Nature Communications, ISSN 2041-1723, 07/2015, Volume 6, Issue 1, p. 7722
Dendrimers are well-defined macromolecules whose highly branched structure is reminiscent of many natural structures, such as trees, dendritic cells, neurons...
CELLS | NANOPARTICLES | ACTIVATION | DESIGN | RECOGNITION | MULTIDISCIPLINARY SCIENCES | MONOCYTES | PHOSPHORUS-CONTAINING DENDRIMERS | Polylysine - pharmacology | Silanes - chemistry | Nanoparticles - chemistry | Biocompatible Materials - chemistry | Humans | Aza Compounds - chemistry | Polylysine - chemistry | Aza Compounds - pharmacology | Biocompatible Materials - pharmacology | Polypropylenes - pharmacology | Molecular Dynamics Simulation | Bone Density Conservation Agents - pharmacology | Monocytes - drug effects | Flow Cytometry | Diphosphonates - chemistry | Dendrimers - chemistry | Polypropylenes - chemistry | Molecular Structure | Dendrimers - pharmacology | Silanes - pharmacology | Diphosphonates - pharmacology | Bone Density Conservation Agents - chemistry | Chemical Sciences | Coordination chemistry
CELLS | NANOPARTICLES | ACTIVATION | DESIGN | RECOGNITION | MULTIDISCIPLINARY SCIENCES | MONOCYTES | PHOSPHORUS-CONTAINING DENDRIMERS | Polylysine - pharmacology | Silanes - chemistry | Nanoparticles - chemistry | Biocompatible Materials - chemistry | Humans | Aza Compounds - chemistry | Polylysine - chemistry | Aza Compounds - pharmacology | Biocompatible Materials - pharmacology | Polypropylenes - pharmacology | Molecular Dynamics Simulation | Bone Density Conservation Agents - pharmacology | Monocytes - drug effects | Flow Cytometry | Diphosphonates - chemistry | Dendrimers - chemistry | Polypropylenes - chemistry | Molecular Structure | Dendrimers - pharmacology | Silanes - pharmacology | Diphosphonates - pharmacology | Bone Density Conservation Agents - chemistry | Chemical Sciences | Coordination chemistry
Journal Article
International Journal of Pharmaceutics, ISSN 0378-5173, 01/2015, Volume 478, Issue 2, pp. 496 - 503
Hydrogels synthesized from poly( -lysine isophthalamide) (PLP) crosslinked with -lysine methyl ester were investigated as drug delivery systems for a wide size...
Oral drug delivery | Amphiphilic | Hydrogels | pH-responsive | Controlled release | COMPLEXATION HYDROGELS | TRANSIT | DESIGN | DRUG-DELIVERY | DOSAGE FORMS | INSULIN | NANOPARTICLES | IN-VITRO | PSEUDO-PEPTIDES | SYSTEMS | PHARMACOLOGY & PHARMACY | Hemolysis - drug effects | Phthalic Acids - chemistry | Dextrans - chemistry | Polylysine - chemistry | Fluorescein-5-isothiocyanate - chemistry | Dextrans - pharmacology | Phthalic Acids - pharmacology | Fluorescein - chemistry | Lysine - analogs & derivatives | Polylysine - pharmacology | Fluorescein-5-isothiocyanate - pharmacology | Administration, Oral | Fluorescein-5-isothiocyanate - analogs & derivatives | Peptide Hydrolases - chemistry | Erythrocytes - drug effects | Animals | Lysine - pharmacology | Fluorescein - pharmacology | Polymers - pharmacology | Drug Liberation | Polymers - chemistry | Sheep | Hydrogels - pharmacology | Lysine - chemistry | Hydrogels - chemistry | Hydrogen-Ion Concentration | Lysine
Oral drug delivery | Amphiphilic | Hydrogels | pH-responsive | Controlled release | COMPLEXATION HYDROGELS | TRANSIT | DESIGN | DRUG-DELIVERY | DOSAGE FORMS | INSULIN | NANOPARTICLES | IN-VITRO | PSEUDO-PEPTIDES | SYSTEMS | PHARMACOLOGY & PHARMACY | Hemolysis - drug effects | Phthalic Acids - chemistry | Dextrans - chemistry | Polylysine - chemistry | Fluorescein-5-isothiocyanate - chemistry | Dextrans - pharmacology | Phthalic Acids - pharmacology | Fluorescein - chemistry | Lysine - analogs & derivatives | Polylysine - pharmacology | Fluorescein-5-isothiocyanate - pharmacology | Administration, Oral | Fluorescein-5-isothiocyanate - analogs & derivatives | Peptide Hydrolases - chemistry | Erythrocytes - drug effects | Animals | Lysine - pharmacology | Fluorescein - pharmacology | Polymers - pharmacology | Drug Liberation | Polymers - chemistry | Sheep | Hydrogels - pharmacology | Lysine - chemistry | Hydrogels - chemistry | Hydrogen-Ion Concentration | Lysine
Journal Article
Biomacromolecules, ISSN 1525-7797, 04/2012, Volume 13, Issue 4, pp. 1024 - 1034
A dual stimulus-responsive mPEG-SS-PLL15-glutaraldehyde star (mPEG-SS-PLL15-star) catiomer is developed and biologically evaluated. The catiomer system...
