Development of a lyophilized plasmid/LPEI polyplex formulation with long-term stability--A step closer from promising technology to application.

Abstract

Cationic polymer/DNA complexes are limited by their instability in aqueous suspensions and usually have to be freshly prepared prior to administration. Thus, the development of isotonic lyophilized polyplex formulations with long-term stability is a desirable goal. Polyplexes based on 22kDa linear polyethylenimine were prepared using a micro-mixer method. Freeze-thawing and lyophilization were performed on a pilot scale freeze-drier. Several excipients (trehalose, sucrose, lactosucrose, dextran, hydroxypropylbetadex or povidone and combinations thereof) at varying concentrations were evaluated for their stabilizing potential against freezing and dehydration induced stresses. For stability testing the lyophilized samples were stored for 6 weeks at 2-8°C, 20°C and 40°C, respectively. Polyplex samples were characterized for particle size, zeta potential, their in vitro transfection efficiency and metabolic activity in Neuro2A cells. In addition, liquid samples were investigated for turbidity and number of sub-visible particles and solid samples were analyzed for residual moisture content, glass transition temperature and sample morphology. L-histidine buffer pH 6.0 was selected as effective buffer. In isotonic formulations with 14% lactosucrose, 10% hydroxypropylbetadex/6.5% sucrose or 10% povidone/6.3% sucrose, particle size was <170nm for all formulations and did not change after storage for 6weeks at 40°C. Polyplexes formulated with lactosucrose or hydroxypropylbetadex/sucrose showed high transfection efficiencies and cellular metabolic activities. Absence of large aggregates was indicated by turbidity and subvisible particle number measurements. The current standard limits for particulate contamination for small volume parenterals were met for all formulations. All samples were amorphous with low residual moisture levels (<1.3%) and high glass transition temperatures (>90°C).

• Authors: Julia Christina Kasper, David Schaffert, Manfred Ogris, Ernst Wagner, Wolfgang Friess
• Journal: Journal of controlled release : official journal of the Controlled Release Society (J Control Release) Vol. 151 Issue 3 Pg. 246-55 (May 10 2011) ISSN: 1873-4995 [Electronic] Netherlands
• PMID: 21223985 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
• Copyright: Copyright © 2011. Published by Elsevier B.V.

Chemical References

• Drug Carriers
• Excipients
• Polyethyleneimine
• Luciferases

Topics

• Animals
• Calorimetry, Differential Scanning
• Cell Culture Techniques
• Cell Line, Tumor
• Chemistry, Pharmaceutical
• Drug Carriers (chemistry)
• Drug Stability
• Excipients (chemistry)
• Freeze Drying
• Luciferases (genetics)
• Mice
• Particle Size
• Pilot Projects
• Plasmids (administration & dosage, genetics)
• Polyethyleneimine (chemistry)
• Surface Properties
• Technology, Pharmaceutical (methods)
• Time Factors
• Transfection
• X-Ray Diffraction