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D T Burns

Publications and source records attributed to D T Burns.

At least 19 recordsLinked to original sources
PubMed2006

A new approach to the determination of air kerma using primary-standard cavity ionization chambers.

A consistent formalism is presented using Monte Carlo calculations to determine the reference air kerma from the measured energy deposition in a primary-standard cavity ionization chamber. A global approach avoiding the use of cavity ionization theory is discussed and its limitations shown in relation to the use of the recommended value for W. The role of charged-particle equilibrium is outlined and the consequent requirements placed on the calculations are detailed. Values for correction factors are presented for the BIPM air-kerma standard for 60Co, making use of the Monte Carlo code PENELOPE, a detailed geometrical model of the BIPM 60Co source and event-by-event electron transport. While the wall correction factor k(wall) = 1.0012(2) is somewhat lower than the existing value, the axial non-uniformity correction k(an) = 1.0027(3) is significantly higher. The use of a point source in the evaluation of k(an) is discussed. A comparison is made of the calculated dose ratio with the Bragg-Gray and Spencer-Attix stopping-power ratios, the results indicating a preference for the Bragg-Gray approach in this particular case. A change to the recommended value for W of up to 2 parts in 10(3) is discussed. The uncertainties arising from the geometrical models, the use of phase-space files, the radiation transport algorithms and the underlying radiation interaction coefficients are estimated.

Air↗
PubMed2000

Analytical chemistry and the law: progress for half a millennium.

Chemistry has been used for the detection of adulteration since the earliest times of recorded history going back at least 3 1/2 millennia. Since the invention of printing the subject is easier to follow. Aspects of law and its application via chemistry in regard to precious metals, food, drink and medicinal materials are reviewed over the last half millennium with particular reference to the U.K.

Chemistry, Analytic↗
PubMed2000

Rapid analysis of ecstasy and related phenethylamines in seized tablets by Raman spectroscopy.

Raman spectroscopy with far-red excitation has been used to study seized, tableted samples of MDMA (N-methyl-3,4-methylenedioxyamphetamine) and related compounds (MDA, MDEA, MBDB, 2C-B and amphetamine sulfate), as well as pure standards of these drugs. We have found that by using far-red (785 nm) excitation the level of fluorescence background even in untreated seized samples is sufficiently low that there is little difficulty in obtaining good quality data with moderate 2 min data accumulation times. The spectra can be used to distinguish between even chemically-similar substances, such as the geometrical isomers MDEA and MBDB, and between different polymorphic/hydrated forms of the same drug. Moreover, these differences can be found even in directly recorded spectra of seized samples which have been bulked with other materials, giving a rapid and non-destructive method for drug identification. The spectra can be processed to give unambiguous identification of both drug and excipients (even when more than one compound has been used as the bulking agent) and the relative intensities of drug and excipient bands can be used for quantitative or at least semi-quantitative analysis. Finally, the simple nature of the measurements lends itself to automatic sample handling so that sample throughputs of 20 samples per hour can be achieved with no real difficulty.

Drug and Narcotic Control↗
PubMed2000

Composition profiling of seized ecstasy tablets by Raman spectroscopy.

Raman spectroscopy with far-red excitation has been investigated as a simple and rapid technique for composition profiling of seized ecstasy (MDMA, N-methyl-3,4-methylenedioxyamphetamine) tablets. The spectra obtained are rich in vibrational bands and allow the active drug and excipient used to bulk the tablets to be identified. Relative band heights can be used to determine drug/excipient ratios and the degree of hydration of the drug while the fact that 50 tablets per hour can be analysed allows large numbers of spectra to be recorded. The ability of Raman spectroscopy to distinguish between ecstasy tablets on the basis of their chemical composition is illustrated here by a sample set of 400 tablets taken from a large seizure of > 50,000 tablets that were found in eight large bags. The tablets are all similar in appearance and carry the same logo. Conventional analysis by GC-MS showed they contained MDMA. Initial Raman studies of samples from each of the eight bags showed that despite some tablet-to-tablet variation within each bag the contents could be classified on the basis of the excipients used. The tablets in five of the bags were sorbitol-based, two were cellulose-based and one bag contained tablets with a glucose excipient. More extensive analysis of 50 tablets from each of a representative series of sample bags have distribution profiles that showed the contents of each bag were approximately normally distributed about a mean value, rather than being mixtures of several discrete types. Two of the sorbitol-containing sample sets were indistinguishable while a third was similar but not identical to these, in that it contained the same excipient and MDMA with the same degree of hydration but had a slightly different MDMA/sorbitol ratio. The cellulose-based samples were badly manufactured and showed considerable tablet-to-tablet variation in their drug/excipient ratio while the glucose-based tablets had a tight distribution in their drug/excipient ratios. The degree of hydration in the MDMA feedstocks used to manufacture the cellulose-, glucose- and sorbitol-based tablets were all different from each other. This study, because it centres on a single seizure of physically similar tablets with the same active drug, highlights the fact that simple physical descriptions coupled with active drug content do not in themselves fully characterize the nature of the seized materials. There is considerable variation in the composition of the tablets within this single seizure and the fact that this variation can be detected from Raman spectra demonstrates that the potential benefits of obtaining highly detailed spectra can indeed translate into information that is not readily available from other methods but would be useful for tracing of drug distribution networks.

