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INTRODUCTION
LIMITATIONS OF CONVENTIONAL LABORATORY TESTS
BIOSENSORS AND DETECTION
EVANESCENT WAVE FIBER-OPTIC BIOSENSORS
FIBER OPTICS BIOSENSORS & BACTERIA DETECTION
REFERENCES

LIMITATIONS OF CONVENTIONAL LABORATORY TESTS:

            Although conventional bacterial testing methods are sensitive, inexpensive and contain qualitative and quantitative information of the microorganisms present in a food sample, they are often very time consuming and require extensive microbiological trainings. Conventional bacteria testing involve five steps: pre-enrichment, selective-enrichment, selective plating, biochemical tests and serological tests. The concept behind these steps is to isolate the targeted microorganisms from other organic and non organic substances and then grow them in culture medium into visible colonies for detection which usually takes 5 to 7 days.

 

            Storage of food for seven days for laboratory results costs food industry millions of dollars.  In many cases when result of a laboratory test is ready, food products are in suppliers’ warehouses or on supermarkets’ shelves. In addition, preparation of culture medium, incubation of plates, biochemical tests and immunodiagnostic test make these methods labor intensive.

 

            Automated systems have enhanced the detection of microorganisms. These automated systems perform the same test as conventional procedures but results are determined within few hours with minimal human interference. The disadvantages of automated devices are that they require pure cultures and operate with large and expensive equipments. Such disadvantages have limited the used of automated devices to hospital laboratories for human clinical applications.

 

Immunofluorescence and enzyme-linked immunosorbent assays (ELISAs) are immno-diagnostic tests that use antibody/antigen binding complex to identify microorganisms Although these tests are quick with high selectivity and specificity, they require at least  bacteria in colony for detection. If  bacteria are not present, culturing in nutrient medium for 1-2 day is needed.

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