In Vivo Analysis of Lipid-Protein Ratios in Human Muscle by Differential X-Ray Absorption Using 109Cd Photons

1972 ◽  
Vol 16 ◽  
pp. 111-123 ◽  
Author(s):  
Luther E. Preuss ◽  
Frank P. Bolin

AbstractTissue's two major components: lipid and protein, are of a primary importance, related as they are to the normal life states. Assay of protein and lipid (fat and lean) in vivo is of certain criticality in human disease states, such as wasting, edema, obesity and other dyscrasias involving body mass and fat-lean balance. Since the elemental composition of lipid and protein molecules differ in a significant and regular fashion, their mass absorption coefficients differ when radiation in the x-ray and lower energy gamma ray region is used. Two monochromatic photons, one in the 20 to 30 keV region, another in the 60 to 100 keV region, can be shown to exhibit an absorption ratio in a two component system of fat and lean which provides for a determination of the component mass ratios. Photons from x-ray machines and isotopic x- and gamma ray sources have been proposed for this. The radionuclide offers qualities of stability, small size and weight, portability, zero power consumption and, generally, a certain economy. The electron capture decay of 109Cd provides a gamma ray at 88 kilovolts and a daughter (Ag) Kα doublet at 22 keV. This fortuitous energy combination is advantageous in this differential absorptiometry. The 109Cd source provides for a stable geometry and calls for the simultaneous measurement of both photons by non-dispersive x-ray spectroscopic techniques. Ten mCi of 109Cd was incorporated into a sealed source, filtered for the silver Kβ1 x-ray (at 24. 942 keV) with 0. 1 mm palladium and collimated with a grazing aperture arrangement. Fat-lean tissue simulating standard samples three cm to ten cm in length and of various component ratios were studied. Component weight percent was determined using a function of the transmitted radiation. Determinations on water (the lean simulator) and polyethylene (the fat Simulator) as well as other materials produced absorption ratios concurring favorably with the known make-up of the Simulators.In vitro dual beam analysis of muscle tissue samples showed a high degree of correlation with the results of ether lipid extractions. Using lipid extraction values as the standard, the x-ray absorptiometric technique produced percentage lipid levels averaging within 0. 5% of the extractions.In vivo measurements of fat content of the triceps muscle area were compared with skinfold thickness measurements of the same area. Coefficient of correlation was 0. 88.

1970 ◽  
Vol 48 (12) ◽  
pp. 1514-1517 ◽  
Author(s):  
D. S. Murty ◽  
K. V. Ramana Rao ◽  
P. Jagam ◽  
V. Lakshminarayana

The evidence obtained for the existence of the K X-ray gamma-ray directional correlation by Perepelkin against the predictions of the theory of Dolginov evoked considerable interest in this field. The electron capture decay of 114Inm is used to advantage in the present investigation with a sum-peak-coincidence scintillation spectrometer. The results obtained are consistent with the theory of Dolginov.


1994 ◽  
Vol 38 ◽  
pp. 615-624
Author(s):  
Bradley E. Patt ◽  
Jan S. Iwanczyk ◽  
Martin P. Tornai ◽  
Craig S. Levin ◽  
Edward J. Hoffman

Abstract A nineteen element mercuric iodide (HgI2) detector array has been developed in order to investigate the potential of using this technology for in-vivo x-ray and gamma-ray imaging. A prototype cross-grid detector array was constructed with hexagonal pixels of 1.9 mm diameter (active area = 3.28 mm2) and 0.2 mm thick septa. The overall detector active area is roughly 65 mm2. A detector thickness of 1.2 mm was used to achieve about 100% efficiency at 60 keV and 67% efficiency at 140 keV The detector fabrication, geometry and structure were optimized for charge collection and to minimize crosstalk between elements. A section of a standard high resolution cast-lead gamma-camera collimator was incorporated into the detector to provide collimation matching the discrete pixel geometry. Measurements of spectral and spatial performance of the array were made using 241-Am and 99m-Tc sources. These measurements were compared with similar measurements made using an optimized single HgI2 x-ray detector with active area of about 3 mm2 and thickness of 500 μm.


2016 ◽  
Vol 57 (3) ◽  
pp. 210-219 ◽  
Author(s):  
Candy Y.P. Ng ◽  
Eva Y. Kong ◽  
Alisa Kobayashi ◽  
Noriyoshi Suya ◽  
Yukio Uchihori ◽  
...  

