Cardiovascular diseases are the first cause of death globally. Their early diagnosis requires ultrasensitive tools enabling the detection of minor structural and functional alterations in small arteries. Such analyses have been traditionally performed with video imaging-based myographs, which helped to investigate the pathophysiology of the microvessels. Since new vascular questions have emerged, substantial modifications are necessary to improve the performance of imaging and tracking software, reducing the cost and minimizing the microvessel cleaning and manipulation. To address these limitations, we present a photonic microsystem fabricated in polydimethylsiloxane and integrating micro-optical elements and a lightguide-cantilever for sub-micrometric analysis of small arteries (between 125 and 400μm of basal diameter). This technology enables simultaneous measurement of arterial distension, stiffness, vasomotion, and heartbeat and without the need for advanced imaging system. The microsystem has a limit of detection of 2μm, five times lower than video imaging-based myographs, is two times more sensitive than them (0.5 μm/mmHg), reduces variability to half and doubles the linear range reported in these myographs. More importantly, it allows the analysis of intact arteries preserving the integrity and function of surrounding tissues. Assays can be conducted in three configurations according to the surrounding tissue: (i) isolated arteries (in vitro) where the surrounding tissue is partially removed, (ii) non-isolated arteries (in vivo) with surrounding tissue partially removed, and (iii) intact arteries in vivo preserving surrounding tissue as well as function and integrity. This technology represents a step forward in the prediction of cardiovascular risk.
English
61 - Medical sciences
Vasos sanguinis; Òptica integrada; Litografia; Vasos sanguíneos; Óptica integrada; Litografía; Blood vessels; Lithography; Integrated optics
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The research leading to these results has received funding from the GISCERV program (NGG-227, Ministerio de Economia y Competitividad) and SOAR project (Convocatoria 2015 de Ayudas Fundación BBVA a Investigadores y Creadores Culturales). This work was partially funded by the European Commission (Contract No. 317916, Liphos), Ministerio de Economía y Competitividad (MINAHE 5 MINECO/ICTI 2013–2016/TEC2014-51940-C2), and EU ERDF (FEDER) funds. XM-B was supported by the Ramón y Cajal program (Spanish Government). VM acknowledges funding from the Danish Heart Foundation (No. 4004-00102B) and the Novo Nordisk Foundation (No. NNF14OC001273). This work has made use of the Spanish ICTS Network MICRONANOFABS (Ministry of Economy, Industry and Competitiveness). We acknowledge support of the publication fee by the CSIC Open Access Publication Support Initiative through its Unit of Information Resources for Research (URICI).
Frontiers in Physiology
info:eu-repo/grantAgreement/ES/1PE/TEC2014-51940-C2
© 2019 Rodríguez-Rodríguez, Ackermann, Plaza, Simonsen, Matchkov, Llobera and Munoz-Berbel. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
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