<?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>2026-06-26T10:56:18Z</responseDate><request verb="GetRecord" identifier="oai:docta.ucm.es:20.500.14352/12759" metadataPrefix="mods">https://docta.ucm.es/rest/oai/request</request><GetRecord><record><header><identifier>oai:docta.ucm.es:20.500.14352/12759</identifier><datestamp>2024-09-02T15:05:39Z</datestamp><setSpec>com_20.500.14352_14</setSpec><setSpec>col_20.500.14352_15</setSpec></header><metadata><mods:mods xmlns:mods="http://www.loc.gov/mods/v3" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:doc="http://www.lyncode.com/xoai" xsi:schemaLocation="http://www.loc.gov/mods/v3 http://www.loc.gov/standards/mods/v3/mods-3-1.xsd">
   <mods:name>
      <mods:namePart>Gómez Ballesteros, Miguel</mods:namePart>
   </mods:name>
   <mods:name>
      <mods:namePart>Andrés Guerrero, Vanesa</mods:namePart>
   </mods:name>
   <mods:name>
      <mods:namePart>Parra Luna, Francisco</mods:namePart>
   </mods:name>
   <mods:name>
      <mods:namePart>Marinich, Jorge</mods:namePart>
   </mods:name>
   <mods:name>
      <mods:namePart>Heras Polo, Beatriz De Las</mods:namePart>
   </mods:name>
   <mods:name>
      <mods:namePart>Molina Martínez, Irene Teresa</mods:namePart>
   </mods:name>
   <mods:name>
      <mods:namePart>Vázquez Lasa, Blanca</mods:namePart>
   </mods:name>
   <mods:name>
      <mods:namePart>San Román Del Barrio, Julio</mods:namePart>
   </mods:name>
   <mods:name>
      <mods:namePart>Herrero Vanrell, María Del Rocío</mods:namePart>
   </mods:name>
   <mods:extension>
      <mods:dateAvailable encoding="iso8601">2023-06-17T12:40:40Z</mods:dateAvailable>
   </mods:extension>
   <mods:extension>
      <mods:dateAccessioned encoding="iso8601">2023-06-17T12:40:40Z</mods:dateAccessioned>
   </mods:extension>
   <mods:originInfo>
      <mods:dateIssued encoding="iso8601">2019-07-19</mods:dateIssued>
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   <mods:identifier type="citation">Gómez Ballesteros, M., Andrés Guerrero, V., Parra Luna, F. et al. «Amphiphilic Acrylic Nanoparticles Containing the Poloxamer Star Bayfit® 10WF15 as Ophthalmic Drug Carriers». Polymers, vol. 11, n.o 7, julio de 2019, p. 1213. DOI.org (Crossref), https://doi.org/10.3390/polym11071213.</mods:identifier>
   <mods:identifier type="citation">Gómez Ballesteros, M., Andrés Guerrero, V., Parra Luna, F. et al. «Amphiphilic Acrylic Nanoparticles Containing the Poloxamer Star Bayfit® 10WF15 as Ophthalmic Drug Carriers». Polymers, vol. 11, n.o 7, julio de 2019, p. 1213. DOI.org (Crossref), https://doi.org/10.3390/polym11071213.</mods:identifier>
   <mods:identifier type="issn">2073-4360</mods:identifier>
   <mods:identifier type="doi">10.3390/polym11071213</mods:identifier>
   <mods:identifier type="uri">https://hdl.handle.net/20.500.14352/12759</mods:identifier>
   <mods:identifier type="officialurl">https://doi.org/10.3390/polym11071213</mods:identifier>
   <mods:abstract>Topical application of drops containing ocular drugs is the preferred non-invasive route to treat diseases that a_ect the anterior segment of the eye. However, the formulation of eye drops is a major challenge for pharmacists since the access of drugs to ocular tissues is restricted by several barriers. Acetazolamide (ACZ) is a carbonic anhydrase inhibitor used orally for the treatment of ocular hypertension in glaucoma. However, large ACZ doses are needed which results in systemic side e_ects. Recently, we synthesized copolymers based on 2-hydroxyethyl methacrylate (HEMA) and a functionalized three-arm poloxamer star (Bayfit-MA). The new material (HEMA/Bayfit-MA) was engineered to be transformed into nanoparticles without the use of surfactants, which represents a significant step forward in developing new ophthalmic drug delivery platforms. Acetazolamide-loaded nanocarriers (ACZ-NPs) were prepared via dialysis (224 +/- 19 nm,  ̶ 17.2 +/- 0.4 mV). The in vitro release rate of ACZ was constant over 24 h (cumulative delivery of ACZ: 83.3 +/- 8.4%). Following standard specifications, ACZ-NPs were not cytotoxic in vitro in cornea, conjunctiva, and macrophages. In normotensive rabbits, ACZ-NPs generated a significant intraocular pressure reduction compared to a conventional solution of ACZ (16.4% versus 9.6%) with the same dose of the hypotensive drug (20 μg). In comparison to previously reported studies, this formulation reduced intraocular pressure with a lower dose of ACZ. In summary, HEMA:Bayfit-MA nanoparticles may be a promising system for ocular topical treatments, showing an enhanced ocular bioavailability of ACZ after a single instillation on the ocular surface.</mods:abstract>
   <mods:language>
      <mods:languageTerm>eng</mods:languageTerm>
   </mods:language>
   <mods:accessCondition type="useAndReproduction">https://creativecommons.org/licenses/by/3.0/es/</mods:accessCondition>
   <mods:accessCondition type="useAndReproduction">open access</mods:accessCondition>
   <mods:accessCondition type="useAndReproduction">Atribución 3.0 España</mods:accessCondition>
   <mods:titleInfo>
      <mods:title>Amphiphilic Acrylic Nanoparticles Containing the Poloxamer Star Bayfit® 10WF15 as Ophthalmic Drug Carriers</mods:title>
   </mods:titleInfo>
   <mods:genre>journal article</mods:genre>
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