Electrospun Nanofiber and Cryogel of Polyvinyl Alcohol Transdermal Patch Containing Diclofenac Sodium: Preparation, Characterization and In Vitro Release Studies

Transdermal drug delivery systems (TDDS) have drawn more interest from pharmaceutical scientists because they could provide steady blood levels and prevent the first-pass metabolism over a longer period. Polyvinyl alcohol (PVA) has been widely used in this application due to its biocompatibility, no...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: Shafizah Sa’adon, Mohamed Nainar Mohamed Ansari, Saiful Izwan Abd Razak, Abdul Halim Mohd Yusof, Ahmad Athif Mohd Faudzi, Suresh Sagadevan, Nadirul Hasraf Mat Nayan, Joseph Sahaya Anand, Khairul Anuar Mat Amin
Formato: article
Lenguaje:EN
Publicado: MDPI AG 2021
Materias:
Acceso en línea:https://doaj.org/article/4227780f80e147639373b37c1736dca7
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
id oai:doaj.org-article:4227780f80e147639373b37c1736dca7
record_format dspace
spelling oai:doaj.org-article:4227780f80e147639373b37c1736dca72021-11-25T18:41:38ZElectrospun Nanofiber and Cryogel of Polyvinyl Alcohol Transdermal Patch Containing Diclofenac Sodium: Preparation, Characterization and In Vitro Release Studies10.3390/pharmaceutics131119001999-4923https://doaj.org/article/4227780f80e147639373b37c1736dca72021-11-01T00:00:00Zhttps://www.mdpi.com/1999-4923/13/11/1900https://doaj.org/toc/1999-4923Transdermal drug delivery systems (TDDS) have drawn more interest from pharmaceutical scientists because they could provide steady blood levels and prevent the first-pass metabolism over a longer period. Polyvinyl alcohol (PVA) has been widely used in this application due to its biocompatibility, non-toxicity, nanofiber and hydrogel-forming ability. Despite those benefits, their morphology would easily be destroyed by continuous water absorption and contribute to burst drug release due to its hydrophilicity. The aim of this study was to prepare the diclofenac sodium (DS)-medicated dual layer PVA patch using a combination of electrospinning and cryogelation (freeze–thaw) methods to improve the physicochemical properties and drug compatibility and investigate the release of the DS-medicated dual layer PVA patch. Morphological observations using scanning electron microscopy (SEM) verified the polymer−polymer interaction between both layers, whereas Fourier transform infrared (FTIR) spectroscopy has demonstrated the compatibility of DS in PVA matrix up to 2% <i>w</i>/<i>v</i> of PVA volume. The DS loads were found amorphously distributed efficaciously in PVA matrix as no visible spectra of DS–PVA interaction were detected. The DS-medicated dual layer PVA patch with a thicker nanofiber layer (3-milliliter running volume), three freeze–thaw cycles and 2% DS loading labeled as 2%DL<sub>B</sub>3C show the lowest swelling capacity (18.47%). The in vitro assessment using Franz diffusion cells showed that the 2%DL<sub>B</sub>3C indicates a better sustained release of DS, with 53.26% of the DS being released after 12 h. The 2%DL<sub>B</sub>3C owned a flux (<i>J</i><sub>ss</sub>) of 0.256 mg/cm<sup>2</sup>/h and a permeability coefficient (K<sub>p</sub>) value of 0.020 cm/h. Thus, the results demonstrate that DS-medicated dual layer PVA patches prepared via a combination of electrospinning and cryogelation are capable of releasing drugs for up to 24 h and can serve as a drug reservoir in the skin, thereby extending the pharmacologic effects of DS.Shafizah Sa’adonMohamed Nainar Mohamed AnsariSaiful Izwan Abd RazakAbdul Halim Mohd YusofAhmad Athif Mohd FaudziSuresh SagadevanNadirul Hasraf Mat NayanJoseph Sahaya AnandKhairul Anuar Mat AminMDPI AGarticleelectrospinningnanofiberscryogelationdiclofenac sodiumpolyvinyl alcoholdual layerPharmacy and materia medicaRS1-441ENPharmaceutics, Vol 13, Iss 1900, p 1900 (2021)
institution DOAJ
collection DOAJ
language EN
topic electrospinning
nanofibers
cryogelation
diclofenac sodium
polyvinyl alcohol
dual layer
Pharmacy and materia medica
RS1-441
spellingShingle electrospinning
nanofibers
cryogelation
diclofenac sodium
polyvinyl alcohol
dual layer
Pharmacy and materia medica
RS1-441
Shafizah Sa’adon
Mohamed Nainar Mohamed Ansari
Saiful Izwan Abd Razak
Abdul Halim Mohd Yusof
Ahmad Athif Mohd Faudzi
Suresh Sagadevan
Nadirul Hasraf Mat Nayan
Joseph Sahaya Anand
Khairul Anuar Mat Amin
Electrospun Nanofiber and Cryogel of Polyvinyl Alcohol Transdermal Patch Containing Diclofenac Sodium: Preparation, Characterization and In Vitro Release Studies
description Transdermal drug delivery systems (TDDS) have drawn more interest from pharmaceutical scientists because they could provide steady blood levels and prevent the first-pass metabolism over a longer period. Polyvinyl alcohol (PVA) has been widely used in this application due to its biocompatibility, non-toxicity, nanofiber and hydrogel-forming ability. Despite those benefits, their morphology would easily be destroyed by continuous water absorption and contribute to burst drug release due to its hydrophilicity. The aim of this study was to prepare the diclofenac sodium (DS)-medicated dual layer PVA patch using a combination of electrospinning and cryogelation (freeze–thaw) methods to improve the physicochemical properties and drug compatibility and investigate the release of the DS-medicated dual layer PVA patch. Morphological observations using scanning electron microscopy (SEM) verified the polymer−polymer interaction between both layers, whereas Fourier transform infrared (FTIR) spectroscopy has demonstrated the compatibility of DS in PVA matrix up to 2% <i>w</i>/<i>v</i> of PVA volume. The DS loads were found amorphously distributed efficaciously in PVA matrix as no visible spectra of DS–PVA interaction were detected. The DS-medicated dual layer PVA patch with a thicker nanofiber layer (3-milliliter running volume), three freeze–thaw cycles and 2% DS loading labeled as 2%DL<sub>B</sub>3C show the lowest swelling capacity (18.47%). The in vitro assessment using Franz diffusion cells showed that the 2%DL<sub>B</sub>3C indicates a better sustained release of DS, with 53.26% of the DS being released after 12 h. The 2%DL<sub>B</sub>3C owned a flux (<i>J</i><sub>ss</sub>) of 0.256 mg/cm<sup>2</sup>/h and a permeability coefficient (K<sub>p</sub>) value of 0.020 cm/h. Thus, the results demonstrate that DS-medicated dual layer PVA patches prepared via a combination of electrospinning and cryogelation are capable of releasing drugs for up to 24 h and can serve as a drug reservoir in the skin, thereby extending the pharmacologic effects of DS.
