17. Posters

Preliminary Dose Measurements on the SCANNEX Low Dose X-Ray Unit

Egbert Hering Nicolene Gentle 
Dept. of Medical Physics, Groote Schuur Hospital and University of Cape Town 

A modified version of the SCANNEX X-ray unit for medical diagnostic purposes has been developed by DEBEX, a Division of De Beers Mining Co. The unit was designed using technology developed for the detection of diamonds in mine workers. One of the prime features of this scanning, slit imaging X-ray unit is the low radiation dose to the patient and personnel. 

A prototype of this unit was installed in the trauma department of Groote Schuur Hospital for clinical and physics trials, enabling us to measure the radiation doses in the primary beam and around the unit. 

Dose measurements were carried out for all possible kV and mA settings with different collimators and added filtration, full and partial scans. 

The doses around the unit were about 3% of those for conventional X-ray units, whereas the patient surface entrance doses ranged from 0.3 to 13% of those for conventional X-rays. 
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Effect of Evening Primrose Oil (EPO) Supplementation on Mouse Tissue Radiation Response

A Hendrikse, F Rahbeeni and G Blekkenhorst 
Dept. Radiation Oncology, Groote Schuur Hospital / University of Cape Town 

Aim:

  1. To determine the effect of EPO supplementation on mouse skin response to radiation.
  2. To determine the effect of EPO supplementation on mouse tumour response to radiation.

Method:

Female, BALB/c mice were fed a standard diet supplement with either EPO or water. For the normal tissue study, mice were fed 10ml EPO daily for 14 days before and then for 4 weeks after their feet were irradiated with graded doses (35Gy - 40Gy) of 60Co gamma radiation. After irradiation feet were assessed daily for signs of moist desquamation and the radiation dose that resulted in moist desquamation in 50% of mice (i.e. the ED50) then determined. For the tumour study, mice were fed EPO daily starting 14 days before tumours were irradiated (30Gy) and ending when the tumours had reached 1.5 times their irradiated size. The tumour growth delay caused by irradiation was then determined. 

Results:

The ED50 for EPO-supplement mice was 37.8Gy; the ED50 for control mice was 36.9Gy. 

The tumour radiation growth delay of mice receiving EPO supplementation increased and was statistically different when compared to that of control mice. 

Conclusion:

EPO supplementation protected normal tissue against but sensitized tumour tissue to irradiation. Possible mechanisms for EPO’s radiation modifying effects are discussed. 
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The Effect of Inhibitors of Energy Metabolism on the Radiation Response of Tumours In Vivo

A.J. Hunter and G.H. Blekkenhorst 

Inhibitors of energy metabolism, 2-deoxyglucose (2DG) and aminooxyacetic acid (AOA) have been used to inhibit energy metabolism, the former inhibiting glycolysis and the latter inhibiting glutaminolysis. Since a supply of energy is required for repair of radiation damage to take place, it was proposed that the presence of these inhibitors would inhibit such repair. Experiments were performed using tumour growth delay assay in 3 tumour types. Contrary to results by previous workers, no statistically significant change in growth delay was found for tumours in mice administered 2DG prior to radiation relative to that for tumours in mice given saline prior to radiation. However, when, AOA was administered together with 2DG a reduction in radiation induced growth delay was found. This suggests that some kind of interaction may exist between glycolysis and glutaminolysis, which may influence energy supply and possibly repair. 
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Rays of Hope: A Radiotherapy Information Video

H Burger and Personnel 
Department of Radiation Oncology, Pretoria Academic Hospital 
J. Taute, VideoTuks, University of Pretoria 

Purpose:

A study performed in our department revealed that a large number of patients did not understand their treatment, despite the fact that information sessions were held. The aim of this study was to develop a more effective means of introducing new patients and their families to radiotherapy treatment. 

Methods:

The department discussed possible methods of communication. A committee representing all professions in the department was elected. Questionnaires completed by patients and staff members were evaluated to determine problem areas. 

Results:

The department elected to make a video to use during information sessions. The main problem identified was the large number of languages spoken by the patients. It was decided to produce the video in such a way that it could be translated into many languages. The script was written in a simple, non-technical way, and included the following areas: 
  • What is cancer?
  • What is radiotherapy?
  • What can a patient expect when radiotherapy is prescribed?
  • What side effects or reactions can occur due to radiotherapy?
  • What other support systems are available to patients?
  • What happens behind the scenes?

