Glycosaminoglycan destabilization of DNA–chitosan polyplexes for gene delivery depends on chitosan chain length and GAG properties

2005 ◽  
Vol 1721 (1-3) ◽  
pp. 44-54 ◽  
Author(s):  
Signe Danielsen ◽  
Sabina Strand ◽  
Catharina de Lange Davies ◽  
Bjørn T. Stokke
Polymers ◽  
2019 ◽  
Vol 11 (8) ◽  
pp. 1236 ◽  
Author(s):  
Delas ◽  
Mock-Joubert ◽  
Faivre ◽  
Hofmaier ◽  
Sandre ◽  
...  

In the context of gene delivery, chitosan has been widely used as a safe and effective polycation to complex DNA, RNA and more recently, siRNA. However, much less attention has been paid to chitosan oligosaccharides (COS) despite their biological properties. This study proposed to carry out a physicochemical study of COS varying in degree of polymerization (DP) from 5 to 50, both from the point of view of the solution properties and the complexing behavior with siRNA. The main parameters studied as a function of DP were the apparent pKa, the solubility versus pH, the binding affinity with siRNA and the colloidal properties of complexes. Some parameters, like the pKa or the binding enthalpy with siRNA, showed a marked transition from DP 5 to DP 13, suggesting that electrostatic properties of COS vary considerably in this range of DP. The colloidal properties of siRNA/COS complexes were affected in a different way by the COS chain length. In particular, COS of relatively high DP (≥50) were required to form small complex particles with good stability.


2010 ◽  
Vol 142 (2) ◽  
pp. 229-237 ◽  
Author(s):  
Rupei Tang ◽  
R. Noelle Palumbo ◽  
Lakshmi Nagarajan ◽  
Emily Krogstad ◽  
Chun Wang

2011 ◽  
Vol 12 (3) ◽  
pp. 721-729 ◽  
Author(s):  
Jostein Malmo ◽  
Kjell M. Vårum ◽  
Sabina P. Strand

Biomolecules ◽  
2022 ◽  
Vol 12 (1) ◽  
pp. 102
Author(s):  
Xiaohong Liu ◽  
Hui Yin ◽  
Xia Song ◽  
Zhongxing Zhang ◽  
Jun Li

Lignin is a natural renewable biomass resource with great potential for applications, while its development into high value-added molecules or materials is rare. The development of biomass lignin as potential nonviral gene delivery carriers was initiated by our group through the “grafting-from” approach. Firstly, the lignin was modified into macroinitiator using 2-bromoisobutyryl bromide. Then cationic polymer chains of poly[2-(dimethylamino)ethyl methacrylate] (PDMAEMA) were grown from the lignin backbone using atom transfer radical polymerization (ATRP) to yield lignin-PDMAEMA graft copolymers (LPs) with branched structure. To gain a deep understanding of the relationship between the nonviral gene transfection efficiency of such copolymers and their structural and compositional factors, herein eight lignin-based macroinitiators with different modification degrees (MDs, from 3.0 to 100%) were synthesized. Initiated by them, a series of 20 LPs were synthesized with varied structural factors such as grafting degree (GD, which is equal to MD, determining the cationic chain number per lignin macromolecule), cationic chain length (represented by number of repeating DMAEMA units per grafted arm or degree of polymerization, DP) as well as the content of N element (N%) which is due to the grafted PDMAEMA chains and proportional to molecular weight of the LPs. The in vitro gene transfection capability of these graft copolymers was evaluated by luciferase assay in HeLa, COS7 and MDA-MB-231cell lines. Generally, the copolymers LP-12 (N% = 7.28, MD = 36.7%, DP = 13.6) and LP-14 (N% = 6.05, MD = 44.4%, DP = 5.5) showed good gene transfection capabilities in the cell lines tested. Overall, the performance of LP-12 was the best among all the LPs in the three cell lines at the N/P ratios from 10 to 30, which was usually several times higher than PEI standard. However, in MDA-MB-231 at N/P ratio of 30, LP-14 showed the best gene transfection performance among all the LPs. Its gene transfection efficiency was ca. 11 times higher than PEI standard at this N/P ratio. This work demonstrated that, although the content of N element (N%) which is due to the grafted PDMAEMA chains primarily determines the gene transfection efficiency of the LPs, it is not the only factor in explaining the performance of such copolymers with the branched structure. Structural factors of these copolymers such as grafting degree and cationic chain length could have a profound effect on the copolymer performance on gene transfection efficiency. Through carefully adjusting these factors, the gene transfection efficiency of the LPs could be modulated and optimized for different cell lines, which could make this new type of biomass-based biomaterial an attractive choice for various gene delivery applications.


2010 ◽  
Vol 79 (3) ◽  
pp. 590-596 ◽  
Author(s):  
Xiaoying Wang ◽  
Sabina P. Strand ◽  
Yumin Du ◽  
Kjell M. Vårum
Keyword(s):  

1999 ◽  
Vol 10 (5) ◽  
pp. 773-780 ◽  
Author(s):  
Takuro Niidome ◽  
Keiko Takaji ◽  
Mamiko Urakawa ◽  
Naoya Ohmori ◽  
Akihiro Wada ◽  
...  

2001 ◽  
Vol 120 (5) ◽  
pp. A710-A710
Author(s):  
S LAL ◽  
J MCLAUGHLIN ◽  
O NIAZ ◽  
G DOCKRAY ◽  
A VARRO ◽  
...  

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