Characterization of chitosan-magnesium aluminum silicate nanocomposite films for buccal delivery of nicotine

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Characterization of chitosan-magnesium aluminum silicate nanocomposite films for buccal delivery of nicotine. / Pongjanyakul, Thaned; Khunawattanakul, Wanwisa; Strachan, Clare J; Gordon, Keith C; Puttipipatkhachorn, Satit; Rades, Thomas.

In: International Journal of Biological Macromolecules, Vol. 55, 2013, p. 24-31.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Pongjanyakul, T, Khunawattanakul, W, Strachan, CJ, Gordon, KC, Puttipipatkhachorn, S & Rades, T 2013, 'Characterization of chitosan-magnesium aluminum silicate nanocomposite films for buccal delivery of nicotine', International Journal of Biological Macromolecules, vol. 55, pp. 24-31. https://doi.org/10.1016/j.ijbiomac.2012.12.043

APA

Pongjanyakul, T., Khunawattanakul, W., Strachan, C. J., Gordon, K. C., Puttipipatkhachorn, S., & Rades, T. (2013). Characterization of chitosan-magnesium aluminum silicate nanocomposite films for buccal delivery of nicotine. International Journal of Biological Macromolecules, 55, 24-31. https://doi.org/10.1016/j.ijbiomac.2012.12.043

Vancouver

Pongjanyakul T, Khunawattanakul W, Strachan CJ, Gordon KC, Puttipipatkhachorn S, Rades T. Characterization of chitosan-magnesium aluminum silicate nanocomposite films for buccal delivery of nicotine. International Journal of Biological Macromolecules. 2013;55:24-31. https://doi.org/10.1016/j.ijbiomac.2012.12.043

Author

Pongjanyakul, Thaned ; Khunawattanakul, Wanwisa ; Strachan, Clare J ; Gordon, Keith C ; Puttipipatkhachorn, Satit ; Rades, Thomas. / Characterization of chitosan-magnesium aluminum silicate nanocomposite films for buccal delivery of nicotine. In: International Journal of Biological Macromolecules. 2013 ; Vol. 55. pp. 24-31.

Bibtex

@article{43cfb066058f4144b552a32cea4e7d1b,
title = "Characterization of chitosan-magnesium aluminum silicate nanocomposite films for buccal delivery of nicotine",
abstract = "The objective of this study was to prepare and characterize chitosan-magnesium aluminum silicate (CS-MAS) nanocomposite films as a buccal delivery system for nicotine (NCT). The effects of the CS-MAS ratio on the physicochemical properties, release and permeation, as well as on the mucoadhesive properties, were investigated. Molecular interactions between the components of the film were also investigated. The results indicated that NCT-loaded CS-MAS films provided a higher NCT content than NCT-loaded films containing only CS. The greater the MAS ratio in the films, the higher the NCT content that was observed because intercalated nanocomposites could be formed by electrostatic interactions of MAS with NCT and CS. These interactions caused an insignificant loss of NCT by evaporation during film drying. The release and permeation of NCT were related to the square root of time, indicating that a diffusion-controlled mechanism via the NCT-MAS complex particles and the film matrix controls NCT release. NCT release and permeation rates decreased with as the MAS ratio of the films was increased. However, the NCT-loaded CS-MAS films may have a potential adhesion to the mucosal membrane. These findings suggest that NCT-loaded CS-MAS films can be used as a buccal NCT delivery system.",
author = "Thaned Pongjanyakul and Wanwisa Khunawattanakul and Strachan, {Clare J} and Gordon, {Keith C} and Satit Puttipipatkhachorn and Thomas Rades",
note = "Copyright {\textcopyright} 2013 Elsevier B.V. All rights reserved.",
year = "2013",
doi = "10.1016/j.ijbiomac.2012.12.043",
language = "English",
volume = "55",
pages = "24--31",
journal = "International Journal of Biological Macromolecules",
issn = "0141-8130",
publisher = "Elsevier",

}

RIS

TY - JOUR

T1 - Characterization of chitosan-magnesium aluminum silicate nanocomposite films for buccal delivery of nicotine

AU - Pongjanyakul, Thaned

AU - Khunawattanakul, Wanwisa

AU - Strachan, Clare J

AU - Gordon, Keith C

AU - Puttipipatkhachorn, Satit

AU - Rades, Thomas

N1 - Copyright © 2013 Elsevier B.V. All rights reserved.

PY - 2013

Y1 - 2013

N2 - The objective of this study was to prepare and characterize chitosan-magnesium aluminum silicate (CS-MAS) nanocomposite films as a buccal delivery system for nicotine (NCT). The effects of the CS-MAS ratio on the physicochemical properties, release and permeation, as well as on the mucoadhesive properties, were investigated. Molecular interactions between the components of the film were also investigated. The results indicated that NCT-loaded CS-MAS films provided a higher NCT content than NCT-loaded films containing only CS. The greater the MAS ratio in the films, the higher the NCT content that was observed because intercalated nanocomposites could be formed by electrostatic interactions of MAS with NCT and CS. These interactions caused an insignificant loss of NCT by evaporation during film drying. The release and permeation of NCT were related to the square root of time, indicating that a diffusion-controlled mechanism via the NCT-MAS complex particles and the film matrix controls NCT release. NCT release and permeation rates decreased with as the MAS ratio of the films was increased. However, the NCT-loaded CS-MAS films may have a potential adhesion to the mucosal membrane. These findings suggest that NCT-loaded CS-MAS films can be used as a buccal NCT delivery system.

AB - The objective of this study was to prepare and characterize chitosan-magnesium aluminum silicate (CS-MAS) nanocomposite films as a buccal delivery system for nicotine (NCT). The effects of the CS-MAS ratio on the physicochemical properties, release and permeation, as well as on the mucoadhesive properties, were investigated. Molecular interactions between the components of the film were also investigated. The results indicated that NCT-loaded CS-MAS films provided a higher NCT content than NCT-loaded films containing only CS. The greater the MAS ratio in the films, the higher the NCT content that was observed because intercalated nanocomposites could be formed by electrostatic interactions of MAS with NCT and CS. These interactions caused an insignificant loss of NCT by evaporation during film drying. The release and permeation of NCT were related to the square root of time, indicating that a diffusion-controlled mechanism via the NCT-MAS complex particles and the film matrix controls NCT release. NCT release and permeation rates decreased with as the MAS ratio of the films was increased. However, the NCT-loaded CS-MAS films may have a potential adhesion to the mucosal membrane. These findings suggest that NCT-loaded CS-MAS films can be used as a buccal NCT delivery system.

U2 - 10.1016/j.ijbiomac.2012.12.043

DO - 10.1016/j.ijbiomac.2012.12.043

M3 - Journal article

C2 - 23298850

VL - 55

SP - 24

EP - 31

JO - International Journal of Biological Macromolecules

JF - International Journal of Biological Macromolecules

SN - 0141-8130

ER -

ID: 44287879