contrast. Otherwise, the CT numbers are low and the measurement error, large. Also, bringing the patient back to the scanner 2 hours later may be inconvenient to both patient and radiologist, and may disrupt case scheduling. This method is, however, less inconvenient than the established blood-level measurement. The dynamic CT method yields a new measure of renal clearance, namely, clearance per unit volume of kidney. The disadvantages of this method are the radiation burden involved in repeated rapid CT scans and the fact that, if renal disease is uneven, a nonrepresentative slice could be chosen. Its advantages are its simplicity and that it can be completed within the first 2 minutes of a CT examination. It may be expected to have an interesting application to situations in which there is known renal disease. Although difficulties are associated with both of these techniques that could prevent their general adoption as clinical routines, they nevertheless should find application in selected patients and should prove useful research tools in the study of renal disease.

Contrast Media↗

New sterically stabilized vesicles based on nonionic surfactant, cholesterol, and poly(ethylene glycol)-cholesterol conjugates.

Monomethoxypoly(ethylene glycol) cholesteryl carbonates (M-PEG-Chol) with polymer chain molecular weights of 1000 (M-PEG1000-Chol) and 2000 (M-PEG2000-Chol) have been newly synthesized and characterized. Their aggregation behavior in mixture with diglycerol hexadecyl ether (C16G2) and cholesterol has been examined by cryotransmission electron microscopy, high-performance gel exclusion chromatography, and quasielastic light scattering. Nonaggregated, stable, unilamellar vesicles were obtained at low polymer levels with optimal shape and size homogeneity at cholesteryl conjugate/ lipids ratios of 10 mol% M-PEG1000-Chol or 5 mol% M-PEG2000-Chol, corresponding to the theoretically predicted brush conformational state of the PEG chains. At 20 mol% M-PEG1000-Chol or 10 mol% M-PEG2000-Chol, the saturation threshold of the C16G2/cholesterol membrane in polymer is exceeded, and open disk-shaped aggregates are seen in coexistence with closed vesicles. Higher levels up to 30 mol% lead to the complete solubilization of the vesicles into disk-like structures of decreasing size with increasing PEG content. This study underlines the bivalent role of M-PEG-Chol derivatives: while behaving as solubilizing surfactants, they provide an efficient steric barrier, preventing the vesicles from aggregation and fusion over a period of at least 2 weeks.

Cholesterol↗

Affinity precipitation of proteins by surfactant-solubilized, ligand-modified phospholipids.

The use of ligand-modified phospholipids solubilized in aqueous solution by nonionic surfactant for affinity precipitation of proteins is described. Avidin was precipitated by contact with solutions in which dimyristoylphosphatidylethanolamine (DMPE) functionalized with biotin (DMPE-B) was solubilized in octaethylene glycol mono-n-dodecyl ether (C12E8) solutions. The nonionic surfactant solubilizes the phospholipid in micelles above its critical micelle concentration (CMC) and in small submicellar aggregates below this concentration. At C12E8 concentrations significantly exceeding its CMC, determined to be about 100 microM, precipitation of avidin by solubilized DMPE-B is not observed. In this regime, binding of protein by DMPE-B was monitored by a hyperchroic shift in the protein's UV-visible spectrum at 231.5 nm. The data were analyzed using a model that considers the four binding sites on the protein to be independent and identical in binding strength for DMPE-B. Below the CMC of C12E8, precipitation is observed and is monitored by increasing turbidity of the solution. The kinetics of precipitation and the aggregate size measured by quasielastic light scattering were analyzed using Smoluchowski kinetics and the Mie scattering theory. These results help establish more completely the factors that influence the precipitation of proteins by ligand-modified phospholipids, and they are helpful in specifying conditions for the precipitation of other proteins.

Avidin↗

An implanted spherical head model exposed to electromagnetic fields at a mobile communication frequency.

Can cellular phones and personal communication systems base station antennas affect the active or passive implantable medical devices adversely? Concerns over the possible harmful effects of nonionizing irradiaton upon implanted medical devices have been present for many years. Key issues to address are the questions of whether mobile phones have a detrimental effect on implants, and how the interaction of the handset with the body can be minimized in order to both alleviate public fears and improve handset antenna performance and new implant designs. This paper presents a thorough investigation of the scattering of an electromagnetic (EM) wave from a perfectly conducting implant (a cylindrical wire and a very thin cylindrical disk) of electrically small radius (of resonant length), embedded eccentrically into a dielectric spherical head model by a dipole antenna (0.4 wavelength) at 900 MHz. The dyadic Green's function (DGF) for spherical vector wave functions is employed. Analytical expressions for the scattered fields of an implant embedded head model is obtained. Numerical results from analytical expressions are computed for this problem and then compared with the results from the same model using the finite-difference time-domain, EMU-FDTD electromagnetic simulator. Good agreement is observed between the analytical results on the proposed method in comparison with the FDTD method.