DRUG | POLYMERS | POLYMER SCIENCE | BIOCHEMISTRY & MOLECULAR BIOLOGY | COMPLEXES | LOW-MOLECULAR-WEIGHT | TRANSFECTION EFFICIENCY | CHEMISTRY, ORGANIC | MICELLES | POLYMERIZATION | POLYETHYLENIMINE | BLOCK-COPOLYMER | DNA POLYPLEXES | Cross-Linking Reagents - pharmacology | Humans | Polyethylene Glycols - chemistry | Polylysine - chemistry | Cross-Linking Reagents - chemical synthesis | Cations - pharmacology | Disulfides - chemistry | Surface Properties | HEK293 Cells | Imines - chemistry | Disulfides - pharmacology | Molecular Structure | Glutaral - chemistry | Polyethylene Glycols - pharmacology | Cations - chemical synthesis | Cell Survival - drug effects | Gene Transfer Techniques | Cations - chemistry | Cross-Linking Reagents - chemistry | Genetic Vectors - chemistry | Oxidation-Reduction | Genetic Vectors - chemical synthesis | Imines - pharmacology | Polylysine - genetics | Particle Size | Genetic Vectors - pharmacology | Glutaral - pharmacology | HeLa Cells
DRUG | POLYMERS | POLYMER SCIENCE | BIOCHEMISTRY & MOLECULAR BIOLOGY | COMPLEXES | LOW-MOLECULAR-WEIGHT | TRANSFECTION EFFICIENCY | CHEMISTRY, ORGANIC | MICELLES | POLYMERIZATION | POLYETHYLENIMINE | BLOCK-COPOLYMER | DNA POLYPLEXES | Cross-Linking Reagents - pharmacology | Humans | Polyethylene Glycols - chemistry | Polylysine - chemistry | Cross-Linking Reagents - chemical synthesis | Cations - pharmacology | Disulfides - chemistry | Surface Properties | HEK293 Cells | Imines - chemistry | Disulfides - pharmacology | Molecular Structure | Glutaral - chemistry | Polyethylene Glycols - pharmacology | Cations - chemical synthesis | Cell Survival - drug effects | Gene Transfer Techniques | Cations - chemistry | Cross-Linking Reagents - chemistry | Genetic Vectors - chemistry | Oxidation-Reduction | Genetic Vectors - chemical synthesis | Imines - pharmacology | Polylysine - genetics | Particle Size | Genetic Vectors - pharmacology | Glutaral - pharmacology | HeLa Cells
Journal Article
Acta Biomaterialia, ISSN 1742-7061, 10/2014, Volume 10, Issue 10, pp. 4206 - 4216
Since the introduction of cell immunoisolation as an alternative to protect transplanted cells from host immune attack, much effort has been made to develop...
Poly(lactic-co-glycolic) acid | Dexamethasone | Alginate Hydrogel-based scaffolds | Cell encapsulation | Xenotransplantation | DRUG | PORCINE SERTOLI-CELLS | STEM-CELLS | MATERIALS SCIENCE, BIOMATERIALS | PLGA-MICROSPHERES | ENGINEERING, BIOMEDICAL | RELEASE | ALGINATE MICROCAPSULES | DELIVERY | FOREIGN-BODY RESPONSE | TISSUE-RESPONSE | Dexamethasone - chemistry | Inflammation - pathology | Polylysine - analogs & derivatives | Capsules - pharmacology | Rats, Inbred F344 | Polyglycolic Acid - pharmacology | Delayed-Action Preparations - chemistry | Male | Polylysine - chemistry | Microspheres | Inflammation - metabolism | Dexamethasone - pharmacology | Delayed-Action Preparations - pharmacology | Cells, Immobilized - transplantation | Lactic Acid - pharmacology | Alginates - pharmacology | Cell Line | Polylysine - pharmacology | Lactic Acid - chemistry | Anti-Inflammatory Agents - pharmacology | Cells, Immobilized - metabolism | Rats | Capsules - chemistry | Cell Transplantation | Animals | Anti-Inflammatory Agents - chemistry | Alginates - chemistry | Polyglycolic Acid - chemistry | Inflammation - prevention & control | Mice | Hydrogels - pharmacology | Hydrogels - chemistry | Surgical implants | Hydrogels | Implantation | Constants | Inflammatory response | Alginates | Proposals | Scaffolds
Poly(lactic-co-glycolic) acid | Dexamethasone | Alginate Hydrogel-based scaffolds | Cell encapsulation | Xenotransplantation | DRUG | PORCINE SERTOLI-CELLS | STEM-CELLS | MATERIALS SCIENCE, BIOMATERIALS | PLGA-MICROSPHERES | ENGINEERING, BIOMEDICAL | RELEASE | ALGINATE MICROCAPSULES | DELIVERY | FOREIGN-BODY RESPONSE | TISSUE-RESPONSE | Dexamethasone - chemistry | Inflammation - pathology | Polylysine - analogs & derivatives | Capsules - pharmacology | Rats, Inbred F344 | Polyglycolic Acid - pharmacology | Delayed-Action Preparations - chemistry | Male | Polylysine - chemistry | Microspheres | Inflammation - metabolism | Dexamethasone - pharmacology | Delayed-Action Preparations - pharmacology | Cells, Immobilized - transplantation | Lactic Acid - pharmacology | Alginates - pharmacology | Cell Line | Polylysine - pharmacology | Lactic Acid - chemistry | Anti-Inflammatory Agents - pharmacology | Cells, Immobilized - metabolism | Rats | Capsules - chemistry | Cell Transplantation | Animals | Anti-Inflammatory Agents - chemistry | Alginates - chemistry | Polyglycolic Acid - chemistry | Inflammation - prevention & control | Mice | Hydrogels - pharmacology | Hydrogels - chemistry | Surgical implants | Hydrogels | Implantation | Constants | Inflammatory response | Alginates | Proposals | Scaffolds
Journal Article
Infection and Immunity, ISSN 0019-9567, 12/2005, Volume 73, Issue 12, pp. 7967 - 7976
