Peptide-Based Nanoparticles for Therapeutic Nucleic Acid Delivery

被引:45
|
作者
Boisguerin, Prisca [1 ]
Konate, Karidia [1 ]
Josse, Emilie [1 ]
Vives, Eric [1 ]
Deshayes, Sebastien [1 ]
机构
[1] Univ Montpellier, PhyMedExp, INSERM U1046, CNRS UMR 9214, F-34295 Montpellier, France
关键词
cell-penetrating peptide; nanoparticle; nucleic acid; delivery; self-assembly; CELL-PENETRATING PEPTIDE; NF-KAPPA-B; SIRNA DELIVERY; GENE DELIVERY; IN-VITRO; DRUG-DELIVERY; TRANSFECTION EFFICIENCY; AMPHIPATHIC PEPTIDE; INTRACELLULAR DELIVERY; CULTURED NEURONS;
D O I
10.3390/biomedicines9050583
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Gene therapy offers the possibility to skip, repair, or silence faulty genes or to stimulate the immune system to fight against disease by delivering therapeutic nucleic acids (NAs) to a patient. Compared to other drugs or protein treatments, NA-based therapies have the advantage of being a more universal approach to designing therapies because of the versatility of NA design. NAs (siRNA, pDNA, or mRNA) have great potential for therapeutic applications for an immense number of indications. However, the delivery of these exogenous NAs is still challenging and requires a specific delivery system. In this context, beside other non-viral vectors, cell-penetrating peptides (CPPs) gain more and more interest as delivery systems by forming a variety of nanocomplexes depending on the formulation conditions and the properties of the used CPPs/NAs. In this review, we attempt to cover the most important biophysical and biological aspects of non-viral peptide-based nanoparticles (PBNs) for therapeutic nucleic acid formulations as a delivery system. The most relevant peptides or peptide families forming PBNs in the presence of NAs described since 2015 will be presented. All these PBNs able to deliver NAs in vitro and in vivo have common features, which are characterized by defined formulation conditions in order to obtain PBNs from 60 nm to 150 nm with a homogeneous dispersity (PdI lower than 0.3) and a positive charge between +10 mV and +40 mV.
引用
收藏
页数:27
相关论文
共 50 条
  • [31] Lipid-based nanoparticles for nucleic acid delivery
    Li, Weijun
    Szoka, Francis C., Jr.
    PHARMACEUTICAL RESEARCH, 2007, 24 (03) : 438 - 449
  • [32] Polyester-based nanoparticles for nucleic acid delivery
    Zhao, Jing
    Weng, Guojun
    Li, Jianjun
    Zhu, Jian
    Zhao, Junwu
    MATERIALS SCIENCE AND ENGINEERING C-MATERIALS FOR BIOLOGICAL APPLICATIONS, 2018, 92 : 983 - 994
  • [33] Unleashing the potential of natural protein based nanoparticles for the delivery of therapeutic nucleic Acid: A comprehensive review
    Yadav, Krishna
    Gnanakani, S. Princely Ebenezer
    Sahu, Kantrol Kumar
    Sucheta
    Dubey, Akhilesh
    Minz, Sunita
    Raza, Wasim
    Pradhan, Madhulika
    INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2025, 669
  • [34] Delivery of proteins and nucleic acids using a non-covalent peptide-based strategy
    Deshayes, Sebastien
    Morris, May
    Heitz, Frederic
    Divita, Gilles
    ADVANCED DRUG DELIVERY REVIEWS, 2008, 60 (4-5) : 537 - 547
  • [35] Peptide-Based Drug Delivery Systems
    Berillo, Dmitriy
    Yeskendir, Adilkhan
    Zharkinbekov, Zharylkasyn
    Raziyeva, Kamila
    Saparov, Arman
    MEDICINA-LITHUANIA, 2021, 57 (11):
  • [36] Peptide-based gene delivery vectors
    Kang, Ziyao
    Meng, Qingbin
    Liu, Keliang
    JOURNAL OF MATERIALS CHEMISTRY B, 2019, 7 (11) : 1824 - 1841
  • [37] Development of a Peptide Nucleic Acid Based siRNA Delivery System
    Naik, Tejal Ulhas
    Sullivan, Millicent O.
    FASEB JOURNAL, 2010, 24
  • [38] Development of a Peptide Nucleic Acid Based siRNA Delivery System
    Naik, Tejal U.
    Sullivan, Millicent O.
    FASEB JOURNAL, 2011, 25
  • [39] Peptide-based capsules for protein delivery
    Li, Yi
    Lock, Lye Lin
    Cui, Honggang
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2016, 252
  • [40] Peptide-Based Vectors for Gene Delivery
    Yang, Juan
    Luo, Guo-Feng
    CHEMISTRY-SWITZERLAND, 2023, 5 (03): : 1696 - 1718