Cell Phone↗

Interaction of nonionic detergents with phospholipids in hepatic microsomes at subsolubilizing concentrations as studied by 31P-NMR.

The effect of low concentrations of nonionic detergents with different critical micelle concentrations such as Triton X-100, Brij 35 and octylglucoside on rabbit liver microsomes is studied by means of 31P-NMR, 1H-NMR, dynamic light scattering and functional investigations. Hexane phosphonic acid diethyl ester was used as a phosphorus membrane probe molecule to monitor the interaction of detergent molecules with microsomal phospholipids by 31P-NMR. This method is more sensitive than 31P-NMR of phospholipids alone and permitted the estimation of the maximum number of detergent molecules which can be incorporated in microsomes without the formation of mixed micelles outside the membrane. These membrane saturation concentrations were determined to be 0.07 (Brij 35), 0.1 (Triton X-100) and 0.4 (octylglucoside) (molar ratio of detergent/total phospholipids). Above these detergent concentrations, mixed micelles consisting of detergent and membrane constituents are formed, coexisting with the microsomes up to the membrane solubilization concentration. The results indicate a dependence of the membrane saturation concentration on the critical micelle concentration of the detergent and a preferential removal of phosphatidylcholine over phosphatidylethanolamine from the microsomes by all detergents studied.

Animals↗

Interaction of nonionic PEO-PPO diblock copolymers with lipid bilayers.

The relationship between the molecular architecture of a series of poly(ethylene oxide)-b-poly(propylene oxide) (PEO-PPO) diblock copolymers and the nature of their interactions with lipid bilayers has been studied using small- and wide-angle X-ray scattering (SAXS and WAXS) and differential scanning calorimetry (DSC). The number of molecular repeat units in the hydrophobic PPO block has been found to be a critical determinant of the nature of diblock copolymer-lipid bilayer association. For dimyristoyl-sn-glycero-3-phosphocholine (DMPC)-based biomembrane structures, polymers whose PPO chain length approximates that of the acyl chains of the lipid bilayer yield highly ordered, expanded lamellar structures consistent with well-integrated (into the lipid bilayer) PPO blocks. Shorter diblock copolymers produce mixed lamellar and nonlamellar mesophases. The thermotropic phase behavior of the polymer-doped membrane systems is highly influenced by the presence and molecular architecture of the diblock copolymer, as evidenced by shifting of the main phase transition to higher temperatures, broadening of the main transition, and the appearance of other features. Studies of temperature-induced changes in the mesophase structure for compositions prepared with well-integrated PEO-PPO polymers indicate that they undergo reversible changes to a nonlamellar structure as the temperature is lowered. Increasing either the number of repeat units in the PEO block or the polymer concentration promotes a greater degree of structural ordering.

Biocompatible Materials↗

Flow cytometric discrimination of mitotic cells: resolution of M, as well as G1, S, and G2 phase nuclei with mithramycin, propidium iodide, and ethidium bromide after fixation with formaldehyde.

Cells in mitosis can be flow cytometrically discriminated from G1, S, and G2 cells by analysis of a nuclear suspension prepared with nonionic detergent, fixed with formaldehyde, and stained with mithramycin, propidium iodide, or ethidium bromide. With these DNA-fluorochromes, the fluorescence is quenched by formaldehyde less in mitotic nuclei than in interphase nuclei. Mitotic nuclei have a 20-40% increased mithramycin fluorescence and 30-60% decreased light scatter in comparison to those of G2 nuclei. There is a high correlation (r = 0.95; P less than 0.001) between microscope counts of mitotic figures in smear preparations of the initial cell suspension and the flow cytometrically estimated fraction of nuclei with increased mithramycin fluorescence. Flow sorting (FACS) demonstrates that the mitotic nuclei are confined to the peak of increased mithramycin fluorescence and decreased light scatter. The method has been applied to cultures of Yoshida ascites tumor cells, JB-1 reticulosarcoma cells, and PHA-stimulated human lymphocytes, incubated in the presence or absence of vinblastine for mitotic arrest. In a heteroploid mixture of fixed Yoshida (near-diploid) and JB-1 (hypotetraploid) nuclei, the mitotic fractions of the two cell lines could be estimated separately when analyzed with mithramycin fluorescence versus light scatter or with mithramycin fluorescence versus propidium iodide fluorescence.

