Constrained and UV-activatable cell-penetrating peptides for intracellular delivery of liposomes.
暂无分享,去创建一个
Gert Storm | Inge J. Minten | Dennis W P M Löwik | Jan C M van Hest | G. Storm | J. V. van Hest | D. Löwik | E. V. van Gaal | M. B. Hansen | I. Minten | Morten B Hansen | Ethlinn van Gaal | Inge Minten | M. Hansen
[1] Jim Euchner. Design , 2014, Catalysis from A to Z.
[2] Gleb B Sukhorukov,et al. Remote control over guidance and release properties of composite polyelectrolyte based capsules. , 2011, Advanced drug delivery reviews.
[3] U. Baxa,et al. Hyperthermia-triggered intracellular delivery of anticancer agent to HER2(+) cells by HER2-specific affibody (ZHER2-GS-Cys)-conjugated thermosensitive liposomes (HER2(+) affisomes). , 2011, Journal of controlled release : official journal of the Controlled Release Society.
[4] Gonen Ashkenasy,et al. Light induced drug delivery into cancer cells. , 2011, Biomaterials.
[5] U. Haberkorn,et al. The pharmacokinetics of cell-penetrating peptides. , 2010, Molecular pharmaceutics.
[6] Roland Brock,et al. Cellular integration of an enzyme-loaded polymersome nanoreactor. , 2010, Angewandte Chemie.
[7] Y. Hori,et al. Photocontrolled compound release system using caged antimicrobial peptide. , 2010, Journal of the American Chemical Society.
[8] M. Perugini,et al. Self-assembly of peptides into spherical nanoparticles for delivery of hydrophilic moieties to the cytosol. , 2010, ACS nano.
[9] J. Boyer,et al. Remote-control photorelease of caged compounds using near-infrared light and upconverting nanoparticles. , 2010, Angewandte Chemie.
[10] G. Wong,et al. Arginine‐rich cell‐penetrating peptides , 2010, FEBS letters.
[11] N. Kaji,et al. Quantum dots labeling using octa-arginine peptides for imaging of adipose tissue-derived stem cells. , 2010, Biomaterials.
[12] A. Eggermont,et al. Hyperthermia and Thermosensitive Liposomes for Improved Delivery of Chemotherapeutic Drugs to Solid Tumors , 2010, Pharmaceutical Research.
[13] Li Shi,et al. Designer nanoparticles: incorporating size, shape and triggered release into nanoscale drug carriers , 2010, Expert opinion on drug delivery.
[14] Wuli Yang,et al. Study on the Intracellular Fate of Tat Peptide-Conjugated Quantum Dots by Spectroscopic Investigation , 2010, Journal of Fluorescence.
[15] Roman I. Koning,et al. Shape and release control of a peptide decorated vesicle through pH sensitive orthogonal supramolecular interactions. , 2009, Journal of the American Chemical Society.
[16] Malar A. Azagarsamy,et al. Enzyme-triggered disassembly of dendrimer-based amphiphilic nanocontainers. , 2009, Journal of the American Chemical Society.
[17] Renjun Pei,et al. Triggered release of an active peptide conjugate from a DNA device by an orally administrable small molecule. , 2009, Angewandte Chemie.
[18] Mauro Ferrari,et al. Nanomedicine—Challenge and Perspectives , 2009 .
[19] S. Bauer,et al. Amphiphilic TiO2 nanotube arrays: an actively controllable drug delivery system. , 2009, Journal of the American Chemical Society.
[20] Juan L. Vivero-Escoto,et al. Photoinduced intracellular controlled release drug delivery in human cells by gold-capped mesoporous silica nanosphere. , 2009, Journal of the American Chemical Society.
[21] K. Tachibana,et al. A novel strategy utilizing ultrasound for antigen delivery in dendritic cell-based cancer immunotherapy. , 2009, Journal of controlled release : official journal of the Controlled Release Society.
[22] G. Fields,et al. Solid phase peptide synthesis utilizing 9-fluorenylmethoxycarbonyl amino acids. , 2009, International journal of peptide and protein research.
[23] W. Stüber,et al. Synthesis of peptide amides by Fmoc-solid-phase peptide synthesis and acid labile anchor groups. , 2009, International journal of peptide and protein research.
[24] W. Stüber,et al. Synthesis and application of acid labile anchor groups for the synthesis of peptide amides by Fmoc-solid-phase peptide synthesis. , 2009, International journal of peptide and protein research.