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INFECTIOUS DISEASES | HUMAN MONOCYTIC CELLS | LIPOTEICHOIC ACID | MURAMYL DIPEPTIDE | HOST RECOGNITION | WALL COMPONENTS | IFN-GAMMA | ADJUVANT ACTIVITY | DIAMINOPIMELIC ACID | IMMUNOLOGY | BACTERIAL PEPTIDOGLYCAN | CUTTING EDGE | Adjuvants, Immunologic - pharmacology | Diaminopimelic Acid - pharmacology | Dendritic Cells - immunology | Humans | RNA, Messenger - analysis | Intracellular Signaling Peptides and Proteins - metabolism | RNA, Messenger - metabolism | Th1 Cells - immunology | Th1 Cells - metabolism | Dendritic Cells - drug effects | Toll-Like Receptors - metabolism | Intracellular Signaling Peptides and Proteins - genetics | Polylysine - pharmacology | Poly I-C - pharmacology | Cytokines - metabolism | Interleukin-12 - metabolism | Nod2 Signaling Adaptor Protein | Adaptor Proteins, Signal Transducing - agonists | Toll-Like Receptors - agonists | Acetylmuramyl-Alanyl-Isoglutamine - pharmacology | Drug Synergism | Diaminopimelic Acid - analogs & derivatives | Intracellular Signaling Peptides and Proteins - agonists | Toll-Like Receptors - genetics | Adaptor Proteins, Signal Transducing - genetics | Lipid A - pharmacology | Nod1 Signaling Adaptor Protein | Adaptor Proteins, Signal Transducing - metabolism | Oligodeoxyribonucleotides - pharmacology | Oligopeptides - pharmacology | Host Response and Inflammation
INFECTIOUS DISEASES | HUMAN MONOCYTIC CELLS | LIPOTEICHOIC ACID | MURAMYL DIPEPTIDE | HOST RECOGNITION | WALL COMPONENTS | IFN-GAMMA | ADJUVANT ACTIVITY | DIAMINOPIMELIC ACID | IMMUNOLOGY | BACTERIAL PEPTIDOGLYCAN | CUTTING EDGE | Adjuvants, Immunologic - pharmacology | Diaminopimelic Acid - pharmacology | Dendritic Cells - immunology | Humans | RNA, Messenger - analysis | Intracellular Signaling Peptides and Proteins - metabolism | RNA, Messenger - metabolism | Th1 Cells - immunology | Th1 Cells - metabolism | Dendritic Cells - drug effects | Toll-Like Receptors - metabolism | Intracellular Signaling Peptides and Proteins - genetics | Polylysine - pharmacology | Poly I-C - pharmacology | Cytokines - metabolism | Interleukin-12 - metabolism | Nod2 Signaling Adaptor Protein | Adaptor Proteins, Signal Transducing - agonists | Toll-Like Receptors - agonists | Acetylmuramyl-Alanyl-Isoglutamine - pharmacology | Drug Synergism | Diaminopimelic Acid - analogs & derivatives | Intracellular Signaling Peptides and Proteins - agonists | Toll-Like Receptors - genetics | Adaptor Proteins, Signal Transducing - genetics | Lipid A - pharmacology | Nod1 Signaling Adaptor Protein | Adaptor Proteins, Signal Transducing - metabolism | Oligodeoxyribonucleotides - pharmacology | Oligopeptides - pharmacology | Host Response and Inflammation
Journal Article
Molecular Pharmaceutics, ISSN 1543-8384, 12/2015, Volume 12, Issue 12, pp. 4226 - 4236
Nucleoside reverse transcriptase inhibitors (NRTIs) are an integral part of the current antiretroviral therapy (ART), which dramatically reduced the mortality...
HIV-1 | macrophages | nucleoside reverse transcriptase inhibitors | prodrugs of zidovudine | humanized mouse (hu-PBL) HIV model | abacavir | nanogel conjugates | mitochondrial toxicity | epsilon-polylysine | lamivudine | MEDICINE, RESEARCH & EXPERIMENTAL | BIODISTRIBUTION | TOXICITY | DELIVERY | ACTIVATED NUCLEOSIDE ANALOGS | NANOPARTICLES | IN-VITRO | ZIDOVUDINE | PHARMACOLOGY & PHARMACY | TYPE-1 | BRAIN | Anti-HIV Agents - pharmacology | Dideoxynucleosides - pharmacology | Polylysine - pharmacology | HIV-1 - drug effects | HIV Reverse Transcriptase - antagonists & inhibitors | Humans | Reverse Transcriptase Inhibitors - pharmacology | Zidovudine - pharmacology | Polyethyleneimine - pharmacology | Hep G2 Cells | Drug Therapy, Combination - methods | Animals | HIV Infections - drug therapy | Lamivudine - pharmacology | Mice | Polyethylene Glycols - pharmacology | Index Medicus | humanized mouse (hu-PBL)HIV model | prodrugs of Zidovudine | Abacavir | Lamivudine
HIV-1 | macrophages | nucleoside reverse transcriptase inhibitors | prodrugs of zidovudine | humanized mouse (hu-PBL) HIV model | abacavir | nanogel conjugates | mitochondrial toxicity | epsilon-polylysine | lamivudine | MEDICINE, RESEARCH & EXPERIMENTAL | BIODISTRIBUTION | TOXICITY | DELIVERY | ACTIVATED NUCLEOSIDE ANALOGS | NANOPARTICLES | IN-VITRO | ZIDOVUDINE | PHARMACOLOGY & PHARMACY | TYPE-1 | BRAIN | Anti-HIV Agents - pharmacology | Dideoxynucleosides - pharmacology | Polylysine - pharmacology | HIV-1 - drug effects | HIV Reverse Transcriptase - antagonists & inhibitors | Humans | Reverse Transcriptase Inhibitors - pharmacology | Zidovudine - pharmacology | Polyethyleneimine - pharmacology | Hep G2 Cells | Drug Therapy, Combination - methods | Animals | HIV Infections - drug therapy | Lamivudine - pharmacology | Mice | Polyethylene Glycols - pharmacology | Index Medicus | humanized mouse (hu-PBL)HIV model | prodrugs of Zidovudine | Abacavir | Lamivudine
Journal Article
Pharmacology and Therapeutics, ISSN 0163-7258, 02/2015, Volume 146, pp. 120 - 131
Although cancer vaccination has yielded promising results in patients, the objective response rates are low. The right choice of adjuvant might improve the...
