Molecular homing and retention of muscle membrane stabilizing copolymers by non-invasive optical imaging in vivo
暂无分享,去创建一个
Mihee M. Kim | F. Bates | T. Lodge | M. Hillmyer | J. Metzger | Dongwoo Hahn | B. Hackel | Nicholas J. Van Zee | Houda Cohen | Addeli Bez Batti Angulski
[1] Beob Soo Kim,et al. Size-tunable PEG-grafted copolymers as a polymeric nanoruler for passive targeting muscle tissues. , 2022, Journal of controlled release : official journal of the Controlled Release Society.
[2] Asher Mullard. Sarepta’s DMD gene therapy falls flat , 2021, Nature reviews. Drug discovery.
[3] Haiyan Chen,et al. Near-infrared small molecular fluorescent dyes for photothermal therapy , 2019, Chinese Chemical Letters.
[4] F. Bates,et al. Cardiac Muscle Membrane Stabilization in Myocardial Reperfusion Injury , 2019, JACC. Basic to translational science.
[5] Lauren M. Aufdembrink,et al. Acute AT1R blockade prevents isoproterenol-induced injury in mdx hearts. , 2019, Journal of molecular and cellular cardiology.
[6] Y. Sham,et al. Muscle membrane integrity in Duchenne muscular dystrophy: recent advances in copolymer-based muscle membrane stabilizers , 2018, Skeletal Muscle.
[7] Y. Sham,et al. All-Atom Molecular Dynamics-Based Analysis of Membrane-Stabilizing Copolymer Interactions with Lipid Bilayers Probed under Constant Surface Tensions. , 2017, The journal of physical chemistry. B.
[8] O. Velev,et al. Investigation of interfacial properties of pure and mixed poloxamers for surfactant-mediated shear protection of mammalian cells. , 2017, Colloids and surfaces. B, Biointerfaces.
[9] Mihee M. Kim,et al. PEO-PPO Diblock Copolymers Protect Myoblasts from Hypo-Osmotic Stress In Vitro Dependent on Copolymer Size, Composition, and Architecture. , 2017, Biomacromolecules.
[10] Mihee M. Kim,et al. Chemical End Group Modified Diblock Copolymers Elucidate Anchor and Chain Mechanism of Membrane Stabilization. , 2017, Molecular pharmaceutics.
[11] Shan Sun,et al. Preventive Effects of Poloxamer 188 on Muscle Cell Damage Mechanics Under Oxidative Stress , 2016, Annals of Biomedical Engineering.
[12] M. Muhammed,et al. Biodistribution of biodegradable polymeric nano-carriers loaded with busulphan and designed for multimodal imaging , 2016, Journal of Nanobiotechnology.
[13] J. Metzger,et al. Sarcomere neutralization in inherited cardiomyopathy: small-molecule proof-of-concept to correct hyper-Ca2+-sensitive myofilaments. , 2016, American Journal of Physiology. Heart and Circulatory Physiology.
[14] F. Bates,et al. Intracoronary Poloxamer 188 Prevents Reperfusion Injury in a Porcine Model of ST-Segment Elevation Myocardial Infarction , 2016, JACC. Basic to translational science.
[15] R. Perlingeiro,et al. Membrane-stabilizing copolymers confer marked protection to dystrophic skeletal muscle in vivo , 2015, Molecular therapy. Methods & clinical development.
[16] J. Wilkinson,et al. Chronic Dosing with Membrane Sealant Poloxamer 188 NF Improves Respiratory Dysfunction in Dystrophic Mdx and Mdx/Utrophin-/- Mice , 2015, PloS one.
[17] R. Neumar,et al. Bundled postconditioning therapies improve hemodynamics and neurologic recovery after 17 min of untreated cardiac arrest. , 2015, Resuscitation.
[18] K. Flanigan. Duchenne and Becker muscular dystrophies. , 2014, Neurologic clinics.
[19] Laura D. Hughes,et al. Choose Your Label Wisely: Water-Soluble Fluorophores Often Interact with Lipid Bilayers , 2014, PloS one.
[20] J. Metzger,et al. Uncoupling of increased cellular oxidative stress and myocardial ischemia reperfusion injury by directed sarcolemma stabilization. , 2014, Journal of molecular and cellular cardiology.
[21] P. Gervais,et al. Exploration of Lipid Metabolism in Relation with Plasma Membrane Properties of Duchenne Muscular Dystrophy Cells: Influence of L-Carnitine , 2012, PloS one.
[22] Songi Han,et al. Nature of interactions between PEO-PPO-PEO triblock copolymers and lipid membranes: (II) role of hydration dynamics revealed by dynamic nuclear polarization. , 2012, Biomacromolecules.
[23] J. Marks,et al. Nature of interactions between PEO-PPO-PEO triblock copolymers and lipid membranes: (I) effect of polymer hydrophobicity on its ability to protect liposomes from peroxidation. , 2012, Biomacromolecules.
[24] Y. Itoyama,et al. Continuous administration of poloxamer 188 reduces overload-induced muscular atrophy in dysferlin-deficient SJL mice , 2012, Neuroscience Research.
[25] P. Turner,et al. Administration of substances to laboratory animals: routes of administration and factors to consider. , 2011, Journal of the American Association for Laboratory Animal Science : JAALAS.
[26] E. Hoffman,et al. Membrane Sealant Poloxamer P188 Protects Against Isoproterenol Induced Cardiomyopathy in Dystrophin Deficient Mice , 2011, BMC cardiovascular disorders.
