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Preparation and Evaluation of Boronate-Linked Nanoassembly for Efficient Gene Delivery

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Part of the book series: Biomaterial Engineering ((BIOENG))

Abstract

Rapid transfection can not only maximize the bioavailability of vector-carried gene prior to exocytosis, but also well match chemotherapy for optimal combinational therapy in view of the rapid chemotherapeutic action. However, little attention has been paid to the “rapid” goal in vector-aided transfection process. This chapter describes a boronate-linked nanoassembly for the rapid transnuclear gene transport and efficient gene transfection in vitro and in vivo. The nanoassembly was constructed on the basis of the pH-reversible covalent boronic acid-diol coupling between 1,3-diol-rich oligoethylenimine (OEI-EHDO) and phenylboronic acid modified cholesterol (Chol-PBA). The obtained results demonstrate that the boronate-linked nanoassembly can lead to rapid and efficient nuclei-tropic delivery and transfection, which may largely rely on the lysosome-acidity induced assembly destruction followed by the easy liberation of gene payloads. Consequently, the nanoassembly-mediated transfection just at 8 h can afford the outcome comparable to that achieved at 48 h by the golden standard of PEI25K, and the transfection efficiency can remain at a high level during 48 h. In addition, the in vitro and in vivo results reveal the strong tolerance to the serum interference and the good biocompatibility of this hydroxyl-rich bio-decomposable nanoassembly.

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References

  • Ahmadi S, Rabiee N, Bagherzadeh M, Elmi F, Fatahi Y, Farjadian F, Baheiraei N, Nasseri B, Rabiee M, Dastjerd NT, Valibeik A, Karimi M, Hamblin MR (2020) Stimulus-responsive sequential release systems for drug and gene delivery. Nano Today 34:100914

    Article  Google Scholar 

  • Boedtkjer E, Pedersen SF (2020) The acidic tumor microenvironment as a driver of cancer. In M. T. Nelson & K. Walsh (Eds.). Annu Rev Physiol 82:103–126

    Article  Google Scholar 

  • Cai WQ, Luo TL, Mao LQ, Wang M (2020) Spatiotemporal delivery of crispr/cas9 genome editing machinery using stimuli-responsive vehicles. Angew Chem Int Ed 133(16):8679–8689

    Article  Google Scholar 

  • DeBerardinis RJ, Chandel NS (2020) We need to talk about the Warburg effect. Nat Metab 2(2):127–129

    Article  Google Scholar 

  • Deverman BE, Ravina BM, Bankiewicz KS, Paul SM, Sah DWY (2018) Gene therapy for neurological disorders: Progress and prospects. Nat Rev Drug Discov 17(9):641–659

    Article  Google Scholar 

  • Dhaliwal A, Zheng G (2019) Improving accessibility of EPR-insensitive tumor phenotypes using EPR-adaptive strategies: designing a new perspective in nanomedicine delivery. Theranostics 9(26):8091–8108

    Article  Google Scholar 

  • Dobson J (2006) Gene therapy progress and prospects: magnetic nanoparticle-based gene delivery. Gene Ther 13(4):283–287

    Article  MathSciNet  Google Scholar 

  • Fang J, Islam W, Maeda H (2020) Exploiting the dynamics of the EPR effect and strategies to improve the therapeutic effects of nanomedicines by using EPR effect enhancers. Adv Drug Deliv Rev 157:142–160

    Article  Google Scholar 

  • Forgac M (2007) Vacuolar ATPases: rotary proton pumps in physiology and pathophysiology. Nat Rev Mol Cell Biol 8(11):917–929

    Article  Google Scholar 

  • Heiden MGV, Cantley LC, Thompson CB (2009) Understanding the Warburg effect: the metabolic requirements of cell proliferation. Science 324(5930):1029–1033

    Article  Google Scholar 

  • Jia HZ, Zhu JY, Wang XL, Cheng H, Chen G, Zhao YF, Zeng X, Feng J, Zhang XZ, Zhuo RX (2014) A boronate-linked linear-hyperbranched polymeric nanovehicle for pH-dependent tumor-targeted drug delivery. Biomaterials 35(19):5240–5249

    Article  Google Scholar 

  • Khandare J, Calderon M, Dagia NM, Haag R (2012) Multifunctional dendritic polymers in nanomedicine: opportunities and challenges. Chem Soc Rev 41(7):2824–2848

    Article  Google Scholar 

  • Kheirolomoom A, Ferrara KW (2007) Cholesterol transport from liposomal delivery vehicles. Biomaterials 28(29):4311–4320

    Article  Google Scholar 

  • Li YP, Xiao WW, Xiao K, Berti L, Luo JT, Tseng HP, Fung G, Lam KS (2012) Well-defined, reversible boronate crosslinked nanocarriers for targeted drug delivery in response to acidic ph values and cis-diols. Angew Chem Int Ed 51(12):2864–2869

    Article  Google Scholar 

  • Li J, Zheng C, Cansiz S, Wu CC, Xu JH, Cui C, Liu Y, Hou WJ, Wang YY, Zhang LQ, Teng IT, Yang HH, Tan WH (2015) Self-assembly of DNA nanohydrogels with controllable size and stimuli-responsive property for targeted gene regulation therapy. J Am Chem Soc 137(4):1412–1415