Conclusion:

A 18 minute video "Rays of Hope" was produced and translated into seven languages, including Afrikaans, English, Sotho, Zulu, Xhosa, French and Portuguese. It is shown in the department on a regular basis, and is also available to patients to take home on a library basis. The video has also been made available to other interested parties outside the hospital. 
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Fetal Dose Estimation during Three Different Diagnostic Radiology Procedures.

N. Falzone, Q. Connell, H. Burger 
Department of Radiation Oncology, Pretoria Academic Hospital 

Purpose:

To determine the fetal dose to a 10 week pregnant woman who had been exposed to radiation during various x-ray examinations. 

Introduction:

In order to come to a correct diagnosis of the patient’s lung pathology chest x-rays, a series of CT scans and pulmonary angiography was indicated. At the same time the results from two different fetal dose estimate techniques were compared for each of the three mentioned procedures. 

Method:

In each of the above mentioned procedures the fetal dose was calculated by two different means: 
  1. ) Existing tabulated data [ NCRP report No. 54, Fetal Dose Estimates for CT Pelvimetry, M.M Moore, D.R. Shearer, Radiology 1989;171 ]
  2. ) TLD’s

Results:

The fetal dose for each procedure is summarised in the table below. 
 
Procedure Existing Data TLD’s
X - rays
0.03 mGy
0.10 mGy *
CT scan
43 mGy
0.43 mGy *
Pulmonary Angiography
35 mGy
0.36 mGy
* Entrance skin dose
Intra Vaginal dose
 

Conclusion:

Calculating fetal doses from existing data gives a very conservative estimate and totally overestimates that physically measured in this case using TLD’s (taking into account the inherent accuracy of TLD’s). This is partially due to the fact that lead aprons were used to shield the patient during the procedures and that care was taken especially during fluoroscopy not to scan low over the abdomen. The fetal dose, worst case scenario (i.e. determined from existing data), was found to be 78 mGy - termination of pregnancies are only indicated at 150 mGy and above. 
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Dose Area Product (DAP) Measurement for Determining Reference Doses in Radiology

P.C. Engel-Hills, E.R. Hering 
Peninsula Technikon and Groote Schuur Hospital 

Purpose:

A study was conducted to measure the dose-area product to patients during barium enema x-ray examinations. The results were compared to similar measurements done in the United Kingdom where the dose-area product is used for reference and investigation dose levels. 

Method:

A dose-area product meter (DAP-meter) was used to measure the dose-area product to patients having a barium enema. Measurements were done on 50 patiets. The 3 centres involved in the study reflected the different types of equipment used for this examination. The results were obtained for various techniques and equipments. 
DAP Readings for Barium Enema
Place 1st quartile Median 3rd quartile
United Kingdom 26 Gy cm2 41 Gy cm2 60 Gy cm2
Western Cape 35 Gy cm2 48 Gy cm2 84 Gy cm2

Conclusion:

A National protocol for DAP measurements in diagnostic radiology is recommended for South Africa. 
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Implementation of Revised Dosimetric Quantities and Dose Limits for Radiation Protection in Medicine

GJJ Korf and WJ Strydom 
Department of Medical Physics, Medunsa 

Objective:

The ICRU Report 39 of 1985 and the ICRP Publication 51 of 1986 introduced four new quantities for use in environmental and individual radiation monitoring. The most pressing need for the recommendations of ICRU 39 was the requirement to implement the change to S.I. units in radiation protection. The aim of this exercise therefore was to implement one of the new dosimetric quantities, namely the ambient dose equivalent H*(d), and to investigate the impact of the use of this quantity on current dose limitations as issued by the national regulatory body while simultaneously examine the validity of these limitations. 

Method:

The H*(10) rate for gamma radiation at various distances from a 137Cs source (661.5 keV) and a 99mTc source (140 keV) were determined with a calibrated Bicron-NE Model PRM510 portable radiation monitor which only offers a built-in H*(10) response. The exposure rates in the same gamma radiation at equal distances were thereafter measured with a calibrated Panoramic Victoreen Model 470A exposure rate meter. The exposure rate readings were converted to air kerma rate with an exposure-air kerma factor of 0.00876 Gy/R. Published values to convert air kerma to H*(10) were used (1.20 SvGy-1 for 137Cs and 1.63 SvGy-1 for 99mTc) and the determined H*(10) rates using the old exposure rate meter were compared with the data gathered with the PRM510 monitor. The results were then applied to one medical radiation protection problem namely dose monitoring during 131I radiotherapy. 

