Cargando…

Synthesis and Formulation of Thermosensitive Drug Carrier for Temperature Triggered Delivery of Naproxen Sodium

Nanospheres and microspheres are known as a multipurpose compounds and are used in various branches of science. Recent controlled delivery systems for drugs are also based on poly-micro and nanospheres. In our study we describe an investigation of the influence of thermosensitive polymer N-isopropyl...

Descripción completa

Detalles Bibliográficos
Autores principales: Gasztych, Monika, Gola, Agnieszka, Kobryń, Justyna, Musiał, Witold
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6274452/
https://www.ncbi.nlm.nih.gov/pubmed/27827936
http://dx.doi.org/10.3390/molecules21111473
_version_ 1783377621592047616
author Gasztych, Monika
Gola, Agnieszka
Kobryń, Justyna
Musiał, Witold
author_facet Gasztych, Monika
Gola, Agnieszka
Kobryń, Justyna
Musiał, Witold
author_sort Gasztych, Monika
collection PubMed
description Nanospheres and microspheres are known as a multipurpose compounds and are used in various branches of science. Recent controlled delivery systems for drugs are also based on poly-micro and nanospheres. In our study we describe an investigation of the influence of thermosensitive polymer N-isopropylacrylamide (NIPA) on the release of the drug naproxen sodium (NS) with a hydrogel hydroxypropyl methylcellulose (HPMC) base. The hydrodynamic diameter (D(H)) of the obtained polymer was measured by using dynamic light scattering (DLS) at a wavelength of 678 nm. Hydrogel formulations of NS were prepared in a specific way ex tempore. NS was sprinkled on the surface of a distilled water, then polymer soluted in water was added. Afterward, HPMC was affixed to the solution. Prepared samples were stored at room temperature for 24 h. Release tests showed that modification of thevcross-linker type influenced the properties of synthesized polymeric particles. The NIPA derivatives obtained via surfactant free precipitation polymerization (SFPP) may be formulated as hydrogel preparations using HPMC. The obtained formulations presented varied half-release times, depending on the type of applied NIPA derivatives in hydrogel formulations. At 18 °C, the release rates were lower comparing to the reference HPMC hydrogel, whereas at 42 °C, the release rates were significantly higher. The synthesized thermosensitive polymers enabled temperature-triggered release of NS.
format Online
Article
Text
id pubmed-6274452
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-62744522018-12-28 Synthesis and Formulation of Thermosensitive Drug Carrier for Temperature Triggered Delivery of Naproxen Sodium Gasztych, Monika Gola, Agnieszka Kobryń, Justyna Musiał, Witold Molecules Article Nanospheres and microspheres are known as a multipurpose compounds and are used in various branches of science. Recent controlled delivery systems for drugs are also based on poly-micro and nanospheres. In our study we describe an investigation of the influence of thermosensitive polymer N-isopropylacrylamide (NIPA) on the release of the drug naproxen sodium (NS) with a hydrogel hydroxypropyl methylcellulose (HPMC) base. The hydrodynamic diameter (D(H)) of the obtained polymer was measured by using dynamic light scattering (DLS) at a wavelength of 678 nm. Hydrogel formulations of NS were prepared in a specific way ex tempore. NS was sprinkled on the surface of a distilled water, then polymer soluted in water was added. Afterward, HPMC was affixed to the solution. Prepared samples were stored at room temperature for 24 h. Release tests showed that modification of thevcross-linker type influenced the properties of synthesized polymeric particles. The NIPA derivatives obtained via surfactant free precipitation polymerization (SFPP) may be formulated as hydrogel preparations using HPMC. The obtained formulations presented varied half-release times, depending on the type of applied NIPA derivatives in hydrogel formulations. At 18 °C, the release rates were lower comparing to the reference HPMC hydrogel, whereas at 42 °C, the release rates were significantly higher. The synthesized thermosensitive polymers enabled temperature-triggered release of NS. MDPI 2016-11-04 /pmc/articles/PMC6274452/ /pubmed/27827936 http://dx.doi.org/10.3390/molecules21111473 Text en © 2016 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC-BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Gasztych, Monika
Gola, Agnieszka
Kobryń, Justyna
Musiał, Witold
Synthesis and Formulation of Thermosensitive Drug Carrier for Temperature Triggered Delivery of Naproxen Sodium
title Synthesis and Formulation of Thermosensitive Drug Carrier for Temperature Triggered Delivery of Naproxen Sodium
title_full Synthesis and Formulation of Thermosensitive Drug Carrier for Temperature Triggered Delivery of Naproxen Sodium
title_fullStr Synthesis and Formulation of Thermosensitive Drug Carrier for Temperature Triggered Delivery of Naproxen Sodium
title_full_unstemmed Synthesis and Formulation of Thermosensitive Drug Carrier for Temperature Triggered Delivery of Naproxen Sodium
title_short Synthesis and Formulation of Thermosensitive Drug Carrier for Temperature Triggered Delivery of Naproxen Sodium
title_sort synthesis and formulation of thermosensitive drug carrier for temperature triggered delivery of naproxen sodium
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6274452/
https://www.ncbi.nlm.nih.gov/pubmed/27827936
http://dx.doi.org/10.3390/molecules21111473
work_keys_str_mv AT gasztychmonika synthesisandformulationofthermosensitivedrugcarrierfortemperaturetriggereddeliveryofnaproxensodium
AT golaagnieszka synthesisandformulationofthermosensitivedrugcarrierfortemperaturetriggereddeliveryofnaproxensodium
AT kobrynjustyna synthesisandformulationofthermosensitivedrugcarrierfortemperaturetriggereddeliveryofnaproxensodium
AT musiałwitold synthesisandformulationofthermosensitivedrugcarrierfortemperaturetriggereddeliveryofnaproxensodium