Fabrication of Electrospun PLA-nHAp Nanocomposite for Sustained Drug Release in Dental and Orthopedic Applications

This study describes the fabrication of nanocomposites using electrospinning technique from poly lactic acid (PLA) and nano-hydroxyapatite (n-HAp). The prepared electrospun PLA-nHAP nanocomposite is intended to be used for drug delivery application. A hydrogen bond in between nHAp and PLA was confir...

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Main Authors: Nishat Anzum Kanak, Md. Shahruzzaman, Md. Sazedul Islam, Makoto Takafuji, Mohammed Mizanur Rahman, Sumaya F. Kabir
Format: Article
Language:English
Published: MDPI AG 2023-05-01
Series:Materials
Subjects:
Online Access:https://www.mdpi.com/1996-1944/16/10/3691
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author Nishat Anzum Kanak
Md. Shahruzzaman
Md. Sazedul Islam
Makoto Takafuji
Mohammed Mizanur Rahman
Sumaya F. Kabir
author_facet Nishat Anzum Kanak
Md. Shahruzzaman
Md. Sazedul Islam
Makoto Takafuji
Mohammed Mizanur Rahman
Sumaya F. Kabir
author_sort Nishat Anzum Kanak
collection DOAJ
description This study describes the fabrication of nanocomposites using electrospinning technique from poly lactic acid (PLA) and nano-hydroxyapatite (n-HAp). The prepared electrospun PLA-nHAP nanocomposite is intended to be used for drug delivery application. A hydrogen bond in between nHAp and PLA was confirmed by Fourier transform infrared (FT-IR) spectroscopy. Degradation study of the prepared electrospun PLA-nHAp nanocomposite was conducted for 30 days both in phosphate buffer solution (PBS) of pH 7.4 and deionized water. The degradation of the nanocomposite occurred faster in PBS in comparison to water. Cytotoxicity analysis was conducted on both Vero cells and BHK-21 cells and the survival percentage of both cells was found to be more than 95%, which indicates that the prepared nanocomposite is non-toxic and biocompatible. Gentamicin was loaded in the nanocomposite via an encapsulation process and the in vitro drug delivery process was investigated in phosphate buffer solution at different pHs. An initial burst release of the drug was observed from the nanocomposite after 1 to 2 weeks for all pH media. After that, a sustained drug release behavior was observed for the nanocomposite for 8 weeks with a release of 80%, 70% and 50% at pHs 5.5, 6.0 and 7.4, respectively. It can be suggested that the electrospun PLA-nHAp nanocomposite can be used as a potential antibacterial drug carrier for sustained drug release in dental and orthopedic sector.
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spelling doaj.art-f7ff61df53ee45b0b2cd286c61656b092023-11-18T02:14:41ZengMDPI AGMaterials1996-19442023-05-011610369110.3390/ma16103691Fabrication of Electrospun PLA-nHAp Nanocomposite for Sustained Drug Release in Dental and Orthopedic ApplicationsNishat Anzum Kanak0Md. Shahruzzaman1Md. Sazedul Islam2Makoto Takafuji3Mohammed Mizanur Rahman4Sumaya F. Kabir5Department of Applied Chemistry and Chemical Engineering, University of Dhaka, Dhaka 1000, BangladeshDepartment of Applied Chemistry and Chemical Engineering, University of Dhaka, Dhaka 1000, BangladeshDepartment of Applied Chemistry and Chemical Engineering, University of Dhaka, Dhaka 1000, BangladeshDepartment of Applied Chemistry and Biochemistry, Kumamoto University, Kumamoto 860-8555, JapanDepartment of Applied Chemistry and Chemical Engineering, University of Dhaka, Dhaka 1000, BangladeshDepartment of Applied Chemistry and Chemical Engineering, University of Dhaka, Dhaka 1000, BangladeshThis study describes the fabrication of nanocomposites using electrospinning technique from poly lactic acid (PLA) and nano-hydroxyapatite (n-HAp). The prepared electrospun PLA-nHAP nanocomposite is intended to be used for drug delivery application. A hydrogen bond in between nHAp and PLA was confirmed by Fourier transform infrared (FT-IR) spectroscopy. Degradation study of the prepared electrospun PLA-nHAp nanocomposite was conducted for 30 days both in phosphate buffer solution (PBS) of pH 7.4 and deionized water. The degradation of the nanocomposite occurred faster in PBS in comparison to water. Cytotoxicity analysis was conducted on both Vero cells and BHK-21 cells and the survival percentage of both cells was found to be more than 95%, which indicates that the prepared nanocomposite is non-toxic and biocompatible. Gentamicin was loaded in the nanocomposite via an encapsulation process and the in vitro drug delivery process was investigated in phosphate buffer solution at different pHs. An initial burst release of the drug was observed from the nanocomposite after 1 to 2 weeks for all pH media. After that, a sustained drug release behavior was observed for the nanocomposite for 8 weeks with a release of 80%, 70% and 50% at pHs 5.5, 6.0 and 7.4, respectively. It can be suggested that the electrospun PLA-nHAp nanocomposite can be used as a potential antibacterial drug carrier for sustained drug release in dental and orthopedic sector.https://www.mdpi.com/1996-1944/16/10/3691electrospunnanocompositedrug releasecytotoxicityhydroxyapatite
spellingShingle Nishat Anzum Kanak
Md. Shahruzzaman
Md. Sazedul Islam
Makoto Takafuji
Mohammed Mizanur Rahman
Sumaya F. Kabir
Fabrication of Electrospun PLA-nHAp Nanocomposite for Sustained Drug Release in Dental and Orthopedic Applications
Materials
electrospun
nanocomposite
drug release
cytotoxicity
hydroxyapatite
title Fabrication of Electrospun PLA-nHAp Nanocomposite for Sustained Drug Release in Dental and Orthopedic Applications
title_full Fabrication of Electrospun PLA-nHAp Nanocomposite for Sustained Drug Release in Dental and Orthopedic Applications
title_fullStr Fabrication of Electrospun PLA-nHAp Nanocomposite for Sustained Drug Release in Dental and Orthopedic Applications
title_full_unstemmed Fabrication of Electrospun PLA-nHAp Nanocomposite for Sustained Drug Release in Dental and Orthopedic Applications
title_short Fabrication of Electrospun PLA-nHAp Nanocomposite for Sustained Drug Release in Dental and Orthopedic Applications
title_sort fabrication of electrospun pla nhap nanocomposite for sustained drug release in dental and orthopedic applications
topic electrospun
nanocomposite
drug release
cytotoxicity
hydroxyapatite
url https://www.mdpi.com/1996-1944/16/10/3691
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