Psychopharmacology, ISSN 0033-3158, 12/2017, Volume 234, Issue 23, pp. 3507 - 3520
Racemic (RS)-amisulpride (Solian®) is an atypical antipsychotic drug used to treat schizophrenia and dysthymia. Blockade of dopamine D2/D3 and/or serotonin...
Drug discrimination | Neurosciences | Amisulpride | Schizophrenia | Isomers | Anxiolytics | Discriminative stimulus | Antipsychotics | Biomedicine | Antidepressants | C57BL/6 mice | Benzamides | Pharmacology/Toxicology | Psychiatry | CORTICAL MEMBRANES | PSYCHIATRY | HIGH-AFFINITY | MAJOR DEPRESSION | D-2 RECEPTORS | NEUROSCIENCES | RECEPTOR ANTAGONIST | LIMBIC SELECTIVITY | 5-HT7 RECEPTOR | PHARMACOLOGY & PHARMACY | MOLECULAR-CLONING | RAT-BRAIN | DOPAMINE-RECEPTORS | Sulpiride - pharmacology | Conditioning, Operant - physiology | Male | Sulpiride - analogs & derivatives | Clozapine - pharmacology | Discrimination Learning - drug effects | Clozapine - chemistry | Conditioning, Operant - drug effects | Antidepressive Agents - chemistry | Anti-Anxiety Agents - chemistry | Antidepressive Agents - pharmacology | Benzamides - pharmacology | Quetiapine Fumarate - pharmacology | Benzamides - chemistry | Quetiapine Fumarate - chemistry | Mice, Inbred C57BL | Chlorpromazine - chemistry | Risperidone - pharmacology | Anti-Anxiety Agents - pharmacology | Chlorpromazine - pharmacology | Risperidone - chemistry | Discrimination Learning - physiology | Animals | Antipsychotic Agents - chemistry | Mice | Antipsychotic Agents - pharmacology | Sulpiride - chemistry | Dosage and administration | Antipsychotic drugs | Comparative analysis | Drug interactions | Antianxiety agents | Stereoisomers | Drugs | Neuroleptics | Olanzapine | Operant conditioning | Mental disorders | Aripiprazole | Benzamide | Metoclopramide | Chlorpromazine | Sulpiride | Serotonin S7 receptors | Psychotropic drugs | Imipramine | Receptors | Bupropion | Mianserin | Risperidone | Dopamine D2 receptors | Drug dosages | Quetiapine | Raclopride | Dopamine | Serotonin | Dopamine D3 receptors | Chlordiazepoxide | Pharmacology | Clozapine | Derivatives | Properties (attributes) | Serotonin receptors
Drug discrimination | Neurosciences | Amisulpride | Schizophrenia | Isomers | Anxiolytics | Discriminative stimulus | Antipsychotics | Biomedicine | Antidepressants | C57BL/6 mice | Benzamides | Pharmacology/Toxicology | Psychiatry | CORTICAL MEMBRANES | PSYCHIATRY | HIGH-AFFINITY | MAJOR DEPRESSION | D-2 RECEPTORS | NEUROSCIENCES | RECEPTOR ANTAGONIST | LIMBIC SELECTIVITY | 5-HT7 RECEPTOR | PHARMACOLOGY & PHARMACY | MOLECULAR-CLONING | RAT-BRAIN | DOPAMINE-RECEPTORS | Sulpiride - pharmacology | Conditioning, Operant - physiology | Male | Sulpiride - analogs & derivatives | Clozapine - pharmacology | Discrimination Learning - drug effects | Clozapine - chemistry | Conditioning, Operant - drug effects | Antidepressive Agents - chemistry | Anti-Anxiety Agents - chemistry | Antidepressive Agents - pharmacology | Benzamides - pharmacology | Quetiapine Fumarate - pharmacology | Benzamides - chemistry | Quetiapine Fumarate - chemistry | Mice, Inbred C57BL | Chlorpromazine - chemistry | Risperidone - pharmacology | Anti-Anxiety Agents - pharmacology | Chlorpromazine - pharmacology | Risperidone - chemistry | Discrimination Learning - physiology | Animals | Antipsychotic Agents - chemistry | Mice | Antipsychotic Agents - pharmacology | Sulpiride - chemistry | Dosage and administration | Antipsychotic drugs | Comparative analysis | Drug interactions | Antianxiety agents | Stereoisomers | Drugs | Neuroleptics | Olanzapine | Operant conditioning | Mental disorders | Aripiprazole | Benzamide | Metoclopramide | Chlorpromazine | Sulpiride | Serotonin S7 receptors | Psychotropic drugs | Imipramine | Receptors | Bupropion | Mianserin | Risperidone | Dopamine D2 receptors | Drug dosages | Quetiapine | Raclopride | Dopamine | Serotonin | Dopamine D3 receptors | Chlordiazepoxide | Pharmacology | Clozapine | Derivatives | Properties (attributes) | Serotonin receptors
Journal Article
Chemical Communications, ISSN 1359-7345, 2015, Volume 51, Issue 41, pp. 8618 - 8621
To understand the structural basis for the Na+-sensitivity of ligand binding to dopamine D2-like receptors, using computational analysis in combination with...