Animals↗

Flow cytometric analysis of the cellular toxicity of tributyltin.

Flow cytometric and light/fluorescence microscopic analyses indicate that tributyltin (TBT) alters the plasma membrane/cytoplasm complex of the murine erythroleukemic cell (MELC) in a dose-dependent and time-dependent manner. The flow cytometric parameter axial light loss, a measure of cell volume, decreases in cells exposed to 5 microM TBT relative to control cells or cells exposed to 50 microM TBT. The flow cytometric parameter 90 degrees light scatter, a function of refractive index and a measure of protein content, increases as a function of TBT concentration above 0.5 microM. Following exposure to TBT concentrations greater than 0.5 microM, but less than 50 microM, DNA distribution across the cell cycle cannot be resolved adequately by flow cytometry. Also, the cells become resistant to solubilization of the cell membrane/cytoplasm complex by nonionic detergents. Relative to logarithmically growing cells, MELC in the stationary phase of the growth cycle and butyric acid-differentiated cells exhibit decreased plasma membrane permeability resulting in increased carboxyfluorescein (CF) retention derived from the intracellular hydrolysis of carboxyfluorescein diacetate (CFDA). Similarly, cells exposed to TBT concentrations below 50 microM exhibit increased cellular CF retention. Viability in terms of CFDA hydrolysis/CF retention and propidium iodide (PI) exclusion is not decreased by exposure to TBT concentrations below 1 microM. At doses between 5 and 50 microM, however, cells exhibit both CF and PI fluorescence simultaneously and are programmed for death. At TBT concentrations greater than 1.0 microM, MELC plasma membrane potential, measured with the cyanine dye, 3,3'-dihexyloxacarbocyanine iodide (DiOC6) decreases at the same time that the uptake of PI is observed. In conjunction with other data, the concentration-dependent increase in CF fluorescence, resistance to detergent-mediated solubilization of the plasma membrane/cytoplasm complex, and increase in 90 degrees light scatter suggest fixation (protein denaturation, cross-linking, etc.) as a mechanism of the toxic action of TBT.

Animals↗

Physicochemical and solubilization properties of N, N-dimethyl-N-(3-dodecylcarbonyloxypropyl)amineoxide: a biodegradable nonionic surfactant.

The physicochemical characteristics of N,N-dimethyl-N-(3-dodecylcar- bonyloxypropyl)amineoxide (DDCPNO), a biodegradable analogue of a N, N-dimethylalkylamine-N-oxide, are compared with those of N, N-dimethyldodecylamine-N-oxide (DDNO) to establish the effect on the properties of DDNO of inserting a propoxy linker between the hydrophobic tail and hydrophilic head region. Surface tension measurements gave a critical micelle concentration of 0.33 mM for DDCPNO compared with a value of 1.57 mM for DDNO, suggesting that the former was the more hydrophobic surfactant. This result was confirmed by laser light scattering studies in which total intensity light scattering indicated the presence of DDCPNO micelles of aggregation number 85.0. Photon correlation spectroscopy studies yielded a limiting hydrodynamic diameter of 4.0 nm in comparison with values of 57.5 and 3.3 nm obtained for the aggregation number and the limiting hydrodynamic size, respectively, of DDNO micelles. Studies demonstrated that neither a dilute aqueous solution of DDCPNO or DDNO exhibited a cloud point within the temperature range 293-373 K. Solubilization studies showed that the capacity of DDCPNO micelles for a range of drugs of varying size and polarity was less than that observed with DDNO micelles at an equivalent surfactant concentration. As a further measure of solubilization, the ability of DDCPNO to form oil-in-water microemulsions with a range of ethyl ester oils was investigated and found to be slightly higher than that achieved with DDNO. Together these studies suggest that the presence of the semipolar linker significantly alters the properties of this low molecular weight surfactant.

Alkanes↗

Transitional steps in the solubilization of protein-containing membranes and liposomes by nonionic detergent.

