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Solid lipid nanoparticles with enteric coating for improving stability, palatability, and oral bioavailability of enrofloxacin
BACKGROUND: The poor palatability, variable oral bioavailability, stimulation to gastric mucosa, and light instability limited the application of enrofloxacin (ENR). The enteric granules combining solid lipid nanoparticles (SLNs) with enteric coating were explored to overcome these disadvantages. MA...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6402439/ https://www.ncbi.nlm.nih.gov/pubmed/30880969 http://dx.doi.org/10.2147/IJN.S183479 |
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author | Li, Chao Zhou, Kaixiang Chen, Dongmei Xu, Wei Tao, Yanfei Pan, Yuanhu Meng, Kuiyu Shabbir, Muhammad Abu Bakr Liu, Qianying Huang, Lingli Xie, Shuyu |
author_facet | Li, Chao Zhou, Kaixiang Chen, Dongmei Xu, Wei Tao, Yanfei Pan, Yuanhu Meng, Kuiyu Shabbir, Muhammad Abu Bakr Liu, Qianying Huang, Lingli Xie, Shuyu |
author_sort | Li, Chao |
collection | PubMed |
description | BACKGROUND: The poor palatability, variable oral bioavailability, stimulation to gastric mucosa, and light instability limited the application of enrofloxacin (ENR). The enteric granules combining solid lipid nanoparticles (SLNs) with enteric coating were explored to overcome these disadvantages. MATERIALS AND METHODS: ENR-loaded SLNs were produced by a hot homogenization and ultrasonic emulsification method and the enteric granules with SLNs as inner core were prepared by wet granulation followed by coating using polyacrylic resin II (PRII). The formulation was optimized by using orthogonal or single factor test screening. RESULTS: The optimal SLNs with loading capacity (LC) and price as inspection indexes were consisted of 10 mL 3% polyvinyl alcohol per 0.8 g ENR and 2.4 g octadecanoic acid. The sizes, LC, polydispersion index, and zeta potential of the SLNs were 308.5±6.3 nm, 15.73%±0.31%, 0.352±0.015, and −22.3 mv, respectively. The best enteric granules were used 15% PRII as coating materials. The release of the enteric granules in simulated intestine fluid (SIF, pH=8) was significantly faster than in simulated gastric fluid (SGF, pH=2) and simultaneously slower than those of SLNs and native ENR. The granules showed good stability in influencing factor experiment. The granules displayed a similar daily feed intake as the control group and higher daily feed intake than ENR powder and single-coating granules. Compared to the ENR soluble powder, the area under the plasma concentration–time curve and mean retention time of the enteric granules after intragastric administration were increased from 4.26±0.85 µg h/mL and 6.80±2.28 hours to 11.24±3.33 µg h/mL and 17.97±4.01 hours, respectively. CONCLUSION: The enteric granules combination SLNs with enteric coating significantly improved the stability, palatability, sustained-release performance and oral bioavailability of ENR. The novel technology will be a potential measure to overcome the similar disadvantages of other drugs. |
format | Online Article Text |
id | pubmed-6402439 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-64024392019-03-16 Solid lipid nanoparticles with enteric coating for improving stability, palatability, and oral bioavailability of enrofloxacin Li, Chao Zhou, Kaixiang Chen, Dongmei Xu, Wei Tao, Yanfei Pan, Yuanhu Meng, Kuiyu Shabbir, Muhammad Abu Bakr Liu, Qianying Huang, Lingli Xie, Shuyu Int J Nanomedicine Original Research BACKGROUND: The poor palatability, variable oral bioavailability, stimulation to gastric mucosa, and light instability limited the application of enrofloxacin (ENR). The enteric granules combining solid lipid nanoparticles (SLNs) with enteric coating were explored to overcome these disadvantages. MATERIALS AND METHODS: ENR-loaded SLNs were produced by a hot homogenization and ultrasonic emulsification method and the enteric granules with SLNs as inner core were prepared by wet granulation followed by coating using polyacrylic resin II (PRII). The formulation was optimized by using orthogonal or single factor test screening. RESULTS: The optimal SLNs with loading capacity (LC) and price as inspection indexes were consisted of 10 mL 3% polyvinyl alcohol per 0.8 g ENR and 2.4 g octadecanoic acid. The sizes, LC, polydispersion index, and zeta potential of the SLNs were 308.5±6.3 nm, 15.73%±0.31%, 0.352±0.015, and −22.3 mv, respectively. The best enteric granules were used 15% PRII as coating materials. The release of the enteric granules in simulated intestine fluid (SIF, pH=8) was significantly faster than in simulated gastric fluid (SGF, pH=2) and simultaneously slower than those of SLNs and native ENR. The granules showed good stability in influencing factor experiment. The granules displayed a similar daily feed intake as the control group and higher daily feed intake than ENR powder and single-coating granules. Compared to the ENR soluble powder, the area under the plasma concentration–time curve and mean retention time of the enteric granules after intragastric administration were increased from 4.26±0.85 µg h/mL and 6.80±2.28 hours to 11.24±3.33 µg h/mL and 17.97±4.01 hours, respectively. CONCLUSION: The enteric granules combination SLNs with enteric coating significantly improved the stability, palatability, sustained-release performance and oral bioavailability of ENR. The novel technology will be a potential measure to overcome the similar disadvantages of other drugs. Dove Medical Press 2019-03-01 /pmc/articles/PMC6402439/ /pubmed/30880969 http://dx.doi.org/10.2147/IJN.S183479 Text en © 2019 Li et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research Li, Chao Zhou, Kaixiang Chen, Dongmei Xu, Wei Tao, Yanfei Pan, Yuanhu Meng, Kuiyu Shabbir, Muhammad Abu Bakr Liu, Qianying Huang, Lingli Xie, Shuyu Solid lipid nanoparticles with enteric coating for improving stability, palatability, and oral bioavailability of enrofloxacin |
title | Solid lipid nanoparticles with enteric coating for improving stability, palatability, and oral bioavailability of enrofloxacin |
title_full | Solid lipid nanoparticles with enteric coating for improving stability, palatability, and oral bioavailability of enrofloxacin |
title_fullStr | Solid lipid nanoparticles with enteric coating for improving stability, palatability, and oral bioavailability of enrofloxacin |
title_full_unstemmed | Solid lipid nanoparticles with enteric coating for improving stability, palatability, and oral bioavailability of enrofloxacin |
title_short | Solid lipid nanoparticles with enteric coating for improving stability, palatability, and oral bioavailability of enrofloxacin |
title_sort | solid lipid nanoparticles with enteric coating for improving stability, palatability, and oral bioavailability of enrofloxacin |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6402439/ https://www.ncbi.nlm.nih.gov/pubmed/30880969 http://dx.doi.org/10.2147/IJN.S183479 |
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