Journal Article
Chemical Communications, ISSN 1359-7345, 05/2015, Volume 51, Issue 41, pp. 8618 - 8621
To understand the structural basis for the Na+-sensitivity of ligand binding to dopamine D2-like receptors, using computational analysis in combination with...
SODIUM-BINDING | ANTAGONIST | INHIBITION | AFFINITY | MEMBRANE | BINDING-SITE CREVICE | PROTEIN-COUPLED RECEPTORS | ALLOSTERIC MODULATION | RESIDUES | CHEMISTRY, MULTIDISCIPLINARY | PIVOTAL ROLE | Sodium - pharmacology | Sulpiride - pharmacology | Sodium - chemistry | Protein Conformation - drug effects | Receptors, Dopamine D3 - chemistry | Receptors, Dopamine D3 - metabolism | Structure-Activity Relationship | Receptors, Dopamine D2 - metabolism | Molecular Dynamics Simulation | Dose-Response Relationship, Drug | Dopamine Antagonists - pharmacology | Salicylamides - chemistry | Receptors, Dopamine D2 - chemistry | Ligands | Benzamides - pharmacology | Molecular Structure | Receptors, Dopamine D3 - antagonists & inhibitors | Dopamine Antagonists - chemistry | Salicylamides - pharmacology | Sulpiride - chemistry | Binding Sites - drug effects | Benzamides - chemistry
SODIUM-BINDING | ANTAGONIST | INHIBITION | AFFINITY | MEMBRANE | BINDING-SITE CREVICE | PROTEIN-COUPLED RECEPTORS | ALLOSTERIC MODULATION | RESIDUES | CHEMISTRY, MULTIDISCIPLINARY | PIVOTAL ROLE | Sodium - pharmacology | Sulpiride - pharmacology | Sodium - chemistry | Protein Conformation - drug effects | Receptors, Dopamine D3 - chemistry | Receptors, Dopamine D3 - metabolism | Structure-Activity Relationship | Receptors, Dopamine D2 - metabolism | Molecular Dynamics Simulation | Dose-Response Relationship, Drug | Dopamine Antagonists - pharmacology | Salicylamides - chemistry | Receptors, Dopamine D2 - chemistry | Ligands | Benzamides - pharmacology | Molecular Structure | Receptors, Dopamine D3 - antagonists & inhibitors | Dopamine Antagonists - chemistry | Salicylamides - pharmacology | Sulpiride - chemistry | Binding Sites - drug effects | Benzamides - chemistry
Journal Article
Colloids and Surfaces B: Biointerfaces, ISSN 0927-7765, 11/2016, Volume 147, pp. 250 - 257
The aim of this study was to assess the effect of -α-tocopheryl polyethylene glycol 1000 succinate (TPGS) on the physicochemical characterization and oral...
Oral absorption | l-sulpiride | Quaternary microcapsule | d-α-tocopheryl polyethylene glycol 1000 succinate | Administered drug dose | L-sulpiride | D-α-tocopheryl polyethylene glycol 1000 succinate | D-alpha-tocopheryl polyethylene glycol 1000 | MATERIALS SCIENCE, BIOMATERIALS | BIOPHARMACEUTICS CLASSIFICATION-SYSTEM | DRUG-DELIVERY SYSTEM | CHEMISTRY, PHYSICAL | VITAMIN-E TPGS | succinate | SOLID LIPID NANOPARTICLES | INTESTINAL-ABSORPTION | SOLUBLE DRUG | BIOPHYSICS | MODEL-DRUG | PARTICLE-SIZE | IN-VIVO EVALUATION | AQUEOUS SOLUBILITY | Povidone - administration & dosage | Surface-Active Agents | Polymers - administration & dosage | Administration, Oral | Solubility | Drug Carriers - administration & dosage | Rats | Biological Availability | Capsules - chemistry | Male | Sulpiride - administration & dosage | Sulpiride - pharmacokinetics | Rats, Sprague-Dawley | Drug Carriers - chemistry | Drug Delivery Systems | Tissue Distribution | Povidone - chemistry | Animals | Sodium Dodecyl Sulfate - chemistry | Vitamin E - administration & dosage | Polymers - chemistry | Vitamin E - chemistry | Sulpiride - chemistry | Sodium Dodecyl Sulfate - administration & dosage | Drugstores | Pharmacy | Polyethylene glycol | Polyols | Carriers | Carriers, Drug | Drugs | Solvents | Absorption | Bioavailability
Oral absorption | l-sulpiride | Quaternary microcapsule | d-α-tocopheryl polyethylene glycol 1000 succinate | Administered drug dose | L-sulpiride | D-α-tocopheryl polyethylene glycol 1000 succinate | D-alpha-tocopheryl polyethylene glycol 1000 | MATERIALS SCIENCE, BIOMATERIALS | BIOPHARMACEUTICS CLASSIFICATION-SYSTEM | DRUG-DELIVERY SYSTEM | CHEMISTRY, PHYSICAL | VITAMIN-E TPGS | succinate | SOLID LIPID NANOPARTICLES | INTESTINAL-ABSORPTION | SOLUBLE DRUG | BIOPHYSICS | MODEL-DRUG | PARTICLE-SIZE | IN-VIVO EVALUATION | AQUEOUS SOLUBILITY | Povidone - administration & dosage | Surface-Active Agents | Polymers - administration & dosage | Administration, Oral | Solubility | Drug Carriers - administration & dosage | Rats | Biological Availability | Capsules - chemistry | Male | Sulpiride - administration & dosage | Sulpiride - pharmacokinetics | Rats, Sprague-Dawley | Drug Carriers - chemistry | Drug Delivery Systems | Tissue Distribution | Povidone - chemistry | Animals | Sodium Dodecyl Sulfate - chemistry | Vitamin E - administration & dosage | Polymers - chemistry | Vitamin E - chemistry | Sulpiride - chemistry | Sodium Dodecyl Sulfate - administration & dosage | Drugstores | Pharmacy | Polyethylene glycol | Polyols | Carriers | Carriers, Drug | Drugs | Solvents | Absorption | Bioavailability