Cancer vaccine | Adjuvant | TLR | Poly(I:C) | Poly-ICLC | Anti-tumor immunity | DENDRITIC CELLS | COMBINED IMMUNIZATION | POLYRIBOINOSINIC-POLYRIBOCYTIDYLIC ACID | OVARIAN-CANCER | TOLL-LIKE RECEPTOR-3 | T-CELL RESPONSES | NK CELLS | L-LYSINE | POLYCYTIDYLIC ACID | PHARMACOLOGY & PHARMACY | PHASE-I | Carboxymethylcellulose Sodium - therapeutic use | Polylysine - pharmacology | Carboxymethylcellulose Sodium - analogs & derivatives | Poly I-C - pharmacology | Adjuvants, Immunologic - pharmacology | Polylysine - analogs & derivatives | Cancer Vaccines - pharmacology | Humans | Polylysine - therapeutic use | Cancer Vaccines - therapeutic use | Animals | Carboxymethylcellulose Sodium - pharmacology | Poly I-C - therapeutic use | Adjuvants, Immunologic - therapeutic use | Cancer vaccines
Cancer vaccine | Adjuvant | TLR | Poly(I:C) | Poly-ICLC | Anti-tumor immunity | DENDRITIC CELLS | COMBINED IMMUNIZATION | POLYRIBOINOSINIC-POLYRIBOCYTIDYLIC ACID | OVARIAN-CANCER | TOLL-LIKE RECEPTOR-3 | T-CELL RESPONSES | NK CELLS | L-LYSINE | POLYCYTIDYLIC ACID | PHARMACOLOGY & PHARMACY | PHASE-I | Carboxymethylcellulose Sodium - therapeutic use | Polylysine - pharmacology | Carboxymethylcellulose Sodium - analogs & derivatives | Poly I-C - pharmacology | Adjuvants, Immunologic - pharmacology | Polylysine - analogs & derivatives | Cancer Vaccines - pharmacology | Humans | Polylysine - therapeutic use | Cancer Vaccines - therapeutic use | Animals | Carboxymethylcellulose Sodium - pharmacology | Poly I-C - therapeutic use | Adjuvants, Immunologic - therapeutic use | Cancer vaccines
Journal Article
The Journal of Physiology, ISSN 0022-3751, 01/2009, Volume 587, Issue 2, pp. 363 - 377
Caffeine, a prototypic bitter stimulus, produces several physiological actions on taste receptor cells that include inhibition of K IR and K V potassium...
BITTER STIMULI | PHYSIOLOGY | POTASSIUM CURRENTS | INTRACELLULAR CALCIUM | RECTIFYING K+ CHANNELS | PATCH-CLAMP | TRANSDUCTION | MAMMALIAN TASTE | NEUROSCIENCES | VOLTAGE-DEPENDENT CURRENTS | SWEET TASTANTS | PIP2 | Taste Buds - physiology | Tetradecanoylphorbol Acetate - pharmacology | Male | Phosphatidylinositol 3-Kinases - antagonists & inhibitors | Phospholipase C beta - antagonists & inhibitors | Delayed Rectifier Potassium Channels - physiology | Protein Kinase C - metabolism | Delayed Rectifier Potassium Channels - drug effects | Estrenes - pharmacology | Pyrrolidinones - pharmacology | Phosphatidylinositol Phosphates - pharmacology | Caffeine - pharmacology | Chromones - pharmacology | Taste Buds - drug effects | Polylysine - pharmacology | Serum Albumin, Bovine - pharmacology | Potassium Channels, Inwardly Rectifying - drug effects | Enzyme Inhibitors - pharmacology | Morpholines - pharmacology | Rats | Taste Buds - cytology | Sulfonamides - pharmacology | Taste - physiology | Calcium-Calmodulin-Dependent Protein Kinase Type 2 - antagonists & inhibitors | Phosphatidylinositol 4,5-Diphosphate - antagonists & inhibitors | Rats, Sprague-Dawley | Patch-Clamp Techniques | Animals | Taste - drug effects | Androstadienes - pharmacology | Potassium Channels, Inwardly Rectifying - physiology | Phosphatidylinositol 4,5-Diphosphate - pharmacology | Phosphatidylinositol 4,5-Diphosphate - biosynthesis | Benzylamines - pharmacology | Physiological aspects | Phosphatidylinositol | Serum albumin | Calcium-binding proteins | Protein kinases | Caffeine | Index Medicus | Neuroscience
BITTER STIMULI | PHYSIOLOGY | POTASSIUM CURRENTS | INTRACELLULAR CALCIUM | RECTIFYING K+ CHANNELS | PATCH-CLAMP | TRANSDUCTION | MAMMALIAN TASTE | NEUROSCIENCES | VOLTAGE-DEPENDENT CURRENTS | SWEET TASTANTS | PIP2 | Taste Buds - physiology | Tetradecanoylphorbol Acetate - pharmacology | Male | Phosphatidylinositol 3-Kinases - antagonists & inhibitors | Phospholipase C beta - antagonists & inhibitors | Delayed Rectifier Potassium Channels - physiology | Protein Kinase C - metabolism | Delayed Rectifier Potassium Channels - drug effects | Estrenes - pharmacology | Pyrrolidinones - pharmacology | Phosphatidylinositol Phosphates - pharmacology | Caffeine - pharmacology | Chromones - pharmacology | Taste Buds - drug effects | Polylysine - pharmacology | Serum Albumin, Bovine - pharmacology | Potassium Channels, Inwardly Rectifying - drug effects | Enzyme Inhibitors - pharmacology | Morpholines - pharmacology | Rats | Taste Buds - cytology | Sulfonamides - pharmacology | Taste - physiology | Calcium-Calmodulin-Dependent Protein Kinase Type 2 - antagonists & inhibitors | Phosphatidylinositol 4,5-Diphosphate - antagonists & inhibitors | Rats, Sprague-Dawley | Patch-Clamp Techniques | Animals | Taste - drug effects | Androstadienes - pharmacology | Potassium Channels, Inwardly Rectifying - physiology | Phosphatidylinositol 4,5-Diphosphate - pharmacology | Phosphatidylinositol 4,5-Diphosphate - biosynthesis | Benzylamines - pharmacology | Physiological aspects | Phosphatidylinositol | Serum albumin | Calcium-binding proteins | Protein kinases | Caffeine | Index Medicus | Neuroscience
