Abstract
Mucoadhesive hybrid polymer/liposome paste is a new drug delivery system presenting controllable and tailorable delivery mechanism. By using mucoadhesive material, the delivery can be more specific and local. Here, we present a study investigating the effect of polymer type, concentration, functional end group, and cross-linking on the release profile of nanoliposomes from polymer pastes. Polymer pastes can be expected to combine the mucoadhesion mechanisms of dry and wet dosage forms but have not been studied extensively. To better understand the mucoadhesion of pastes, we investigated a series of pastes based on the same polymer and used different chemical modifications that can produce interactions at different levels. Native and thiolated polymers presented enhanced mucoadhesion in a wet environment in comparison to acrylated polymers which dissolved rapidly because of the enhanced solubility of PEG chains in water. Paste cross-linking resulted in a sustained release profile compared to non–cross-linked pastes. Pectin-SH pastes, especially 3% (w/v), showed a linear liposomal release profile which is ascribed to the combination of ionic cross-linking and disulfide bridging. By configuring the polymer type or concentration, we can control the release mechanisms and achieve distinct inherent properties which can be applied for diverse medical applications.
Original language | English |
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Pages (from-to) | 3814-3822 |
Number of pages | 9 |
Journal | Journal of Pharmaceutical Sciences |
Volume | 108 |
Issue number | 12 |
DOIs | |
State | Published - Dec 2019 |
Bibliographical note
Publisher Copyright:© 2019 American Pharmacists Association®
Funding
This work was supported by the Israel Ministry of Science and Technology (3-11878), Jerusalem, Israel. The support of the Israel Innovation Authoroty (Kamin Project 63379) is highly appreciated. This work was supported by the Israel Ministry of Science and Technology (3-11878), Jerusalem, Israel. The support of the Israel Innovation Authoroty (Kamin Project 63379) is highly appreciated. The authors wish to thank Ariela Tarnapolsky, Maayan Biton, and Noi Breger for participating in the experiments.
Funders | Funder number |
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Israel Innovation Authoroty | 63379 |
Israel Ministry of Science and Technology | 3-11878 |
Ministry of science and technology, Israel |
Keywords
- drug delivery system
- liposome
- mucoadhesive
- polymer