US 4241046A
· Papahadjopoulos et al.
· 1980
[cited by applicant]
KR 20110114952A
· 2011
[cited by applicant]
WO 2000003683A2
· 2000
[cited by applicant]
WO 2010110471A1
· 2010
[cited by applicant]
Somiya et al., One-step scalable preparation method for non-cationic liposomes with high siRNA content, May 28, 2015, Internation Journal of Pharmaceutics, 490, 316-323 (Year: 2015).
[cited by examiner]
Nakamura et al., Octaarginine-modified multifunctional envelope-type nano device for siRNA, Mar. 23, 2007, Journal of Controlled Release, 119, 360-367. (Year: 2007).
[cited by examiner]
Jiang et al., Gene delivery to tumor cells by cationic polymeric nanovectors coupled to folic acid and the cell-penetrating peptide octaarginine, Jun. 28, 2011, Biomaterials, 32, 7253-7262 (Year: 2011).
[cited by examiner]
Torchilin et al., Cell transfection in vitro and in vivo with nontoxic TAT peptide-liposome-DNA complexes, Feb. 18, 2003, Proceedings of the National Academy of Sciences, 100, 1972-1977 (Year: 2003).
[cited by examiner]
Khalil, I.A. et al., High density of octaarginine stimulates macropinocytosis leading to efficient intracellular trafficking for gene expression, 2006, Journal of Biological Chemistry, vol. 281, 3544-3551 (Year: 2006).
[cited by examiner]
Bochicchio, S. et al., Liposomes as siRNA delivery vectors, 2014, Current Drug Metabolism, vol. 15, 882-892 (Year: 2014).
[cited by examiner]
Pattni et al., New developments in liposomal drug delivery, Chemical Reviews, 2015, 10938-66, 115.
[cited by applicant]
Aryasomayajula et al., Multifunctional Liposomes, Cancer Nanotechnology, 2017, 41-61, Springer.
[cited by applicant]
Johnson et al., Single bilayer liposomes, Biochimica et Biophysica Acta (BBA)-Biomembranes, 1971, 820-6, 233.
[cited by applicant]
Bunker et al., Rational design of liposomal drug delivery systems, a review: combined experimental and computational studies of lipid membranes, liposomes and their PEGylation, Biochimica et Biophysica Acta (BBA)-Biomem…
[cited by applicant]
Sercombe et al., Advances and challenges of liposome assisted drug delivery, Frontiers in Pharmacology, 2015, 286, 6.
[cited by applicant]
Noble et al., Ligand-targeted liposome design: challenges and fundamental considerations, Trends in Biotechnology, 2014, 32-45, 32.
[cited by applicant]
Miller AD, Cationic liposomes for gene therapy, Angewandte Chemie International Edition, 1998, 1768-85, 37.
[cited by applicant]
Saul et al., A dual-ligand approach for enhancing targeting selectivity of therapeutic nanocarriers, Journal of Controlled Release, 2006, 277-87, 114.
[cited by applicant]
Zylberberg et al., Engineering liposomal nanoparticles for targeted gene therapy, Gene Therapy, 2017, 441, 24.
[cited by applicant]
Garg et al., Liposomes: targeted and controlled delivery system, Drug Delivery Letters 2014, 62-71, 4.
[cited by applicant]
Wasungu et al., Cationic lipids, lipoplexes and intracellular delivery of genes, Journal of Controlled Release 2006, 255-64, 116.
[cited by applicant]
Antipina et al., Molecular mechanism of calcium-induced adsorption of DNA on zwitterionic phospholipid membranes, The Journal of Physical Chemistry, Apr. 20, 2015, 6638-45, 119.
[cited by applicant]
Koren et al., Cell-penetrating peptides: breaking through to the other side, Trends in Molecular Medicine, 2012, 385-93, 18.
[cited by applicant]
Yang et al., Cell-penetrating peptide induces leaky fusion of liposomes containing late endosome-specific anionic lipid, Biophysical Journal, 2010, 2525-33, 99.
[cited by applicant]
Schmidt et al., Arginine-rich cell-penetrating peptides, FEBS Letters, 2010, 1806-13, 584.
[cited by applicant]
Somiya et al., One-step scalable preparation method for non-cationic liposomes with high siRNA content, International Journal of Pharmaceutics, 2015, 316-23, 490.
[cited by applicant]
Fisher et al., Improving the efficacy of liposome-mediated vascular gene therapy via lipid surface modifications, Journal of Surgical Research, 2017, 136-44, 219.