Membrane solubilization by dodecyl maltoside was studied, using Ca(2+)-ATPase membranes and liposome preparations as prototypes of biological membranes. In equilibrium dialysis experiments, transition from saturable incorporation of monomeric detergent into the membrane to cooperative binding already occurred at a free detergent concentration about 50% of the cmc. This transition was discontinuous for unilamellar liposomes of dioleoylphosphatidylcholine, but gradual for Ca(2+)-ATPase membranes and multilayered liposomes of sarcoplasmic reticulum lipid. Equilibrium detergent binding by Ca(2+)-ATPase membranes (expressed on the basis of lipid content) was the same as for detergent binding by multilamellar liposomes of sarcoplasmic reticulum lipid. Equilibration involving cooperative binding was considerably delayed (for many days) if detergent was presented gradually to the membranous preparations in nonmicellar form by diffusion across the dialysis membrane, while equilibration of detergent occurred rapidly if detergent in micellar form was added directly to the membrane preparations. In contrast, equilibration was rapid in both directions if detergent was added at levels below that required to initiate cooperative binding. Detergent interaction resulted in a biphasic decrease in light scattering of Ca(2+)-ATPase membranes. The first of these decreases coincided with the onset of cooperative binding, while the second one was associated with a decreased sedimentability during ultracentrifugation, i.e., with usual criteria of solubilization. The concentration at which this occurred corresponded to the level of free detergent at which lipid, after detergent solubilization, segregated from detergent after gel chromatography.(ABSTRACT TRUNCATED AT 250 WORDS)

Animals↗

[Spiral computerized tomography in the study of renal neoplasms in children].

INTRODUCTION: Different kinds of pediatric renal tumors are known, the commonest of which is Wilms' tumor or nephroblastoma; other less common tumors are nephroblastomatosis, rhabdoid malignant tumor, clear cell sarcoma, congenital mesoblastic nephroma and multilocular cystic nephroma. However, the diagnostic imaging features of all these neoplasms are very similar. Ultrasonography (US) and Computed Tomography (CT) have currently a preminent role in the diagnostic evaluation of these conditions, compared to conventional radiology. The use of Spiral Computed Tomography (spiral CT) has definitely improved the efficacy of CT and we report on the advantages of this technique in both diagnosing and staging pediatric renal tumors. MATERIAL AND METHODS: We examined 11 children with renal masses, 5 boys and 6 girls, whose age ranged 3 days to 10 years. All of them were submitted to US and CT; an abdominal plain film was previously obtained in 5 cases. Five patients were examined with conventional CT scaning, while the other 6 patients were submitted to spiral CT. CT examinations were always performed before and after i.v. administration of nonionic contrast medium (3 mL/kg). Contrast medium injection was performed manually in most cases; a mechanical injector was used only for older children, with 1 mL/s injection rate. Volume scan started at the end of manual or mechanical injection, or in some cases with a 70-second delay from the beginning of the mechanical injection. Spiral CT examinations were performed with 5-mm collimation thickness, 10 mm/s table speed (pitch = 2), 5-mm reconstruction intervals. In 4 of 6 cases studied with spiral CT a simple sedation of the patients was necessary. RESULTS: In 4 patients the abdominal plain film provided diagnostic information based on indirect signs such as bowel loops displacement by the tumor; it showed also some calcifications within the lesion in 1 of these cases and it was negative in 1 case. US allowed to detect the tumor and to evaluate its site, size and morphology in all patients. However, this technique is inaccurate in detecting abdominal lymph nodes involvement and failed to show two small cortical lesions in the contralateral kidney. CT always allowed to confirm the renal origin of the tumor, clearly showing the mass morphology and size and its intra- and extrarenal spread; moreover this technique evaluated the densitometric pattern of the mass before and after contrast medium administration. Compared to conventional CT, the spiral technique improved the enhancement of the lesion and abdominal vessels; the latter were better studied using multiplanar reconstructions (MPR). Furthermore, spiral CT detected a peritumoral pseudocapsule in 3 cases, a 5-mm lesion of the contralateral kidney in 1 case and abdominal lymph nodes involvement in 1 case. Angiography was performed in 2 patients to assess the presence of hemorrhagic components within the lesion and the possibility of preoperative embolization. DISCUSSION: CT is currently the technique of choice in the diagnosis and staging of renal masses in children, since it allows to recognize lesion site, size and densitometric patterns and provides an excellent visualization of surrounding structures (vessels and lymph nodes). Spiral CT further improves the examination quality, reducing the sedation time and requiring lower radiation doses. The use of MPR improves the depiction of great vessels and permits to detect venous thrombosis. Finally, synchronous lesions in the contralateral kidney and metastases to the liver and lungs are more easier to show.

