methods for impurity profiling of heroin and cocaine - United Nations ...
methods for impurity profiling of heroin and cocaine - United Nations ...
methods for impurity profiling of heroin and cocaine - United Nations ...
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Data h<strong>and</strong>ling, interpretation <strong>of</strong> results <strong>and</strong> data collections 49<br />
bulk <strong>of</strong> the <strong>heroin</strong> <strong>and</strong> other alkaloidal bases are retained in the aqueous phase<br />
while extracting many <strong>of</strong> the alkaloidal-related amidic compounds into an organic<br />
phase. High-resolution capillary gas chromatograms <strong>of</strong> these extracts are typically<br />
quite complex <strong>and</strong> many analysts have found that visual comparison <strong>of</strong> the<br />
overlaid chromatograms is the most efficient direct comparison method (see annex<br />
II, tables 1 <strong>and</strong> 2, <strong>for</strong> a listing <strong>of</strong> many <strong>of</strong> the known alkaloidal compounds found<br />
in <strong>heroin</strong> <strong>and</strong> <strong>cocaine</strong>).<br />
B. Interpretation <strong>of</strong> results<br />
Irrespective <strong>of</strong> the equipment <strong>and</strong> s<strong>of</strong>tware available in a laboratory carrying out,<br />
or planning to carry out, <strong>impurity</strong> <strong>pr<strong>of</strong>iling</strong>, the results have to be interpreted carefully,<br />
taking all relevant considerations into account, including analytical implications<br />
<strong>of</strong> illicit processing <strong>and</strong> distribution, as well as those arising, <strong>for</strong> example,<br />
from differences in storage conditions. Experience in the interpretation <strong>of</strong> <strong>pr<strong>of</strong>iling</strong><br />
results can only be built gradually, but good analytical skills <strong>and</strong> knowledge<br />
<strong>of</strong> relevant chemistry are essential. In addition, <strong>for</strong> analytical results to be operationally<br />
useful, they have to be communicated in an adequate way to the requesting<br />
authority. The <strong>United</strong> <strong>Nations</strong> manual Drug Characterization/Impurity Pr<strong>of</strong>iling:<br />
Background <strong>and</strong> Concepts [5] provides an overview <strong>of</strong> relevant practical aspects<br />
related to the interpretation <strong>of</strong> results, addressing the following areas:<br />
(a) The significance <strong>of</strong> chemical similarities <strong>and</strong> differences between<br />
drug samples;<br />
(b) Establishing specific links between two or more samples;<br />
(c) Establishing drug distribution patterns;<br />
(d) Identifying the source <strong>of</strong> drug samples:<br />
(i) Natural <strong>and</strong> semi-synthetic drugs;<br />
(ii) Synthetic drugs;<br />
(e) Identifying <strong>and</strong> characterizing the specific starting materials employed<br />
in cl<strong>and</strong>estine drug manufacture.<br />
C. Approach to setting up <strong>pr<strong>of</strong>iling</strong> data collections<br />
As explained previously, the availability <strong>of</strong> appropriate databases is critical <strong>for</strong><br />
both types <strong>of</strong> comparison, case-to-case comparisons <strong>for</strong> evidential purposes <strong>and</strong><br />
retrospective comparisons <strong>for</strong> intelligence purposes. A recommended approach to<br />
the compilation <strong>of</strong> a <strong>pr<strong>of</strong>iling</strong> data collection is as follows:<br />
(a) Generate a data bank <strong>of</strong> comparison data (i.e. analytical data plus any<br />
appropriate physical data). (The samples used <strong>for</strong> generating compari-