Results:

The two instruments agreed on average within 14.3 % with each other for the determined ambient dose equivalent rate for 137Cs gamma radiation. The air kerma to H*(10) conversion factor depends on energy but has a near constant value of approximately 1.21 SvGy-1 for gamma energies in the range of 180 – 1000 keV. When using a new survey instrument which has a built-in H*(d) response during assessments of patients who received a therapeutic dose of 131I and wished to be discharged from isolation, a maximum detected value for H*(10) of 26.5 m Svh-1 at a distance of 1m from the patient will comply with the current allowable exposure rate of 2.5 mRh-1 at a distance of 1m from the patient. 

Conclusion:

It is now more than ten years after the new ICRU dosimetric quantities were introduced, primarily to promote the change to S.I. units in radiation protection. Maybe it is time for South Africa to not only implement these quantities in health regulations concerning 131I-therapy, but also to consider the revision of the current dose limitations by introducing a minimum age for 131I-therapy and to take into account the latest allowable dose limits for members of the public. 
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Radiation dosimetry of craniopagus twins during Tc99m-DTPA and Tc99m-HMPAO studies.

AC Chamberlain, *MM Sathekge, *RP Clauss. 
Department of Medical Physics, *Department of Nuclear Medicine, Medunsa 

Introduction:

Occipitally coupled Siamese twins were presented at GaRunkuwa hospital for separation. Due to the large number of investigations the twins had to undergo it was desired to estimate the dose received by the twins during these investigations. 

Aim:

The aim of the study is to estimate the dose received by craniopagus twins during Tc99m-DTPA and Tc99m-HMPAO investigations. 

Method:

Exponential curves were fitted to the data acquired from the studies. The residence times were calculated from the rate constants of the curves and the initial activities in the organs. The residence times were supplied to the MIRDOSE3 program and the doses calculated using the newborn phantom. 

Results:

The results are summarised in the table below. 
 
Estimated Dose (mGy)
DTPA
Day 1
DTPA
Day 6
HMPAO
Day 11
HMPAO
Day 14
Total Dose (mGy)
Twin 1
Body
0.13
0.14 
6.8 
4.2 
11.27 
Brain
0.05 
0.08 
12.5 
17.63 
Thyroid
5.34 
3.9 
274 
129 
412.24 
Liver
0.14 
0.18 
25.2 
13.1 
38.62 
Gut, Gall Bladder, Kidney
0.75 
2.85 
285 
71.5 
360.1 
Bladder
1.75 
1.75 
14.6 
7.6 
25.7 
Twin 2
Body
0.13 
0.14 
3.2 
8.4 
11.87 
Brain
0.05 
0.08 
2.7 
15.9 
18.73 
Thyroid
5.34 
3.9 
288 
322 
619.24 
Liver
0.14 
0.18 
13.6 
56.2 
70.12 
Gut, Gall Bladder, Kidney
0.75 
2.85 
68.9 
286 
358.5 
Bladder
1.75 
1.75 
6.2 
15.6 
25.3 
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Simple Method of Measuring Glomerular Filtration Rate below 30 ml/min

A.J. White, S.S. Bakhane, A.Chamberlain, W.J. Strydom 
Dept Medical Physics, MEDUNSA 

The recommended technique for measurment of glomerular filtration rate (GFR) less than 30 ml/min requires the counting of plasma and urine samples. An alternative method is described to give a body surface area (BSA) normalised GFR measurement (GFRn) which requires a single injection of Tc-99m DTPA and the counting of two blood plasma samples. No other measurement such as BSA or injected dose is needed. 

The theoretical background was described and mathematical analysis of errors due to enlarged or reduced patients extracellular volume (ECV) was performed. 

The method was tested on patients referred for conventional Tc-99m DTPA renography and a Cr-51 EDTA BSA normalised GFR measurement (GFRn a) by the slope intercept technique. Simultaneous measurement of GFRn with Tc-99m DTPA and GFRn a on 28 patients whose GFR was less than 50 ml/min were selected for analysis. Taking GFRn a as standard, the GFRn method was found to be accurate for a normal size ECV but was in error for an enlarged or reduced ECV. For GFR less than 30 ml/min these errors were acceptably small. 