[25] H. Devalapally,et al. Multi-functional nanocarriers for targeted delivery of drugs and genes. , 2008, Journal of controlled release : official journal of the Controlled Release Society.
[26] Andrea J. Hanson,et al. Mechanistic studies of the triggered release of liposomal contents by matrix metalloproteinase-9. , 2008, Journal of the American Chemical Society.
[27] Zhuang Liu,et al. PEGylated nanographene oxide for delivery of water-insoluble cancer drugs. , 2008, Journal of the American Chemical Society.
[28] H. Dai,et al. Targeted single-wall carbon nanotube-mediated Pt(IV) prodrug delivery using folate as a homing device. , 2008, Journal of the American Chemical Society.
[29] S. Kelley,et al. Cell-penetrating peptides as delivery vehicles for biology and medicine. , 2008, Organic & biomolecular chemistry.
[30] S. Ganta,et al. A review of stimuli-responsive nanocarriers for drug and gene delivery. , 2008, Journal of controlled release : official journal of the Controlled Release Society.
[31] S. Futaki,et al. Cellular internalization and distribution of arginine-rich peptides as a function of extracellular peptide concentration, serum, and plasma membrane associated proteoglycans. , 2008, Bioconjugate chemistry.
[32] William R. Dichtel,et al. Enzyme-responsive snap-top covered silica nanocontainers. , 2008, Journal of the American Chemical Society.
[33] V. Torchilin,et al. Tatp-mediated intracellular delivery of pharmaceutical nanocarriers. , 2007, Biochemical Society transactions.
[34] W. Jiskoot,et al. Cytosolic Delivery of Liposomally Targeted Proteins Induced by Photochemical Internalization , 2007, Pharmaceutical Research.
[35] S. Libutti,et al. Pulsed-High Intensity Focused Ultrasound and Low Temperature–Sensitive Liposomes for Enhanced Targeted Drug Delivery and Antitumor Effect , 2007, Clinical Cancer Research.
[36] Jeffrey I. Zink,et al. Photo-Driven Expulsion of Molecules from Mesostructured Silica Nanoparticles , 2007 .
[37] Dominic J. Glover,et al. Histone-mediated transduction as an efficient means for gene delivery. , 2007, Molecular therapy : the journal of the American Society of Gene Therapy.
[38] V. Torchilin,et al. Design, synthesis, and characterization of pH-sensitive PEG-PE conjugates for stimuli-sensitive pharmaceutical nanocarriers: the effect of substitutes at the hydrazone linkage on the ph stability of PEG-PE conjugates. , 2007, Bioconjugate chemistry.
[39] J. F. Stoddart,et al. Design and optimization of molecular nanovalves based on redox-switchable bistable rotaxanes. , 2007, Journal of the American Chemical Society.
[40] Vladimir P Torchilin,et al. Enhanced transfection of tumor cells in vivo using “Smart” pH-sensitive TAT-modified pegylated liposomes , 2007, Journal of drug targeting.
[41] S. Frokjaer,et al. Phospholipase A2 Sensitive Liposomes for Delivery of Small Interfering RNA (siRNA) , 2007, Journal of liposome research.
[42] V. Torchilin,et al. “Smart” Drug Carriers: PEGylated TATp-Modified pH-Sensitive Liposomes , 2007, Journal of liposome research.
[43] D. Schmaljohann. Thermo- and pH-responsive polymers in drug delivery. , 2006, Advanced drug delivery reviews.
[44] V. Torchilin,et al. "SMART" drug delivery systems: double-targeted pH-responsive pharmaceutical nanocarriers. , 2006, Bioconjugate chemistry.
[45] Rajesh Subramaniam,et al. Formulation of photocleavable liposomes and the mechanism of their content release. , 2006, Organic & biomolecular chemistry.
[46] R. Fischer,et al. Break on through to the Other Side—Biophysics and Cell Biology Shed Light on Cell‐Penetrating Peptides , 2005, Chembiochem : a European journal of chemical biology.
[47] Victor S-Y Lin,et al. Stimuli-responsive controlled-release delivery system based on mesoporous silica nanorods capped with magnetic nanoparticles. , 2005, Angewandte Chemie.
[48] V. Torchilin. Recent advances with liposomes as pharmaceutical carriers , 2005, Nature Reviews Drug Discovery.
[49] W. Jiskoot,et al. OVCAR-3 cells internalize TAT-peptide modified liposomes by endocytosis. , 2004, Biochimica et biophysica acta.