[cited by applicant]
Kim et al., Enhanced siRNA delivery using cationic liposomes with new polyarginine-conjugated PEG-lipid, International Journal of Pharmaceutics, 2010, 141-7, 392.
[cited by applicant]
Kogure et al., Development of a non- viral multifunctional envelope-type nano device by a novel lipid film hydration method, Journal of Controlled Release 2004, 317-23, 98.
[cited by applicant]
Lee et al., Topology of surface ligands on liposomes: characterization based on the terms, incorporation ratio, surface anchor density, and reaction yield, Biological and Pharmaceutical Bulletin, 2016, 1983-94, 39.
[cited by applicant]
Uster et al., Insertion of poly (ethylene glycol) derivatized phospholipid into pre-formed liposomes results in prolonged in vivo circulation time, FEBS Letters, 1996, 243-6, 386.
[cited by applicant]
Sułkowski et al., The influence of temperature, cholesterol content and pH on liposome stability, Journal of Molecular Structure, 2005, 737-47, 744.
[cited by applicant]
Iden et al., In vitro and in vivo comparison of immunoliposomes made by conventional coupling techniques with those made by a new post-insertion approach, Biochimica et Biophysica Acta (BBA)-Biomembranes, 2001, 207-16, …
[cited by applicant]
Moreira et al., Use of the post-insertion technique to insert peptide ligands into pre-formed stealth liposomes with retention of binding activity and cytotoxicity, Pharmaceutical Research, 2002, 265-9, 19.
[cited by applicant]
Nakamura et al., Octaarginine-modified multifunctional envelope-type nano device for siRNA, Journal of Controlled Release, 2007, 360-7, 119.
[cited by applicant]
Zhang et al., Cationic lipids and polymers mediated vectors for delivery of siRNA, Journal of Controlled Release, 2007, 1-10, 123.
[cited by applicant]
Torchilin VP. Multifunctional nanocarriers, Advanced Drug Delivery Reviews, 2012, 302-15, 64.
[cited by applicant]
Gao et al., Cell-penetrating peptide-based intelligent liposomal systems for enhanced drug delivery, Current pharmaceutical biotechnology, 2014, 210-9, 15.
[cited by applicant]
Copolovici et al., Cell-penetrating peptides: design, synthesis, and applications, ACS Nano, 2014, 1972-94, 8.
[cited by applicant]
Karmali et al., Cationic liposomes as non-viral carriers of gene medicines: resolved issues, open questions, and future promises, Medicinal Research Reviews, 2007, 696-722, 27.
[cited by applicant]
Safinya et al., Cationic liposome-nucleic acid complexes for gene delivery and gene silencing, New Journal of Chemistry, 2014, 5164-72, 38.
[cited by applicant]
Kogure et al., Multifunctional envelope-type nano device (MEND) as a non-viral gene delivery system, Advanced Drug Delivery Reviews, 2008, 559-71, 60.
[cited by applicant]
33. Soenen et al., Addressing the problem of cationic lipid-mediated toxicity: the magnetoliposome model, Biomaterials, 2009, 3691-701, 30.
[cited by applicant]
Holland et al., Poly (ethylene glycol)—lipid conjugates regulate the calcium-induced fusion of liposomes composed of phosphatidylethanolamine and phosphatidylserine, Biochemistry, 1996, 2618-24, 35.
[cited by applicant]
El-Sayed et al., Delivery of macromolecules using arginine-rich cell-penetrating peptides: ways to overcome endosomal entrapment, The AAPS Journal, 2009, 13-22, 11.
[cited by applicant]
Chan et al., Endosomal escape and transfection efficiency of PEGylated cationic liposome-DNA complexes prepared with an acid-labile PEG-lipid, Biomaterials, 2012, 4928-35, 33.
[cited by applicant]
Mattern-Schain et al., Cell mimetic liposomal nanocarriers for tailored delivery of vascular therapeutics, Chemistry and Physics of Lipids, 2019, 149-57, 218.
[cited by applicant]
International Search Report and Written Opinion, PCT/US2019/042600, Nov. 21, 2019 (11 pages).
[cited by applicant]
Extended European Search Report , Application No. 19840350.3, Jul. 6, 2022 (147 pages).
[cited by applicant]
Bruno, Using drug-excipient interactions for siRNA delivery, Advanced Drug Delivery Reviews, Sep. 14, 2011, p. 1210-1226, vol. 63.
[cited by applicant]