A Modified Jaffe Test for Determination of Paralytic Shellfish Poison

1959 ◽  
Vol 42 (2) ◽  
pp. 399-404
Author(s):  
E F McFarren ◽  
E J Schantz ◽  
J E Campbell ◽  
K H Lewis
1994 ◽  
Vol 11 (1) ◽  
pp. 39-56 ◽  
Author(s):  
H. P. Van Egmond ◽  
H. J. van den Top ◽  
W. E. Paulsch ◽  
X. Goenaga ◽  
M. R. Vieytes

1977 ◽  
Vol 34 (4) ◽  
pp. 559-563 ◽  
Author(s):  
R. M. Gershey ◽  
R. A. Nevé ◽  
D. L. Musgrave ◽  
P. B. Reichardt

Saxitoxin, the paralytic shellfish poison, can be conveniently determined by colorimetry after hydrogen peroxide oxidation and reaction of the resultant guanidine with biacetyl. This colorimetric method has been used to assay saxitoxin quantitatively at concentrations down to 0.5 μg/ml. Saxitoxin levels in the Alaskan butter clam (Saxidomus gigantea) have also been determined by this test coupled with a preliminary chromatographic cleanup procedure. Key words: saxitoxin, paralytic shellfish poison, colorimetry, Alaskan butter clam (Saxidomus gigantea)


1958 ◽  
Vol 41 (1) ◽  
pp. 168-177
Author(s):  
E F McFarren ◽  
E J Schantz ◽  
J E Campbell ◽  
K H Lewis

2016 ◽  
Vol 60 (4) ◽  
pp. 447-451 ◽  
Author(s):  
Mirosław Michalski ◽  
Jacek Osek

Abstract Introduction: Growing consumption of shellfish is associated with an increased risk of food poisoning. The study was carried out on live bivalve molluscs available on the Polish market between 2009 and 2013. Material and Methods: ELISA was used for the determination of the following marine biotoxins: paralytic shellfish poison (PSP), amnaesic shellfish poison (ASP), and diarrhoeic shellfish poison (DSP). The molluscs, of which seven species were examined, were obtained from wholesale companies and markets. Results: Marine biotoxins were detected below the permitted levels in 67.6% of the samples. The maximum amounts of PSP and ASP biotoxins were found in great scallops (532.6 μg/kg and 1.0 mg/kg respectively) and the peak for DSP was in blue mussels (107 μg/kg). Conclusion: The analysis of toxicological status of raw bivalve molluscs available on the market in Poland indicates that they are safe for consumers.


2014 ◽  
Vol 97 (2) ◽  
pp. 492-497 ◽  
Author(s):  
Andrew D Turner ◽  
Monika Dhanji-Rapkova ◽  
Clothilde Baker ◽  
Myriam Algoet

Abstract AOAC Official Method 2005.06 precolumn oxidation LC-fluorescence detection method has been used for many years for the detection and quantitation of paralytic shellfish poisoning (PSP) toxins in bivalve molluscs. After extensive single- and multiple-laboratory validation, the method has been slowly gaining acceptance worldwide as a useful and practical tool for official control testing. In Great Britain, the method has become routine since 2008, with no requirement since then for reverting back to the bioassay reference method. Although the method has been refined to be semiautomated, faster, and more reproducible, the quantitation step can be complex and time-consuming. An alternative approach was developed to utilize the qualitative screening results for generatinga semiquantitative results assessment. Data obtained over 5 years enabled the comparison of semiquantitative and fully quantitative PSP results in over 15 000 shellfish samples comprising eight different species showed that the semiquantitative approach resulted in over-estimated paralytic shellfish toxin levels by an average factor close to two in comparison with the fully quantified levels. No temporal trends were observed in the data or relating to species type, with the exception of surf clams. The comparison suggested a semiquantitative threshold of 800 μg saxitoxin (STX) eq/kg should provide a safe limitfor the determination of samples to be forwarded to full quantitation. However, the decision was taken to halve this limit to include an additional safety factor of 2, resulting in the use of a semiquantitative threshold of 400 μg STX eq/kg. Implementation of the semiquantitative method into routine testing would result in a significant reduction in the numbers of samples requiring quantitation and have a positive impact on the overall turnaround of reported PSP results. The refined method would be appropriate for any monitoring laboratory faced with high throughput requirements.


1991 ◽  
Vol 56 (6) ◽  
pp. 1572-1575 ◽  
Author(s):  
YUJI NAGASHIMA ◽  
TAMAO NOGUCHI ◽  
MUNEHIKO TANAKA ◽  
KANEHISA HASHIMOTO

1966 ◽  
Vol 8 (2) ◽  
pp. 286-294 ◽  
Author(s):  
James S. Watts ◽  
J. Reilly ◽  
F.M. DaCosta ◽  
S. Krop

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