Hallucinogens↗
PubMed1998

Ion recombination corrections for the NACP parallel-plate chamber in a pulsed electron beam.

The NACP electron chamber is one of three parallel-plate chambers recommended for use in the UK. Measurements with this chamber type have indicated a problem in determining the recombination correction. This is due to a variation of the ionization current I with polarizing voltage V which deviates from the accepted Boag theory. It is shown that there is a chamber-dependent threshold voltage below which the NACP chamber follows the Boag theory. Above this voltage the chamber should be used with caution, although it is still possible to correct for the dependence of the chamber response on the dose per pulse. The existence of such deviations from theory demonstrates the usefulness of the 1/I against 1/V plot and the limitations of the Boag two-voltage analysis. Values for the initial recombination and the coefficient of general recombination are measured for several NACP chambers. It is shown that from these one can derive a value for the effective plate separation and the collector radius of each chamber. Differences in the behaviour of NACP chambers manufactured by Scanditronix and Dosetek are discussed and the implications of free-electron collection are considered.

Electrons↗
PubMed1996

R50 as a beam quality specifier for selecting stopping-power ratios and reference depths for electron dosimetry.

For electron beam reference dosimetry in radiotherapy, it is shown that by choosing the reference depth as dref = 0.6R(50)-0.1 cm, where R50 is the half-value depth in centimeters, the Spencer-Attix water-to-air stopping-power ratio at dref is given by (Llp)airw = 1.2534 - 0.1487 (R50)0.2144. This is derived from data for (Llp)airw obtained from realistic Monte Carlo simulations for 24 clinical beams. The rms deviation of this expression from the Monte Carlo calculations is 0.16%, with a maximum deviation of 0.26%. This approach fully takes into account the spectral differences between real electron beams of the same R50 and allows an absorbed-dose calibration at a standards laboratory to be easily and accurately transferred to a reference clinical beam. Using a single parameter to specify (Llp)airw, rather than the two parameters (R50 and depth) needed when the reference depth is chosen as the depth of dose maximum, has the potential to greatly simplify electron beam dosimetry protocols and allows the use of a similar formalism for photon and electron beam dosimetry. For use in converting a depth-ionization curve into a depth-dose curve, a somewhat less accurate but general expression for (Llp)w(air) as a function of R50 and depth is presented.

Biophysical Phenomena↗
PubMed1995

A new method to determine ratios of electron stopping powers to an improved accuracy.

A new method is presented to determine the ratio of electron stopping powers which is effective in the transfer of absorbed dose from one medium to another. The method involves an accurate measurement of the electron range in each of the media combined with a full Monte Carlo simulation of each experimental geometry. For the specific case of graphite and water, the uncertainty attainable is estimated to be around +/- 0.5% at the 95% confidence level, which is approximately a factor of three better than the best methods currently in use.

Biophysical Phenomena↗
PubMed1994

Cyclodextrins as versatile chiral recognition reagents for use in a variety of optical and separative analyses.

A short overview is presented covering the actual and potential use of cyclodextrins and some of their derivatives in analytical chemistry. The contributions in separation science, including HPLC, GC, CE and MEKC are noted, together with applications in circular dichroism and luminescence techniques, including fluorescence and phosphorescence.

Chemistry Techniques, Analytical↗