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Preformulation Study of Electrospun Haemanthamine-Loaded Amphiphilic Nanofibers Intended for a Solid Template for Self-Assembled Liposomes

Haemanthamine (HAE) has been proven as a potential anticancer agent. However, the therapeutic use of this plant-origin alkaloid to date is limited due to the chemical instability and poorly water-soluble characteristics of the agent. To overcome these challenges, we developed novel amphiphilic elect...

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Autores principales: Viet Nguyen, Khan, Laidmäe, Ivo, Kogermann, Karin, Lust, Andres, Meos, Andres, Viet Ho, Duc, Raal, Ain, Heinämäki, Jyrki, Thi Nguyen, Hoai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6835215/
https://www.ncbi.nlm.nih.gov/pubmed/31569535
http://dx.doi.org/10.3390/pharmaceutics11100499
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author Viet Nguyen, Khan
Laidmäe, Ivo
Kogermann, Karin
Lust, Andres
Meos, Andres
Viet Ho, Duc
Raal, Ain
Heinämäki, Jyrki
Thi Nguyen, Hoai
author_facet Viet Nguyen, Khan
Laidmäe, Ivo
Kogermann, Karin
Lust, Andres
Meos, Andres
Viet Ho, Duc
Raal, Ain
Heinämäki, Jyrki
Thi Nguyen, Hoai
author_sort Viet Nguyen, Khan
collection PubMed
description Haemanthamine (HAE) has been proven as a potential anticancer agent. However, the therapeutic use of this plant-origin alkaloid to date is limited due to the chemical instability and poorly water-soluble characteristics of the agent. To overcome these challenges, we developed novel amphiphilic electrospun nanofibers (NFs) loaded with HAE, phosphatidylcholine (PC) and polyvinylpyrrolidone (PVP), and intended for a stabilizing platform (template) of self-assembled liposomes of the active agent. The NFs were fabricated with a solvent-based electrospinning method. The chemical structure of HAE and the geometric properties, molecular interactions and physical solid-state properties of the NFs were investigated using nuclear magnetic resonance (NMR) spectroscopy, scanning electron microscopy (SEM), photon correlation spectroscopy (PCS), Fourier transform infrared (FTIR) spectroscopy, X-ray powder diffraction (XRPD) and differential scanning calorimetry (DSC), respectively. An in-house dialysis-based dissolution method was used to investigate the drug release in vitro. The HAE-loaded fibers showed a nanoscale size ranging from 197 nm to 534 nm. The liposomes with a diameter between 63 nm and 401 nm were spontaneously formed as the NFs were exposed to water. HAE dispersed inside liposomes showed a tri-modal dissolution behavior. In conclusion, the present amphiphilic NFs loaded with HAE are an alternative approach for the formulation of a liposomal drug delivery system and stabilization of the liposomes of the present alkaloid.
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spelling pubmed-68352152019-11-25 Preformulation Study of Electrospun Haemanthamine-Loaded Amphiphilic Nanofibers Intended for a Solid Template for Self-Assembled Liposomes Viet Nguyen, Khan Laidmäe, Ivo Kogermann, Karin Lust, Andres Meos, Andres Viet Ho, Duc Raal, Ain Heinämäki, Jyrki Thi Nguyen, Hoai Pharmaceutics Article Haemanthamine (HAE) has been proven as a potential anticancer agent. However, the therapeutic use of this plant-origin alkaloid to date is limited due to the chemical instability and poorly water-soluble characteristics of the agent. To overcome these challenges, we developed novel amphiphilic electrospun nanofibers (NFs) loaded with HAE, phosphatidylcholine (PC) and polyvinylpyrrolidone (PVP), and intended for a stabilizing platform (template) of self-assembled liposomes of the active agent. The NFs were fabricated with a solvent-based electrospinning method. The chemical structure of HAE and the geometric properties, molecular interactions and physical solid-state properties of the NFs were investigated using nuclear magnetic resonance (NMR) spectroscopy, scanning electron microscopy (SEM), photon correlation spectroscopy (PCS), Fourier transform infrared (FTIR) spectroscopy, X-ray powder diffraction (XRPD) and differential scanning calorimetry (DSC), respectively. An in-house dialysis-based dissolution method was used to investigate the drug release in vitro. The HAE-loaded fibers showed a nanoscale size ranging from 197 nm to 534 nm. The liposomes with a diameter between 63 nm and 401 nm were spontaneously formed as the NFs were exposed to water. HAE dispersed inside liposomes showed a tri-modal dissolution behavior. In conclusion, the present amphiphilic NFs loaded with HAE are an alternative approach for the formulation of a liposomal drug delivery system and stabilization of the liposomes of the present alkaloid. MDPI 2019-09-29 /pmc/articles/PMC6835215/ /pubmed/31569535 http://dx.doi.org/10.3390/pharmaceutics11100499 Text en © 2019 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
Viet Nguyen, Khan
Laidmäe, Ivo
Kogermann, Karin
Lust, Andres
Meos, Andres
Viet Ho, Duc
Raal, Ain
Heinämäki, Jyrki
Thi Nguyen, Hoai
Preformulation Study of Electrospun Haemanthamine-Loaded Amphiphilic Nanofibers Intended for a Solid Template for Self-Assembled Liposomes
title Preformulation Study of Electrospun Haemanthamine-Loaded Amphiphilic Nanofibers Intended for a Solid Template for Self-Assembled Liposomes
title_full Preformulation Study of Electrospun Haemanthamine-Loaded Amphiphilic Nanofibers Intended for a Solid Template for Self-Assembled Liposomes
title_fullStr Preformulation Study of Electrospun Haemanthamine-Loaded Amphiphilic Nanofibers Intended for a Solid Template for Self-Assembled Liposomes
title_full_unstemmed Preformulation Study of Electrospun Haemanthamine-Loaded Amphiphilic Nanofibers Intended for a Solid Template for Self-Assembled Liposomes
title_short Preformulation Study of Electrospun Haemanthamine-Loaded Amphiphilic Nanofibers Intended for a Solid Template for Self-Assembled Liposomes
title_sort preformulation study of electrospun haemanthamine-loaded amphiphilic nanofibers intended for a solid template for self-assembled liposomes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6835215/
https://www.ncbi.nlm.nih.gov/pubmed/31569535
http://dx.doi.org/10.3390/pharmaceutics11100499
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