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Comprehensive evaluation of carboxylated nanodiamond as a topical drug delivery system

The best strategy in the development of topical drug delivery systems may be to facilitate the permeation of drugs without any harmful effects, while staying on the skin surface and maintaining stability of the system. Nanodiamonds (NDs) play a key role with their excellent physicochemical propertie...

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Autores principales: Lim, Dae Gon, Kim, Ki Hyun, Kang, Eunah, Lim, Sun Hee, Ricci, Jeremy, Sung, Si Kwon, Kwon, Myoung Taek, Jeong, Seong Hoon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4887070/
https://www.ncbi.nlm.nih.gov/pubmed/27307736
http://dx.doi.org/10.2147/IJN.S104859
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author Lim, Dae Gon
Kim, Ki Hyun
Kang, Eunah
Lim, Sun Hee
Ricci, Jeremy
Sung, Si Kwon
Kwon, Myoung Taek
Jeong, Seong Hoon
author_facet Lim, Dae Gon
Kim, Ki Hyun
Kang, Eunah
Lim, Sun Hee
Ricci, Jeremy
Sung, Si Kwon
Kwon, Myoung Taek
Jeong, Seong Hoon
author_sort Lim, Dae Gon
collection PubMed
description The best strategy in the development of topical drug delivery systems may be to facilitate the permeation of drugs without any harmful effects, while staying on the skin surface and maintaining stability of the system. Nanodiamonds (NDs) play a key role with their excellent physicochemical properties, including high biocompatibility, physical adsorption, reactive oxygen species (ROS) scavenging capability, and photostabilizing activity. Z-average sizes of carboxylated ND (ND–COOH) agglutinate decreased significantly as the pH increased. Fluorescein-conjugated ND was observed only on the stratum corneum, and no sample diffused into the dermal layer even after 48 hours. Moreover, ND–COOH and ND–COOH/eugenol complex did not show significant toxic effects on murine macrophage cells. ND improved in vitro skin permeation >50% acting as a “drug reservoir” to maintain a high drug concentration in the donor chamber, which was supported by quartz crystal microbalance results. Moreover, ND–COOH could adsorb a drug amount equivalent to 80% of its own weight. A photostability study showed that ND–COOH increased the photostability ~47% with regard to rate constant of the eugenol itself. A significant decrease in ROS was observed in the ND–COOH and ND–COOH/eugenol complex compared with the negative control during intracellular ROS assay. Moreover, ROS and cupric reducing antioxidant capacity evaluation showed that ND–COOH had synergistic effects of antioxidation with eugenol. Therefore, ND–COOH could be used as an excellent topical drug delivery system with improved permeability, higher stability, and minimized safety issue.
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spelling pubmed-48870702016-06-15 Comprehensive evaluation of carboxylated nanodiamond as a topical drug delivery system Lim, Dae Gon Kim, Ki Hyun Kang, Eunah Lim, Sun Hee Ricci, Jeremy Sung, Si Kwon Kwon, Myoung Taek Jeong, Seong Hoon Int J Nanomedicine Original Research The best strategy in the development of topical drug delivery systems may be to facilitate the permeation of drugs without any harmful effects, while staying on the skin surface and maintaining stability of the system. Nanodiamonds (NDs) play a key role with their excellent physicochemical properties, including high biocompatibility, physical adsorption, reactive oxygen species (ROS) scavenging capability, and photostabilizing activity. Z-average sizes of carboxylated ND (ND–COOH) agglutinate decreased significantly as the pH increased. Fluorescein-conjugated ND was observed only on the stratum corneum, and no sample diffused into the dermal layer even after 48 hours. Moreover, ND–COOH and ND–COOH/eugenol complex did not show significant toxic effects on murine macrophage cells. ND improved in vitro skin permeation >50% acting as a “drug reservoir” to maintain a high drug concentration in the donor chamber, which was supported by quartz crystal microbalance results. Moreover, ND–COOH could adsorb a drug amount equivalent to 80% of its own weight. A photostability study showed that ND–COOH increased the photostability ~47% with regard to rate constant of the eugenol itself. A significant decrease in ROS was observed in the ND–COOH and ND–COOH/eugenol complex compared with the negative control during intracellular ROS assay. Moreover, ROS and cupric reducing antioxidant capacity evaluation showed that ND–COOH had synergistic effects of antioxidation with eugenol. Therefore, ND–COOH could be used as an excellent topical drug delivery system with improved permeability, higher stability, and minimized safety issue. Dove Medical Press 2016-05-26 /pmc/articles/PMC4887070/ /pubmed/27307736 http://dx.doi.org/10.2147/IJN.S104859 Text en © 2016 Lim 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
Lim, Dae Gon
Kim, Ki Hyun
Kang, Eunah
Lim, Sun Hee
Ricci, Jeremy
Sung, Si Kwon
Kwon, Myoung Taek
Jeong, Seong Hoon
Comprehensive evaluation of carboxylated nanodiamond as a topical drug delivery system
title Comprehensive evaluation of carboxylated nanodiamond as a topical drug delivery system
title_full Comprehensive evaluation of carboxylated nanodiamond as a topical drug delivery system
title_fullStr Comprehensive evaluation of carboxylated nanodiamond as a topical drug delivery system
title_full_unstemmed Comprehensive evaluation of carboxylated nanodiamond as a topical drug delivery system
title_short Comprehensive evaluation of carboxylated nanodiamond as a topical drug delivery system
title_sort comprehensive evaluation of carboxylated nanodiamond as a topical drug delivery system
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4887070/
https://www.ncbi.nlm.nih.gov/pubmed/27307736
http://dx.doi.org/10.2147/IJN.S104859
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