Abstract In vivo neutron-induced radioadaptive response (RAR) was studied using zebrafish ( Danio rerio ) embryos. The Neutron exposure Accelerator System for Biological Effect Experiments (NASBEE) facility at the National Institute of Radiological Sciences (NIRS), Japan, was employed to provide 2-MeV neutrons. Neutron doses of 0.6, 1, 25, 50 and 100 mGy were chosen as priming doses. An X-ray dose of 2 Gy was chosen as the challenging dose. Zebrafish embryos were dechorionated at 4 h post fertilization (hpf), irradiated with a chosen neutron dose at 5 hpf and the X-ray dose at 10 hpf. The responses of embryos were assessed at 25 hpf through the number of apoptotic signals. None of the neutron doses studied could induce RAR. Non-induction of RAR in embryos having received 0.6- and 1-mGy neutron doses was attributed to neutron-induced hormesis, which maintained the number of damaged cells at below the threshold for RAR induction. On the other hand, non-induction of RAR in embryos having received 25-, 50- and 100-mGy neutron doses was explained by gamma-ray hormesis, which mitigated neutron-induced damages through triggering high-fidelity DNA repair and removal of aberrant cells through apoptosis. Separate experimental results were obtained to verify that high-energy photons could disable RAR. Specifically, 5- or 10-mGy X-rays disabled the RAR induced by a priming dose of 0.88 mGy of alpha particles delivered to 5-hpf zebrafish embryos against a challenging dose of 2 Gy of X-rays delivered to the embryos at 10 hpf.


Antibiotics ◽  
2020 ◽  
Vol 9 (1) ◽  
pp. 25 ◽  
Author(s):  
Ioannis Ketikidis ◽  
Christina N. Banti ◽  
Nikolaos Kourkoumelis ◽  
Constantinos G. Tsiafoulis ◽  
Christina Papachristodoulou ◽  
...  

Conjugation of penicillin G (PenH) with silver(I) ions forms a new CoMeD (conjugate of metal with a drug) with formula [Ag(pen)(CH3OH)]2 (PenAg). PenAg was characterized by a plethora of physical and spectroscopic techniques, which include in the solid state m.p.; elemental analysis; X-ray fluorescence (XRF) spectroscopy; scanning electron microscopy (SEM); energy-dispersive X-ray spectroscopy (EDX); FT-IR; and in solution: attenuated total reflection spectroscopy (FT-IR-ATR), UV–Vis, 1H NMR, and atomic absorption (AA). The structure of PenAg was determined by NMR spectroscopy. Silver(I) ions coordinate to the carboxylic group of PenH, while secondary intra-molecular interactions are developed through (i) the nitrogen atom of the amide group in MeOD-d4 or (ii) the sulfur atom in the thietane ring in deuterated dimethyl sulfoxide DMSO-d6. The antibacterial activities of PenAg and the sodium salt of penicillin (PenNa) (the formulation which is clinically used) against Gram positive (Staphylococcus epidermidis (S. epidermidis) and Staphylococcus aureus (S. aureus)) and Gram negative (Pseudomonas aeruginosa (P. aeuroginosa PAO1)) bacteria were evaluated by the means of minimum inhibitory concentration (MIC), minimum bactericidal concentration (MBC), and inhibition zone (IZ). PenAg inhibits the growth of the Gram negative bacterial strain P. aeuroginosa with a MIC value of 23.00 ± 2.29 μM, in contrast to PenNa, which shows no such activity (>2 mM). The corresponding antimicrobial activities of PenAg against the Gram positive bacteria S. epidermidis and S. aureus are even better than those of PenNa. Moreover, PenAg exhibits no in vivo toxicity against Artemia salina at concentration up to 300 μΜ. The wide therapeutic window and the low toxicity, make PenAg a possible candidate for the development of a new antibiotic.


2021 ◽  
pp. 002203452110268
Author(s):  
R.M. Sulyanto ◽  
M. Kang ◽  
S. Srirangapatanam ◽  
M. Berger ◽  
F. Candamo ◽  
...  

Silver diamine fluoride (SDF) is a dental biomaterial used to arrest dental caries. To better understand SDF’s mechanism of action, we examined the localization of silver within the tissues of SDF-treated teeth. Carious primary teeth fixed within 2 min of SDF application (SDF-minutes, n = 3), at 3 wk after SDF application in vivo (SDF-weeks, n = 4), and at 2 y after multiple SDF applications in vivo (SDF-multiple, n = 1) were investigated in this study. Carious primary teeth without SDF application (no-SDF, n = 3) served as controls. Mineral density and structural analyses were performed via micro–X-ray computed tomography and scanning electron microscopy. Elemental analyses were performed through X-ray fluorescence microprobe and energy-dispersive X-ray spectroscopic techniques. SDF-treated teeth revealed higher X-ray–attenuated surface and subsurface regions within carious lesions, and similar regions were not present in no-SDF teeth. Regions of higher mineral density correlated with regions of silver abundance in SDF-treated teeth. The SDF penetration depth was approximated to 0.5 ± 0.02 mm and 0.6 ± 0.05 mm (mean ± SD) for SDF-minutes and SDF-weeks specimens, respectively. A higher percentage of dentin tubular occlusion by silver or calcium phosphate particles was observed in primary teeth treated with SDF-weeks as compared with SDF-minutes. Elemental analysis also revealed zinc abundance in carious lesions and around the pulp chamber. SDF-weeks teeth had significantly increased tertiary dentin than SDF-minutes and no-SDF teeth. These results suggest that SDF treatment on primary teeth affected by caries promotes pathologic biomineralization by altering their physicochemical properties, occluding dentin tubules, and increasing tertiary dentin volume. These seemingly serendipitous effects collectively contribute to the cariostatic activity of SDF.