Journal Article
Drug Development and Industrial Pharmacy, ISSN 0363-9045, 09/2017, Volume 43, Issue 9, pp. 1530 - 1538
Objective: The aim of the current investigation was at enhancing the oral biopharmaceutical behavior; solubility and intestinal permeability of amisulpride...
Amisulpride | non-everted gut sac model | bioenhancers | ex vivo permeability testing | self-nanoemulsifying | ternary phase diagrams | DESIGN | CHEMISTRY, MEDICINAL | SNEDDS | TRANSDERMAL DELIVERY | EXCIPIENTS | ORAL ABSORPTION | DISSOLUTION | PHARMACOLOGY & PHARMACY | Administration, Oral | Emulsions - chemistry | Solubility | Biological Availability | Polyethylene Glycols - chemistry | Sulpiride - administration & dosage | Permeability | Chemistry, Pharmaceutical | Particle Size | Sulpiride - analogs & derivatives | Excipients - chemistry | Ethylene Glycols - chemistry | Drug Liberation | Surface-Active Agents - chemistry | Ethylene Glycols - administration & dosage | Drug Delivery Systems - methods | Sulpiride - chemistry | Intestinal Absorption - physiology
Amisulpride | non-everted gut sac model | bioenhancers | ex vivo permeability testing | self-nanoemulsifying | ternary phase diagrams | DESIGN | CHEMISTRY, MEDICINAL | SNEDDS | TRANSDERMAL DELIVERY | EXCIPIENTS | ORAL ABSORPTION | DISSOLUTION | PHARMACOLOGY & PHARMACY | Administration, Oral | Emulsions - chemistry | Solubility | Biological Availability | Polyethylene Glycols - chemistry | Sulpiride - administration & dosage | Permeability | Chemistry, Pharmaceutical | Particle Size | Sulpiride - analogs & derivatives | Excipients - chemistry | Ethylene Glycols - chemistry | Drug Liberation | Surface-Active Agents - chemistry | Ethylene Glycols - administration & dosage | Drug Delivery Systems - methods | Sulpiride - chemistry | Intestinal Absorption - physiology
Journal Article
Drug Development and Industrial Pharmacy, ISSN 0363-9045, 09/2017, Volume 43, Issue 9, pp. 1539 - 1547
Objective: The current investigation is focused on the formulation and in vivo evaluation of optimized solid self-nanoemulsifying drug delivery systems...
pharmacokinetics | Nanoemulsions | tableting | solid-state characterization | solid self-nanoemulsifying drug delivery systems | VITRO | IMPROVE | CHEMISTRY, MEDICINAL | FORMULATION | PLASMA | DISSOLUTION | WATER-SOLUBLE DRUGS | ORAL BIOAVAILABILITY | DOUBLE-BLIND | PHARMACOLOGY & PHARMACY | DRUG-DELIVERY SYSTEMS | IN-VIVO EVALUATION | Rabbits | Administration, Oral | Emulsions - chemistry | Tablets - pharmacokinetics | Biological Availability | Polyethylene Glycols - chemistry | Ethylene Glycols - pharmacokinetics | Sulpiride - administration & dosage | Sulpiride - pharmacokinetics | Chemistry, Pharmaceutical | Drug Carriers | Particle Size | Sulpiride - analogs & derivatives | Animals | Ethylene Glycols - chemistry | Tablets - chemistry | Surface-Active Agents - chemistry | Ethylene Glycols - administration & dosage | Drug Delivery Systems - methods | Sulpiride - chemistry
pharmacokinetics | Nanoemulsions | tableting | solid-state characterization | solid self-nanoemulsifying drug delivery systems | VITRO | IMPROVE | CHEMISTRY, MEDICINAL | FORMULATION | PLASMA | DISSOLUTION | WATER-SOLUBLE DRUGS | ORAL BIOAVAILABILITY | DOUBLE-BLIND | PHARMACOLOGY & PHARMACY | DRUG-DELIVERY SYSTEMS | IN-VIVO EVALUATION | Rabbits | Administration, Oral | Emulsions - chemistry | Tablets - pharmacokinetics | Biological Availability | Polyethylene Glycols - chemistry | Ethylene Glycols - pharmacokinetics | Sulpiride - administration & dosage | Sulpiride - pharmacokinetics | Chemistry, Pharmaceutical | Drug Carriers | Particle Size | Sulpiride - analogs & derivatives | Animals | Ethylene Glycols - chemistry | Tablets - chemistry | Surface-Active Agents - chemistry | Ethylene Glycols - administration & dosage | Drug Delivery Systems - methods | Sulpiride - chemistry
Journal Article
ACS Chemical Neuroscience, ISSN 1948-7193, 07/2017, Volume 8, Issue 7, pp. 1543 - 1553
Neuroleptic drugs are widely applied in effective treatment of schizophrenia and related disorders. The lipophilic character of neuroleptics means that they...