Child↗

Solubilizing effects caused by the nonionic surfactant dodecylmaltoside in phosphatidylcholine liposomes.

The interaction of the nonionic surfactant dodecylmaltoside (DM) with phosphatidylcholine liposomes was investigated. Permeability alterations were detected as a change in 5(6)-carboxyfluorescein released from the interior of vesicles and bilayer solubilization as a decrease in the static light scattered by liposome suspensions. This surfactant showed higher capacity to saturate and solubilize PC liposomes and greater affinity with these structures than those reported for the octyl glucoside. At subsolubilizing level an initial maximum in the bilayer/water partitioning (K) followed by an abrupt decrease of this parameter occurred as the effective molar ratio of surfactant to phospholipid in bilayers (Re) rose. However, at solubilizing level a direct dependence was established between both parameters. A direct correlation took place in the initial interaction steps (Re up to 0.28) between the growth of vesicles, their fluidity, and Re. A similar direct dependence was established during solubilization (Re range from 0.9 to 1.7) between the decrease in both the surfactant-PC aggregate size, the light scattering of the system, and Re (composition of aggregates). The fact that the free DM concentration at subsolubilizing and solubilizing levels showed values lower than and similar to its critical micelle concentration indicates that permeability alterations and solubilization were determined, respectively, by the action of surfactant monomer and by the formation of mixed micelles.

Fluoresceins↗

Radio frequency electromagnetic fields: cancer, mutagenesis, and genotoxicity.

We present critiques of epidemiologic studies and experimental investigations, published mostly in peer-reviewed journals, on cancer and related effects from exposure to nonionizing electromagnetic fields in the nominal frequency range of 3 kHz to 300 GHz of interest to Subcommittee 4 (SC4) of the International Committee on Electromagnetic Safety (ICES). The major topics discussed are presented under the headings Epidemiologic and Other Findings on Human Exposure, Mammals Exposed In Vivo, Mammalian Live Tissues and Cell Preparations Exposed In Vitro, and Mutagenesis and Genotoxicity in Microorganisms and Fruit Flies. Under each major topic, we present minireviews of papers on various specific endpoints investigated. The section on Epidemiologic and Other Findings on Human Exposure is divided into two subsections, the first on possible carcinogenic effects of exposure from emitters not in physical contact with the populations studied, for example, transmitting antennas and other devices. Discussed in the second subsection are studies of postulated carcinogenic effects from use of mobile phones, with prominence given to brain tumors from use of cellular and cordless telephones in direct physical contact with an ear of each subject. In both subsections, some investigations yielded positive findings, others had negative findings, including papers directed toward experimentally verifying positive findings, and both were reported in a few instances. Further research on various important aspects may resolve such differences. Overall, however, the preponderance of published epidemiologic and experimental findings do not support the supposition that in vivo or in vitro exposures to such fields are carcinogenic.

Animals↗

Interactions between a nonionic gemini surfactant and cyclodextrins investigated by small-angle neutron scattering.

The microstructure of complexes between hydroxypropyl-cyclodextrins (HPCDs) (alpha, beta, and gamma) and a novel gemini surfactant has been investigated by small-angle neutron scattering (SANS). This nonionic hetero-gemini surfactant (denoted NIHG750) contains two hydrophobic groups and two hydrophilic groups. One is a methyl-capped polyoxyethylene chain with 16 oxyethylene units and the other is a secondary hydroxyl group. Various form factor models have been considered for fitting the SANS data. Spherical aggregates (25 to 40 A) with a size slightly larger than that of NIHG750 micelles (about 23 A) appear in mixed systems. These could be micellar aggregates partly covered with a few cyclodextrin molecules. In addition, the results indicate rod formation (r approximately 8 A, L approximately 70 A) for the NIHG-HPCD complexes. This result is consistent with the threading of HPCDs onto NIHG750 to such an extent that the surfactant molecule takes an extended conformation at high levels of HPCD. Also, the results indicate that HPCDs may interact with the oxyethylene groups of the spherical micellar aggregates leading to an increase in micelle size and a gradual transformation to rod-shaped aggregates. The tendency to form rods increases in the order gamma-CD<alpha-CD<beta-CD. An increase in HPCD concentration results in an increased amount of rods in the system. All spherical aggregates disappear at relative amounts of HPbetaCD above 4 to 5 (molar ratio). However, for HPalphaCD and HPgammaCD spherical aggregates coexist with rod shaped aggregates in the whole range of concentrations investigated here.

Cyclodextrins↗