Hydrogel Micro-/Nanosphere Coated by a Lipid Bilayer: Preparation and Microscopic Probing
The result of polymeric nanogels and lipid vesicles interaction—lipobeads—can be considered as multipurpose containers for future therapeutic applications, such as targeted anticancer chemotherapy with superior tumor response and minimum side effects. In this work, micrometer sized lipobeads were sy...
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doaj-1f2154ea4b434ff5abc629e39ac9fab72020-11-24T23:58:46ZengMDPI AGGels2310-28612017-02-0131710.3390/gels3010007gels3010007Hydrogel Micro-/Nanosphere Coated by a Lipid Bilayer: Preparation and Microscopic ProbingSarah Rahni0Sergey Kazakov1Department of Chemistry & Physical Sciences, Pace University, 861 Bedford Road, Pleasantville, NY 10570, USADepartment of Chemistry & Physical Sciences, Pace University, 861 Bedford Road, Pleasantville, NY 10570, USAThe result of polymeric nanogels and lipid vesicles interaction—lipobeads—can be considered as multipurpose containers for future therapeutic applications, such as targeted anticancer chemotherapy with superior tumor response and minimum side effects. In this work, micrometer sized lipobeads were synthesized by two methods: (i) mixing separately prepared microgels made of poly(N-isopropylacrylamide) (PNIPA) and phospholipid vesicles of micrometer or nanometer size and (ii) polymerization within the lipid vesicles. For the first time, a high vacuum scanning electron microscopy was shown to be suitable for a quick validation of the structural organization of wet lipobeads and their constituents without special sample preparation. In particular, the structural difference of microgels prepared by thermal and UV-polymerization in different solvents was revealed and three types of giant liposomes were recognized under high vacuum in conjunction with their size, composition, and method of preparation. Importantly, the substructure of the hydrogel core and multi- and unilamellar constructions of the peripheral lipid part were explicitly distinguished on the SEM images of lipobeads, justifying the spontaneous formation of a lipid bilayer on the surface of microgels and evidencing an energetically favorable structural organization of the hydrogel/lipid bilayer assembly. This key property can facilitate lipobeads’ preparation and decrease technological expenses on their scaled production. The comparison of the SEM imaging with the scanning confocal and atomic force microscopies data are also presented in the discussion.http://www.mdpi.com/2310-2861/3/1/7lipid bilayerlipid vesicleshydrogelssupramolecular assemblylipobeadsdrug delivery systems |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Sarah Rahni Sergey Kazakov |
spellingShingle |
Sarah Rahni Sergey Kazakov Hydrogel Micro-/Nanosphere Coated by a Lipid Bilayer: Preparation and Microscopic Probing Gels lipid bilayer lipid vesicles hydrogels supramolecular assembly lipobeads drug delivery systems |
author_facet |
Sarah Rahni Sergey Kazakov |
author_sort |
Sarah Rahni |
title |
Hydrogel Micro-/Nanosphere Coated by a Lipid Bilayer: Preparation and Microscopic Probing |
title_short |
Hydrogel Micro-/Nanosphere Coated by a Lipid Bilayer: Preparation and Microscopic Probing |
title_full |
Hydrogel Micro-/Nanosphere Coated by a Lipid Bilayer: Preparation and Microscopic Probing |
title_fullStr |
Hydrogel Micro-/Nanosphere Coated by a Lipid Bilayer: Preparation and Microscopic Probing |
title_full_unstemmed |
Hydrogel Micro-/Nanosphere Coated by a Lipid Bilayer: Preparation and Microscopic Probing |
title_sort |
hydrogel micro-/nanosphere coated by a lipid bilayer: preparation and microscopic probing |
publisher |
MDPI AG |
series |
Gels |
issn |
2310-2861 |
publishDate |
2017-02-01 |
description |
The result of polymeric nanogels and lipid vesicles interaction—lipobeads—can be considered as multipurpose containers for future therapeutic applications, such as targeted anticancer chemotherapy with superior tumor response and minimum side effects. In this work, micrometer sized lipobeads were synthesized by two methods: (i) mixing separately prepared microgels made of poly(N-isopropylacrylamide) (PNIPA) and phospholipid vesicles of micrometer or nanometer size and (ii) polymerization within the lipid vesicles. For the first time, a high vacuum scanning electron microscopy was shown to be suitable for a quick validation of the structural organization of wet lipobeads and their constituents without special sample preparation. In particular, the structural difference of microgels prepared by thermal and UV-polymerization in different solvents was revealed and three types of giant liposomes were recognized under high vacuum in conjunction with their size, composition, and method of preparation. Importantly, the substructure of the hydrogel core and multi- and unilamellar constructions of the peripheral lipid part were explicitly distinguished on the SEM images of lipobeads, justifying the spontaneous formation of a lipid bilayer on the surface of microgels and evidencing an energetically favorable structural organization of the hydrogel/lipid bilayer assembly. This key property can facilitate lipobeads’ preparation and decrease technological expenses on their scaled production. The comparison of the SEM imaging with the scanning confocal and atomic force microscopies data are also presented in the discussion. |
topic |
lipid bilayer lipid vesicles hydrogels supramolecular assembly lipobeads drug delivery systems |
url |
http://www.mdpi.com/2310-2861/3/1/7 |
work_keys_str_mv |
AT sarahrahni hydrogelmicronanospherecoatedbyalipidbilayerpreparationandmicroscopicprobing AT sergeykazakov hydrogelmicronanospherecoatedbyalipidbilayerpreparationandmicroscopicprobing |
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1725449855867813888 |