Journal Article
Antimicrobial Agents and Chemotherapy, ISSN 0066-4804, 06/2005, Volume 49, Issue 6, pp. 2329 - 2335
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Photosensitizing Agents - chemistry | Escherichia coli - drug effects | Porphyrins - chemistry | Photosensitizing Agents - metabolism | Polylysine - chemistry | Candida albicans - metabolism | Porphyrins - metabolism | Candida albicans - growth & development | Rose Bengal - pharmacology | Rose Bengal - metabolism | Microbial Sensitivity Tests | Polylysine - metabolism | Tolonium Chloride - metabolism | Photosensitizing Agents - pharmacology | Rose Bengal - chemistry | Candida albicans - drug effects | Light | Escherichia coli - metabolism | Radiation-Sensitizing Agents - chemistry | Escherichia coli - growth & development | Staphylococcus aureus - metabolism | Polylysine - pharmacology | Radiation-Sensitizing Agents - pharmacology | Porphyrins - pharmacology | Tolonium Chloride - chemistry | Radiation-Sensitizing Agents - metabolism | Tolonium Chloride - pharmacology | Staphylococcus aureus - drug effects | Staphylococcus aureus - growth & development | Mechanisms of Action | Physiological Effects
Photosensitizing Agents - chemistry | Escherichia coli - drug effects | Porphyrins - chemistry | Photosensitizing Agents - metabolism | Polylysine - chemistry | Candida albicans - metabolism | Porphyrins - metabolism | Candida albicans - growth & development | Rose Bengal - pharmacology | Rose Bengal - metabolism | Microbial Sensitivity Tests | Polylysine - metabolism | Tolonium Chloride - metabolism | Photosensitizing Agents - pharmacology | Rose Bengal - chemistry | Candida albicans - drug effects | Light | Escherichia coli - metabolism | Radiation-Sensitizing Agents - chemistry | Escherichia coli - growth & development | Staphylococcus aureus - metabolism | Polylysine - pharmacology | Radiation-Sensitizing Agents - pharmacology | Porphyrins - pharmacology | Tolonium Chloride - chemistry | Radiation-Sensitizing Agents - metabolism | Tolonium Chloride - pharmacology | Staphylococcus aureus - drug effects | Staphylococcus aureus - growth & development | Mechanisms of Action | Physiological Effects
Journal Article
Antimicrobial Agents and Chemotherapy, ISSN 0066-4804, 04/2012, Volume 56, Issue 4, pp. 1756 - 1761
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LISTERIA-MONOCYTOGENES | GARDNERELLA-VAGINALIS | IN-VITRO | DESIGN | BACILLUS-SUBTILIS | VIRUS TYPE-1 EXPRESSION | ANAEROBIC-BACTERIA | MICROBIOLOGY | PHARMACOLOGY & PHARMACY | INFECTION | DRUG-COMBINATION | PREGNANCY | Polylysine - pharmacology | Humans | Bacteria - drug effects | Peptides, Cyclic - pharmacology | Monoglycerides - pharmacology | Arginine - analogs & derivatives | Drug Synergism | Microbial Sensitivity Tests | Lactobacillus - drug effects | Vaginosis, Bacterial - microbiology | Arginine - pharmacology | Bacteriocins - pharmacology | Female | Laurates - pharmacology | Anti-Bacterial Agents - pharmacology | Gardnerella vaginalis - drug effects | Kinetics | Susceptibility
LISTERIA-MONOCYTOGENES | GARDNERELLA-VAGINALIS | IN-VITRO | DESIGN | BACILLUS-SUBTILIS | VIRUS TYPE-1 EXPRESSION | ANAEROBIC-BACTERIA | MICROBIOLOGY | PHARMACOLOGY & PHARMACY | INFECTION | DRUG-COMBINATION | PREGNANCY | Polylysine - pharmacology | Humans | Bacteria - drug effects | Peptides, Cyclic - pharmacology | Monoglycerides - pharmacology | Arginine - analogs & derivatives | Drug Synergism | Microbial Sensitivity Tests | Lactobacillus - drug effects | Vaginosis, Bacterial - microbiology | Arginine - pharmacology | Bacteriocins - pharmacology | Female | Laurates - pharmacology | Anti-Bacterial Agents - pharmacology | Gardnerella vaginalis - drug effects | Kinetics | Susceptibility
Journal Article
Antimicrobial Agents and Chemotherapy, ISSN 0066-4804, 2017, Volume 61, Issue 10
The mammalian and microbial cell selectivity of synthetic and biosynthetic cationic polymers has been investigated. Among the polymers with peptide backbones,...
