Screening, synthesis, and applications of "lipidoids", a novel class of molecules developed for the delivery of RNAi therapeutics

RNAi therapeutics represent a fundamentally new way of treating disease, permitting the selective abrogation of protein production at the genetic level. As nucleic acids do not readily enter cells, carriers are utilized to enhance uptake. While viruses are extremely efficient, concerns about their safety has led to the desire to engineer novel synthetic vectors. We have developed chemical methods using a combinatorial approach that has resulted in the synthesis of a large library of structurally-diverse compounds (1,200 in total), termed "lipidoids", without the need to use solvents, catalysts, or protection/deprotection steps. The members of this library were screened for the ability to transfect mammalian cells in vitro. The top-performing compounds were formulated for in vivo administration and resulted in durable, potent, and specific knockdown of reporter and therapeutically-relevant genes in four distinct species, including non-human primates. Local and systemic administration effectively silenced target genes in three different tissue types. In addition to reducing protein expression by directing cleavage of target mRNA through delivery of siRNA, lipidoids were shown to mediate upregulation of proteins by derpressing miRNA targets through delivery of anti-miR. Finally, inspection of the chemical functional groups common to the top-performing lipidoids from the first library informed the synthesis of a second-generation library. The dramatic increase in percentage of effective materials from this second library (52% as opposed to 3%) confirmed that a convergence of structure has been identified.

Department dc:contributor.department

Massachusetts Institute of Technology. Dept. of Chemistry.

Grantor dc:publisher

Massachusetts Institute of Technology

Year dc:date.issued

2008

Author dc:creator

• Goldberg, Michael Solomon

Advisor dc:contributor.advisor

• Robert Langer.

• Chemistry.

Statement dc:rights

• M.I.T. theses are protected by copyright. They may be viewed from this source for any purpose, but reproduction or distribution in any format is prohibited without written permission. See provided URL for inquiries about permission.

Licence dc:rights.uri

• http://dspace.mit.edu/handle/1721.1/7582

Language dc:language.iso

eng

Handle dc:identifier.uri

http://hdl.handle.net/1721.1/43765

OAI identifier oai:identifier

oai:dspace.mit.edu:1721.1/43765