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. 2016 Mar 9;9:162–164. doi: 10.1007/s12265-016-9684-2

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© The Author(s) 2016

Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.

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Fig. 1 — a (i) A schematic illustration of the development of the NO-releasing polymer and transmission electron microscopy image of the particles, size and morphology of the NO-releasing polymers as determined by (ii) dynamic light scattering and (iii) scanning electron microscopy at ×3035. b NO release from different concentrations of NO-releasing polymers (NO-RPs). Measurements were recorded using NO measuring electrode over a period of 20 min. c NO release pharmacokinetics from the NO-releasing polymers (NO-RPs). Measurements were recorded using NO measuring electrode over a period of 8 h. d Effect of NO-releasing polymer (NO-RP) on pre-contracted pulmonary artery from control mice and mice with pulmonary arterial hypertension. Data represents mean ± SEM for n = 3 from three animals. Statistical significance was determined by two-way ANOVA followed by a Bonferroni post hoc test (*p < 0.05)