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. 2015 Nov 26;13(12):7087–7112. doi: 10.3390/md13127057

Table 1.

Summary of methods applicable to the detection of CI producing phytoplankton and shellfish CIs.

Method Advantages Disadvantages
Microscopy
  • Detection of Alexandrium genus

  • Fulfils requirement of legislation

  • Identification to species too time consuming for routine analysis

Particle counting methods
  • Potential for more rapid enumeration than by manual cell count

  • Morphology of causative species prevents easy enumeration

  • Little evidence of suitability for field situations

  • Sample preservation compromises detection

Molecular techniques
  • Enables species identification

  • Methods still research based without application to official testing as yet

  • Sample preparation can be time consuming

  • Some required fixatives difficult to use in a monitoring context

Mouse bioassay (MBA)
  • Direct toxicity assessment in the animal

  • History of use and prevention of sickness

  • Qualitative

  • Possible interferences

  • No indication of toxin profile

  • Ethical issues

  • Variable performance

  • Not validated

Fluorescence polarization (competitive)
  • Quick

  • Technically easy

  • Some toxicity assessment (only for the targeted mechanism of action)

  • No indication of toxicity for toxins with a different mode of action

  • No information on toxic profile

  • Dependent on availability of receptors from Torpedo marmorata electric organ

  • Validation data limited

  • Standards required to test performance for other analogues

Fluorescence polarization (direct)
  • As competitive FP

  • More sensitive than the competitive assay

  • Easier than competitive FP

  • As competitive assay

  • Tested only in one shellfish species for one SPX

Solid-phase receptor-based assays (RBA)
  • Simple, sensitive, rapid

  • Good performance in collaborative study

  • Promising fluorescence-based binding assay

  • Variable affinity for BTX metabolites

  • Requirement for animal tissues and radiolabel

  • Matrix effects

  • Limited development to date with fluorescence-based binding assay

HPLC-UV
  • Can be automated

  • Quantitative method

  • Low specificity

  • Standards required for some CIs

  • Not validated

LC-MS(MS)
  • Can be automated

  • Highly specific

  • Sensitive

  • Toxin profile information available

  • Expensive instrumentation

  • Lack of availability of all relevant standards

  • No indication of toxicity