<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-06-08T10:18:33Z</responseDate><request verb="GetRecord" identifier="oai:docta.ucm.es:20.500.14352/119954" metadataPrefix="marc">https://docta.ucm.es/rest/oai/request</request><GetRecord><record><header><identifier>oai:docta.ucm.es:20.500.14352/119954</identifier><datestamp>2025-05-09T23:50:48Z</datestamp><setSpec>com_20.500.14352_14</setSpec><setSpec>col_20.500.14352_15</setSpec></header><metadata><record xmlns="http://www.loc.gov/MARC21/slim" xmlns:dcterms="http://purl.org/dc/terms/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:doc="http://www.lyncode.com/xoai" xsi:schemaLocation="http://www.loc.gov/MARC21/slim http://www.loc.gov/standards/marcxml/schema/MARC21slim.xsd">
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      <subfield code="a">Raposo González, Rafaela</subfield>
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      <subfield code="a">González Burgos, Elena María</subfield>
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      <subfield code="a">Serrano López, Dolores Remedios</subfield>
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      <subfield code="a">Brayan J. Anaya</subfield>
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      <subfield code="a">Aytug Kara</subfield>
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      <subfield code="a">Tirado, Diego F.</subfield>
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      <subfield code="a">Lalatsa, A.</subfield>
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      <subfield code="c">2025</subfield>
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      <subfield code="a">Pulmonary drug delivery is crucial for treating respiratory diseases, requiring precise particle engineering for optimal therapeutic efficacy. This study demonstrates a novel integration of 3D-printed microfluidic micromixers
with spray drying technology to produce inhalable azithromycin (AZM) microparticles targeting lung delivery. The formulation demonstrated effective deep lung deposition at both 30 L/min and 60 L/min flow rates. At 30 L/
min, AZM-loaded microparticles achieved enhanced performance with 1.2-fold higher Fine Particle Fraction (FPF) &lt; 5 µm and 1.4-fold higher FPF &lt; 3 µm compared to 60 L/min. Microparticles (25 mg) can deliver an
efficacious dose of AZM to the lung, exceeding the reported epidemiological cut-off for Haemophilus influenzae (4mg/L) by approximately five-fold while maintaining high human bronchial epithelial cell viability (> 94 %). The
antibacterial efficacy against H. influenzae was confirmed, demonstrating the therapeutic potential against lung pathogens. The successful deep lung deposition at both air flow rates reflects the robustness of the formulation
design, making it suitable for diverse patient populations with varying inspiratory capabilities, including children and elderly patients.</subfield>
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      <subfield code="a">Anaya BJ, Kara A, Raposo R, Tirado DF, Lalatsa A, González-Burgos E, et al. Integration of 3D-printed micromixers and spray drying for pulmonary delivery of antimicrobial microparticles. International Journal of Pharmaceutics 2025;674:125493. https://doi.org/10.1016/j.ijpharm.2025.125493.</subfield>
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      <subfield code="a">10.1016/j.ijpharm.2025.125493</subfield>
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      <subfield code="a">https://hdl.handle.net/20.500.14352/119954</subfield>
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      <subfield code="a">https://doi.org/10.1016/j.ijpharm.2025.125493</subfield>
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      <subfield code="a">Integration of 3D-Printed Micromixers and Spray Drying for Pulmonary Delivery of Antimicrobial Microparticles</subfield>
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