Synthesis and Evaluation of Symmetrically PEG‐Decorated Triglycerides of Fatty Acid as Drug‐Encapsulating Agents. Issue 4 (3rd December 2014)
- Record Type:
- Journal Article
- Title:
- Synthesis and Evaluation of Symmetrically PEG‐Decorated Triglycerides of Fatty Acid as Drug‐Encapsulating Agents. Issue 4 (3rd December 2014)
- Main Title:
- Synthesis and Evaluation of Symmetrically PEG‐Decorated Triglycerides of Fatty Acid as Drug‐Encapsulating Agents
- Authors:
- Elkin, Igor
Rabanel, Jean‐Michel
Aoun, Valéry
Hildgen, Patrice - Abstract:
- <abstract abstract-type="main" xml:lang="en"> <title> <x xml:space="preserve">Abstract</x> </title> <p>New symmetrically poly(ethylene glycol) (PEG)‐decorated triglycerides of fatty acid are synthesized and proposed as drug‐encapsulation systems. A method of effective grafting of PEG on secondary hydroxy groups located on long alkyl chains by the use of a short spacer represented by succinic acid is elaborated. Synthesis of new derivatives of triacylglycerols of fatty acids (TAG) based on the triolein standard and commercial olive oil, with PEG chains of different lengths (1000, 550, and 220 Da) is performed. MTT assay on the murine macrophage cell line RAW‐262.7 shows the absence of cytotoxic effects caused by the obtained products. Encapsulation tests using itraconazole (ITZ) as a hydrophobic drug model are carried out. The influence of the PEG chain length, as well as of the presence of ITZ on the size of micelles, are studied by the dynamic light scattering (DLS) method. The reduced cytotoxicity observed on <italic>Candida albicans</italic> cells of ITZ formulated with the PEG‐decorated TAG versus the free drug indicates that the systems may be promising to increase the duration of drug release and to reduce toxic side effects. <boxed-text content-type="graphic" position="anchor" orientation="portrait"><graphic position="anchor" mimetype="image" xlink:href="ark:/27927/pgh3wcj294r" orientation="portrait" xlink:type="simple" xmlns:xlink="http://www.w3.org/1999/xlink"<abstract abstract-type="main" xml:lang="en"> <title> <x xml:space="preserve">Abstract</x> </title> <p>New symmetrically poly(ethylene glycol) (PEG)‐decorated triglycerides of fatty acid are synthesized and proposed as drug‐encapsulation systems. A method of effective grafting of PEG on secondary hydroxy groups located on long alkyl chains by the use of a short spacer represented by succinic acid is elaborated. Synthesis of new derivatives of triacylglycerols of fatty acids (TAG) based on the triolein standard and commercial olive oil, with PEG chains of different lengths (1000, 550, and 220 Da) is performed. MTT assay on the murine macrophage cell line RAW‐262.7 shows the absence of cytotoxic effects caused by the obtained products. Encapsulation tests using itraconazole (ITZ) as a hydrophobic drug model are carried out. The influence of the PEG chain length, as well as of the presence of ITZ on the size of micelles, are studied by the dynamic light scattering (DLS) method. The reduced cytotoxicity observed on <italic>Candida albicans</italic> cells of ITZ formulated with the PEG‐decorated TAG versus the free drug indicates that the systems may be promising to increase the duration of drug release and to reduce toxic side effects. <boxed-text content-type="graphic" position="anchor" orientation="portrait"><graphic position="anchor" mimetype="image" xlink:href="ark:/27927/pgh3wcj294r" orientation="portrait" xlink:type="simple" xmlns:xlink="http://www.w3.org/1999/xlink" /></boxed-text></p> </abstract> … (more)
- Is Part Of:
- Macromolecular chemistry and physics. Volume 216:Issue 4(2015:Feb.)
- Journal:
- Macromolecular chemistry and physics
- Issue:
- Volume 216:Issue 4(2015:Feb.)
- Issue Display:
- Volume 216, Issue 4 (2015)
- Year:
- 2015
- Volume:
- 216
- Issue:
- 4
- Issue Sort Value:
- 2015-0216-0004-0000
- Page Start:
- 427
- Page End:
- 438
- Publication Date:
- 2014-12-03
- Subjects:
- Polymers -- Periodicals
Polymerization -- Periodicals
Synthetic products -- Periodicals
Macromolecules -- Periodicals
547.7 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1521-3935 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/macp.201400486 ↗
- Languages:
- English
- ISSNs:
- 1022-1352
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5330.398000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 3528.xml