Simple and inexpensive immunoassay-based diagnostic tests

Simple and inexpensive yet sensitive and robust diagnostic tests are critically needed for resource-poor settings to enable timely diagnosis and effective use of limited health care resources. Current tests are often too expensive, too slow, or have compromised clinical performance, and they often require health care professional to perform the test. In addition, most assays are not intended to be used in extreme environmental conditions, but their performance may be affected by high temperatures and humidity often encountered in resource-poor settings. This review provides an overview of current immunoassay technologies and their advantages and limitations with respect to their feasibility to resource-poor settings. Future trends of immunoassay development for decentralized testing are also discussed. Homogeneous assays as such are out of the scope of this article because they are generally not yet sensitive enough or otherwise less feasible for inexpensive rapid diagnostic tests.     

Non-plasma bonding of PDMS for inexpensive fabrication of microfluidic devices

In this video, we demonstrate how to use the neuron microfluidic device without plasma bonding. In some cases it may be desirable to reversibly bond devices to the Corning No. 1 cover glass. This could be due, perhaps, to a plasma cleaner not being available. In other instances, it may be desirable to remove the device from the glass after the culturing of neurons for certain types of microscopy or for immunostaining, though it is not necessary to remove the device for immunostaining since the neurons can be stained in the device. Some researchers, however, still prefer to remove the device. In this case, reversible bonding of the device to the cover glass makes that possible. There are some disadvantages to non-plasma bonding of the devices in that not as tight of a seal is formed. In some cases axons may grow under the grooves rather than through them. Also, because the glass and PDMS are hydrophobic, liquids do not readily enter the device making it necessary at times to force media and other reagents into the device. Liquids will enter the device via capillary action, but it takes significantly longer as compared to devices that have been plasma bonded. The plasma cleaner creates temporary hydrophilic charges on the glass and device that facilitate the flow of liquids through the device after bonding within seconds. For non-plasma bound devices, liquid flow through the devices takes several minutes. It is also important to note that the devices to be used with non-plasma bonding need to be sterilized first, whereas plasma treated devices do not need to be sterilized prior to use because the plasma cleaner will sterilize them.     

Simple fabrication of gold nanobelts and patterns

Gold nanobelts are of interest in several areas; however, there are only few methods available to produce these belts. We report here on a simple evaporation induced self-assembly (EISA) method to produce porous gold nanobelts with dimensions that scale across nanometer (thickness ～80 nm) and micrometer (width ～20 μm), to decimeter (length ～0.15 m). The gold nanobelts are well packed on the beaker wall and can be easily made to float on the surface of the solution for depositing onto other substrates. Microscopy showed that gold nanobelts had a different structure on the two sides of the belt; the density of gold nanowires on one side was greater than on the other side. Electrical measurements showed that these nanobelts were sensitive to compressive or tensile forces, indicating a potential use as a strain sensor. The patterned nanobelts were further used as a template to grow ZnO nanowires for potential use in applications such as piezo-electronics.     

Simple and inexpensive devices to measure heart rates of incubating birds

ABSTRACT Heart rate is a useful physiological index for studies of stress, locomotion, and activity patterns. Measuring heart rates of birds without the need to handle individuals is desirable when trapping is problematic or may cause unwanted disturbance. Heart‐rate recorders housed in dummy eggs offer an effective solution, but the usefulness of previously described devices is limited by their size, complex construction, and reliance on analog media. We constructed egg‐based, heart‐rate monitors through simple modifications of inexpensive, commercially available MP3 players and Bluetooth headsets. We compared the merits of each device during tests in the laboratory, an aviary, and the field in 2008. Field testing was undertaken at Presqu’ile Provincial Park, Ontario, Canada, where we recorded heart rates of Common Terns (Sterna hirundo), Caspian Terns (Hydroprogne caspia), and Ring‐billed Gulls (Larus delawarensis). Birds incubated dummy eggs normally, with no differences in behavior (all P > 0.05) when incubating either wired (MP3 players) or wireless (Bluetooth) devices. MP3 devices were more reliable in the field. Bluetooth devices often lost pairing with laptop computers (33% of files analyzed contained no signal), produced files with more obscuring noise, and only two could be deployed simultaneously with a single computer; there was no limit on how many MP3 devices could be deployed simultaneously. Common Terns, the smallest of our three focal species, had significantly higher (P < 0.001) mean heart rates (268.6 ± 9.3 beats per min [bpm]) than either Ring‐billed Gulls (198.0 ± 7.1 bpm) or Caspian Terns (204.2 ± 8.0 bpm). Heart rates of all three species were consistent with those reported or predicted from previous studies. The MP3 devices we describe provide investigators with a simple, inexpensive, and minimally invasive way to digitally record heart rates of birds of almost any size.     

Simple, inexpensive method for controlled freezing of cell cultures

[This corrects the article on p. 616 in vol. 27.].     

Simple, inexpensive method for controlled freezing of cell cultures

We have devised a system for controlled cooling of living cells which eliminates the need for complicated, expensive equipment but allows excellent recovery of viable cells after storage in liquid nitrogen.     

Generation of density gradients. Approximations to equivolumetric gradients for zonal rotors

The use of a “density gradient generating function” allows the concentration profile of a density gradient to be written explicitly in terms of the required distribution of sedimentation coefficients in place of the previous implicit formulations. This function, which is easily implemented in a computer program, permits calculation of density gradients for a number of applications. This approach is applied to computation of a variety of equivolumetric gradients of sucrose for zonal rotors and yields a formula for the calibration of such gradients. An accurate approximation has been found which allows the generation of virtually all equivolumetric gradients of sucrose for a given rotor using a single program for the gradient generator employed; the adjustment for different particle densities and for different concentrations at the top of the gradient is made by varying only the initial and final concentrations of sucrose used.     

Simple, inexpensive attainment and measurement of very high cooling and warming rates

We have developed a simple, inexpensive system (<$300 US) for measuring cooling and warming rates of small (∼ 0.1 μl) aqueous samples at rates as high as 10⁵ °C/min. The measurement system itself, can track rates approaching one million °C/min. For temperature sensing, a Type T thermocouple with 50 μm wire was used. The thermocouple output voltage was read with an inexpensive USB based digital oscilloscope interfaced to a laptop computer, and the raw data were processed with MS Excel.     

Buoyant density sedimentation of macromolecules in sodium iothalamate density gradients.

Nucleic acids, bacteriophages, phage capsids, and a DNA-capsid complex have been centrifuged to an equilibrium buoyant density in sodium iothalamate density gradients. Nucleic acids have comparatively high hydrations and are less dense than proteins in these gradients. Sodium iothalamate gradients can be used to separate DNA from RNA, single-chain DNA from double-chain DNA and to separate bacteriophage T7 and λ deletion mutants from the respective wild-type phage.The DNA packaged in bacteriophage T7 appears to be less hydrated than free DNA in sodium iothalamate gradients. There is evidence that the hydration of DNA packaged in phage T7 is restricted by the volume of the phage head. The total volume of phage T7 was estimated to be 1.32 × 10⁻¹⁶ ml. The volume available to package phage T7 DNA was estimated to be 2.2 times the volume of the B form of T7 DNA.