Journal of Pharmacy and Pharmacology. VOLUME 48 1996 SUBJECT INDEX

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Journal of Pharmacy and Pharmacology. VOLUME 48 1996 SUBJECT INDEX

Auteurs :

Source :

• Journal of Pharmacy and Pharmacology [ 0022-3573 ] ; 1996-12.

RBID : ISTEX:DC2CB750207C5C2B0BFE76D2E14A8021151F6A6F

English descriptors

• Teeft :
  • Abdominal constriction, Absorption enhancers, Acetylcholinesterase inhibition, Adenosine receptor antagonist, Aerosol propellent suspensions, Alanine aminotransferase, Albumin mrna, Amino acids, Analogue, Antagonist, Antibacterial activity, Anticonvulsant activity, Antidiarrhoeal activity, Antihypertensive drugs, Antimicrobial activity, Antinociceptive activity, Antistaphylococcal effect, Antithrombotic activity, Antitumour activity, Antitussive activity, Antiviral activity, Arginine vasopressin, Arginine vasopressin analogues, Aspartate aminotransferase, Atopic dermatitis, Bead products, Benzoic acid, Biliary excretion, Bioavailability, Biodegradable implants, Biological activity, Biological fluids, Blood levels, Blood pressure, Blood pressure control, Bothropsjararaca venom, Brain surgery, Buccal patches, Bunitrolol enantiomers, Bupivacaine kinetics, Butylated hydroxyanisole, Caffeine concentration, Calcium channel blockers, Calcium movement, Calcium polycarbophil, Calcium sources, Candida albicans, Carbopol polymers, Cardiac muscles, Cardiovascular effects, Cephalosporin sugar interactions, Cerebrospinal fluid, Cetiedil enantiomers, Chinese medicines, Cholinesterase inhibitors, Cinnamoyl derivatives, Circadian variation, Cisplatin, Cisplatin treatment, Cissampelos sympodialis eichl, Collagen degradation, Collagen peptides, Colloidal bismuth subcitrate, Coronary arteries, Coronary dilator derivatives, Cough potentiation, Coumarin binding, Cyclosporin, Cytoprotective mechanism, Dapsone, Dapsone analogues, Dapsone metabolite, Decomposition kinetics, Deferens, Derivative, Diabetes mellitus, Diclofenac, Diclofenac disposition, Diclofenac sodium, Dipeptoid mimetics, Dizocilpine enantiomers, Drug aggregates, Drug delivery, Enantiomer, Endothelial cell permeability, Energy analysis, Erythropoietin synthesis, Eschericha coli, Excretion, Fatty acids, Fatty alcohols, Foetal sera, Fragmentation pathway, Frequency distribution, Fructose intolerance, Furanpropanoic acid, Gaba release, Gall bladder, Gastrointestinal tract, Glycyrrhetic acid, Hallux abduct0 valgus, Heckel analysis, Heparin fragment, Hepatic growth factor, Heterotheca inuloides, Hplc determinations, Human erythrocytes, Human lymphocytes, Human polymorphonuclear function, Human response, Human serum albumin, Human skin, Human synovial tissues, Hydrophilic matrix, Hypercholesterolaemic rabbits, Hyperthyroid rats, Hypolipaemic drugs, Ibuproxam derivatives, Immunological detection, Immunopharmacological activity, Immunosorbent assay, Immunosuppressive activity, Incorporating fluorescein, Indomethacin, Industrial view, Inhibition, Inhibitor, Interactive mixtures, Interleukin, Interleukin production, Intestinal, Intestinal absorption, Intestinal bbmv, Intestinal secretion, Intrapulmonary investigation, Intravenous magnolol, Irreversible opioid antagonists, Isopropyl myristate, Kinetics, Leukocyte migration, Lipid microspheres, Lipid peroxidation, Liposome, Liver failure, Liver microsomes, Local tolerance, Lyase activity, Lysosomal enzymes, Magnetizable support beads, Medical aerosols, Membrane emulsification, Metabolism, Methadone withdrawal, Methyl parahydroxybenzoate, Microbicidal activity, Microcapsule injection, Microdialysis, Microsomal debromination, Microsomal metabolism, Microspheres, Molecular characterization, Molecular modelling, Monoamine oxidase inhibitors, Monophasic release, Mouse brain, Mucosal epithelial cells, Myocardial cells, Nanc bronchoconstriction, Naproxen, Nasal products, Nasal transport, Neonate piglets, Neostriatal dopamine, Neostriatal release, Neural network simulation, Neurosedative effects, Nicorandil treatment, Nicotinic acid, Nicotinic receptor antagonists, Niosomal plumbagin, Nitric oxide donors, Nitrofurantoin suspensions, Nucleic acids, Ocular bioavailability, Ocular drug delivery, Oestrogen receptors, Oral bioavailability, Oral cavity, Organophosphorus compounds, Osteotropic drug delivery, Oxidative metabolism, Palmitoyl carnitine, Palmitoyl carnitine derivatives, Paracetamol, Paracetamol overdose, Peptide, Peptide hormones, Percutaneous delivery, Perfused, Peritoneal transport, Permeability, Permeation, Pharmacokinetics, Pharmacy view, Phosphatidylcholine secretion, Phosphoglycerate kinase inhibitors, Phospholipid affinity, Phyllanthus, Phyllanthus caroliniensis, Phyllanthus urinaria, Physicochemical properties, Pilocarpine prodrug, Piperonyl butoxide, Platelet, Platelet aggregation, Poly acid copolymers, Polyethylene glycols, Portal vein contractile force, Powder plug formation, Preformulation studies, Preservative efficacy tests, Pressor responses, Pulmonary catabolism, Purinoceptor antagonists, Pyridine derivatives, Qsar study, Rabbit aorta, Rabbit colon, Rat, Rauwolfia ligustrina, Receptor, Receptor antagonist, Rectal irritation, Relaxant effect, Renal, Renal accumulation, Renal haemodynamics, Renal transplant patients, Renal uptake kinetics, Resistance profiles, Rotary tablet press, Salicylate disposition, Saturable function, Scalp hair, Scoparia dulcis, Screening cytochrome, Sickingia williamsii, Signal transduction mechanisms, Silver ions, Smoker rats, Snake skin, Spasmolytic action, Stability properties, Staphylococcus aureus, Stereospecific synthesis, Striatal slices, Subcellular distribution, Subcutaneous injections, Subject index, Sucrose laurate, Sulphonamidobenzophenone oximes, Sulphonylurea preparations, Surfactant effect, Synovial tissues, Tagetes patula, Tetrahydroprotoberberine alkaloids, Thioperamide protein binding, Thromboxane receptor antagonist, Thromboxane synthetase inhibitor, Toxicodynamic analysis, Transdermal, Transdermal absorption, Transdermal drug delivery, Triamcinolone acetonide, Tricyclic antidepressants, Triiodothyronine clearance, Unbound serum valproic acid concentration, Unilamellar liposomes, Urinary excretion profile, Uterine relaxation, Uterus, Vanilloid receptor, Warfarin binding, Xanthone derivatives.

Url:

• https://api.istex.fr/ark:/67375/WNG-BLVMR8ML-G/fulltext.pdf

DOI: 10.1111/j.2042-7158.1996.tb03925.x

Affiliations:

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