[50] K. Burgess,et al. Syntheses and Activities of New C10 β-Turn Peptidomimetics , 2004 .
[51] A. Kutateladze,et al. Dithiane-Based Photolabile Amphiphiles: Toward Photolabile Liposomes1,2 , 2003 .
[52] R. Nolte,et al. Vesicles and polymerized vesicles from thiophene-containing rod-coil block copolymers. , 2003, Angewandte Chemie.
[53] W. Jiskoot,et al. Functional Characterization of an Endosome-disruptive Peptide and Its Application in Cytosolic Delivery of Immunoliposome-entrapped Proteins* , 2002, The Journal of Biological Chemistry.
[54] L. Chaloin,et al. Improvement of porphyrin cellular delivery and activity by conjugation to a carrier peptide. , 2001, Bioconjugate chemistry.
[55] V. Torchilin,et al. TAT peptide on the surface of liposomes affords their efficient intracellular delivery even at low temperature and in the presence of metabolic inhibitors , 2001, Proceedings of the National Academy of Sciences of the United States of America.
[56] F. Muggia,et al. Liposomal encapsulated anthracyclines: new therapeutic horizons , 2001, Current oncology reports.
[57] F. Szoka,et al. Cholesterol phosphate derivatives: synthesis and incorporation into a phosphatase and calcium-sensitive triggered release liposome. , 1998, Bioconjugate chemistry.
[58] N. Mullah,et al. Poly(ethylene glycol)-grafted liposomes with oligopeptide or oligosaccharide ligands appended to the termini of the polymer chains. , 1997, Bioconjugate chemistry.
[59] A. Gabizon,et al. Sterically stabilized liposomes: improvements in pharmacokinetics and antitumor therapeutic efficacy. , 1991, Proceedings of the National Academy of Sciences of the United States of America.
[60] T M Allen,et al. Liposomes containing synthetic lipid derivatives of poly(ethylene glycol) show prolonged circulation half-lives in vivo. , 1991, Biochimica et biophysica acta.
[61] G Gregoriadis,et al. Influence of surface hydrophilicity of liposomes on their interaction with plasma protein and clearance from the circulation: studies with poly(ethylene glycol)-coated vesicles. , 1991, Biochimica et biophysica acta.
[62] G Blume,et al. Liposomes for the sustained drug release in vivo. , 1990, Biochimica et biophysica acta.
[63] Kazuo Maruyama,et al. Amphipathic polyethyleneglycols effectively prolong the circulation time of liposomes , 1990, FEBS letters.
[64] G. Fields,et al. Solid Phase Peptide Synthesis Utilizing 9-Fluorenylmethoxycarbonylamino Acids , 1990 .
[65] Carl O. Pabo,et al. Cellular uptake of the tat protein from human immunodeficiency virus , 1988, Cell.
[66] D. Friend,et al. Endocytosis of liposomes and intracellular fate of encapsulated molecules: Encounter with a low pH compartment after internalization in coated vesicles , 1983, Cell.
[67] R Blumenthal,et al. Design of liposomes for enhanced local release of drugs by hyperthermia. , 1978, Science.
[68] F. Szoka,et al. Procedure for preparation of liposomes with large internal aqueous space and high capture by reverse-phase evaporation. , 1978, Proceedings of the National Academy of Sciences of the United States of America.
[69] S. Fleischer,et al. Two dimensional thin layer chromatographic separation of polar lipids and determination of phospholipids by phosphorus analysis of spots , 1970, Lipids.
[70] E. Kaiser,et al. Color test for detection of free terminal amino groups in the solid-phase synthesis of peptides. , 1970, Analytical biochemistry.
[71] Tayyaba Hasan,et al. Intracellular drug delivery by poly(lactic-co-glycolic acid) nanoparticles, revisited. , 2009, Molecular pharmaceutics.
[72] Xenophon E. Verykios,et al. A Light-Actuated Nanovalve Derived from a Channel Protein , 2005 .
[73] K. Burgess,et al. Syntheses and activities of new C10 beta-turn peptidomimetics. , 2004, The Journal of organic chemistry.
[74] P. Cullis,et al. Liposomal doxorubicin. , 1996, Journal of drug targeting.
[75] M. Green,et al. Autonomous functional domains of chemically synthesized human immunodeficiency virus tat trans-activator protein. , 1988, Cell.
[76] A. A. Spector,et al. Binding of long-chain fatty acids to bovine serum albumin. , 1969, Journal of lipid research.