Antimicrobial activity | Membrane selectivity | Cell selectivity | Rapid bactericidal activity | Cationic polymers | Superior biocompatibility index | Topical bacterial infections | superior biocompatibility index | EFFICACY | cationic polymers | rapid bactericidal activity | BIOFILMS | MICROBIOLOGY | antimicrobial activity | cell selectivity | membrane selectivity | ANTISEPTICS | STRATEGIES | STAPHYLOCOCCUS | PEPTIDES | WOUNDS | RESISTANCE | CHLORHEXIDINE | PHARMACOLOGY & PHARMACY | topical bacterial infections | POVIDONE-IODINE | Cell Line | Polylysine - pharmacology | Rabbits | Staphylococcal Infections - drug therapy | Keratitis - microbiology | Pseudomonas Infections - drug therapy | Humans | Antimicrobial Cationic Peptides - pharmacology | Polyethyleneimine - pharmacology | Aziridines - pharmacology | Pseudomonas aeruginosa - drug effects | Microbial Sensitivity Tests | Animals | Candida albicans - drug effects | Candidiasis - drug therapy | Fibroblasts - drug effects | Allylamine - pharmacology | Polymers - chemistry | Anti-Bacterial Agents - pharmacology | Staphylococcus aureus - drug effects | Keratitis - drug therapy | Cell Membrane - drug effects | Disease Models, Animal
Antimicrobial activity | Membrane selectivity | Cell selectivity | Rapid bactericidal activity | Cationic polymers | Superior biocompatibility index | Topical bacterial infections | superior biocompatibility index | EFFICACY | cationic polymers | rapid bactericidal activity | BIOFILMS | MICROBIOLOGY | antimicrobial activity | cell selectivity | membrane selectivity | ANTISEPTICS | STRATEGIES | STAPHYLOCOCCUS | PEPTIDES | WOUNDS | RESISTANCE | CHLORHEXIDINE | PHARMACOLOGY & PHARMACY | topical bacterial infections | POVIDONE-IODINE | Cell Line | Polylysine - pharmacology | Rabbits | Staphylococcal Infections - drug therapy | Keratitis - microbiology | Pseudomonas Infections - drug therapy | Humans | Antimicrobial Cationic Peptides - pharmacology | Polyethyleneimine - pharmacology | Aziridines - pharmacology | Pseudomonas aeruginosa - drug effects | Microbial Sensitivity Tests | Animals | Candida albicans - drug effects | Candidiasis - drug therapy | Fibroblasts - drug effects | Allylamine - pharmacology | Polymers - chemistry | Anti-Bacterial Agents - pharmacology | Staphylococcus aureus - drug effects | Keratitis - drug therapy | Cell Membrane - drug effects | Disease Models, Animal
Journal Article
Macromolecular Bioscience, ISSN 1616-5187, 09/2014, Volume 14, Issue 9, pp. 1222 - 1238
Wellâdefined amphiphilic polymers of the ABA and ABC type are synthesized, where A is poly(Lâlysine hydrochloride) (PLL), B is poly(Îłâbenzylâ(d7) Lâglutamate)...
nanotechnology | pancreatic cancer | nanoparticles | polymersomes | polypeptides | Nanoparticles | Polypeptides | Pancreatic cancer | Polymersomes | Nanotechnology | MATERIALS SCIENCE, BIOMATERIALS | POLYMER SCIENCE | VESICLES | BIOCHEMISTRY & MOLECULAR BIOLOGY | DOXORUBICIN | MICELLES | NANO | POLYETHYLENIMINATED FUNCTIONAL POLYMERS | IN-VIVO | SYSTEMS | DEGRADABLE CHIMERIC POLYMERSOMES | POLYOXYPROPYLENEDIAMINES | Paclitaxel - pharmacology | Pancreatic Neoplasms - metabolism | Antibiotics, Antineoplastic - pharmacology | Nanoparticles - chemistry | Humans | Polyethylene Glycols - chemistry | Polylysine - chemistry | Doxorubicin - chemistry | Drug Carriers - chemistry | Pancreatic Neoplasms - drug therapy | Polyglutamic Acid - analogs & derivatives | Paclitaxel - chemistry | Polyglutamic Acid - pharmacology | Antibiotics, Antineoplastic - chemistry | Polyethylene Glycols - pharmacology | Polylysine - pharmacology | Pancreatic Neoplasms - pathology | Antineoplastic Agents, Phytogenic - chemistry | Drug Carriers - chemical synthesis | Polyglutamic Acid - chemical synthesis | Drug Carriers - pharmacology | Polyglutamic Acid - chemistry | Polylysine - chemical synthesis | Cell Line, Tumor | Polyethylene Glycols - chemical synthesis | Antineoplastic Agents, Phytogenic - pharmacology | Doxorubicin - pharmacology | Drug Screening Assays, Antitumor | Invertebrates | Index Medicus | Surgical implants | Vesicles | Asymmetry | Hydrochlorides | Biocompatibility | In vitro testing | Polymers | Doxorubicin | Cancer
nanotechnology | pancreatic cancer | nanoparticles | polymersomes | polypeptides | Nanoparticles | Polypeptides | Pancreatic cancer | Polymersomes | Nanotechnology | MATERIALS SCIENCE, BIOMATERIALS | POLYMER SCIENCE | VESICLES | BIOCHEMISTRY & MOLECULAR BIOLOGY | DOXORUBICIN | MICELLES | NANO | POLYETHYLENIMINATED FUNCTIONAL POLYMERS | IN-VIVO | SYSTEMS | DEGRADABLE CHIMERIC POLYMERSOMES | POLYOXYPROPYLENEDIAMINES | Paclitaxel - pharmacology | Pancreatic Neoplasms - metabolism | Antibiotics, Antineoplastic - pharmacology | Nanoparticles - chemistry | Humans | Polyethylene Glycols - chemistry | Polylysine - chemistry | Doxorubicin - chemistry | Drug Carriers - chemistry | Pancreatic Neoplasms - drug therapy | Polyglutamic Acid - analogs & derivatives | Paclitaxel - chemistry | Polyglutamic Acid - pharmacology | Antibiotics, Antineoplastic - chemistry | Polyethylene Glycols - pharmacology | Polylysine - pharmacology | Pancreatic Neoplasms - pathology | Antineoplastic Agents, Phytogenic - chemistry | Drug Carriers - chemical synthesis | Polyglutamic Acid - chemical synthesis | Drug Carriers - pharmacology | Polyglutamic Acid - chemistry | Polylysine - chemical synthesis | Cell Line, Tumor | Polyethylene Glycols - chemical synthesis | Antineoplastic Agents, Phytogenic - pharmacology | Doxorubicin - pharmacology | Drug Screening Assays, Antitumor | Invertebrates | Index Medicus | Surgical implants | Vesicles | Asymmetry | Hydrochlorides | Biocompatibility | In vitro testing | Polymers | Doxorubicin | Cancer
Journal Article
Molecular Pharmaceutics, ISSN 1543-8384, 10/2009, Volume 6, Issue 5, pp. 1562 - 1572
Polymer conjugates of camptothecin (CPT) have been pursued as a solution to the difficulties present in treating cancers with CPT and its derivatives. Covalent...