The GFRn method may be useful when poor renal function is observed during conventional scintigraphic renography and a GFR measurement is required for confirmation. The injected renographic dose can be used for the measurement and at least 15 minutes will be available after renography to arrange for blood sampling. 
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Normalisation of Glomerular Filtration Rate in Adults and Children: Body Surface Area or Extracellular Fluid?

S Ghoorun, W I D Rae 
Department of Medical Physics, Addington Hospital, Durban 

Introduction:

The accurate assessment of glomerular filtration rate requires a normalisation method for standardisation and comparison between individuals of different sizes. The aim of this study was to investigate the validity of expressing GFR in relation to extracellular fluid volume and to compare this value to GFR normalised to body surface area. 

Method:

A dataset consisting of 1099 patients was used in the analysis. This was divided into 1018 adults and 81 children. GFR was measured using the two sample blood technique following bolus intravenous injection of 99mTc-DTPA (1). At our institution, the Du Bois formula (2) is used for the calculation of body surface area in adults and children. However the Du Bois formula is considered inappropriate especially in the case of children and therefore part of this study involved comparing the Du Bois formula to the Haycock formula (3) for determining body surface area. 

Results:

The calculation of BSA using the two different equations was almost identical with a correlation coefficient of 0.983 in adults and 0.997 in children. The Du Bois formula was thus used in all further computations. GFR normalised to ECV correlated well in adults with GFR normalised to BSA with a correlation coefficient of 0.946. In children this did not correlate well and the correlation coefficient was 0.698. 

Conclusion:

  1. The Du Bois formula for the calculation of body surface area correlates well with the Haycock formula in children and in adults and can therefore be used for the normalisation of GFR.
  2. Extracellular volume can be used as the normalisation variable in adults.
  3. Body surface area is the most accurate parameter for the normalisatiion of GFR in children.

References:

  1. Russell CD, Bischoff PG, Kontzen FN, et al: Measurement of glomerular filtration rate: Single injection plasma clearance method without urine collection. Journal of Nuclear Medicine 26: 1243-1247,1985
  2. Du Bois D and Du Bois EF: A formula to estimate the approximate surface area if height and weight are known. Arch Intern Med 17: 863,1916
  3. Haycock GB, Chir B, Schwartz GJ, Wisotsky DH: Geometric method for measuring body surface area. Journal of Pediatrics 93: 62,1978
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Left Ventricular Ejection Fraction Normal Values

W I D Rae, Z Mahomed, S Ghoorun. 
Department of Medical Physics, Addington Hospital, Durban. 

Introduction:

Left ventricular ejection fractions (LVEF) are clinically useful in assessing the function of the left ventricle and are widely used. LVEF normal ranges are specific for the gamma camera system used for the acquisition and the software being used for the analysis (1). These normal ranges cannot be reliably assumed from other centres as the calculation of LVEF varies significantly for different software and different manufacturers. This study was done using a patient set of 242 consecutive patients to obtain an estimate of the normal range of LVEF for this centre. 

Method:

A set of 242 consecutive patients presenting with a variety of diagnoses was studied. LVEF studies were acquired as gated Left Anterior Oblique (LAO) blood pool images on a Siemens Orbiter Gamma Camera (2). Three standard methods of image data filtration (No filter, Tempero-spatial, and Wiener) were used when analysing all patients and the results were studied for each of 7 diagnostic groups. The heart rate and body mass index (BMI) were recorded for most patients. If the analysis failed using the "semi-automatic" analysis option then "manual" analysis was done. Regression analysis was done to determine the relationship between the LVEFs derived using the different analysis techniques. LVEF dependence on the heart rate, age and BMI of patients was also tested. 

Results:

The difference between "semi-automatic" and "manual", could not be assessed. The results (using no filtration) formed three groups when they were plotted as a histogram. These had peaks around 30%, 50%, and 70%. For female patients the diagnostic class "pre-chemotherapy" (normal patients?) had a mean of 62± 12%. For male patients the same diagnostic class had a mean of 65± 7%. This did not appear to be strongly dependent upon BMI or age. The dependence upon heart rate was not significant for the range 40 to 100 beats per minute. 