calorimetry | drug-membrane interactions | Neuroleptics | liposomes | ζ potential | EPR | PLASMA-MEMBRANES | CHEMISTRY, MEDICINAL | BIOCHEMISTRY & MOLECULAR BIOLOGY | drug membrane interactions | zeta potential | BLOOD-BRAIN-BARRIER | NEUROSCIENCES | LIPID-BILAYERS | CHLORPROMAZINE INTERACTION | ANTIPSYCHOTIC-DRUGS | TITRATION CALORIMETRY | RAT-BRAIN | WATER PENETRATION | PHOSPHOLIPID-BILAYERS | HYDROPHOBIC BARRIER | Protons | Sulpiride - pharmacology | Benzodiazepines - pharmacology | Electron Spin Resonance Spectroscopy | Models, Chemical | Membranes, Artificial | Phosphatidylcholines - chemistry | Sulpiride - analogs & derivatives | Thermodynamics | Phosphatidylglycerols - chemistry | Antipsychotic Agents - chemistry | Thioridazine - pharmacology | Water - chemistry | Benzodiazepines - chemistry | Thioridazine - chemistry | Calorimetry | Molecular Structure | Antipsychotic Agents - pharmacology | Sulpiride - chemistry | Dynamic Light Scattering
calorimetry | drug-membrane interactions | Neuroleptics | liposomes | ζ potential | EPR | PLASMA-MEMBRANES | CHEMISTRY, MEDICINAL | BIOCHEMISTRY & MOLECULAR BIOLOGY | drug membrane interactions | zeta potential | BLOOD-BRAIN-BARRIER | NEUROSCIENCES | LIPID-BILAYERS | CHLORPROMAZINE INTERACTION | ANTIPSYCHOTIC-DRUGS | TITRATION CALORIMETRY | RAT-BRAIN | WATER PENETRATION | PHOSPHOLIPID-BILAYERS | HYDROPHOBIC BARRIER | Protons | Sulpiride - pharmacology | Benzodiazepines - pharmacology | Electron Spin Resonance Spectroscopy | Models, Chemical | Membranes, Artificial | Phosphatidylcholines - chemistry | Sulpiride - analogs & derivatives | Thermodynamics | Phosphatidylglycerols - chemistry | Antipsychotic Agents - chemistry | Thioridazine - pharmacology | Water - chemistry | Benzodiazepines - chemistry | Thioridazine - chemistry | Calorimetry | Molecular Structure | Antipsychotic Agents - pharmacology | Sulpiride - chemistry | Dynamic Light Scattering
Journal Article
AAPS PharmSciTech, ISSN 1530-9932, 4/2017, Volume 18, Issue 3, pp. 654 - 670
In this study, an optimized epichlorohydrin-crosslinked semi-interpenetrating polymer network xerogel matrix system (XePoMas) for the controlled delivery of...
