» Articles » PMID: 11451027

Water-soluble and Low Molecular Weight Chitosan-based Plasmid DNA Delivery

Overview
Journal Pharm Res
Specialties Pharmacology
Pharmacy
Date 2001 Jul 14
PMID 11451027
Citations 28
Authors
Affiliations
Soon will be listed here.
Abstract

Purpose: Chitosan, a natural cationic polysaccharide, is a candidate non-viral vector for gene delivery because of its high positive charges and low cytotoxicity. In this study, low molecular weight chitosan (LMWC, molecular weight of 22 kDa) was characterized and evaluated as a gene carrier.

Methods: Plasmid/LMWC complex was analyzed in 1% agarose gel electrophoresis. To confirm that the LMWC protected plasmids from nuclease. DNase I protection assays were performed. pSV-beta-galactosidase plasmid/LMWC complex was transfected into 293T cells and transfection efficiency was evaluated by beta-galactosidase assay. Cytotoxicity of LMWC was determined by MTT assay.

Results: Unlike high molecular weight chitosan (HMWC), LMWC is highly water soluble, and can form complex with plasmids in physiological buffer. The plasmid DNA was completely retarded at a weight ratio of 1:2 (plasmid:LMWC) in 1% agarose gel. DNase I protection assay showed that plasmids were protected from DNase-I over 60 min. The most efficient transfection was obtained at a weight ratio of 1:3 (plasmid:LMWC). The transfection efficiency of LMWC was significantly higher than naked DNA and higher than poly-L-lysine (PLL). MTT assay showed that LMWC was less cytotoxic than PLL.

Conclusions: LMWC is non-toxic and has higher transfection efficiency than PLL. Therefore, LMWC will be useful in the development of safe gene carriers.

Citing Articles

Hyper-Branched Cationic Cyclodextrin Polymers for Improving Plasmid Transfection in 2D and 3D Spheroid Cells.

Khazaei Monfared Y, Mahmoudian M, Cecone C, Caldera F, Haiaty S, Heidari H Pharmaceutics. 2022; 14(12).

PMID: 36559184 PMC: 9785855. DOI: 10.3390/pharmaceutics14122690.


Interleukin-12 Plasmid DNA Delivery by -[(2-Hydroxy-3-trimethylammonium)propyl]chitosan-Based Nanoparticles.

Dehshahri A, Khalvati B, Taheri Z, Safari F, Mohammadinejad R, Heydari A Polymers (Basel). 2022; 14(11).

PMID: 35683849 PMC: 9182864. DOI: 10.3390/polym14112176.


Polysaccharide-Drug Conjugates: A Tool for Enhanced Cancer Therapy.

Yadav N, Francis A, Priya V, Patil S, Mustaq S, Khan S Polymers (Basel). 2022; 14(5).

PMID: 35267773 PMC: 8912870. DOI: 10.3390/polym14050950.


Synthesis and Characterization of Chitosan-Based Nanodelivery Systems to Enhance the Anticancer Effect of Sorafenib Drug in Hepatocellular Carcinoma and Colorectal Adenocarcinoma Cells.

Ruman U, Buskaran K, Pastorin G, Masarudin M, Fakurazi S, Hussein M Nanomaterials (Basel). 2021; 11(2).

PMID: 33669332 PMC: 7920308. DOI: 10.3390/nano11020497.


Tiny miRNAs Play a Big Role in the Treatment of Breast Cancer Metastasis.

Teo A, Xiang X, Le M, Wong A, Zeng Q, Wang L Cancers (Basel). 2021; 13(2).

PMID: 33477629 PMC: 7831489. DOI: 10.3390/cancers13020337.


References
1.
Wagner E, Plank C, Zatloukal K, Cotten M, Birnstiel M . Influenza virus hemagglutinin HA-2 N-terminal fusogenic peptides augment gene transfer by transferrin-polylysine-DNA complexes: toward a synthetic virus-like gene-transfer vehicle. Proc Natl Acad Sci U S A. 1992; 89(17):7934-8. PMC: 49829. DOI: 10.1073/pnas.89.17.7934. View

2.
Cotten M, Wagner E . Non-viral approaches to gene therapy. Curr Opin Biotechnol. 1993; 4(6):705-10. DOI: 10.1016/0958-1669(93)90053-y. View

3.
Wu C, Wilson J, Wu G . Targeting genes: delivery and persistent expression of a foreign gene driven by mammalian regulatory elements in vivo. J Biol Chem. 1989; 264(29):16985-7. View

4.
Midoux P, Mendes C, Legrand A, Raimond J, Mayer R, Monsigny M . Specific gene transfer mediated by lactosylated poly-L-lysine into hepatoma cells. Nucleic Acids Res. 1993; 21(4):871-8. PMC: 309219. DOI: 10.1093/nar/21.4.871. View

5.
Richardson S, Kolbe H, Duncan R . Potential of low molecular mass chitosan as a DNA delivery system: biocompatibility, body distribution and ability to complex and protect DNA. Int J Pharm. 1999; 178(2):231-43. DOI: 10.1016/s0378-5173(98)00378-0. View