Conclusion:

The range of the LVEFs at our hospital using currently standard analysis techniques for a set of apparently normal individuals is about 62± 12% for females and 65± 7% for males. A suggested useful normal range of 50% to 70% is appropriate for routine use. 

References:

  1. Franken, P.R.; Deconinck, F.; Bourguignon, M.H.; Busemann Sokole, E. and contributors to the ENCD, European variability of left ventricular ejection fraction from gated blood pool studies. J. Nuc. Med. Proceedings, Proceedings of 44th Annual Congress, San Antonio, Texas, No. 725, 168P, June 1997.
  2. Siemens Operating Instructions. Clinical Protocols for ICON-Volume 1, Rev. 06, February 1996.
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I am a Medical Physicist

W I D Rae. 
Department of Medical Physics, Addington Hospital, Durban. 

Aim:

Medical Physics, after many years as a profession, is often not well understood by the public, or by Medical Practitioners. This series of 3 accessible posters presents a Medical Physicist’s activities. Each is aimed at a sector of the general public with its own interests and information needs. The presentation aims to be more easily accessible than booklets (1) and long documents, and is directed at a wide audience. 

Content:

Poster 1 is a friendly general overview of Medical Physics, as would be given to a stranger, or a child. The vocabulary is non-technical and simple illustrations are used to present Medical Physicist involvement in hospitals. 

Poster 2 contains more information and is slightly less accessible. The information gives more insight into making on career choices. 

Poster 3 is a more formal presentation of the profession of Medical Physics. A brief outline of the scope of practice is included (2). An example calculation is also given (3). 

Conclusion:

This non-technical overview of the tasks of a Medical Physicist is presented in 3 accessible posters aimed at readers needing information for general interest, scholarly projects, and in-depth career path choices. 

References:

  1. Institute of Physics and Engineering in Medicine, "Physics in Engineering and Medicine", Ed. P.N.T. Wells, 1997.
  2. Department of National Health and Population Developement, "Regulations Defining The Scope Of The Profession Of Medical Physicist", Government Gazette No. 11152, pg. 46-47, 26 February 1988.
  3. Johns, H.E.; Cunningham, J.R. "The Physics of Radiology", IV Ed., 1983, Charles C Thomas.
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Quality Control for Diffusion Imaging in MRI

M. D. Rana, W.I.D. Rae 
Department of Medical Physics, Addington Hospital 

Introduction

To measure movement of intra- and extracellular water molecules for diffusion imaging, will require optimum performance from the MRI unit. Measurement of certain parameters mentioned below will monitor the stringent requirements set down for diffusion imaging. 

Method

To achieve peak performance from the GE Signal Horizon 1.5T Echo Speed, two GE phantoms and a phased array head coil was used. Parameters measured will predict the accuracy of the magnetic field homogeneity, magnetic field gradients in x,y,z plane, magnetic and RF shielding, and transmitter and receiver RF. 

Specific imaging parameter (1) used are : 

  1. Resonance Frequency
  2. Signal to Noise ratio
  3. Spatial linearity
  4. Spatial resolutio
  5. Slice thickness 
  6. Slice separation
  7. a 5 step diffusion gradient in all 3 planes simultaneously (x,y,z) and in individual plane x,y,z in steps of 0.4 mT m-1.
To quality control tests takes 1.5 hr which is done on a weekly basis. 

Results

The results showed good stability of the MRI unit and parameters (i) to (vi) were within specifications set down by AAPM (1). However diffusion coefficients were affected by temperature but showed <5% variation in a particular direction and temperature. 

Discussion

Variation in diffusion coefficients are representative of phase variation along a particular axis and ultimately reflect in variation of magnetic field gradient and magnetic field corrections along that axis. 

Conclusion

Quality control is important for conventional imaging, MRA, spectrocopy and also for research projects like diffusion imaging. With more experience and better understanding quality control tests will have to be simplified so as to replace insensitive and too cumbersome tests. 

References:

  1. Price R R, Axel L, et al, Med Phys 11.7(2) Mar/Apr 1990 287 - 295
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Progressively Reduced Sm-153-EDTMP Uptake in Normal Bone after Multiple Applications; A Non-Human Primate Study

I Dormehl1, W Louw2, R Milner3, F Schneeweiss4, U Karl5, G Schmitt5
1) AEC Institute for Life Sciences, University of Pretoria 
2) Atomic Energy Corporation, Pelindaba 
3) Veterinary Faculty, Onderstepoort 
4) Institute for Medicine, Jülich 
5) Clinic for Radiotherapy, University of Düsseldorf 

Re-application of Sm-153-EDTMP for maintained palliation of metastatic bone pain in patients was found to be progressively less effective. Does EDTMP exert a blocking function, limiting access to bone tissue on re-application? 

