(481d) An Injection-Molded Device for Purification of Nucleic Acids From Whole Blood Using Isotachophoresis

An
Injection-Molded Device for Purification of

Nucleic
Acids from Whole Blood using Isotachophoresis

Lewis A. Marshall, Anita Rogacs, Carl Meinhart, and Juan
G. Santiago

Stanford University

Stanford, CA 94305, USA

We have designed a new microfluidic chip to simplify nucleic
acid preparation from biological samples such as whole blood. We previously
demonstrated the application of isotachophoresis (ITP) for sample preparation.¹
We here describe the design of an injection molded plastic device capable
of purifying DNA from a 25 µL sample of whole blood lysate under 40 min.

We have targeted samples with volumes between 2-25 µL
in an attempt to address an unmet need in sample preparation. Solid phase
extraction (SPE) kits for purification of nucleic acids work well for sample
volumes of 100-1000 µL, and nucleic acid yields of several nanograms.
However, they exhibit poor extraction efficiency for samples of low volume and smaller
nucleic acid yields. ITP does not rely on surface adsorption, and so can operate
on samples with a wide range of volumes and nucleic acid content. Our new
device enables ITP purification of samples in this critical volume range while
simplifying device operation. We have also maximized device throughput by
adjusting our chemistry and protocol and considering the sample volume
processing rate as a cost function..

This new device is pictured in Figure 1. This custom device is fabricated from injection molded Topas cyclic olefin copolymer (COC) or poly(methyl
methacrylate) (PMMA). The device was fabricated by the
microfluidics foundry Microfluidic Chipshop GmbH of
Jenna, Germany. The injection molded layer
contains channels with a nominal cross-section of
2 mm x 150 µm, a total length of 16 cm. The injection molded layer is capped by a thin, transparent plastic
film to enable imaging into the channel.

We've included novel features in this chip to improve the
device loading process. To simplify set up of the initial interface between the
sample and the separation buffer, we've developed a specialized capillary barrier
structure that provides passive valving for sequential
loading of liquids into the device. This structure is shown in Figure 2. In addition to incorporating this
passive valving system for device loading, we have
incorporated the use of gels in the buffering reservoirs to suppress pressure
driven flow. This simplifies loading by making the device performance robust to
uneven fluid levels in the reservoirs.

We used this device to extract DNA from whole blood lysate
samples. A visualization of the separation process is shown in Figure 3. Here, we separate two
fluorescent dyes with mobilities similar to DNA and a contaminating protein
species. The analyte dye focuses into a sharp band and elutes into the
extraction reservoir, while the contaminating species lags behind and within the
channel for later disposal.

We verified the purity of our extracted samples from species
that inhibit polymerase chain reaction (PCR) by performing quantitative PCR (qPCR) and comparing the results with those collected from
samples extracted using a commercial SPE DNA purification kit. Sample qPCR data is shown in Figure
4.

By introducing a standard injection molded device for
purification of samples using ITP, we have created a method of performing
sample preparation at a relevant scale using ITP. This system addresses an
unmet need in sample preparation of nucleic acids by providing an alternative
method for processing samples with low nucleic acid content.

Figure
1. Image of the new injection molded device. For
imaging, the device was filled with colored liquid to improve contrast. The
sample channel (red) can hold a 25 µL sample. The
separation channel (blue) holds 28 µL separation
buffer. There are buffering reservoirs for both the leading and trailing
electrolyte (LE and TE). These buffering reservoirs contain a gel with high
buffering capacity gel to maintain a constant pH in the channel while
suppressing pressure-driven flow. An air outlet with specialized capillary
structures is included to ease the loading process, as shown in Figure 2.

Figure
2. Capillary loading structures near the vacuum
port. The capillary structures allow set-up of a fluid interface without
wasting sample or trapping bubbles. a. The separation channel is initially filled
with the (red) separation buffer, which wets up to the surface of the capillary
barrier. b. The sample is applied to the sample channel, and a -0.1 psig vacuum is
applied to the air outlet to draw the sample into the channel. c. The sample
wets the separation buffer, causing it to break through the barrier. d. The liquids
form a sharp interface, and flow up to the final fluid stop barrier.

Figure 3. An
experimental image of separation of two dyes overlaid with the device schematic.
Two dyes, Alexa Fluor 488 (AF) and fluorescein (FL) are loaded as the sample.
When current is applied, the AF focuses to the ITP interface, while the FL remains
behind as an unfocused zone. The AF is about to elute into the extraction
reservoir, while the FL remains behind in the channel.

Figure 4. qPCR results. We performed qPCR
with samples extracted from whole blood using isotachophoresis. The extracted
DNA amplified consistently, and at the predicted temperature for the amplified
sequence (not shown). The results were comparable to qPCR
amplification of calibration samples with template DNA extracted from blood
using a commercially available SPE kit. We performed negative controls using
whole blood lysate, water, and the separation buffer as templates, and observed
no amplification.

REFERENCES:

1.     "Purification of nucleic acids from whole blood
using isotachophoresis," Persat, A., Marshall, L. A., and
Santiago, J. G. Analytical
Chemistry 81, 9507 (2009).