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Microstereolithography-fabricated microneedles for fluid sampling of histamine-contaminated tuna




































            Figure  2.  Optical micrographs of the microstereolithography-fabricated  microneedles  (A–C), including  (A)  a front view of the
            microneedles showing the trapezoidal cutouts, (B) a top view of the microneedles showing the thin pyramidal geometries and the
            staggered orientation, (C) an angled view of the microneedle array; the scale bars in these images are 2 mm. In (D) a microneedle is
            inserted into a fresh piece of tuna. After removal in (E), indentations of the hand-applied microneedle array are noted in the tuna
            sample. An example of a positive test is shown in (F); in this figure, a lateral flow test strip was placed in the sample chamber and
            was allowed to develop after incubating in diluent. The diluent washed over a microneedle array that had sampled a piece of hista-
            mine-spiked tuna.

            The following formulas were used to compare results   variance and n 1 and n 2 as the number of samples for
            from the tuna samples and establish the difference of   the  microneedle sampling system procedure and the
            means confidence interval:                         manufacturer-described  procedure  measurements, re-
                                                               spectively. Upon calculating the confidence intervals,
                                       t
                                    +
                                            S
                C ..I Upper =  (M −  1  M 2  ) ( 0.95  )( M 1 M−  2 )    (3.1)   if the range of the interval spans both  positive and
                                                               negative values, no statistical difference exists be-
                                    −
                                       t
                C .. I Lower =  (M −  1  M 2  ) ( 0.95  )( M 1 M−  2  )    (3.2)   tween  the  two  means  within  the  indicated  level  of
                                            S
                                                               confidence.
                                   S   2    S   2            Using this  method,  the confidence intervals com-
                       S M −     =     1      +     2         (3.3)
                         1 M
                            2
                                   n 1     n 2             paring  the  difference of  means  for  the  microneedle
                                                               sampling system procedure and the manufacturer-de-
            The upper and lower limits of the confidence interval   scribed  procedure were compared. For  the  negative
            were calculated using Equations 3.1 and 3.2, with M 1   control with PBS, the 95% C.I. range was calculated
            and  M 2  representing the means of the  microneedle   to be −0.14  ≥ S M  ≥−10.76, with  a difference of
                                                                              1 M−
                                                                                 2
            sampling system procedure and  manufacturer-descr-  means of −5.45.  Based  on  this  calculation,  a  slight
                                  ®
            ibed procedure Accuscan  reading ratios, respectively.   statistical difference was noted  between  the test  me-
            The t 0.95 value is the t-table value at 95% confidence   thods for PBS. When examining the 0.5 mg/mL test
            level. The  S M 1 M−  2    represents the standard deviation   comparison, the 95% C.I. range was  −  3.96 ≥  S
                                                                                                         1 M−
                                                                                                       M
                                                                                                            2
            for the difference of means; it was calculated by use of   ≥− 4.21, with a difference of means of  0.13−  . Look-
                                          2
                                                  2
            Equation 3.3. In this  equation,  S   and  S   are the   ing at the 1.0  mg/mL values, the 95% C.I. spanned
                                          1
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            76                          International Journal of Bioprinting (2016)–Volume 2, Issue 1
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