scholarly journals a PENERAPAN KIMIA FORENSIK: PENGGUNAAN POLONIUM (210PO) SEBAGAI RACUN DILIHAT DARI SEGI TOKSIKOLOGI

2021 ◽  
Vol 2 (2) ◽  
pp. 38-45
Author(s):  
Endro Tri Susdarwono

This study intends to provide a description of how the use of polonium-210 (210Po) as a poison in terms of toxicology. This research is a qualitative research, the type of research uses comprehensive analytic studies and analytical normative approaches. Polonium-210 is created in nuclear reactors. This element is very radioactive which if swallowed even a little is very fatal. After entering the blood tissue, the element mainly targets the liver and kidneys and bone marrow. After 210Po is absorbed into the body, the whole body is basically targeted. The dose given and the sensitivity of individual tissues determine the level of damage throughout the body. Unlike most heavy metals, 210 Po accumulates in soft tissue rather than bone. Polonium (210Po) is a producer of very active alpha particles, but only becomes toxic when entering the body. If entered into the human body, toxic effects are often fatal, even at very small doses. Most of the initial dose is quickly excreted in the feces and urine, but the rest is distributed to the soft tissues of the body.

PEDIATRICS ◽  
1977 ◽  
Vol 59 (2) ◽  
pp. 305-308
Author(s):  
Derek Harwood-Nash ◽  
Herman Grossman ◽  
Alvin Felman ◽  
John Kirkpatrick ◽  
Leonard Swischuk

Computerized tomography (CT), a technique conceptualized by Oldendorf in 19611 and developed by Hounsfield2 of EMI-Tronics Inc. (EMI) Central Research Laboratories, has proven to be a successful innovation in neuroradiology. Reviews by Ambrose3 in England and by Baker et al.4 and by New et al.5 in the United States have clearly demonstrated the value of this new modality in neuroradiological diagnosis. In 1975 Houser et al.6 and Harwood-Nash et al.7 provided the initial clinical and radiological data about CT in infants and children. More recently this technique has been extended to the study of tissues and organs in the body other than those in the head. This has been accomplished by modification of the original machine into a whole-body CT system. Early reviews by Ledley et al.8 and by Alfidi et al.9 suggest a significant potential for diagnosis of lesions in the abdomen, pelvis, and thorax. The advantages of CT are that it is less invasive than standard special diagnostic radiological procedures and that for the first time it provides in vivo information regarding the content and the characteristics of tissue composing organs and masses. DESCRIPTION OF EQUIPMENT In conventional radiography an image is made on radiographic film by an attenuated X-ray beam. In passing through a core of tissue, each ray of the beam is attenuated as it is absorbed and scattered by the tissue in its path. The intensity of the transmitted ray depends on the sum total of X-ray attenuation by all the different soft tissues in its path.


1959 ◽  
Vol 14 (6) ◽  
pp. 1009-1012 ◽  
Author(s):  
T. H. Allen ◽  
B. E. Welch ◽  
T. T. Trujillo ◽  
J. E. Roberts

Except for bone mineral, the body is shown to belong to the same water:fat:protein system as its soft tissues. Hence, an equation verified with a variety of freshly isolated tissues can be used to estimate the body fat and the so-called total tissue solids. On the average, there are 0.784 kg of water/kg of body weight less bone mineral and fat. However, this water content probably fluctuates between extremes of 0.816 and 0.752, in accordance with the time elapsing since imbibing much water. This causes the density of the tissues in the fat-free, bone mineral-free body to range from 1.050 to 1.071. Combined simultaneous measurements of water, density and bone mineral, therefore, are required for the estimation of fat and tissue solids. Bone mineral occurs in the proportion of about one part to three parts of tissue solids, irrespective of ranges in quantities of fat and water among 30 healthy persons. Submitted on June 15, 1959


Paleobiology ◽  
1993 ◽  
Vol 19 (1) ◽  
pp. 107-135 ◽  
Author(s):  
Derek E. G. Briggs ◽  
Amanda J. Kear

