A novel class of cationic gemini surfactants showing efficient in vitro gene transfection properties

2000 ◽  
pp. 1253-1254 ◽  
Author(s):  
Patrick Camilleri ◽  
Andreas Kremer ◽  
Andrew J. Edwards ◽  
Kevin H. Jennings ◽  
Owen Jenkins ◽  
...  
2012 ◽  
Vol 15 (4) ◽  
pp. 548 ◽  
Author(s):  
Waleed Mohammed-Saeid ◽  
Deborah Michel ◽  
Anas El-Aneed ◽  
Ronald E Verrall ◽  
Nicholas H Low ◽  
...  

Purpose. Cationic gemini surfactants have been studied as non-viral vectors for gene therapy. Clinical applications of cationic lipid/DNA lipoplexes are restricted by their instability in aqueous formulations. In this work, we investigated the influence of lyophilization on the essential physiochemical properties and in vitro transfection of gemini surfactant-lipoplexes. Additionally, we evaluated the feasibility of lyophilization as a technique for preparing lipoplexes with long term stability. Methods. A gemini surfactant [12-7NH-12] and plasmid DNA encoding for interferon-γ were used to prepare gemini surfactant/pDNA [P/G] lipoplexes. Helper lipid DOPE [L] was incorporated in all formulation producing a [P/G/L] system. Sucrose and trehalose were utilized as stabilizing agents. To evaluate the ability of lyophilization to improve the stability of gemini surfactant-based lipoplexes, four lyophilized formulations were stored at 25˚C for three months. The formulations were analyzed at different time-points for physiochemical properties and in vitro transfection. Results. The results showed that both sucrose and trehalose provided anticipated stabilizing effect. The transfection efficiency of the lipoplexes increased 2-3 fold compared to fresh formulations upon lyophilization. This effect can be attributed to the improvement of DNA compaction and changes in the lipoplex morphology due to the lyophilization/rehydration cycles. The physiochemical properties of the lyophilized formulations were maintained throughout the stability study. All lyophilized formulations showed a significant loss of gene transfection activity after three months of storage. Nevertheless, no significant losses of transfection efficiency were observed for three formulations after two months storage at 25 ˚C. Conclusion. Lyophilization significantly improved the physical stability of gemini surfactant-based lipoplexes compared to liquid formulations. As well, lyophilization improved the transfection efficiency of the lipoplexes. The loss of transfection activity upon storage is most probably due to the conformational changes in the supramolecular structure of the lipoplexes as a function of time and temperature rather than to DNA degradation. This article is open to POST-PUBLICATION REVIEW. Registered readers (see “For Readers”) may comment by clicking on ABSTRACT on the issue’s contents page.


Langmuir ◽  
2002 ◽  
Vol 18 (6) ◽  
pp. 2426-2429 ◽  
Author(s):  
Kevin H. Jennings ◽  
Ian C. B. Marshall ◽  
Michael J. Wilkinson ◽  
Andreas Kremer ◽  
Anthony J. Kirby ◽  
...  

2018 ◽  
Vol 9 (1) ◽  
pp. 4-11 ◽  
Author(s):  
Aparna Bansal ◽  
Himanshu

Introduction: Gene therapy has emerged out as a promising therapeutic pave for the treatment of genetic and acquired diseases. Gene transfection into target cells using naked DNA is a simple and safe approach which has been further improved by combining vectors or gene carriers. Both viral and non-viral approaches have achieved a milestone to establish this technique, but non-viral approaches have attained a significant attention because of their favourable properties like less immunotoxicity and biosafety, easy to produce with versatile surface modifications, etc. Literature is rich in evidences which revealed that undoubtedly, non–viral vectors have acquired a unique place in gene therapy but still there are number of challenges which are to be overcome to increase their effectiveness and prove them ideal gene vectors. Conclusion: To date, tissue specific expression, long lasting gene expression system, enhanced gene transfection efficiency has been achieved with improvement in delivery methods using non-viral vectors. This review mainly summarizes the various physical and chemical methods for gene transfer in vitro and in vivo.


2004 ◽  
Vol 96 (2) ◽  
pp. 309-323 ◽  
Author(s):  
Tony Azzam ◽  
Hagit Eliyahu ◽  
Arik Makovitzki ◽  
Michal Linial ◽  
Abraham J Domb

2010 ◽  
Vol 55 (11) ◽  
pp. 4775-4779 ◽  
Author(s):  
Iqrar Ahmad Khan ◽  
Ahmad Jahan Khanam ◽  
Ziya Ahmad Khan ◽  
Kabir-ud-Din

Langmuir ◽  
2012 ◽  
Vol 28 (33) ◽  
pp. 11979-11987 ◽  
Author(s):  
Qi Zhang ◽  
Zhinong Gao ◽  
Feng Xu ◽  
Shuxin Tai ◽  
Xueguo Liu ◽  
...  

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