Biochemistry, general | xerogel matrix | Biotechnology | semi-interpenetrating polymer network | Biomedicine | bioavailability | Pharmacy | gellan gum | Pharmacology/Toxicology | poly(ethylene oxide) | sulpiride | CONTROLLED DRUG-DELIVERY | INTESTINAL-ABSORPTION | MATRIX TABLETS | SYSTEMS | PHARMACOLOGY & PHARMACY | CELL | RELEASE KINETICS | Polysaccharides, Bacterial - chemistry | Chemistry, Pharmaceutical - methods | Administration, Oral | Biological Availability | Delayed-Action Preparations - chemistry | Polyethylene Glycols - chemistry | Epichlorohydrin - metabolism | Drug Liberation - drug effects | Delayed-Action Preparations - metabolism | Epichlorohydrin - chemistry | Animals | Swine | Polymers - chemistry | Drug Delivery Systems - methods | Sulpiride - chemistry | Sulpiride - metabolism | Drugs | Polysaccharides | Drug delivery systems | Analysis | Epoxy resins | Ethylene oxide | Vehicles
Biochemistry, general | xerogel matrix | Biotechnology | semi-interpenetrating polymer network | Biomedicine | bioavailability | Pharmacy | gellan gum | Pharmacology/Toxicology | poly(ethylene oxide) | sulpiride | CONTROLLED DRUG-DELIVERY | INTESTINAL-ABSORPTION | MATRIX TABLETS | SYSTEMS | PHARMACOLOGY & PHARMACY | CELL | RELEASE KINETICS | Polysaccharides, Bacterial - chemistry | Chemistry, Pharmaceutical - methods | Administration, Oral | Biological Availability | Delayed-Action Preparations - chemistry | Polyethylene Glycols - chemistry | Epichlorohydrin - metabolism | Drug Liberation - drug effects | Delayed-Action Preparations - metabolism | Epichlorohydrin - chemistry | Animals | Swine | Polymers - chemistry | Drug Delivery Systems - methods | Sulpiride - chemistry | Sulpiride - metabolism | Drugs | Polysaccharides | Drug delivery systems | Analysis | Epoxy resins | Ethylene oxide | Vehicles
Journal Article
European Journal of Pharmaceutical Sciences, ISSN 0928-0987, 12/2018, Volume 125, pp. 102 - 109
Three types of ionically crosslinked (with citric acid) chitosan discs were loaded with the highly water- soluble drug, sodium salicylate (SS) and the poorly...
Triggered erosion | Synchronized release rates | Dual drug platform | Multifactorial definitive screening design | Crosslinked chitosan | VITRO | SULPIRIDE | CANCER | DELIVERY | IN-VIVO ANALYSIS | MATRICES | PHARMACOLOGY & PHARMACY | ABSORPTION | Salicylic Acid - chemistry | Citric Acid - chemistry | Chitosan - chemistry | Cross-Linking Reagents - chemistry | Drug Design | Drug Liberation | Indomethacin - chemistry | Hydrogels - chemistry | Drug Delivery Systems | Crosslinked polymers | Indomethacin | Analysis | Citric acid | Calcium chloride
Triggered erosion | Synchronized release rates | Dual drug platform | Multifactorial definitive screening design | Crosslinked chitosan | VITRO | SULPIRIDE | CANCER | DELIVERY | IN-VIVO ANALYSIS | MATRICES | PHARMACOLOGY & PHARMACY | ABSORPTION | Salicylic Acid - chemistry | Citric Acid - chemistry | Chitosan - chemistry | Cross-Linking Reagents - chemistry | Drug Design | Drug Liberation | Indomethacin - chemistry | Hydrogels - chemistry | Drug Delivery Systems | Crosslinked polymers | Indomethacin | Analysis | Citric acid | Calcium chloride
Journal Article
Journal of Pharmacological Sciences, ISSN 1347-8613, 02/2017, Volume 133, Issue 2, pp. 110 - 113
We previously demonstrated that (CTS), a traditional herbal formula called medicine, improves diabetes-induced cognitive deficits. In the present study, we...
Monoamine | Chotosan | Antidepressants | DEMENTIA | AMELIORATION | GEISSOSCHIZINE METHYL-ETHER | PHARMACOLOGY & PHARMACY | ANIMAL-MODEL | YOKUKANSAN | RECEPTORS | BRAIN | COGNITIVE DEFICITS | Ketanserin - pharmacology | Sulpiride - pharmacology | Pyridines - chemistry | Ketanserin - chemistry | Metergoline - chemistry | Drugs, Chinese Herbal - pharmacology | Male | Piperazines - chemistry | Imipramine - chemistry | Piperazines - pharmacology | Yohimbine - chemistry | Locomotion | Animals | Serotonin Agents - pharmacology | Dopamine Agents - pharmacology | Fenclonine - chemistry | Antidepressive Agents - pharmacology | Mice | Pyridines - pharmacology | Swimming | Imipramine - pharmacology | Medicine, Kampo | Sulpiride - chemistry | Disease Models, Animal | Care and treatment | Medicine, Botanic | Patient outcomes | Depression, Mental | Serotoninergic mechanisms | Medicine, Herbal | Dopaminergic mechanisms | Health aspects | Methods
Monoamine | Chotosan | Antidepressants | DEMENTIA | AMELIORATION | GEISSOSCHIZINE METHYL-ETHER | PHARMACOLOGY & PHARMACY | ANIMAL-MODEL | YOKUKANSAN | RECEPTORS | BRAIN | COGNITIVE DEFICITS | Ketanserin - pharmacology | Sulpiride - pharmacology | Pyridines - chemistry | Ketanserin - chemistry | Metergoline - chemistry | Drugs, Chinese Herbal - pharmacology | Male | Piperazines - chemistry | Imipramine - chemistry | Piperazines - pharmacology | Yohimbine - chemistry | Locomotion | Animals | Serotonin Agents - pharmacology | Dopamine Agents - pharmacology | Fenclonine - chemistry | Antidepressive Agents - pharmacology | Mice | Pyridines - pharmacology | Swimming | Imipramine - pharmacology | Medicine, Kampo | Sulpiride - chemistry | Disease Models, Animal | Care and treatment | Medicine, Botanic | Patient outcomes | Depression, Mental | Serotoninergic mechanisms | Medicine, Herbal | Dopaminergic mechanisms | Health aspects | Methods
Journal Article
Journal of Pharmaceutical and Biomedical Analysis, ISSN 0731-7085, 02/2014, Volume 89, pp. 111 - 117
We report an effective and a quantitative analysis method for one of pharmaceuticals, sulpiride, in river water by online solid phase extraction (SPE)...
