Synthesis and characterization of vincristine loaded folic acid–chitosan conjugated nanoparticles

Vincristine is an anticancer drug used to treat different types of cancer. However, vincristine has been reported to become resistant against some cancer such as small cell lung cancer cell lines due to decreased uptake, increased drug efflux etc. To increase the uptake, vincristine loaded folic aci...

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Main Authors: Raj Kumar Salar, Naresh Kumar
Format: Article
Language:English
Published: Tomsk Polytechnic University 2016-12-01
Series:Resource-Efficient Technologies
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S2405653716300410
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spelling doaj-cd92656551b448078e60b7b1b30a41232020-11-25T02:11:47ZengTomsk Polytechnic UniversityResource-Efficient Technologies2405-65372016-12-012419921410.1016/j.reffit.2016.10.006Synthesis and characterization of vincristine loaded folic acid–chitosan conjugated nanoparticlesRaj Kumar SalarNaresh KumarVincristine is an anticancer drug used to treat different types of cancer. However, vincristine has been reported to become resistant against some cancer such as small cell lung cancer cell lines due to decreased uptake, increased drug efflux etc. To increase the uptake, vincristine loaded folic acid–chitosan conjugated nanoparticles were synthesized using ionic gelation method at pH 2.5. 1H-NMR confirmed conjugation of folic acid with chitosan. Blank folic acid–chitosan conjugated nanoparticles had an average size of 897.5 ± 0.90 nm, a polydispersity index of 0.738 ± 0.30 and zeta potential of +11.2 ± 0.43 mV and found to increase in vincristine loaded folic acid−chitosan nanoparticles at different formulations due to loading of vincristine in folic acid–chitosan conjugated nanoparticles. Fourier Transform Infrared Spectroscopy (FTIR) revealed different functional groups and loading of vincristine in chitosan nanoparticles. X-ray diffraction (XRD) was performed to confirm the crystalline nature of the drug after loading and face centered cubic (FCC) structure of nanoparticles. In vitro drug release study showed slow and sustained release of vincristine in phosphate buffered saline at pH 6.7. Scanning Electron Microscopy (SEM) revealed spherical and rough surface of nanoparticles. Transmission Electron Microscopy (TEM) confirmed loading of vincristine and size range of nanoparticles from 4.24 to 300 nm. Spectrophotometric analysis depicted maximum encapsulation efficiency and loading capacity of 81.25% and 10.31%, respectively. Since cancer cells express folate receptors on their surface, these vincristine loaded folic acid–chitosan conjugated nanoparticles could be used for targeted delivery against resistant cancer with some modifications.http://www.sciencedirect.com/science/article/pii/S2405653716300410ChitosanFolic acidNanoparticlesVincristine
collection DOAJ
language English
format Article
sources DOAJ
author Raj Kumar Salar
Naresh Kumar
spellingShingle Raj Kumar Salar
Naresh Kumar
Synthesis and characterization of vincristine loaded folic acid–chitosan conjugated nanoparticles
Resource-Efficient Technologies
Chitosan
Folic acid
Nanoparticles
Vincristine
author_facet Raj Kumar Salar
Naresh Kumar
author_sort Raj Kumar Salar
title Synthesis and characterization of vincristine loaded folic acid–chitosan conjugated nanoparticles
title_short Synthesis and characterization of vincristine loaded folic acid–chitosan conjugated nanoparticles
title_full Synthesis and characterization of vincristine loaded folic acid–chitosan conjugated nanoparticles
title_fullStr Synthesis and characterization of vincristine loaded folic acid–chitosan conjugated nanoparticles
title_full_unstemmed Synthesis and characterization of vincristine loaded folic acid–chitosan conjugated nanoparticles
title_sort synthesis and characterization of vincristine loaded folic acid–chitosan conjugated nanoparticles
publisher Tomsk Polytechnic University
series Resource-Efficient Technologies
issn 2405-6537
publishDate 2016-12-01
description Vincristine is an anticancer drug used to treat different types of cancer. However, vincristine has been reported to become resistant against some cancer such as small cell lung cancer cell lines due to decreased uptake, increased drug efflux etc. To increase the uptake, vincristine loaded folic acid–chitosan conjugated nanoparticles were synthesized using ionic gelation method at pH 2.5. 1H-NMR confirmed conjugation of folic acid with chitosan. Blank folic acid–chitosan conjugated nanoparticles had an average size of 897.5 ± 0.90 nm, a polydispersity index of 0.738 ± 0.30 and zeta potential of +11.2 ± 0.43 mV and found to increase in vincristine loaded folic acid−chitosan nanoparticles at different formulations due to loading of vincristine in folic acid–chitosan conjugated nanoparticles. Fourier Transform Infrared Spectroscopy (FTIR) revealed different functional groups and loading of vincristine in chitosan nanoparticles. X-ray diffraction (XRD) was performed to confirm the crystalline nature of the drug after loading and face centered cubic (FCC) structure of nanoparticles. In vitro drug release study showed slow and sustained release of vincristine in phosphate buffered saline at pH 6.7. Scanning Electron Microscopy (SEM) revealed spherical and rough surface of nanoparticles. Transmission Electron Microscopy (TEM) confirmed loading of vincristine and size range of nanoparticles from 4.24 to 300 nm. Spectrophotometric analysis depicted maximum encapsulation efficiency and loading capacity of 81.25% and 10.31%, respectively. Since cancer cells express folate receptors on their surface, these vincristine loaded folic acid–chitosan conjugated nanoparticles could be used for targeted delivery against resistant cancer with some modifications.
topic Chitosan
Folic acid
Nanoparticles
Vincristine
url http://www.sciencedirect.com/science/article/pii/S2405653716300410
work_keys_str_mv AT rajkumarsalar synthesisandcharacterizationofvincristineloadedfolicacidchitosanconjugatednanoparticles
AT nareshkumar synthesisandcharacterizationofvincristineloadedfolicacidchitosanconjugatednanoparticles
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