This investigation concerns the pharmaconetics and bone localisation of Sm-153-EDTMP in the normal baboon during three successive applications (6 week intervals) each with two different concentrations of EDTMP (0.7 EDTMP mg/kg, normal; and 1.4 EDTMP mg/kg). Two groups of six baboons were used, one for each concentration. Scintigraphy included a two hour dynamic study (1 min frames) following 111 MBq Sm-153-EDTMP i.v. Static images (4 min) followed hourly at 2 till 5 hours. Time-activity curves were obtained for the heart, kidney and liver, and relative bone to background uptake from the static images. Blood and urine clearance curves were obtained. Comparisons were drawn (Student’s t-test) between successive applications, and between the two concentrations. Partial blocking appears with the lower EDTMP concentration, significant after the third application (P<0.05). The first application of the high concentration indicates lower uptake in the bone than the lower one, pointing to blocking by the high concentration, however not with subsequent re-applications. Re-application of the high EDTMP-concentration could reduce levels of serum calcium, increase parathyroid hormone level, triggering osteoblastic activity and bone remodeling, thus partially off-setting blocking which was hence clearer at the low concentration. 
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Re-188-HEDP as a Therapeutic Bone Agent - Preparation, Experimental Pharmocokinetic and Biodistribution Studies in the Normal Baboon Model

W Louw1, I Dormehl2, R Milner3, F Schneeweiss4, F Chaparro5, E Killian5, J Wagener1 
1Atomic Energy Corporation, Pelindaba, 2AEC Institute for Life Sciences, University of Pretoria, 3Faculty of Veterinary Surgery, Onderstepoort, 4Institut für Medizin, Jülich, 5Pretoria Biomedical Research Centre. 

A variety of bone-seeking radiopharmaceuticals, including 32P, 89Sr, 153Sm-EDTMP and 186Re-HEDP have been used to treat patients with skeletal metastases. 188Re-HEDP (Rhenium-188-hydroxyethylidene diphosphonate) is an attractive alternative for therapeutic use. 188Re (t½ 16.9 hr; b - 2.1 MeV, g 103 keV 15%) has a shorter physical half-life than both 153Sm and 186Re which allows for higher doses (compared with the longer lived radionuclides). 188Re is also available from an in-house generator system (similar to the current 99mTc-generator). Na 188ReO4- was obtained from an 185 000 MBq ORNL alumina-based 188W/188Re-generator system by elution with 0.9% NaCl. To make 188Re-HEDP, 1.0 ml K ReO4- solution (1.0 mg/ml) and up to 2960 MBq, 188ReO4- in 5.0 ml eluate was added to a vial containing 75.0 mg HEDP, 10.0 mg ascorbic acid and 20 mg SnCl2•2H2O. The whole mixture (pH 3.5) was heated for 15 min (» 100 ° C), allowed to cool, whereafter 3.0 ml of 1.0 M sodium citrate (pH 7.0) was added to adjust the pH to 5 - 6. Radiochemical purity (> 99.0%) was determined by instant thin-layer chromatography on silica gel impregnated glass fibre sheets using acetone as solvent. (188Re-HEDP stays at the origin (Rf = 0) while ReO4- was at Rf 0.8). 

In this study the pharmocokinetics and biodistribution of 188Re-HEDP was investigated using the baboon experimental model (which answers many of the criteria of parallelism to the human). With the baboons (n = 6) under pentobaritone anaesthesia both dynamic (one frame/min for 30 min) and subsequent static scintigraphic studies (5 min acquisition; hourly form 2 - 4 hours), were performed after bolus i.v. injection of sterilised 185 MBq 188Re-HEDP, with the HEDP adjusted to a dose of 1.0 mg/kg body weight. Blood and urine samples were collected at 120 min and later at 20 min intervals for 4 hours and then analysed. Time-activity curves were obtained for the heart, kidney, liver, and relative bone to background uptake from the static images. Blood and urine clearance curves were obtained. 

