Handbook of Herbs and Spices - Volume 3

(sharon) #1

48 Handbook of herbs and spices


MRMs require a great deal of time to perform, thereby reducing the number of


samples analysed and the speed of analysis. For example, certain foods, such as those


with high concentrations of fats and oils, are difficult to analyse in a timely manner.


Single residue methods (SRMs) are another category that depend on a number of


different techniques and vary widely in terms of reliability, efficiency, throughput


(samples per day), degree of validation, and practicality for regulatory use. Because


SRMs have been developed by the private sector for submission to EPA as part of the


tolerance setting process, a method exists for every pesticide with a tolerance. Most


SRMs, like MRMs, are based on GC using the full array of element specific detectors.


Although less efficient than MRMs, SRMs are necessary to monitor those pesticides


that cannot be detected by MRMs. SRMs are generally not considered adequate for


routine monitoring by the regulatory agencies, though FDA uses them. To monitor


one pesticide with an SRM is considered inefficient when an MRM can measure


many pesticides using the same resources. In addition, SRMs vary widely even for


chemicals of the same class, so a laboratory needs a wide array of glassware, evaporative


devices, chromatography, and detectors to use the SRMs available.


There is a third class of methods, namely the semi-quantitative and qualitative


methods, that range widely in their ability to quantify the chemical present in a sample.


Semi-quantitative methods indicate the range of pesticide residue concentration in a


sample, while qualitative methods show whether or not a particular pesticide exists


above detectable limits. These methods use technologies like thin layer chromatography


(TLC), enzyme inhibition, and immunoassay, all of which can be moved from the


laboratory into the field without losing their ability to detect pesticides. The enzyme


inhibition-based colour reactions make spots and bands of pesticide residues on thin


layer chromatographic plates visible, in order to measure the pesticide residue either


visually or with instruments. Such techniques are being used for cholinesterase-


inhibiting insecticides and photosynthesis-inhibiting herbicides. Because sophisticated


instrumentation is not required they are relatively inexpensive compared to quantitative


methods. The benefits of these methods are their low cost, speed, or ease of use and


more number of samples that could be analysed. Nevertheless, neither FDA nor FSIS


is currently using these methods for pesticides. A drawback of semi-quantitative


methods is that they do not provide the degree of accuracy necessary for enforcement


action, as in a court of law. Violations found by a semi-quantitative method would have


to be verified by a quantitative analytical method – or maybe two.


As techniques are improved by changes in instrument and hardware design, bringing


about more sensitive, selective, and reproducible devices, their costs usually increase,


particularly when automated sample handling and data manipulation are included.


These additional costs translate into higher costs to implement contemporary pesticide


methodologies for varied herbal samples. Supercritical fluid chromatography (SFC)


is a new technique of chromatographic separation used in the regulatory analysis of


pesticide residues in food. With super fluids as the solvent phase, SFC can chromatograph


chemicals that cannot be handled by gas chromatography because of their non-


volatility or thermal instability. Many detectors designed for GC can also be used in


SFC, such as the flame ionisation, the nitrogen-phosphorus, and the atomic emission


spectrometric as well as the UV absorbance detectors. New analytical methods are


needed to expand the range of pesticide analytes that can be detected in plant derived


food products like herbals in a more efficient process.


Some of these advanced technologies include gas or liquid chromatography/mass


spectrometry (or tandem mass spectrometry), solid phase extraction, laser-induced

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