A series of experiments was carried out to investigate the nature and controls (oxygen, microbial populations, agitation) on the degradation of soft tissues. Decay was monitored in terms of morphological change, weight loss, and change in chemical composition in the polychaete Nereis virens. Polychaetes include a range of tissue types of differing chemical composition and preservation potential: muscle, cuticle, setae, and jaws. Regardless of conditions, all the muscle had broken down and fluid loss through the ruptured cuticle had reduced the carcass to two dimensions within 8 days at 20°C. In most cases some cuticle, in addition to the jaws and setae, remained after 30 days. Where oxygen was completely eliminated, the rate of decay of the more volatile issues was significantly reduced. The degree of both osmotic uptake of water by the carcass and changes in water pH differed depending on whether the system was open or closed to oxygen diffusion. Autolytic and chemical processes are not sufficient to fully degrade the carcass in the absence of bacteria. Where internal bacteria are present, the presence or absence of water column bacteria made little difference to decay rate. Initial degradation (in the first 3 days) affects mainly the lipid fraction and the collagen of the cuticle. Later decay reduces the nonsoluble protein and increases the relative proportion of refractory structural components (tanned chitin and collagen) to more than 95% by day 30. Thus, only the sclerotized tissues are likely to survive beyond 30 days in the absence of early diagenetic mineralization. The sequence of degradation predicted from the relative decay resistance of macromolecules in the sedimentary record (protein → carbohydrate → lipid) is not, therefore, a consistent indicator of the preservation potential of structural tissues which incorporate them.The experiments reveal five stages in the decay of polychaete carcasses; whole/shriveled, flaccid, unsupported gut, cuticle sac, jaws and setae. All are represented in the fossil record. This allows an estimation of how far decay proceeded before it was halted by the fossilization process. The most complete preservations occur in the Cambrian where the Burgess Shale preserves evidence of muscle tissues. Traces of the gut and cuticle are more widely preserved, as at Mazon Creek, Grès à Voltzia, Solnhofen, and Hakel. Preservation varies within Konservat-Lagerstätten. The most common whole body preservation includes only the more recalcitrant tissues, jaws (where present) and setae, with an impression of the body outline. The stage of decay can be used as a taphonomic threshold, to provide an indication of how significantly the diversity of an exceptionally preserved biota is likely to have been reduced by taphonomic loss.


PeerJ ◽  
2016 ◽  
Vol 4 ◽  
pp. e1432 ◽  
Author(s):  
Charlotte A. Brassey ◽  
Thomas G. O’Mahoney ◽  
Andrew C. Kitchener ◽  
Phillip L. Manning ◽  
William I. Sellers

The external appearance of the dodo (Raphus cucullatus,Linnaeus, 1758) has been a source of considerable intrigue, as contemporaneous accounts or depictions are rare. The body mass of the dodo has been particularly contentious, with the flightless pigeon alternatively reconstructed as slim or fat depending upon the skeletal metric used as the basis for mass prediction. Resolving this dichotomy and obtaining a reliable estimate for mass is essential before future analyses regarding dodo life history, physiology or biomechanics can be conducted. Previous mass estimates of the dodo have relied upon predictive equations based upon hind limb dimensions of extant pigeons. Yet the hind limb proportions of dodo have been found to differ considerably from those of their modern relatives, particularly with regards to midshaft diameter. Therefore, application of predictive equations to unusually robust fossil skeletal elements may bias mass estimates. We present a whole-body computed tomography (CT) -based mass estimation technique for application to the dodo. We generate 3D volumetric renders of the articulated skeletons of 20 species of extant pigeons, and wrap minimum-fit ‘convex hulls’ around their bony extremities. Convex hull volume is subsequently regressed against mass to generate predictive models based upon whole skeletons. Our best-performing predictive model is characterized by high correlation coefficients and low mean squared error (a= − 2.31,b= 0.90,r2= 0.97, MSE = 0.0046). When applied to articulated composite skeletons of the dodo (National Museums Scotland, NMS.Z.1993.13; Natural History Museum, NHMUK A.9040 and S/1988.50.1), we estimate eviscerated body masses of 8–10.8 kg. When accounting for missing soft tissues, this may equate to live masses of 10.6–14.3 kg. Mass predictions presented here overlap at the lower end of those previously published, and support recent suggestions of a relatively slim dodo. CT-based reconstructions provide a means of objectively estimating mass and body segment properties of extinct species using whole articulated skeletons.


Blood ◽  
2014 ◽  
Vol 124 (21) ◽  
pp. 3740-3740
Author(s):  
Lawrence D Mayer ◽  
Nicole Sadowski ◽  
Paul Tardi ◽  
Xiaowei Xie ◽  
Donna Cabral-Lilly ◽  
...  