[27] I. Graham,et al. Chronic systemic therapy with low-dose morpholino oligomers ameliorates the pathology and normalizes locomotor behavior in mdx mice. , 2011, Molecular therapy : the journal of the American Society of Gene Therapy.
[28] J. Kornegay,et al. Chronic administration of membrane sealant prevents severe cardiac injury and ventricular dilatation in dystrophic dogs. , 2010, The Journal of clinical investigation.
[29] Soojin Lim,et al. NIR dyes for bioimaging applications. , 2010, Current opinion in chemical biology.
[30] Akinori Nakamura,et al. Efficacy of systemic morpholino exon‐skipping in duchenne dystrophy dogs , 2009, Annals of neurology.
[31] M. Carignano,et al. Effects of block copolymer's architecture on its association with lipid membranes: experiments and simulations. , 2007, The Journal of chemical physics.
[32] Raphael C. Lee,et al. Structural and functional recovery of electropermeabilized skeletal muscle in-vivo after treatment with surfactant poloxamer 188. , 2007, Biochimica et biophysica acta.
[33] A. Rabinowitz,et al. Systemic delivery of morpholino oligonucleotide restores dystrophin expression bodywide and improves dystrophic pathology , 2006, Nature Medicine.
[34] S. Day,et al. Dystrophic heart failure blocked by membrane sealant poloxamer , 2005, Nature.
[35] C. Porter,et al. Subcutaneous drug delivery and the role of the lymphatics. , 2005, Drug discovery today. Technologies.
[36] A. Rabinowitz,et al. Systemic delivery of antisense oligoribonucleotide restores dystrophin expression in body-wide skeletal muscles. , 2005, Proceedings of the National Academy of Sciences of the United States of America.
[37] Raphael C. Lee,et al. Poloxamer 188 prevents acute necrosis of adult skeletal muscle cells following high-dose irradiation. , 2004, Burns : journal of the International Society for Burn Injuries.
[38] D. Duan,et al. Full-length dystrophin expression in half of the heart cells ameliorates beta-isoproterenol-induced cardiomyopathy in mdx mice. , 2004, Human molecular genetics.
[39] Raphael C. Lee,et al. Subcutaneous tri‐block copolymer produces recovery from spinal cord injury , 2004, Journal of neuroscience research.
[40] M. Firestone,et al. Small-angle X-ray scattering study of the interaction of poly(ethylene oxide)-b-poly(propylene oxide)-b-poly(ethylene oxide) triblock copolymers with lipid bilayers. , 2003, Biomacromolecules.
[41] Alexander V Kabanov,et al. Pluronic block copolymers as modulators of drug efflux transporter activity in the blood-brain barrier. , 2003, Advanced drug delivery reviews.
[42] Ka Yee C. Lee,et al. Comparative Study of Poloxamer Insertion into Lipid Monolayers , 2003 .
[43] R. Emanuele,et al. Distribution, metabolism, and excretion of a novel surface-active agent, purified poloxamer 188, in rats, dogs, and humans. , 2002, Journal of pharmaceutical sciences.
[44] Alexander V Kabanov,et al. Pluronic block copolymers as novel polymer therapeutics for drug and gene delivery. , 2002, Journal of controlled release : official journal of the Controlled Release Society.
[45] P. Culbreth,et al. Pharmacokinetics of a novel surface‐active agent, purified poloxamer 188, in rat, rabbit, dog and man , 2002, Biopharmaceutics & drug disposition.
[46] Raphael C. Lee,et al. Direct observation of poloxamer 188 insertion into lipid monolayers. , 2002, Biophysical journal.
[47] S. Shaikh,et al. Lipid phase separation in phospholipid bilayers and monolayers modeling the plasma membrane. , 2001, Biochimica et biophysica acta.
[48] Raphael C. Lee,et al. Surfactant Sealing of Membranes Permeabilized by Ionizing Radiation , 2000, Radiation research.
[49] B. Mokri,et al. Duchenne dystrophy: Electron microscopic findings pointing to a basic or early abnormality in the plasma membrane of the muscle fiber , 1998, Neurology.
[50] M. Steinberg,et al. RheothRx (poloxamer 188) injection for the acute painful episode of sickle cell disease: a pilot study. , 1997, Blood.
[51] R. Gibbons,et al. Beneficial effects of RheothRx injection in patients receiving thrombolytic therapy for acute myocardial infarction. Results of a randomized, double-blind, placebo-controlled trial. , 1996, Circulation.
[52] M. Toner,et al. Effectiveness of Poloxamer 188 in Arresting Calcein Leakage from Thermally Damaged Isolated Skeletal Muscle Cells a , 1994, Annals of the New York Academy of Sciences.
[53] R. Lee,et al. Surfactant-induced sealing of electropermeabilized skeletal muscle membranes in vivo. , 1992, Proceedings of the National Academy of Sciences of the United States of America.
[54] C. M. Bates,et al. 50th Anniversary Perspective: Block Polymers—Pure Potential , 2017 .
[55] Xi-ping Chen,et al. Poloxamer-188 Can Attenuate Blood–Brain Barrier Damage to Exert Neuroprotective Effect in Mice Intracerebral Hemorrhage Model , 2014, Journal of Molecular Neuroscience.
[56] A. Ossipov,et al. Duchenne muscular dystrophy , 2004 .