Microtiter plate

"Microplate" redirects here. For the geographical use, see list of tectonic plates.
Microtiter plates with 96, 384 and 1536 wells

A microtiter plate (spelled Microtiter is a registered trade name in the United States) or microplate or microwell plate or multiwell,[1] is a flat plate with multiple "wells" used as small test tubes. The microplate has become a standard tool in analytical research and clinical diagnostic testing laboratories. A very common usage is in the enzyme-linked immunosorbent assay (ELISA), the basis of most modern medical diagnostic testing in humans and animals.

A microplate typically has 6, 24, 96, 384 or 1536 sample wells arranged in a 2:3 rectangular matrix. Some microplates have even been manufactured with 3456 or 9600 wells, and an "array tape" product has been developed that provides a continuous strip of microplates embossed on a flexible plastic tape.[2]

Each well of a microplate typically holds somewhere between tens of nanolitres[3][4][5] to several millilitres of liquid. They can also be used to store dry powder or as racks to support glass tube inserts. Wells can be either circular or square. For compound storage applications, square wells with close fitting silicone cap-mats are preferred. Microplates can be stored at low temperatures for long periods, may be heated to increase the rate of solvent evaporation from their wells and can even be heat-sealed with foil or clear film. Microplates with an embedded layer of filter material were developed in the early 1980s by several companies, and today, there are microplates for just about every application in life science research which involves filtration, separation, optical detection, storage, reaction mixing, cell culture and detection of antimicrobial activity. [6]

The enormous growth in studies of whole live cells has led to an entirely new range of microplate products which are "tissue culture treated" especially for this work. The surfaces of these products are modified using an oxygen plasma discharge to make their surfaces more hydrophilic so that it becomes easier for adherent cells to grow on the surface which would otherwise be strongly hydrophobic.

Liquid handling robot for 96 wells

A number of companies have developed robots to specifically handle microplates. These robots may be liquid handlers which aspirate or dispense liquid samples from and to these plates, or "plate movers" which transport them between instruments, plate stackers which store microplates during these processes, plate hotels for longer term storage, plate washers for processing plates, plate thermal sealers for applying heat seals, de-sealers for removing heat seals, or microplate incubators to ensure constant temperature during testing. Instrument companies have designed plate readers which can detect specific biological, chemical or physical events in samples stored in these plates.

Manufacture and composition

Microplates are manufactured in a variety of materials. The most common is polystyrene, used for most optical detection microplates. It can be coloured white by the addition of titanium dioxide for optical absorbance or luminescence detection or black by the addition of carbon for fluorescent biological assays. Polypropylene is used for the construction of plates subject to wide changes in temperature, such as storage at -80 °C and thermal cycling. It has excellent properties for the long-term storage of novel chemical compounds. Polycarbonate is cheap and easy to mould and has been used for disposable microplates for the polymerase chain reaction (PCR) method of DNA amplification. Cyclo-olefins are now being used to provide microplates which transmit ultraviolet light for use in newly developed assays. There are also microplates constructed from solid pieces of glass and quartz for special applications.

The most common manufacturing process is injection molding, used for polystyrene, polypropylene and cyclo-olefin ( no such Material, however microplates are made from a variety of Polymers to resist a wide temperature and chemical resistance. There are also plates made from Glass, a combination of Plastic and with a glass bottom. Vacuum forming can be used with many other plastics such as polycarbonate. Composite microplates, In addition filter bottom platesSPE plates and even some advanced PCR plate designs use multiple components which are moulded separately and later assembled into a finished product. ELISA plates may now be assembled from twelve separate strips of eight wells, making it easier to only partially use a plate. This saves cost for the scientist.

History

A commercial microplate washer

The earliest microplate was created in 1951 by a Hungarian, Dr. Gyula Takátsy, who machined 6 rows of 12 "wells" in Lucite.[7][8] However, common usage of the microplate began in the late 1950s when John Liner in USA had introduced a molded version. By 1990 there were more than 15 companies producing a wide range of microplates with different features. It was estimated that 125 million microplates were used in 2000 alone. The word "Microtiter" is a registered trademark of Cooke Engineering Company, and Thermo Electron OY is the last listed owner of the trademark (U.S. Trademark 72,128,338.) It is now more usual to use the generic term "microplate".

Other tradenames for Microplates include Viewplate, Unifilter introduced in the early 1990s by Polyfiltronics and sold by Packard Instrument which is now part of Perkin Elmer

In 1996, the Society for Biomolecular Screening (SBS), later known as Society for Biomolecular Sciences, began an initiative to create a standard definition of a microtiter plate. A series of standards was proposed in 2003 and published by the American National Standards Institute (ANSI) on behalf of the SBS. The standards govern various characteristics of a microplate including well dimensions (e.g. diameter, spacing and depth) as well as plate properties (e.g. dimensions and rigidity) (typical dimension ~5"x3.33"), which allows interoperability between microplates, instrumentation and equipment from different suppliers, and is particularly important in laboratory automation. In 2010, the Society for Biomolecular Sciences merged with the Association for Laboratory Automation (ALA) to form a new organisation, the Society for Laboratory Automation and Screening (SLAS). Henceforth, the microplate standards are known as ANSI/SLAS standards.

References

  1. ↑ http://www.corporeality.net/museion/category/medical-scientific-instruments/
  2. ↑ Elaine May (2007-06-15). "Array Tape for Miniaturized Genotyping". Genetic Engineering & Biotechnology News (Mary Ann Liebert, Inc.). p. 22. Retrieved 2008-07-06. (subtitle) Processing hundreds of microplate equivalents without complex plate-handling equipment
  3. ↑ Lindström, Sara; Eriksson, Malin; Vazin, Tandis; Sandberg, Julia; Lundeberg, Joakim; Frisén, Jonas; Andersson-Svahn, Helene (2009-01-01). "High-density microwell chip for culture and analysis of stem cells". PloS One 4 (9): e6997. doi:10.1371/journal.pone.0006997. ISSN 1932-6203. PMC 2736590. PMID 19750008.
  4. ↑ Weibull, Emilie; Antypas, Haris; Kjäll, Peter; Brauner, Annelie; Andersson-Svahn, Helene; Richter-Dahlfors, Agneta (2014-09-01). "Bacterial nanoscale cultures for phenotypic multiplexed antibiotic susceptibility testing". Journal of Clinical Microbiology 52 (9): 3310–3317. doi:10.1128/JCM.01161-14. ISSN 1098-660X. PMC 4313156. PMID 24989602.
  5. ↑ Lindström, Sara; Larsson, Rolf; Svahn, Helene Andersson (2008-03-01). "Towards high-throughput single cell/clone cultivation and analysis". Electrophoresis 29 (6): 1219–1227. doi:10.1002/elps.200700536. ISSN 0173-0835. PMID 18288779.
  6. ↑ Inglin, Raffael C. (2015). "High-throughput screening assays for antibacterial and antifungal activities of Lactobacillus species". Journal of Microbiological Methods 114 (July 2015): 26-29. doi:10.1016/j.mimet.2015.04.011.
  7. ↑ Farkas E. "Microtitrations in serology and virology – a citation-classic commentary on the use of spiral loops in serological and virological micro-methods by Takatsy, G." (PDF). CC/Life Sci (30): 10-10 Jul 27 1992.
  8. ↑ Takatsy G (1950). "Uj modszer sorozatos higitasok gyors es pontos elvegzesere" [A rapid and accurate method for serial dilutions]. Kiserl. Orvostud. 5: 393–7.

External links

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