Solid phase extraction | Interval recognition | Pharmaceutical | Molecular imprinting | Sulpiride | MULTIPLE PHARMACEUTICALS | CHEMISTRY, ANALYTICAL | PERSONAL CARE PRODUCTS | FEATHER MEAL | REENTRY | LIQUID-CHROMATOGRAPHY | DRUGS | SURFACE | PREVIOUSLY UNRECOGNIZED ROUTE | PHARMACOLOGY & PHARMACY | CATALYSTS | SOLID-PHASE EXTRACTION | Chromatography, High Pressure Liquid - methods | Solvents - chemistry | Water Pollutants, Chemical - chemistry | Fresh Water - chemistry | Water Pollutants, Chemical - analysis | Molecular Imprinting - methods | Adsorption | Rivers - chemistry | Solid Phase Extraction - methods | Polymers - chemistry | Fresh Water - analysis | Chromatography, Liquid - methods | Mass Spectrometry - methods | Sulpiride - chemistry | Polymers | Polymer industry | Usage | Analysis | Nitriles | Liquid chromatography | Mass spectrometry
Solid phase extraction | Interval recognition | Pharmaceutical | Molecular imprinting | Sulpiride | MULTIPLE PHARMACEUTICALS | CHEMISTRY, ANALYTICAL | PERSONAL CARE PRODUCTS | FEATHER MEAL | REENTRY | LIQUID-CHROMATOGRAPHY | DRUGS | SURFACE | PREVIOUSLY UNRECOGNIZED ROUTE | PHARMACOLOGY & PHARMACY | CATALYSTS | SOLID-PHASE EXTRACTION | Chromatography, High Pressure Liquid - methods | Solvents - chemistry | Water Pollutants, Chemical - chemistry | Fresh Water - chemistry | Water Pollutants, Chemical - analysis | Molecular Imprinting - methods | Adsorption | Rivers - chemistry | Solid Phase Extraction - methods | Polymers - chemistry | Fresh Water - analysis | Chromatography, Liquid - methods | Mass Spectrometry - methods | Sulpiride - chemistry | Polymers | Polymer industry | Usage | Analysis | Nitriles | Liquid chromatography | Mass spectrometry
Journal Article
Therapeutic Drug Monitoring, ISSN 0163-4356, 2017, Volume 39, Issue 2, pp. 109 - 117
Background: There is a poor correlation between total concentrations of proton-accepting compounds (most basic drugs) in unstimulated oral fluid and in plasma....
Amisulpride | Oral fluid | Plasma:oral fluid distribution | Clozapine | TDM | METABOLITES | SERUM | MS/MS | SALIVA | WHOLE-BLOOD | amisulpride | ANTIPSYCHOTICS | plasma:oral fluid distribution | oral fluid | DRUGS | clozapine | PHARMACOLOGY & PHARMACY | TOXICOLOGY | MEDICAL LABORATORY TECHNOLOGY | BINDING | Antipsychotic Agents - blood | Humans | Middle Aged | Body Fluids - chemistry | Male | Clozapine - analogs & derivatives | Drug Monitoring - methods | Mouth - chemistry | Sulpiride - analogs & derivatives | Young Adult | Tandem Mass Spectrometry | Antipsychotic Agents - chemistry | Clozapine - chemistry | Plasma - chemistry | Adult | Female | Aged | Clozapine - blood | Chromatography, Liquid - methods | Sulpiride - chemistry | Sulpiride - blood | Index Medicus
Amisulpride | Oral fluid | Plasma:oral fluid distribution | Clozapine | TDM | METABOLITES | SERUM | MS/MS | SALIVA | WHOLE-BLOOD | amisulpride | ANTIPSYCHOTICS | plasma:oral fluid distribution | oral fluid | DRUGS | clozapine | PHARMACOLOGY & PHARMACY | TOXICOLOGY | MEDICAL LABORATORY TECHNOLOGY | BINDING | Antipsychotic Agents - blood | Humans | Middle Aged | Body Fluids - chemistry | Male | Clozapine - analogs & derivatives | Drug Monitoring - methods | Mouth - chemistry | Sulpiride - analogs & derivatives | Young Adult | Tandem Mass Spectrometry | Antipsychotic Agents - chemistry | Clozapine - chemistry | Plasma - chemistry | Adult | Female | Aged | Clozapine - blood | Chromatography, Liquid - methods | Sulpiride - chemistry | Sulpiride - blood | Index Medicus
Journal Article
AAPS PharmSciTech, ISSN 1530-9932, 8/2018, Volume 19, Issue 6, pp. 2658 - 2671
Amisulpride (AMS) is an atypical antipsychotic agent used for the treatment of schizophrenia. The effect of different variables, i.e., the type of...