Abstract Background: CPX-351 is a liposomal formulation co-encapsulating Cyt and Daun, that delivers the drugs in vivo at a 5:1 molar ratio shown to be synergistic preclinically. Clinically, CPX-351 has provided evidence of promising improvements in patient outcomes, most notably in elderly newly diagnosed high risk (secondary) AML and in unfavorable risk first relapse adult AML where statistically significant increases in overall survival where observed in two randomized, controlled Phase 2 studies. In patients, CPX-351 displays a volume of distribution equal to the plasma volume and first order elimination with a half-life of > 24h for both drugs while maintaining the circulating Cyt:Daun molar ratio near 5:1. This is in contrast to the two drugs as conventionally administered in non-liposomal (NL) aqueous solution form where very rapid drug elimination is observed. Comparison of tissue distribution over time between CPX-351 and NL Cyt:Daun was performed in rats to better understand the pharmacodynamic relationships for CPX-351 in the context of what is known for the non-liposomal (NL) drugs, particularly as it relates to tissues relevant to efficacy and drug toxicity. Methods: Duplicate batches utilizing either [14C]Daun or [14C]Cyt CPX-351 or saline solutions of like labeled Cyt+Daun were prepared. Long-Evans rats received single IV bolus doses of either 15 units/kg (15 mg/kg Cyt + 6.64 mg/kg Daun) CPX-351, or a saline solution of 300 mg/kg Cyt + 10 mg/kg Daun. These doses were selected based on allometric scaling to reflect the respective clinical doses of CPX-351 and non-infusional Cyt:Daun treatment regimens. Animals were sacrificed at the designated time points post-dose and were frozen in a dry-ice/hexane bath in preparation for QWBA procedures. The tissue distribution of test article-derived radioactivity was determined using QWBA. Exposure of Cyt and Daun to a wide range of tissues was estimated based on the tissue density of [14C]Cyt-derived or [14C]Daun-derived radioactivity from QWBA section images. Tissue drug exposure comparisons between CPX-351 and NL Cyt:Daun were performed using Cmax and AUC0-t values. Results: The rapid tissue distribution of Cyt and Daun following injection of the NL form of the combination was reflected by the recovery of <5% of either drug in the plasma 15 minutes after injection and tissue/plasma AUC0-t ratios that were >1 and >10 for [14C]Cyt and [14C]Daun, respectively, for the majority of tissues studied. In contrast, for CPX-351 virtually all of the injected Cyt and Daun was present in the plasma between 0.25-1.0 hours and corresponding tissue/plasma AUC0-t ratios in the majority of tissues were <0.05 and <0.2 for [14C]Cyt and [14C]Daun, respectively. These differences were readily apparent in the QWBA section images. For the NL form of the combination, [14C]Cyt and [14C]Daun were widely distributed throughout the body shortly after injection. Following CPX-351 administration, radioactivity was more limited to discreet tissues and organs. Distribution of Cyt into tissues after CPX-351 administration was reduced as well as much slower than after NL Cyt injection as reflected by markedly lower Cmax values in all non-vascular tissues as well as lower AUC values in a majority of tissues. Comparing [14C]Daun distribution for CPX-351 vs NL Daun revealed a slower removal from the blood/plasma compartment and gradual distribution to tissues for CPX-351 with a similar general tissue profile as for NL drug with the notable increases in exposure to spleen, liver, testis and bone marrow. Bone marrow levels of Cyt and Daun peaked at 24h post CPX-351 injection and persisted for several days at anti-leukemic concentrations; drug levels present in the marrow at 96h were well above the CPX-351 IC50 values previously observed with fresh AML patient blast samples. In contrast, bone marrow Cyt concentrations fell below detectable limits within 24h after administration of NL drug. Conclusions: CPX-351 shifts the exposure of Cyt and Daun away from most non-hematologic tissues compared to NL drug treatment. Importantly, CPX-351 accumulates and persists in the bone marrow for over 4 days at concentrations known to have anti-leukemic activity against AML blasts. Taken together, these results provide additional biologic rationale that support the clinical improvements in both efficacy and safety seen for CPX-351 in randomized trials compared to conventional Cyt + Daun treatment. Disclosures Mayer: Celator: Employment, Equity Ownership, Patents & Royalties. Sadowski:Xenobiotic Laboratories: Employment. Tardi:Celator Pharmaceuticals: Employment, Equity Ownership. Xie:Celator Pharmaceuticals: Employment, Equity Ownership. Cabral-Lilly:Ceator Pharmaceuticals: Employment, Equity Ownership. Heller:Xenobiotic Laboratories: Employment, Research Funding.