format article
author Shafizah Sa’adon
Mohamed Nainar Mohamed Ansari
Saiful Izwan Abd Razak
Abdul Halim Mohd Yusof
Ahmad Athif Mohd Faudzi
Suresh Sagadevan
Nadirul Hasraf Mat Nayan
Joseph Sahaya Anand
Khairul Anuar Mat Amin
author_facet Shafizah Sa’adon
Mohamed Nainar Mohamed Ansari
Saiful Izwan Abd Razak
Abdul Halim Mohd Yusof
Ahmad Athif Mohd Faudzi
Suresh Sagadevan
Nadirul Hasraf Mat Nayan
Joseph Sahaya Anand
Khairul Anuar Mat Amin
author_sort Shafizah Sa’adon
title Electrospun Nanofiber and Cryogel of Polyvinyl Alcohol Transdermal Patch Containing Diclofenac Sodium: Preparation, Characterization and In Vitro Release Studies
title_short Electrospun Nanofiber and Cryogel of Polyvinyl Alcohol Transdermal Patch Containing Diclofenac Sodium: Preparation, Characterization and In Vitro Release Studies
title_full Electrospun Nanofiber and Cryogel of Polyvinyl Alcohol Transdermal Patch Containing Diclofenac Sodium: Preparation, Characterization and In Vitro Release Studies
title_fullStr Electrospun Nanofiber and Cryogel of Polyvinyl Alcohol Transdermal Patch Containing Diclofenac Sodium: Preparation, Characterization and In Vitro Release Studies
title_full_unstemmed Electrospun Nanofiber and Cryogel of Polyvinyl Alcohol Transdermal Patch Containing Diclofenac Sodium: Preparation, Characterization and In Vitro Release Studies
title_sort electrospun nanofiber and cryogel of polyvinyl alcohol transdermal patch containing diclofenac sodium: preparation, characterization and in vitro release studies
publisher MDPI AG
publishDate 2021
url https://doaj.org/article/4227780f80e147639373b37c1736dca7
work_keys_str_mv AT shafizahsaadon electrospunnanofiberandcryogelofpolyvinylalcoholtransdermalpatchcontainingdiclofenacsodiumpreparationcharacterizationandinvitroreleasestudies
AT mohamednainarmohamedansari electrospunnanofiberandcryogelofpolyvinylalcoholtransdermalpatchcontainingdiclofenacsodiumpreparationcharacterizationandinvitroreleasestudies
AT saifulizwanabdrazak electrospunnanofiberandcryogelofpolyvinylalcoholtransdermalpatchcontainingdiclofenacsodiumpreparationcharacterizationandinvitroreleasestudies
AT abdulhalimmohdyusof electrospunnanofiberandcryogelofpolyvinylalcoholtransdermalpatchcontainingdiclofenacsodiumpreparationcharacterizationandinvitroreleasestudies
AT ahmadathifmohdfaudzi electrospunnanofiberandcryogelofpolyvinylalcoholtransdermalpatchcontainingdiclofenacsodiumpreparationcharacterizationandinvitroreleasestudies
AT sureshsagadevan electrospunnanofiberandcryogelofpolyvinylalcoholtransdermalpatchcontainingdiclofenacsodiumpreparationcharacterizationandinvitroreleasestudies
AT nadirulhasrafmatnayan electrospunnanofiberandcryogelofpolyvinylalcoholtransdermalpatchcontainingdiclofenacsodiumpreparationcharacterizationandinvitroreleasestudies
AT josephsahayaanand electrospunnanofiberandcryogelofpolyvinylalcoholtransdermalpatchcontainingdiclofenacsodiumpreparationcharacterizationandinvitroreleasestudies
AT khairulanuarmatamin electrospunnanofiberandcryogelofpolyvinylalcoholtransdermalpatchcontainingdiclofenacsodiumpreparationcharacterizationandinvitroreleasestudies
_version_ 1718410767187836928