A novel tyrosine-modified low molecular weight polyethylenimine (P10Y) for efficient siRNA delivery in vitro and in vivo

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• 作者：Alexander Ewe^a ; Susanne Przybylski^b ; Jana Burkhardt^b ; Andreas Janke^c ; Dietmar Appelhans^c ; Achim Aigner^a ; ^{achim.aigner@medizin.uni-leipzig.de" class="auth_mail" title="E-mail the corresponding author}
• 关键词：AFM ; atomic force microscopy ; dH2O ; distilled water ; eGFP ; enhanced green fluorescent protein ; FCS ; fetal calf serum ; HN ; Hepes-NaCl ; i.p. ; intraperiotoneal ; i.v. ; intranvenous ; LDH ; lactate dehydrogenase ; Luc ; luciferase ; PEI ; polyethylenimine ; RLU ; relative light units ; RNAi ; RNA interference ; siRNA ; small interfering RNA ; Y ; tyrosine
• 刊名：Journal of Controlled Release
• 出版年：2016
• 出版时间：28 May 2016
• 年：2016
• 卷：230
• 期：Complete
• 页码：13-25
• 全文大小：1263 K

文摘

The delivery of nucleic acids, particularly of small RNA molecules like siRNAs for the induction of RNA interference (RNAi), still represents a major hurdle with regard to their application in vivo. Possible therapeutic applications thus rely on the development of efficient non-viral gene delivery vectors. While low molecular weight polyethylenimines (PEIs) have been successfully explored, the introduction of chemical modifications offers an avenue towards the development of more efficient vectors.

In this paper, we describe the synthesis of a novel tyrosine-modified low-molecular weight polyethylenimine (P10Y) for efficient siRNA complexation and delivery. The comparison with the respective parent PEI reveals that knockdown efficacies are considerably enhanced by the tyrosine modification, as determined in different reporter cell lines, without appreciable cytotoxicity. We furthermore identify optimal conditions for complex preparation as well as for storing or lyophilization of the complexes without loss of biological activity. Beyond reporter cell lines, P10Y/siRNA complexes mediate the efficient knockdown of endogenous target genes and, upon knockdown of the anti-apoptotic oncogene survivin, tumor cell inhibitory effects in different carcinoma cell lines. Pushing the system further towards its therapeutic in vivo application, we demonstrate in mice the delivery of intact siRNAs and distinct biodistribution profiles upon systemic (intravenous or intraperitoneal) injection. No adverse effects (hepatotoxicity, immunostimulation/alterations in immunophenotype, weight loss) are observed. More importantly, profound tumor-inhibitory effects in a melanoma xenograft mouse model are observed upon systemic application of P10Y/siRNA complexes for survivin knockdown, indicating the therapeutic efficacy of P10Y/siRNA complexes.

Taken together, we (i) establish tyrosine-modified PEI (P10Y) as efficient platform for siRNA delivery in vitro and in vivo, (ii) identify optimal preparation and storage conditions as well as (iii) physicochemical and biological properties of P10Y complexes, and (iv) demonstrate their applicability as siRNA therapeutic in vivo (v) in the absence of adverse effects.