2020 ◽  
Author(s):  
Erik John Woods ◽  
Aubrey M. Sherry ◽  
John R. Woods ◽  
James W. Hardin ◽  
Michael LaFontaine ◽  
...  

Abstract Background Deceased organ donors represent an untapped source of therapeutic bone marrow (BM) that can be recovered in 3–5 times the volume of that obtained from living donors, tested for quality, cryopreserved, and banked indefinitely for future on-demand use. However, a challenge for a future BM banking system built to a genetically diverse scale, will be to manage the prolonged ischemia times that inevitably occur, when bones procured at geographically-dispersed locations are shipped to distant facilities for processing. The goals of this study were: (a) to quantify, under realistic and scaled procurement and shipping conditions, the relationship between ischemia time and the quality of hematopoietic stem and progenitor cells (HSPCs) derived from deceased-donor BM; (b) to identify ischemia-time boundaries beyond which HSPC quality is adversely affected; and (c) to investigate whole-body cooling as a strategy for preserving cell viability and function. Methods Seventy-five bones from 62 deceased donors were analyzed for CD34 + viability following their exposure to various periods of warm-ischemia time (WIT), cold-ischemia time (CIT), and body-cooling time (BCT). Regression models were developed to quantify the independent associations of WIT, CIT, and BCT, with the viability and function of recovered HSPCs. Results Results demonstrate that under “real-world” scenarios: (a) combinations of warm- and cold-ischemia times favorable to the recovery of high-quality HSPCs are achievable (e.g., CD34 + cell viabilities in the range of 80–90% were commonly observed); (b) cooling the body prior to bone recovery is detrimental to cell viability (e.g., CD34 + viability < 73% with, vs. >89% without body cooling); and (c) vertebral bodies (VBs) are a superior source of HSPCs compared to ilia (IL) (e.g., %CD34 + viability > 80% when VBs were the source, vs. <74% when IL were the source). Conclusions Our quantitative models can be used to formulate ischemia-time tolerance limits and HSPC quality-acceptance criteria, and to inform an emerging BM banking system seeking to institute data-driven industry standards.


2000 ◽  
Vol 39 (06) ◽  
pp. 174-179 ◽  
Author(s):  
N. Manthey ◽  
F. Berger ◽  
H. Sommer ◽  
T. Pfluger ◽  
K. Hahn ◽  
...  

SummaryAt modern MRI tomographs the whole body can be screened for bone marrow metastases within 45 min. Aim of this study was to evaluate the diagnostic advantages and disadvantages of a whole-body bone marrow MRI protocol using Turbo Short Tau Inversion Recovery [STIR] sequences in comparison to planar bone scintigraphy (SZ). Patients and methods: In order to screen for bone metastases within two weeks SZ and whole-body MRI with Turbo-STIR-sequences were performed in 20 patients with known breast cancer. For further evaluation five regions were defined: scull, spine including the pelvis, femora, humeri and ribs including scapulae and sternum. Results: In 9/20 patients neither with SZ nor with MRI bone metastases were detected (staging M0). Among the remaining 11 patients SZ detected 109 and MRI 150 lesions which were typical for bone metastases. All of these 11 patients were staged Ml correspondingly with both methods. Within the thorax (ribs, sternum, scapulae) MRI discovered only 6/17 and within the scull 0/6 lesions which were suspicious for metastases in SZ. Inversely MRI identified much more metastatic lesions than SZ within the femora (20/16), the humeri (14/12) and the spine including the pelvis (110/58). Conclusions: Susceptibility-, truncation*, chemical-shift-, third arm- and particularly pulsation artifacts along with the impossibility to chose slice orientation equally advantageous for all regions of the body cause impaired image quality of MRI whole body scanning. Therefore, concerning the detection rate of bone metastases within the thorax (ribs, sternum and scapulae) and the scull, conventional Turbo-STIR-MRI whole-body scans are even less accurate than conventional planar bone scintigraphy in those regions.


