Characterization and toxicity of citral incorporated with nanostructured lipid carrier

The nanoparticle as a cancer drug delivery vehicle is rapidly under investigation due to its promising applicability as a novel drug delivery system for anticancer agents. This study describes the development, characterization and toxicity studies of a nanostructured lipid carrier (NLC) system for c...

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Main Authors: Mohammed Alitheen, Noorjahan Banu, How, Chee Wun, Mohamad, Nurul Elyani, Zamberi, Nur Rizi, Yeap, Swee Keong, Nordin, Noraini, Abdullah, Rasedee, Masarudin, Mas Jaffri, Abu, Nadiah, Heshu, Sulaiman Rahman
Format: Article
Language:English
Published: PeerJ 2018
Online Access:http://psasir.upm.edu.my/id/eprint/73363/1/CITRAL.pdf
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author Mohammed Alitheen, Noorjahan Banu
How, Chee Wun
Mohamad, Nurul Elyani
Zamberi, Nur Rizi
Yeap, Swee Keong
Nordin, Noraini
Abdullah, Rasedee
Masarudin, Mas Jaffri
Abu, Nadiah
Heshu, Sulaiman Rahman
author_facet Mohammed Alitheen, Noorjahan Banu
How, Chee Wun
Mohamad, Nurul Elyani
Zamberi, Nur Rizi
Yeap, Swee Keong
Nordin, Noraini
Abdullah, Rasedee
Masarudin, Mas Jaffri
Abu, Nadiah
Heshu, Sulaiman Rahman
author_sort Mohammed Alitheen, Noorjahan Banu
collection UPM
description The nanoparticle as a cancer drug delivery vehicle is rapidly under investigation due to its promising applicability as a novel drug delivery system for anticancer agents. This study describes the development, characterization and toxicity studies of a nanostructured lipid carrier (NLC) system for citral. Citral was loaded into the NLC using high pressure homogenization methods. The characterizations of NLCcitral were then determined through various methods. Based on Transmission Electron Microscope (TEM) analysis, NLC-Citral showed a spherical shape with an average diameter size of 54.12 ± 0.30 nm and a polydipersity index of 0.224 ± 0.005. The zeta potential of NLC-Citral was −12.73 ± 0.34 mV with an entrapment efficiency of 98.9 ± 0.124%, and drug loading of 9.84 ± 0.041%. Safety profile of the formulation was examined via in vitro and in vivo routes to study its effects toward normal cells. NLC-Citral exhibited no toxic effects towards the proliferation of mice splenocytes. Moreover, no mortality and toxic signs were observed in the treated groups after 28 days of treatment. There were also no significant alterations in serum biochemical analysis for all treatments. Increase in immunomodulatory effects of treated NLC-Citral and Citral groups was verified from the increase in CD4/CD3 and CD8/CD3 T cell population in both NLC-citral and citral treated splenocytes. This study suggests that NLC is a promising drug delivery system for citral as it has the potential in sustaining drug release without inducing any toxicity.
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spelling upm.eprints-733632020-11-27T19:52:18Z http://psasir.upm.edu.my/id/eprint/73363/ Characterization and toxicity of citral incorporated with nanostructured lipid carrier Mohammed Alitheen, Noorjahan Banu How, Chee Wun Mohamad, Nurul Elyani Zamberi, Nur Rizi Yeap, Swee Keong Nordin, Noraini Abdullah, Rasedee Masarudin, Mas Jaffri Abu, Nadiah Heshu, Sulaiman Rahman The nanoparticle as a cancer drug delivery vehicle is rapidly under investigation due to its promising applicability as a novel drug delivery system for anticancer agents. This study describes the development, characterization and toxicity studies of a nanostructured lipid carrier (NLC) system for citral. Citral was loaded into the NLC using high pressure homogenization methods. The characterizations of NLCcitral were then determined through various methods. Based on Transmission Electron Microscope (TEM) analysis, NLC-Citral showed a spherical shape with an average diameter size of 54.12 ± 0.30 nm and a polydipersity index of 0.224 ± 0.005. The zeta potential of NLC-Citral was −12.73 ± 0.34 mV with an entrapment efficiency of 98.9 ± 0.124%, and drug loading of 9.84 ± 0.041%. Safety profile of the formulation was examined via in vitro and in vivo routes to study its effects toward normal cells. NLC-Citral exhibited no toxic effects towards the proliferation of mice splenocytes. Moreover, no mortality and toxic signs were observed in the treated groups after 28 days of treatment. There were also no significant alterations in serum biochemical analysis for all treatments. Increase in immunomodulatory effects of treated NLC-Citral and Citral groups was verified from the increase in CD4/CD3 and CD8/CD3 T cell population in both NLC-citral and citral treated splenocytes. This study suggests that NLC is a promising drug delivery system for citral as it has the potential in sustaining drug release without inducing any toxicity. PeerJ 2018 Article PeerReviewed text en http://psasir.upm.edu.my/id/eprint/73363/1/CITRAL.pdf Mohammed Alitheen, Noorjahan Banu and How, Chee Wun and Mohamad, Nurul Elyani and Zamberi, Nur Rizi and Yeap, Swee Keong and Nordin, Noraini and Abdullah, Rasedee and Masarudin, Mas Jaffri and Abu, Nadiah and Heshu, Sulaiman Rahman (2018) Characterization and toxicity of citral incorporated with nanostructured lipid carrier. PeerJ. pp. 1-19. ISSN 2167-8359 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5756616/pdf/peerj-06-3916.pdf 10.7717/peerj.3916
spellingShingle Mohammed Alitheen, Noorjahan Banu
How, Chee Wun
Mohamad, Nurul Elyani
Zamberi, Nur Rizi
Yeap, Swee Keong
Nordin, Noraini
Abdullah, Rasedee
Masarudin, Mas Jaffri
Abu, Nadiah
Heshu, Sulaiman Rahman
Characterization and toxicity of citral incorporated with nanostructured lipid carrier
title Characterization and toxicity of citral incorporated with nanostructured lipid carrier
title_full Characterization and toxicity of citral incorporated with nanostructured lipid carrier
title_fullStr Characterization and toxicity of citral incorporated with nanostructured lipid carrier
title_full_unstemmed Characterization and toxicity of citral incorporated with nanostructured lipid carrier
title_short Characterization and toxicity of citral incorporated with nanostructured lipid carrier
title_sort characterization and toxicity of citral incorporated with nanostructured lipid carrier
url http://psasir.upm.edu.my/id/eprint/73363/1/CITRAL.pdf
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