Fluorinated Acid-Labile Branched Hydroxyl-Rich Nanosystems for Flexible and Robust Delivery of Plasmids.

Nucleic acid-based therapy specially needs a safe and robust delivery vector. Herein, a novel fluorinated acid-labile branched hydroxyl-rich polycation (ARP-F) is proposed for the flexible and effective delivery nanovector of different plasmids including reporter genes and the Cas9 plasmid. Acid-responsive polycation (ARP) with plentiful ortho ester linkages and hydroxyl groups is first synthesized via a facile one-pot ring-opening polymerization, followed by decoration of fluorinated alkyl chains onto ARP to achieve ARP-F. ARP-F possesses good pH-responsive degradability, biocompatibility, and its preliminary transfection ability evaluated by reporter plasmids pRL-CMV (encoding Renilla luciferase) and pEGFP-N1 (encoding enhanced green fluorescent protein) is also excellent. CRISPR-Cas9 (clustered regularly interspaced short palindromic repeat/CRISPR-associated nuclease 9) technology is a potent genome-editing tool. The subsequent delivery of pCas9-surv (one typical all-in-one Cas9 plasmid) mediated by ARP-F exhibits impressive in vitro and in vivo tumor inhibition performances. In addition, the combination of ARP-F/pCas9-surv with temozolomide could further enhance tumor inhibition activities by increasing the sensitivity of cancer cells to anticancer drugs. Such high-performance polycation would provide a very promising means to produce efficient delivery nanovectors of versatile plasmids.

[1]  Qiang Zhang,et al.  Surface-engineered dendrimers in gene delivery. , 2015, Chemical reviews.

[2]  George M. Church,et al.  Heritable genome editing in C. elegans via a CRISPR-Cas9 system , 2013, Nature Methods.

[3]  Daniel G. Anderson,et al.  Therapeutic genome editing by combined viral and non-viral delivery of CRISPR system components in vivo , 2016, Nature Biotechnology.

[4]  Wenjun Yang,et al.  Disulfide cross-linked low generation dendrimers with high gene transfection efficacy, low cytotoxicity, and low cost. , 2012, Journal of the American Chemical Society.

[5]  Weihang Ji,et al.  Synthesis and characterization of new poly(ortho ester amidine) copolymers for nonviral gene delivery. , 2011, Polymer.

[6]  W. Sessa,et al.  Cell-permeable peptides improve cellular uptake and therapeutic gene delivery of replication-deficient viruses in cells and in vivo , 2003, Nature Medicine.

[7]  Yu Wang,et al.  Self-Assembled Fluorodendrimers Combine the Features of Lipid and Polymeric Vectors in Gene Delivery. , 2015, Angewandte Chemie.

[8]  Mingming Wang,et al.  A fluorinated dendrimer achieves excellent gene transfection efficacy at extremely low nitrogen to phosphorus ratios , 2014, Nature Communications.

[9]  E. Bender Gene therapy: Industrial strength , 2016, Nature.

[10]  T. Zhao,et al.  Bioapplications of hyperbranched polymers. , 2015, Chemical Society reviews.

[11]  Jennifer A. Doudna,et al.  Biology and Applications of CRISPR Systems: Harnessing Nature’s Toolbox for Genome Engineering , 2016, Cell.

[12]  Xiaodong Wang,et al.  DFF, a Heterodimeric Protein That Functions Downstream of Caspase-3 to Trigger DNA Fragmentation during Apoptosis , 1997, Cell.

[13]  D. Thompson,et al.  Decitabine nanoconjugate sensitizes human glioblastoma cells to temozolomide. , 2015, Molecular pharmaceutics.

[14]  Yong Wang,et al.  A Reduction and pH Dual‐Sensitive Polymeric Vector for Long‐Circulating and Tumor‐Targeted siRNA Delivery , 2014, Advanced materials.

[15]  Yulin Li,et al.  PGMA‐Based Star‐Like Polycations with Plentiful Hydroxyl Groups Act as Highly Efficient miRNA Delivery Nanovectors for Effective Applications in Heart Diseases , 2016, Advanced materials.

[16]  Fujian Xu,et al.  Versatile types of hydroxyl-rich polycationic systems via O-heterocyclic ring-opening reactions: From strategic design to nucleic acid delivery applications , 2017 .

[17]  Bingran Yu,et al.  Reduction-responsive multifunctional hyperbranched polyaminoglycosides with excellent antibacterial activity, biocompatibility and gene transfection capability. , 2016, Biomaterials.

[18]  Istv�n T. Horv�th,et al.  Facile Catalyst Separation Without Water: Fluorous Biphase Hydroformylation of Olefins , 1994, Science.

[19]  D. Ding,et al.  Amphiphilic semiconducting polymer as multifunctional nanocarrier for fluorescence/photoacoustic imaging guided chemo-photothermal therapy. , 2017, Biomaterials.

[20]  I. Horváth,et al.  Facile Catalyst Separation Without Water: Fluorous Biphase Hydroformylation of Olefins , 1994, Science.

[21]  Zhangyong Hong,et al.  Targeted Delivery of CRISPR/Cas9‐Mediated Cancer Gene Therapy via Liposome‐Templated Hydrogel Nanoparticles , 2017, Advanced functional materials.