Camptothecin | Dendrimer | Drug delivery | PEG | Poly(L-lysine) | Colon carcinoma | DRUG-DELIVERY | TUNABLE MOLECULAR-WEIGHT | MACROMOLECULAR THERAPEUTICS | colon carcinoma | poly(L-lysine) | camptothecin | TUMOR-BEARING MICE | dendrimer | PHARMACOLOGY & PHARMACY | LYSINE DENDRIMERS | BOW-TIE HYBRIDS | ADVANCED SOLID MALIGNANCIES | POLYETHYLENE-GLYCOL | PHASE-I | BIOLOGICAL APPLICATIONS | Polylysine - analogs & derivatives | Humans | Camptothecin - chemical synthesis | Tissue Distribution | Female | Molecular Structure | Dendrimers - pharmacology | Camptothecin - analogs & derivatives | Polyethylene Glycols - pharmacology | Camptothecin - pharmacokinetics | Polylysine - pharmacology | Antineoplastic Agents, Phytogenic - chemical synthesis | Dendrimers - pharmacokinetics | Polyethylene Glycols - pharmacokinetics | Dendrimers - chemical synthesis | Drug Carriers - chemical synthesis | Polylysine - pharmacokinetics | Antineoplastic Agents, Phytogenic - toxicity | HT29 Cells | Animals | Mice, Nude | Polylysine - chemical synthesis | Cell Line, Tumor | Mice | Mice, Inbred BALB C | Polyethylene Glycols - chemical synthesis | Antineoplastic Agents, Phytogenic - pharmacology | Camptothecin - pharmacology | Neoplasms, Experimental - drug therapy | Drug Screening Assays, Antitumor | Index Medicus | drug delivery
Camptothecin | Dendrimer | Drug delivery | PEG | Poly(L-lysine) | Colon carcinoma | DRUG-DELIVERY | TUNABLE MOLECULAR-WEIGHT | MACROMOLECULAR THERAPEUTICS | colon carcinoma | poly(L-lysine) | camptothecin | TUMOR-BEARING MICE | dendrimer | PHARMACOLOGY & PHARMACY | LYSINE DENDRIMERS | BOW-TIE HYBRIDS | ADVANCED SOLID MALIGNANCIES | POLYETHYLENE-GLYCOL | PHASE-I | BIOLOGICAL APPLICATIONS | Polylysine - analogs & derivatives | Humans | Camptothecin - chemical synthesis | Tissue Distribution | Female | Molecular Structure | Dendrimers - pharmacology | Camptothecin - analogs & derivatives | Polyethylene Glycols - pharmacology | Camptothecin - pharmacokinetics | Polylysine - pharmacology | Antineoplastic Agents, Phytogenic - chemical synthesis | Dendrimers - pharmacokinetics | Polyethylene Glycols - pharmacokinetics | Dendrimers - chemical synthesis | Drug Carriers - chemical synthesis | Polylysine - pharmacokinetics | Antineoplastic Agents, Phytogenic - toxicity | HT29 Cells | Animals | Mice, Nude | Polylysine - chemical synthesis | Cell Line, Tumor | Mice | Mice, Inbred BALB C | Polyethylene Glycols - chemical synthesis | Antineoplastic Agents, Phytogenic - pharmacology | Camptothecin - pharmacology | Neoplasms, Experimental - drug therapy | Drug Screening Assays, Antitumor | Index Medicus | drug delivery
Journal Article
Human Gene Therapy, ISSN 1043-0342, 08/1996, Volume 7, Issue 12, pp. 1437 - 1446
We have examined the complement-activating properties of synthetic cationic molecules and their complexes with DNA. Commonly used gene delivery vehicles...