Biochemistry, general | Biotechnology | amisulpride | Biomedicine | liposomes | Pharmacy | Pharmacology/Toxicology | atypical antipsychotic | double loading | cyclodextrins | SYSTEM | MEMBRANE CONTACTOR | DRUG-DELIVERY | STABILITY | SCHIZOPHRENIA | RELEASE | RECEPTOR ANTAGONIST | CYCLODEXTRIN COMPLEXES | INTEGRITY | LIMBIC SELECTIVITY | PHARMACOLOGY & PHARMACY | 2-Hydroxypropyl-beta-cyclodextrin - metabolism | Rats, Wistar | Tablets | Amisulpride | Drug Carriers - administration & dosage | Biological Availability | Male | Sulpiride - administration & dosage | Drug Carriers - chemistry | Sulpiride - analogs & derivatives | Drug Liberation - physiology | Drug Evaluation, Preclinical - methods | Drug Carriers - metabolism | beta-Cyclodextrins - metabolism | Rats | 2-Hydroxypropyl-beta-cyclodextrin - administration & dosage | Antipsychotic Agents - administration & dosage | Particle Size | Animals | Antipsychotic Agents - chemistry | beta-Cyclodextrins - chemistry | 2-Hydroxypropyl-beta-cyclodextrin - chemistry | Antipsychotic Agents - metabolism | Liposomes | Sulpiride - chemistry | Sulpiride - metabolism
Biochemistry, general | Biotechnology | amisulpride | Biomedicine | liposomes | Pharmacy | Pharmacology/Toxicology | atypical antipsychotic | double loading | cyclodextrins | SYSTEM | MEMBRANE CONTACTOR | DRUG-DELIVERY | STABILITY | SCHIZOPHRENIA | RELEASE | RECEPTOR ANTAGONIST | CYCLODEXTRIN COMPLEXES | INTEGRITY | LIMBIC SELECTIVITY | PHARMACOLOGY & PHARMACY | 2-Hydroxypropyl-beta-cyclodextrin - metabolism | Rats, Wistar | Tablets | Amisulpride | Drug Carriers - administration & dosage | Biological Availability | Male | Sulpiride - administration & dosage | Drug Carriers - chemistry | Sulpiride - analogs & derivatives | Drug Liberation - physiology | Drug Evaluation, Preclinical - methods | Drug Carriers - metabolism | beta-Cyclodextrins - metabolism | Rats | 2-Hydroxypropyl-beta-cyclodextrin - administration & dosage | Antipsychotic Agents - administration & dosage | Particle Size | Animals | Antipsychotic Agents - chemistry | beta-Cyclodextrins - chemistry | 2-Hydroxypropyl-beta-cyclodextrin - chemistry | Antipsychotic Agents - metabolism | Liposomes | Sulpiride - chemistry | Sulpiride - metabolism
Journal Article
AAPS PharmSciTech, ISSN 1865-1372, 10/2014, Volume 15, Issue 5, pp. 1292 - 1306
The current study involved the development of a novel sustained release crosslinked semi-IPN xerogel matrix tablet prepared by chemical crosslinking of...
Biochemistry, general | Biotechnology | semi-interpenetrating polymer network | Biomedicine | epichlorohydrin | sustained release | Pharmacy | matrix tablet | Pharmacology/Toxicology | sulpiride | GELLAN GUM | BEHAVIOR | POLYMER ELECTROLYTES | MECHANICAL-PROPERTIES | GRANULES | TABLETS | PHARMACOLOGY & PHARMACY | DRUG-DELIVERY SYSTEMS | WATER | Polysaccharides, Bacterial - chemistry | Excipients | Powders | Cross-Linking Reagents - chemistry | Hardness Tests | Solubility | Polyethylene Glycols - chemistry | Sulpiride - administration & dosage | Chemistry, Pharmaceutical | Antipsychotic Agents - administration & dosage | Epichlorohydrin - chemistry | Algorithms | Antipsychotic Agents - chemistry | Delayed-Action Preparations | Sulpiride - chemistry | Drugs | Polysaccharides | Drug delivery systems | Crosslinked polymers | Epoxy resins | Electron microscopy | Vehicles
Biochemistry, general | Biotechnology | semi-interpenetrating polymer network | Biomedicine | epichlorohydrin | sustained release | Pharmacy | matrix tablet | Pharmacology/Toxicology | sulpiride | GELLAN GUM | BEHAVIOR | POLYMER ELECTROLYTES | MECHANICAL-PROPERTIES | GRANULES | TABLETS | PHARMACOLOGY & PHARMACY | DRUG-DELIVERY SYSTEMS | WATER | Polysaccharides, Bacterial - chemistry | Excipients | Powders | Cross-Linking Reagents - chemistry | Hardness Tests | Solubility | Polyethylene Glycols - chemistry | Sulpiride - administration & dosage | Chemistry, Pharmaceutical | Antipsychotic Agents - administration & dosage | Epichlorohydrin - chemistry | Algorithms | Antipsychotic Agents - chemistry | Delayed-Action Preparations | Sulpiride - chemistry | Drugs | Polysaccharides | Drug delivery systems | Crosslinked polymers | Epoxy resins | Electron microscopy | Vehicles
Journal Article
Science of the Total Environment, ISSN 0048-9697, 10/2015, Volume 530-531, pp. 434 - 444
Attenuation of pharmaceuticals due to natural sunlight is expected to be an important removal pathway in wastewater treatment plants using treatment lagoon...
