Construction of a Novel Magnetic Targeting Anti-Tumor Drug Delivery System: Cytosine Arabinoside-Loaded Bacterial Magnetosome

To ease the side effects triggered by cytosine arabinoside (Ara-C) for acute leukemia treatment, a novel magnetic targeting anti-tumor drug delivery system was constructed through bacterial magnetosomes (BMs) from Magnetospirillum magneticum AMB-1 combined with Ara-C by crosslinking of genipin (GP)....

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Main Authors: Wenguo Wu, Aizheng Chen, Shenjian Wu, Maobin Xie, Shibin Wang, Qiongjia Deng, Yuangang Liu
Format: Article
Language:English
Published: MDPI AG 2013-09-01
Series:Materials
Subjects:
Online Access:http://www.mdpi.com/1996-1944/6/9/3755
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spelling doaj-112b7d216cf9486ba041ed17759b70542020-11-24T21:05:29ZengMDPI AGMaterials1996-19442013-09-01693755376310.3390/ma6093755Construction of a Novel Magnetic Targeting Anti-Tumor Drug Delivery System: Cytosine Arabinoside-Loaded Bacterial MagnetosomeWenguo WuAizheng ChenShenjian WuMaobin XieShibin WangQiongjia DengYuangang LiuTo ease the side effects triggered by cytosine arabinoside (Ara-C) for acute leukemia treatment, a novel magnetic targeting anti-tumor drug delivery system was constructed through bacterial magnetosomes (BMs) from Magnetospirillum magneticum AMB-1 combined with Ara-C by crosslinking of genipin (GP). The results showed that Ara-C could be bonded onto the membrane surface of BMs effectively through chemical crosslinking induced by dual hand reagents GP. The average diameters of BMs and Ara-C-coupled BMs (ABMs) were 42.0 ± 8.6 and 72.7 ± 6.0 nm respectively, and the zeta potentials (−38.1 ± 9.1) revealed that these systems were stable, confirming the stability of the system. The optimal encapsulation efficiency and drug loading were 89.05% ± 2.33% and 47.05% ± 0.64% respectively when crosslinking reaction lasted for 72 h. The system also presented long-term stability and release behaviors without initial burst release (Ara-C could be released 80% within three months). Our results indicate that BMs have great potential in biomedical and clinical fields as a novel anti-tumor drug carrier.http://www.mdpi.com/1996-1944/6/9/3755cytosine arabinosidemagnetosomegenipindrug release
collection DOAJ
language English
format Article
sources DOAJ
author Wenguo Wu
Aizheng Chen
Shenjian Wu
Maobin Xie
Shibin Wang
Qiongjia Deng
Yuangang Liu
spellingShingle Wenguo Wu
Aizheng Chen
Shenjian Wu
Maobin Xie
Shibin Wang
Qiongjia Deng
Yuangang Liu
Construction of a Novel Magnetic Targeting Anti-Tumor Drug Delivery System: Cytosine Arabinoside-Loaded Bacterial Magnetosome
Materials
cytosine arabinoside
magnetosome
genipin
drug release
author_facet Wenguo Wu
Aizheng Chen
Shenjian Wu
Maobin Xie
Shibin Wang
Qiongjia Deng
Yuangang Liu
author_sort Wenguo Wu
title Construction of a Novel Magnetic Targeting Anti-Tumor Drug Delivery System: Cytosine Arabinoside-Loaded Bacterial Magnetosome
title_short Construction of a Novel Magnetic Targeting Anti-Tumor Drug Delivery System: Cytosine Arabinoside-Loaded Bacterial Magnetosome
title_full Construction of a Novel Magnetic Targeting Anti-Tumor Drug Delivery System: Cytosine Arabinoside-Loaded Bacterial Magnetosome
title_fullStr Construction of a Novel Magnetic Targeting Anti-Tumor Drug Delivery System: Cytosine Arabinoside-Loaded Bacterial Magnetosome
title_full_unstemmed Construction of a Novel Magnetic Targeting Anti-Tumor Drug Delivery System: Cytosine Arabinoside-Loaded Bacterial Magnetosome
title_sort construction of a novel magnetic targeting anti-tumor drug delivery system: cytosine arabinoside-loaded bacterial magnetosome
publisher MDPI AG
series Materials
issn 1996-1944
publishDate 2013-09-01
description To ease the side effects triggered by cytosine arabinoside (Ara-C) for acute leukemia treatment, a novel magnetic targeting anti-tumor drug delivery system was constructed through bacterial magnetosomes (BMs) from Magnetospirillum magneticum AMB-1 combined with Ara-C by crosslinking of genipin (GP). The results showed that Ara-C could be bonded onto the membrane surface of BMs effectively through chemical crosslinking induced by dual hand reagents GP. The average diameters of BMs and Ara-C-coupled BMs (ABMs) were 42.0 ± 8.6 and 72.7 ± 6.0 nm respectively, and the zeta potentials (−38.1 ± 9.1) revealed that these systems were stable, confirming the stability of the system. The optimal encapsulation efficiency and drug loading were 89.05% ± 2.33% and 47.05% ± 0.64% respectively when crosslinking reaction lasted for 72 h. The system also presented long-term stability and release behaviors without initial burst release (Ara-C could be released 80% within three months). Our results indicate that BMs have great potential in biomedical and clinical fields as a novel anti-tumor drug carrier.
topic cytosine arabinoside
magnetosome
genipin
drug release
url http://www.mdpi.com/1996-1944/6/9/3755
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