[22]  Jin Chang,et al.  PLGA/polymeric liposome for targeted drug and gene co-delivery. , 2010, Biomaterials.

[23]  B. Wang,et al.  Linear polycations by ring-opening polymerization as non-viral gene delivery vectors. , 2013, Biomaterials.

[24]  Robert Langer,et al.  A combinatorial polymer library approach yields insight into nonviral gene delivery. , 2008, Accounts of chemical research.

[25]  Israel Steinfeld,et al.  Chemically modified guide RNAs enhance CRISPR-Cas genome editing in human primary cells , 2015, Nature Biotechnology.

[26]  Sung Wan Kim,et al.  Current status of polymeric gene delivery systems. , 2006, Advanced drug delivery reviews.

[27]  E. Neil,et al.  Towards the nonstick egg: designing fluorous proteins. , 2000, Chemistry & biology.

[28]  Kailash C Gupta,et al.  Novel polyethylenimine-derived nanoparticles for in vivo gene delivery , 2013, Expert opinion on drug delivery.

[29]  M. R. Imam,et al.  Self-organizable vesicular columns assembled from polymers dendronized with semifluorinated Janus dendrimers act as reverse thermal actuators. , 2012, Journal of the American Chemical Society.

[30]  Gang Bao,et al.  CRISPR/Cas9-Based Genome Editing for Disease Modeling and Therapy: Challenges and Opportunities for Nonviral Delivery. , 2017, Chemical reviews.

[31]  Hongwei Duan,et al.  Dendronized Semiconducting Polymer as Photothermal Nanocarrier for Remote Activation of Gene Expression. , 2017, Angewandte Chemie.

[32]  Yen-Ling Lin,et al.  Development of Degradable, pH‐Sensitive Star Vectors for Enhancing the Cytoplasmic Delivery of Nucleic Acids , 2013 .

[33]  D. Altieri,et al.  A novel anti-apoptosis gene, survivin, expressed in cancer and lymphoma , 1997, Nature Medicine.

[34]  J. Doudna,et al.  The new frontier of genome engineering with CRISPR-Cas9 , 2014, Science.

[35]  Fujian Xu,et al.  A Facile Strategy to Prepare Hyperbranched Hydroxyl-Rich Polycations for Effective Gene Therapy. , 2016, ACS applied materials & interfaces.

[36]  Xingyu Jiang,et al.  Thermo-triggered Release of CRISPR-Cas9 System by Lipid-Encapsulated Gold Nanoparticles for Tumor Therapy. , 2018, Angewandte Chemie.

[37]  Xiurui Zhu,et al.  A non-viral CRISPR/Cas9 delivery system for therapeutically targeting HBV DNA and pcsk9 in vivo , 2017, Cell Research.

[38]  Bingran Yu,et al.  Well‐Defined Protein‐Based Supramolecular Nanoparticles with Excellent MRI Abilities for Multifunctional Delivery Systems , 2016 .

[39]  Michael R Hamblin,et al.  Smart micro/nanoparticles in stimulus-responsive drug/gene delivery systems. , 2016, Chemical Society reviews.

[40]  Chao Wang,et al.  Self-assembled DNA nanoclews for the efficient delivery of CRISPR-Cas9 for genome editing. , 2015, Angewandte Chemie.

[41]  D. Altieri,et al.  Anti-apoptosis gene, survivin, and prognosis of neuroblastoma , 1998, The Lancet.

[42]  T. Xia,et al.  Effective Codelivery of lncRNA and pDNA by Pullulan‐Based Nanovectors for Promising Therapy of Hepatocellular Carcinoma , 2016 .

[43]  Jinhui Wang,et al.  Reversibly cross-linked polyplexes enable cancer-targeted gene delivery via self-promoted DNA release and self-diminished toxicity. , 2015, Biomacromolecules.

[44]  Jianghong Rao,et al.  Real-time imaging of oxidative and nitrosative stress in the liver of live animals for drug-toxicity testing , 2014, Nature Biotechnology.

[45]  Anirvan Ghosh,et al.  Efficient genome editing in the mouse brain by local delivery of engineered Cas9 ribonucleoprotein complexes , 2017, Nature Biotechnology.

[46]  J. Keith Joung,et al.  Efficient Delivery of Genome-Editing Proteins In Vitro and In Vivo , 2014, Nature Biotechnology.

[47]  Irene Georgakoudi,et al.  Efficient delivery of genome-editing proteins using bioreducible lipid nanoparticles , 2016, Proceedings of the National Academy of Sciences.

[48]  David R. Liu,et al.  Efficient Delivery of Genome-Editing Proteins In Vitro and In Vivo , 2015 .

[49]  Jin Wang,et al.  Anionic Lipid, pH-Sensitive Liposome-Gold Nanoparticle Hybrids for Gene Delivery - Quantitative Research of the Mechanism. , 2015, Small.

[50]  Xian‐Zheng Zhang,et al.  Hyperbranched-hyperbranched polymeric nanoassembly to mediate controllable co-delivery of siRNA and drug for synergistic tumor therapy. , 2015, Journal of controlled release : official journal of the Controlled Release Society.

[51]  Peng Wang,et al.  Genome Editing for Cancer Therapy: Delivery of Cas9 Protein/sgRNA Plasmid via a Gold Nanocluster/Lipid Core–Shell Nanocarrier , 2017, Advanced science.