Transformation products | High-resolution mass spectrometry | Sewage | Lagoon | Photolysis | Pharmaceuticals | ENVIRONMENTAL SCIENCES | REMOVAL | WASTE-WATER | PHOTODEGRADATION | CARBAMAZEPINE | MICROPOLLUTANTS | Desipramine - analysis | Sulpiride - analogs & derivatives | Environmental Monitoring | Sulpiride - analysis | Antidepressive Agents - analysis | Desipramine - chemistry | Waste Water - chemistry | Antidepressive Agents - chemistry | Water Pollutants, Chemical - chemistry | Water Pollutants, Chemical - analysis | Sulpiride - chemistry | Purification | Wastewater | Mass spectrometry | Antidepressants, Tricyclic | Index Medicus | Miljövetenskap | Environmental Sciences
Transformation products | High-resolution mass spectrometry | Sewage | Lagoon | Photolysis | Pharmaceuticals | ENVIRONMENTAL SCIENCES | REMOVAL | WASTE-WATER | PHOTODEGRADATION | CARBAMAZEPINE | MICROPOLLUTANTS | Desipramine - analysis | Sulpiride - analogs & derivatives | Environmental Monitoring | Sulpiride - analysis | Antidepressive Agents - analysis | Desipramine - chemistry | Waste Water - chemistry | Antidepressive Agents - chemistry | Water Pollutants, Chemical - chemistry | Water Pollutants, Chemical - analysis | Sulpiride - chemistry | Purification | Wastewater | Mass spectrometry | Antidepressants, Tricyclic | Index Medicus | Miljövetenskap | Environmental Sciences
Journal Article
16.
Full Text
Efficacy of surface charge in targeting pegylated nanoparticles of sulpiride to the brain
European Journal of Pharmaceutics and Biopharmaceutics, ISSN 0939-6411, 2010, Volume 74, Issue 3, pp. 442 - 450
The objective of the study was to formulate sulpiride-loaded nanoparticles (NPs) that can improve bioretention and achieve dose reduction by passively...
Nanoparticles | Surface charge | Adsorption | Microscopy | Pegylation | Albumin | Cationized bovine serum albumin | CNS | Drug targeting | Sulpiride | Blood–brain barrier | DRUG | BARRIER | DELIVERY | Blood-brain barrier | PHARMACOLOGY & PHARMACY | Injections, Intravenous | Nanoparticles - chemistry | Male | Polyethylene Glycols - chemistry | Sulpiride - administration & dosage | Drug Carriers - chemistry | Brain - metabolism | Tissue Distribution | Cattle | Maleimides - chemical synthesis | Surface Properties | Drug Compounding | Serum Albumin, Bovine - chemistry | Microscopy, Electron, Scanning | Sulpiride - urine | Rats | Sulpiride - pharmacokinetics | Rats, Sprague-Dawley | Brain - drug effects | Particle Size | Polyesters - chemistry | Animals | Polyethylene Glycols - chemical synthesis | Maleimides - chemistry | Drug Delivery Systems - methods | Sulpiride - blood
Nanoparticles | Surface charge | Adsorption | Microscopy | Pegylation | Albumin | Cationized bovine serum albumin | CNS | Drug targeting | Sulpiride | Blood–brain barrier | DRUG | BARRIER | DELIVERY | Blood-brain barrier | PHARMACOLOGY & PHARMACY | Injections, Intravenous | Nanoparticles - chemistry | Male | Polyethylene Glycols - chemistry | Sulpiride - administration & dosage | Drug Carriers - chemistry | Brain - metabolism | Tissue Distribution | Cattle | Maleimides - chemical synthesis | Surface Properties | Drug Compounding | Serum Albumin, Bovine - chemistry | Microscopy, Electron, Scanning | Sulpiride - urine | Rats | Sulpiride - pharmacokinetics | Rats, Sprague-Dawley | Brain - drug effects | Particle Size | Polyesters - chemistry | Animals | Polyethylene Glycols - chemical synthesis | Maleimides - chemistry | Drug Delivery Systems - methods | Sulpiride - blood
Journal Article