DEPENDENT PHAGOCYTOSIS | MEDICINE, RESEARCH & EXPERIMENTAL | CELLS | POLYMERIC IMMUNOGLOBULIN RECEPTOR | K DB BIOTECHNOLOGY & APPLIED MICROBIOLOGY | K KM GENETICS & HEREDITY | THERAPY | INVIVO | TRANSFERRIN | K QA MEDICINE, RESEARCH & EXPERIMENTAL | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | IN-VIVO | PLASMID DNA | GENETICS & HEREDITY | CATIONIC LIPOSOME COMPLEXES | EXPRESSION | Glycine - analogs & derivatives | Fatty Acids, Monounsaturated - pharmacology | Injections, Intravenous | Genetic Vectors - administration & dosage | DNA, Recombinant - administration & dosage | Humans | Polylysine - chemistry | Quaternary Ammonium Compounds - chemistry | Glycine - chemistry | Cations - pharmacology | DNA, Recombinant - chemical synthesis | Fatty Acids, Monounsaturated - chemistry | Complement Activation - drug effects | Spermine - analogs & derivatives | Gene Transfer Techniques | Polylysine - pharmacology | Cations - chemistry | Genetic Vectors - chemistry | Spermine - chemistry | Phospholipids - chemistry | Phospholipids - pharmacology | Liposomes - chemistry | Animals | Genetic Vectors - pharmacology | Glycine - pharmacology | Phosphatidylethanolamines - pharmacology | Spermine - pharmacology | DNA, Recombinant - pharmacology | Sheep - blood | Phosphatidylethanolamines - chemistry | Quaternary Ammonium Compounds - pharmacology
DEPENDENT PHAGOCYTOSIS | MEDICINE, RESEARCH & EXPERIMENTAL | CELLS | POLYMERIC IMMUNOGLOBULIN RECEPTOR | K DB BIOTECHNOLOGY & APPLIED MICROBIOLOGY | K KM GENETICS & HEREDITY | THERAPY | INVIVO | TRANSFERRIN | K QA MEDICINE, RESEARCH & EXPERIMENTAL | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | IN-VIVO | PLASMID DNA | GENETICS & HEREDITY | CATIONIC LIPOSOME COMPLEXES | EXPRESSION | Glycine - analogs & derivatives | Fatty Acids, Monounsaturated - pharmacology | Injections, Intravenous | Genetic Vectors - administration & dosage | DNA, Recombinant - administration & dosage | Humans | Polylysine - chemistry | Quaternary Ammonium Compounds - chemistry | Glycine - chemistry | Cations - pharmacology | DNA, Recombinant - chemical synthesis | Fatty Acids, Monounsaturated - chemistry | Complement Activation - drug effects | Spermine - analogs & derivatives | Gene Transfer Techniques | Polylysine - pharmacology | Cations - chemistry | Genetic Vectors - chemistry | Spermine - chemistry | Phospholipids - chemistry | Phospholipids - pharmacology | Liposomes - chemistry | Animals | Genetic Vectors - pharmacology | Glycine - pharmacology | Phosphatidylethanolamines - pharmacology | Spermine - pharmacology | DNA, Recombinant - pharmacology | Sheep - blood | Phosphatidylethanolamines - chemistry | Quaternary Ammonium Compounds - pharmacology
Journal Article
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Effect of functionalization of multilayered polyelectrolyte films on motoneuron growth
Biomaterials, ISSN 0142-9612, 2005, Volume 26, Issue 5, pp. 545 - 554
We studied in vitro cell-substrate interaction of motoneurons with functionalized polylectrolyte films. Thin polylectrolyte films were built on glass by...
Surface modification | Bioactivity | Growth factors | Nerve regeneration | Cell spreading | THIN-FILMS | MATERIALS SCIENCE, BIOMATERIALS | growth factors | ENGINEERING, BIOMEDICAL | surface modification | DEPOSITION | cell spreading | GUIDANCE | ADSORPTION | LAYERS | SEMAPHORINS | MOLECULES | IN-VITRO | bioactivity | CHONDROSARCOMA CELLS | nerve regeneration | SURFACES | Anions - pharmacology | Humans | DNA, Complementary - genetics | Nanostructures | Kidney | Brain-Derived Neurotrophic Factor - pharmacology | Polyglutamic Acid - pharmacology | Transfection | Neurites - ultrastructure | Motor Neurons - cytology | Microscopy, Atomic Force | Spinal Cord - cytology | Motor Neurons - drug effects | Semaphorin-3A - genetics | Polylysine - pharmacology | Cell Culture Techniques - instrumentation | Cells, Cultured | Semaphorin-3A - pharmacology | Materials Testing | Polyethyleneimine - pharmacology | Cell Adhesion - drug effects | Sulfonic Acids - pharmacology | Semaphorin-3A - administration & dosage | Brain-Derived Neurotrophic Factor - administration & dosage | Tissue Engineering - instrumentation | Polyamines - pharmacology | Animals | Image Processing, Computer-Assisted | Spectrum Analysis - methods | Polymers - pharmacology | Electrolytes - pharmacology | Mice
Surface modification | Bioactivity | Growth factors | Nerve regeneration | Cell spreading | THIN-FILMS | MATERIALS SCIENCE, BIOMATERIALS | growth factors | ENGINEERING, BIOMEDICAL | surface modification | DEPOSITION | cell spreading | GUIDANCE | ADSORPTION | LAYERS | SEMAPHORINS | MOLECULES | IN-VITRO | bioactivity | CHONDROSARCOMA CELLS | nerve regeneration | SURFACES | Anions - pharmacology | Humans | DNA, Complementary - genetics | Nanostructures | Kidney | Brain-Derived Neurotrophic Factor - pharmacology | Polyglutamic Acid - pharmacology | Transfection | Neurites - ultrastructure | Motor Neurons - cytology | Microscopy, Atomic Force | Spinal Cord - cytology | Motor Neurons - drug effects | Semaphorin-3A - genetics | Polylysine - pharmacology | Cell Culture Techniques - instrumentation | Cells, Cultured | Semaphorin-3A - pharmacology | Materials Testing | Polyethyleneimine - pharmacology | Cell Adhesion - drug effects | Sulfonic Acids - pharmacology | Semaphorin-3A - administration & dosage | Brain-Derived Neurotrophic Factor - administration & dosage | Tissue Engineering - instrumentation | Polyamines - pharmacology | Animals | Image Processing, Computer-Assisted | Spectrum Analysis - methods | Polymers - pharmacology | Electrolytes - pharmacology | Mice
Journal Article