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Published September 17, 2013 | Supplemental Material
Journal Article Open

A microfluidic device for dry sample preservation in remote settings

Abstract

This paper describes a microfluidic device for dry preservation of biological specimens at room temperature that incorporates chemical stabilization matrices. Long-term stabilization of samples is crucial for remote medical analysis, biosurveillance, and archiving, but the current paradigm for transporting remotely obtained samples relies on the costly "cold chain" to preserve analytes within biospecimens. We propose an alternative approach that involves the use of microfluidics to preserve samples in the dry state with stabilization matrices, developed by others, that are based on self-preservation chemistries found in nature. We describe a SlipChip-based device that allows minimally trained users to preserve samples with the three simple steps of placing a sample at an inlet, closing a lid, and slipping one layer of the device. The device fills automatically, and a pre-loaded desiccant dries the samples. Later, specimens can be rehydrated and recovered for analysis in a laboratory. This device is portable, compact, and self-contained, so it can be transported and operated by untrained users even in limited-resource settings. Features such as dead-end and sequential filling, combined with a "pumping lid" mechanism, enable precise quantification of the original sample's volume while avoiding overfilling. In addition, we demonstrated that the device can be integrated with a plasma filtration module, and we validated device operations and capabilities by testing the stability of purified RNA solutions. These features and the modularity of this platform (which facilitates integration and simplifies operation) would be applicable to other microfluidic devices beyond this application. We envision that as the field of stabilization matrices develops, microfluidic devices will be useful for cost-effectively facilitating remote analysis and biosurveillance while also opening new opportunities for diagnostics, drug development, and other medical fields.

Additional Information

© 2013 The Royal Society of Chemistry. Received 22 Jun 2013, Accepted 15 Aug 2013; First published online 17 Sep 2013. This work was funded in part by DARPA Cooperative Agreement No. HR0011-11-2-0006 (for plasma filtration and integration) and by NIH grant No. R01EB012946 administered by the National Institute of Biomedical Imaging and Bioengineering (for initial concept development). This paper does not necessarily reflect the position or policy of the U.S. government or these agencies, and no official endorsement should be inferred. The authors would like to thank the Millard and Muriel Jacobs Genetics and Genomics Laboratory for access to its bioanalyzer, Liang Li for discussions about pumping and device fabrication, Qichao Pan for work on the bibliography, discussions about stabilization, and initial tests of drying on a previous version of the device, Bing Sun and Stephanie McCalla for their help in setting up RT-PCR quantification, Yu-Hsiang Hsu, Liang Ma and Alexander Tucker-Schwartz for discussions about device design and properties, Rolf Muller and Judy Muller-Cohn at Biomatrica Inc. for useful discussions about sample preservation, and Whitney Robles for contributions to writing and editing this manuscript. Disclosure: R.F.I. and F.S. have a financial interest in SlipChip Corp.

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