The results of this study showed that there is a highly selective Re-188 uptake in the skeletal system as well as a low non-target uptake and rapid clearance in non-osseous tissue. 
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Breast Tangential Fields: Penumbral Dose to Lung

Mary Jean Scott, Hillbrow Hospital 
Roy Lakier, Johannesburg/Hillbrow Hospitals and the University of the Witwatersrand 

It has been considered best to treat breast tangential fields, either with a half-field block or independent jaws or to angle the fields so that the posterior beam edges are co-linear. This has been true on both Cobalt teletherapy units and on linear accelerators. 

However, if patients are treated with either modality on the basis of clinical skin markings, as would be the case in very advanced carcinoma of the breast, Dose-Volume Histograms, as produced by a Helax treatment planning system, show that there is very little difference between the three modes of treatment. 

Comparisons of the three possible treatments will be given for both modalities. 
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Calculation of Distances within and between Reconstructed SPECT Tomographic Slices

I H Boyd 
Department of Radiation Services, University of the Witwatersrand. 

When distances have to be calculated within or between SPECT tomographic slices, the usual procedure is to obtain the distance in pixels from the image and convert it to absolute units using the pixel width, which is usually supplied as an output parameter of the reconstruction group of images. 

Unexpected results were obtained with certain combinations of acquisition and reconstruction parameters on one manufacturer's dual head gamma. These results prompted this investigation in which SPECT images were acquired of a simple arrangement of point sources, known distances apart. These images were acquired and reconstructed with a various combinations of the relevant parameters and the separation of the source images was calculated and compared with actual values. 

The results revealed two important facts: 

  1. for transaxial slices the pixel width parallel with the axis of rotation is that of the acquisition group. Thus the slice width is unaffected by the values of the reconstruction parameters.
  2. for slices in the coronal, sagittal and oblique planes, the pixel width is that of the expected reconstruction group except when the following combination of parameters applies:

  3. acquisition frame size: 128 x 128 reconstruction frame size: 64 x 64 reconstruction zoom factor: less than 2.0 
Within this parameter domain, the rules for transaxial slices apply, leading to a distortion of the image. 
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The Radiotoxicity of 4-[123I]-IODOANTIPYRINE in Normal and Cancer Cells

B.S. Smit, J.P. Slabbert and J.H. Langenhoven 
National Accelerator Centre 

The high-LET effects of short range Auger electrons is a possible means to inactivate tumor cells. Presently it is of great interest to quantify Auger electron damage in relation to the inherent radiosensitivity of cells. In this work the induction of micronuclei from intracellular and extracellular disintegrations of 123I were followed in an ovarian cancer cell type (DMBA) and a normal cell line (CHO-K1). Extracellular disintegrations of the radionuclide is effected by exposing the cells to [123I]NaI and cellular uptake ensured by using 4-[123I]-iodoantipyrine. Cell exposure to 4-[123I]-iodoantipyrine after 10 half- lives had no measurable effect, indicating that any biological damage from the chemical compound is insignificant. By contrast, high micronuclei frequencies were noted in both cell types when exposed to radioactive 123I. Extracellular disintegrations of the nucleid consistently yield lower levels of biological damage compared to when cells were exposed to 4-[123I]- iodoantipyrine. 
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Development of a Production Procedure for 139Ce at NAC

F.M. Nortier, F.J. Haasbroek, S.J. Mills, G.F. Steyn and T.N. van der Walt 
National Accelerator Centre 

Long-lived (137.64 d) 139Ce is well-known as a laboratory standard for the calibration of g-ray detectors. Since it emits only one g-ray (165.857 keV) in the optimum energy range for detection with a gamma camera this radioisotope also has a high potential for use in calibration sources for SPET. In order to explore this possibility a production procedure for 139Ce was developed at the NAC and an experimental 139Ce line source was prepared for employment in a scanning line source assembly developed by the Department of Biophysics, UOFS, Bloemfontein. 

No suitable cross-section data for the cyclotron production of 139Ce could be found in the literature. Therefore, the excitation function (see Fig. 1) for the production of 139Ce in the bombardment of praseodymium with protons up to 100 MeV was measured in this work. Subsequently, a Pr-metal target was designed and manufactured and several high-current production runs were executed with the 66 MeV proton beam. The yields obtained agree very well with the expected thick-target yield as determined from the measured excitation function data. 

Fig. 1 139Ce yield in the bombardment of praseodymium with protons.
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