1999 ◽  
Vol 09 (03n04) ◽  
pp. 279-289
Author(s):  
Satoshi Harada ◽  
Koichiro Sera ◽  
Shyoji Futatsugawa ◽  
Hirobumi Oikawa ◽  
Yoshiharu Tamakawa

The interactions between mitochondrial and nuclear Mg concentration for the development of radiation-induced apoptosis were tested IN VIVO in Sarcoma-180 in BALB/c mice. The frequency of apoptosis was expressed as a percentage of TUNEL reactivity in the 5 microscopic views under 400 times magnification, and Mg concentration in either mitochondria or nucleus was measured by Particle Induced X-ray Emission (PIXE), on 3, 6, 9, 12 and 24 hours after the 10 or 20 Gy of 60 Co gamma ray radiation, to the mice with or without the 0.01 mMOL MgCl 2 oral administration. There were proximal increases of apoptosis, which peaked on 9 hours after radiation. The Mg concentration of mitochondria strongly correlated with frequency of apoptosis from 3 to 9 hrs after radiation, and that of the nucleus strongly correlated with frequency of apoptosis from 6 to 24 hours after radiation. The oral administration of MgCl 2 did not change those correlations. The two steps are considered: 1st) signaling from mitochondria to nucleus involving Mg on induction of apoptosis; and 2nd) removal of apoptosis involving nuclear Mg .


Author(s):  
N.K.R. Smith ◽  
K.E. Hunter ◽  
P. Mobley ◽  
L.P. Felpel

Electron probe energy dispersive x-ray microanalysis (XRMA) offers a powerful tool for the determination of intracellular elemental content of biological tissue. However, preparation of the tissue specimen , particularly excitable central nervous system (CNS) tissue , for XRMA is rather difficult, as dissection of a sample from the intact organism frequently results in artefacts in elemental distribution. To circumvent the problems inherent in the in vivo preparation, we turned to an in vitro preparation of astrocytes grown in tissue culture. However, preparations of in vitro samples offer a new and unique set of problems. Generally, cultured cells, growing in monolayer, must be harvested by either mechanical or enzymatic procedures, resulting in variable degrees of damage to the cells and compromised intracel1ular elemental distribution. The ultimate objective is to process and analyze unperturbed cells. With the objective of sparing others from some of the same efforts, we are reporting the considerable difficulties we have encountered in attempting to prepare astrocytes for XRMA.Tissue cultures of astrocytes from newborn C57 mice or Sprague Dawley rats were prepared and cultured by standard techniques, usually in T25 flasks, except as noted differently on Cytodex beads or on gelatin. After different preparative procedures, all samples were frozen on brass pins in liquid propane, stored in liquid nitrogen, cryosectioned (0.1 μm), freeze dried, and microanalyzed as previously reported.


1987 ◽  
Vol 48 (C9) ◽  
pp. C9-367-C9-370
Author(s):  
C. B. COLLINS ◽  
F. DAVANLOO ◽  
T. S. BOWEN ◽  
J. J. COOGAN
Keyword(s):  

2003 ◽  
Vol 8 (5-6) ◽  
pp. 60-64
Author(s):  
A.I. Arkhangelsky ◽  
◽  
Yu.D. Kotov ◽  
P.Yu. Chistiakov ◽  
◽  
...  

2020 ◽  
Author(s):  
Marat Korsik ◽  
Edwin Tse ◽  
David Smith ◽  
William Lewis ◽  
Peter J. Rutledge ◽  
...  

<p></p><p>We have discovered and studied a <i>tele</i>substitution reaction in a biologically important heterocyclic ring system. Conditions that favour the <i>tele</i>-substitution pathway were identified: the use of increased equivalents of the nucleophile or decreased equivalents of base, or the use of softer nucleophiles, less polar solvents and larger halogens on the electrophile. Using results from X-ray crystallography and isotope labelling experiments a mechanism for this unusual transformation is proposed. We focused on this triazolopyrazine as it is the core structure of the <i>in vivo </i>active anti-plasmodium compounds of Series 4 of the Open Source Malaria consortium.</p> <p> </p> <p>Archive of the electronic laboratory notebook with the description of all conducted experiments and raw NMR data could be accessed via following link <a href="https://ses.library.usyd.edu.au/handle/2123/21890">https://ses.library.usyd.edu.au/handle/2123/21890</a> . For navigation between entries of laboratory notebook please use file "Strings for compounds in the article.pdf" that works as a reference between article codes and notebook codes, also this file contain SMILES for these compounds. </p><br><p></p>


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