    Article  Google Scholar 

  • Li YW, Yue SZ, Cao JY, Zhu CZ, Wang YX, Hai X, Song WL, Bi S (2020) Ph-responsive DNA nanomicelles for chemo-gene synergetic therapy of anaplastic large cell lymphoma. Theranostics 10(18):8250–8263

    Article  Google Scholar 

  • Lo YL, Chang CH, Wang CS, Yang MH, Lin AMY, Hong CJ, Tseng WH (2020) Peg-coated nanoparticles detachable in acidic microenvironments for the tumor-directed delivery of chemo- and gene therapies for head and neck cancer. Theranostics 10(15):6695–6714

    Article  Google Scholar 

  • Luo XH, Huang FW, Qin SY, Wang HF, Feng J, Zhang XZ, Zhuo RX (2011) A strategy to improve serum-tolerant transfection activity of polycation vectors by surface hydroxylation. Biomaterials 32(36):9925–9939

    Article  Google Scholar 

  • Mohammadinejad R, Dehshahri A, Madamsetty VS, Zahmatkeshan M, Tavakol S, Makvandi P, Khorsandi D, Pardakhty A, Ashrafizadeh M, Afshar EG, Zarrabi A (2020) In vivo gene delivery mediated by non-viral vectors for cancer therapy. J Control Release 325:249–275

    Article  Google Scholar 

  • Piotrowski-Daspit AS, Kauffman AC, Bracaglia LG, Saltzman WM (2020) Polymeric vehicles for nucleic acid delivery. Adv Drug Deliv Rev 156:119–132

    Article  Google Scholar 

  • Shim MS, Kwon YJ (2012) Stimuli-responsive polymers and nanomaterials for gene delivery and imaging applications. Adv Drug Deliv Rev 64(11):1046–1058

    Article  Google Scholar 

  • Wu MY, Meng QS, Chen Y, Zhang LX, Li ML, Cai XJ, Li YP, Yu PC, Zhang LL, Shi JL (2016) Large pore-sized hollow mesoporous organosilica for redox-responsive gene delivery and synergistic cancer chemotherapy. Adv Mater 28(10):1963–1969

    Article  Google Scholar 

  • Yang B, Jia HZ, Wang XL, Chen S, Zhang XZ, Zhuo RX, Feng J (2014a) Self-assembled vehicle construction via boronic acid coupling and host-guest interaction for serum-tolerant DNA transport and pH-responsive drug delivery. Adv Healthc Mater 3(4):596–608

    Article  Google Scholar 

  • Yang B, Lv Y, Zhu JY, Han Y, Jia HZ, Chen WH, Feng J, Zhang XZ, Zhuo RX (2014b) A pH-responsive drug nanovehicle constructed by reversible attachment of cholesterol to pegylated poly(l-lysine) via catechol-boronic acid ester formation. Acta Biomater 10(8):3686–3695

    Article  Google Scholar 

  • Yin H, Kanasty RL, Eltoukhy AA, Vegas AJ, Dorkin JR, Anderson DG (2014) Non-viral vectors for gene-based therapy. Nat Rev Genet 15(8):541–555

    Article  Google Scholar 

  • Zhang M, Guo XL, Wang MF, Liu KH (2020a) Tumor microenvironment-induced structure changing drug/gene delivery system for overcoming delivery -associated challenges. J Control Release 323:203–224

    Article  Google Scholar 

  • Zhang RJ, Liu RF, Liu C, Pan LN, Qi YT, Cheng J, Guo JW, Jia Y, Ding J, Zhang JX, Hu HY (2020b) A pH/ROS dual-responsive and targeting nanotherapy for vascular inflammatory diseases. Biomaterials 230:119605

    Article  Google Scholar 

  • Zhu JY, Lei Q, Yang B, Jia HZ, Qiu WX, Wang XL, Zeng X, Zhuo RX, Feng J, Zhang XZ (2015) Efficient nuclear drug translocation and improved drug efficacy mediated by acidity-responsive boronate-linked dextran/cholesterol nanoassembly. Biomaterials 52:281–290

    Article  Google Scholar 

  • Zhu JY, Zeng X, Qin SY, Wan SS, Jia HZ, Zhuo RX, Feng J, Zhang XZ (2016) Acidity-responsive gene delivery for "superfast" nuclear translocation and transfection with high efficiency. Biomaterials 83:79–92

    Article  Google Scholar 

  • Zhu JY, Wan SS, Zheng DW, Lei Q, Zhuo RX, Feng J, Zhang XZ (2017) Propelled transnuclear gene transport achieved through intracellularly redox-responsive and acidity-accelerative decomposition of supramolecular florescence-quenchable vectors. ACS Appl Mater Interfaces 9(1):255–265

    Article  Google Scholar 

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Correspondence to Jun Feng or Xian-Zheng Zhang .

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Zhu, JY., Feng, J., Zhang, XZ. (2021). Preparation and Evaluation of Boronate-Linked Nanoassembly for Efficient Gene Delivery. In: Tian, H., Chen, X. (eds) Gene Delivery. Biomaterial Engineering. Springer, Singapore. https://doi.org/10.1007/978-981-33-6198-0_23-1

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  • DOI: https://doi.org/10.1007/978-981-33-6198-0_23-1

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  • Publisher Name: Springer, Singapore

  • Print ISBN: 978-981-33-6198-0

  • Online ISBN: 978-981-33-6198-0

  • eBook Packages: Springer Reference EngineeringReference Module Computer Science and Engineering

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