Author(s):  
X. Gary Tan ◽  
Robert N. Saunders ◽  
Amit Bagchi

Current understanding of blast induced traumatic brain injury (TBI) mechanisms is incomplete and limits the development of protective and therapeutic measures. Animal testing has been used as a surrogate for human testing. The correlation of animals to human responses is not well understood with a limited set of experimental data, because of ethical concerns and cost of live animal tests. The validated computational animal models can be used to supplement and improve the granularity of available data at a significantly reduced cost. A whole-body porcine high-fidelity computational model was developed based on the image data. The hyper-viscoelastic model was used for soft tissues to capture the rate dependence and large strain nonlinearity of the material. The shock wave interaction with a porcine subject in a shock tube was simulated using computational fluid dynamics (CFD) models, via a combination of 1-D, 2-D and 3-D numerical techniques. The shock wave loads were applied to the exterior of the porcine finite element (FE) model to simulate the pressure wave transmission through the body and capture its biomechanical response. The CFD and FE problems are solved using the explicit Eulerian and Lagrangian solvers, respectively, in the DoD Open Source code CoBi. The computational models were validated by comparing the simulation results with experimental data at specific instrumented locations. The predicted brain tissue stress-strain fields were used to determine the areas susceptible to blast induced TBI by using published mechanical injury thresholds. The validated porcine model can be used to better understand TBI and how injury in animals corresponds to injury in humans. The coupled Eurlerian and Lagrangian approaches developed in this paper can be extended to other simulations to improve the solution accuracy.


1976 ◽  
Vol 15 (05) ◽  
pp. 248-253
Author(s):  
A. K. Basu ◽  
S. K. Guha ◽  
B. N. Tandon ◽  
M. M. Gupta ◽  
M. ML. Rehani

SummaryThe conventional radioisotope scanner has been used as a whole body counter. The background index of the system is 10.9 counts per minute per ml of sodium iodide crystal. The sensitivity and derived sensitivity parameters have been evaluated and found to be suitable for clinical studies. The optimum parameters for a single detector at two positions above the lying subject have been obtained. It has been found that for the case of 131I measurement it is possible to assay a source located at any point in the body with coefficient of variation less than 5%. To add to the versatility, a fixed geometry for in-vitro counting of large samples has been obtained. The retention values obtained by the whole body counter have been found to correlate with those obtained by in-vitro assay of urine and stool after intravenous administration of 51Cr-albumin.


2020 ◽  
Vol 99 (5) ◽  
pp. 478-482
Author(s):  
N. P. Setko ◽  
A. G. Setko ◽  
Ekaterina V. Bulycheva ◽  
A. V. Tyurin ◽  
E. Yu. Kalinina

Introduction. Changes in the body of children and adolescents aimed at adapting to environmental factors are determined by genetic polymorphism in xenobiotic biotransformation genes, determining the degree of susceptibility of the child’s body to pollutants, which is the basis of modern personalized preventive medicine when managing risks to the health of the child population under the influence of environmental factors. Material and methods. Trace elements, including heavy metals, lead and cadmium, were determined in the hair of 256 practically healthy teenagers by atomic absorption spectrophotometry. Depending on the level of content of the latter, two groups of adolescents were formed to determine six genes of the cytochrome P-450 family. Group 1 consisted of adolescents whose cadmium lead content exceeded the average Russian indices. The second group included adolescents whose heavy metals were above the level of average Russian standards. Results. Studies have shown that in adolescents of the 1st group, compared with the data of adolescents of the 2nd group, an increase in the number of carriers of two mutant alleles at the locus rs 1048943 (gene CYP1A1) is 3.08 times, rs 464621 (gene CYP1A1) is 1. 8 times; locus rs 2069522 (CYP1A2 gene) 3.63 times; locus rs 1799853 (CYP2C9 * 2 gene) 4.5 times; locus rs 1057910 (gene CYP2C9 * 3) 3.8 times and locus rs 2279343 (gene CYP2B6) 4.25 times. Moreover, carriers of two normal alleles in adolescents of the first group at the locus rs 1048943 (gene CYP1A1) were 5.14 times; locus rs 2279343 (CYP2B6 gene) was 6.5 fold less than among adolescents of the 2nd group; and at the locus rs 464621 (gene CYP1A1), rs 2069522 (gene CYP1A2), rs 1799853 (gene CYP2C9 * 2), rs 1057910 (gene CYP2C9 * 3) there were no carriers of normal homozygotes. Conclusion. Group 1 adolescents with heavy metal contamination of the body are carriers significantly in a greater number of pathological mutations in the genes of the cytochrome P-450 detoxification system in comparison with data from group 2 adolescents.


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