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Hollow silica capsules for amphiphilic transport and sustained delivery of antibiotic and anticancer drugs

Hollow mesoporous silica capsules (HMSC) are potential drug transport vehicles due to their biocompatibility, high loading capacity and sufficient stability in biological milieu. Herein, we report the synthesis of ellipsoid-shaped HMSC (aspect ratio ∼2) performed using hematite particles as solid te...

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Autores principales: Gessner, Isabel, Krakor, Eva, Jurewicz, Anna, Wulff, Veronika, Kling, Lasse, Christiansen, Silke, Brodusch, Nicolas, Gauvin, Raynald, Wortmann, Laura, Wolke, Martina, Plum, Georg, Schauss, Astrid, Krautwurst, John, Ruschewitz, Uwe, Ilyas, Shaista, Mathur, Sanjay
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9082457/
https://www.ncbi.nlm.nih.gov/pubmed/35542120
http://dx.doi.org/10.1039/c8ra03716g
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author Gessner, Isabel
Krakor, Eva
Jurewicz, Anna
Wulff, Veronika
Kling, Lasse
Christiansen, Silke
Brodusch, Nicolas
Gauvin, Raynald
Wortmann, Laura
Wolke, Martina
Plum, Georg
Schauss, Astrid
Krautwurst, John
Ruschewitz, Uwe
Ilyas, Shaista
Mathur, Sanjay
author_facet Gessner, Isabel
Krakor, Eva
Jurewicz, Anna
Wulff, Veronika
Kling, Lasse
Christiansen, Silke
Brodusch, Nicolas
Gauvin, Raynald
Wortmann, Laura
Wolke, Martina
Plum, Georg
Schauss, Astrid
Krautwurst, John
Ruschewitz, Uwe
Ilyas, Shaista
Mathur, Sanjay
author_sort Gessner, Isabel
collection PubMed
description Hollow mesoporous silica capsules (HMSC) are potential drug transport vehicles due to their biocompatibility, high loading capacity and sufficient stability in biological milieu. Herein, we report the synthesis of ellipsoid-shaped HMSC (aspect ratio ∼2) performed using hematite particles as solid templates that were coated with a conformal silica shell through cross-condensation reactions. For obtaining hollow silica capsules, the iron oxide core was removed by acidic leaching. Gas sorption studies on HMSC revealed mesoscopic pores (main pore width ∼38 Å) and a high surface area of 308.8 m(2) g(−1). Cell uptake of dye-labeled HMSC was confirmed by incubating them with human cervical cancer (HeLa) cells and analyzing the internalization through confocal microscopy. The amphiphilic nature of HMSC for drug delivery applications was tested by loading antibiotic (ciprofloxacin) and anticancer (curcumin) compounds as model drugs for hydrophilic and hydrophobic therapeutics, respectively. The versatility of HMSC in transporting hydrophilic as well as hydrophobic drugs and a pH dependent drug release over several days under physiological conditions was demonstrated in both cases by UV-vis spectroscopy. Ciprofloxacin-loaded HMSC were additionally evaluated towards Gram negative (E. coli) bacteria and demonstrated their efficacy even at low concentrations (10 μg ml(−1)) in inhibiting complete bacterial growth over 18 hours.
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spelling pubmed-90824572022-05-09 Hollow silica capsules for amphiphilic transport and sustained delivery of antibiotic and anticancer drugs Gessner, Isabel Krakor, Eva Jurewicz, Anna Wulff, Veronika Kling, Lasse Christiansen, Silke Brodusch, Nicolas Gauvin, Raynald Wortmann, Laura Wolke, Martina Plum, Georg Schauss, Astrid Krautwurst, John Ruschewitz, Uwe Ilyas, Shaista Mathur, Sanjay RSC Adv Chemistry Hollow mesoporous silica capsules (HMSC) are potential drug transport vehicles due to their biocompatibility, high loading capacity and sufficient stability in biological milieu. Herein, we report the synthesis of ellipsoid-shaped HMSC (aspect ratio ∼2) performed using hematite particles as solid templates that were coated with a conformal silica shell through cross-condensation reactions. For obtaining hollow silica capsules, the iron oxide core was removed by acidic leaching. Gas sorption studies on HMSC revealed mesoscopic pores (main pore width ∼38 Å) and a high surface area of 308.8 m(2) g(−1). Cell uptake of dye-labeled HMSC was confirmed by incubating them with human cervical cancer (HeLa) cells and analyzing the internalization through confocal microscopy. The amphiphilic nature of HMSC for drug delivery applications was tested by loading antibiotic (ciprofloxacin) and anticancer (curcumin) compounds as model drugs for hydrophilic and hydrophobic therapeutics, respectively. The versatility of HMSC in transporting hydrophilic as well as hydrophobic drugs and a pH dependent drug release over several days under physiological conditions was demonstrated in both cases by UV-vis spectroscopy. Ciprofloxacin-loaded HMSC were additionally evaluated towards Gram negative (E. coli) bacteria and demonstrated their efficacy even at low concentrations (10 μg ml(−1)) in inhibiting complete bacterial growth over 18 hours. The Royal Society of Chemistry 2018-07-10 /pmc/articles/PMC9082457/ /pubmed/35542120 http://dx.doi.org/10.1039/c8ra03716g Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Gessner, Isabel
Krakor, Eva
Jurewicz, Anna
Wulff, Veronika
Kling, Lasse
Christiansen, Silke
Brodusch, Nicolas
Gauvin, Raynald
Wortmann, Laura
Wolke, Martina
Plum, Georg
Schauss, Astrid
Krautwurst, John
Ruschewitz, Uwe
Ilyas, Shaista
Mathur, Sanjay
Hollow silica capsules for amphiphilic transport and sustained delivery of antibiotic and anticancer drugs
title Hollow silica capsules for amphiphilic transport and sustained delivery of antibiotic and anticancer drugs
title_full Hollow silica capsules for amphiphilic transport and sustained delivery of antibiotic and anticancer drugs
title_fullStr Hollow silica capsules for amphiphilic transport and sustained delivery of antibiotic and anticancer drugs
title_full_unstemmed Hollow silica capsules for amphiphilic transport and sustained delivery of antibiotic and anticancer drugs
title_short Hollow silica capsules for amphiphilic transport and sustained delivery of antibiotic and anticancer drugs
title_sort hollow silica capsules for amphiphilic transport and sustained delivery of antibiotic and anticancer drugs
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9082457/
https://www.ncbi.nlm.nih.gov/pubmed/35542120
http://dx.doi.org/10.1039/c8ra03716g
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