Design of an anti‐inflammatory composite nanosystem and evaluation of its potential for ocular drug delivery. Issue 8 (4th July 2013)
- Record Type:
- Journal Article
- Title:
- Design of an anti‐inflammatory composite nanosystem and evaluation of its potential for ocular drug delivery. Issue 8 (4th July 2013)
- Main Title:
- Design of an anti‐inflammatory composite nanosystem and evaluation of its potential for ocular drug delivery
- Authors:
- Du Toit, Lisa C.
Govender, Thirumala
Carmichael, Trevor
Kumar, Pradeep
Choonara, Yahya E.
Pillay, Viness - Abstract:
- <abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <p>This study compared two specific embodiments of an ocular nanosystem (NS): one portraying a purely polymeric system, referred to as the chitosan–poly(<italic>ε</italic>‐caprolactone) nanosystem, and the other based on a composite lipoidal–polymeric NS architecture utilizing phospholipids—the lipoidal–chitosan–poly(<italic>ε</italic>‐caprolactone) nanosystem. Investigations undertaken were implicit to warrant inclusion in an implantable system for the intelligent treatment of inflammatory disorders (specifically ocular afflictions). Results obtained highlighted the enhanced efficacy of both NS to an indomethacin suspension in terms of tissue permeation, cell uptake, and anti‐inflammatory activity. Furthermore, the size (134.3 vs. 140.7 nm); surface charge (+49.4 vs. +55.7 mV); drug incorporation efficiency (75.00% vs. 67.20%); flux across the retinal pigment epithelium–choroid–sclera (0.002951 vs. 0.001255 mg cm <sup>−2</sup> h<sup>−1</sup>); anti‐inflammatory efficacy, demonstrated by a decrease in 4‐chloro‐7‐nitrobenzo‐2‐oxa‐1, 3‐diazole complex formation (0.0031 vs. 0.0023 mmol L<sup>−1</sup>) and decrease in NFκB formation (decrease in relative optical density of 0.2027 vs. 0.2420); and enhanced inflammatory cell uptake, visualized via high‐speed fluorescence and confocal microscopy, all highlighted the enhanced potential of the lipoidal system compared with the purely polymeric NS for potentially<abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <p>This study compared two specific embodiments of an ocular nanosystem (NS): one portraying a purely polymeric system, referred to as the chitosan–poly(<italic>ε</italic>‐caprolactone) nanosystem, and the other based on a composite lipoidal–polymeric NS architecture utilizing phospholipids—the lipoidal–chitosan–poly(<italic>ε</italic>‐caprolactone) nanosystem. Investigations undertaken were implicit to warrant inclusion in an implantable system for the intelligent treatment of inflammatory disorders (specifically ocular afflictions). Results obtained highlighted the enhanced efficacy of both NS to an indomethacin suspension in terms of tissue permeation, cell uptake, and anti‐inflammatory activity. Furthermore, the size (134.3 vs. 140.7 nm); surface charge (+49.4 vs. +55.7 mV); drug incorporation efficiency (75.00% vs. 67.20%); flux across the retinal pigment epithelium–choroid–sclera (0.002951 vs. 0.001255 mg cm <sup>−2</sup> h<sup>−1</sup>); anti‐inflammatory efficacy, demonstrated by a decrease in 4‐chloro‐7‐nitrobenzo‐2‐oxa‐1, 3‐diazole complex formation (0.0031 vs. 0.0023 mmol L<sup>−1</sup>) and decrease in NFκB formation (decrease in relative optical density of 0.2027 vs. 0.2420); and enhanced inflammatory cell uptake, visualized via high‐speed fluorescence and confocal microscopy, all highlighted the enhanced potential of the lipoidal system compared with the purely polymeric NS for potentially targeting inflammatory disorders of the posterior segment of the eye. Mechanics energy relationships revealed the favorable hydrophilic–lipophilic balance of the composite NS compared with the purely polymeric NS. © 2013 Wiley Periodicals, Inc. and the American Pharmacists Association J Pharm Sci 102:2780–2805, 2013</p> </abstract> … (more)
- Is Part Of:
- Journal of pharmaceutical sciences. Volume 102:Issue 8(2013:Aug.)
- Journal:
- Journal of pharmaceutical sciences
- Issue:
- Volume 102:Issue 8(2013:Aug.)
- Issue Display:
- Volume 102, Issue 8 (2013)
- Year:
- 2013
- Volume:
- 102
- Issue:
- 8
- Issue Sort Value:
- 2013-0102-0008-0000
- Page Start:
- 2780
- Page End:
- 2805
- Publication Date:
- 2013-07-04
- Subjects:
- Pharmacy -- Periodicals
615.1 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1520-6017 ↗
http://www.jpharmsci.org/issues ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/jps.23650 ↗
- Languages:
- English
- ISSNs:
- 0022-3549
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5031.900000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 3412.xml