Synthesis, physico-chemical properties and biomedical applications of poly(amidoamine)s
Identifieur interne : 001432 ( Main/Merge ); précédent : 001431; suivant : 001433Synthesis, physico-chemical properties and biomedical applications of poly(amidoamine)s
Auteurs : Paolo Ferruti [Italie] ; Maria Antonietta Marchisio [Italie] ; Rolando Barbucci [Italie]Source :
- Polymer [ 0032-3861 ] ; 1985.
English descriptors
- Teeft :
- Amido groups, Amine, Aminic, Aminic groups, Aminic nitrogens, Amino, Amino acids, Amino nitrogens, Ammonium salts, Aqueous media, Aqueous solution, August, Average charge, Barbucci, Barone, Basic nitrogens, Basic strength, Basicity, Basicity constants, Bertoglio riolo, Biomedical, Biomedical applications, Carbonyl groups, Casolaro, Catalytic activity, Catalytic power, Chem, Chemical applications, Complex formation, Conference issue, Conformational freedom, Conformational transition, Contact time, Corresponding models, Crosslinked, Crosslinking, Crosslinking agent, Crosslinking agents, Crosslinking units, Dacron, Ferruti, First group, First protonation, Form complexes, Further reactions, Heavy metal ions, Heparin, Heparinization studies, Large extent, Last step, Linear polymer, Linear polymers, Linear portion, Linear portions, Macromolecular chain, Macromolecule, Main chain, Metal ions, Monomeric units, N2ll, Naoh, Other hand, Other words, Pergamon press, Phosphate buffer, Polym, Polymer, Polymer acts, Polymeric, Polymeric amines, Polymerization process, Practical applications, Previous study, Protamine sulphate, Protonation, Protonation constants, Protonation enthalpies, Reaction steps, Resin, Results show, Retentive power, Same monomeric unit, Second group, Second protonation, Side substituents, Similar results, Spectrophotometric measurements, Stability constants, Substantial independence, Tertiary, Various materials, Viscosimetric titrations, Whole macromolecule.
Abstract
The aim of this article is to provide a comprehensive survey on synthesis, chemical and physico-chemical properties, and applications in several fields, including the biomedical field, of a family of tertiary amino polymers, the poly(amido-amine)s.
Url:
DOI: 10.1016/0032-3861(85)90309-X
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<profileDesc><textClass><keywords scheme="Teeft" xml:lang="en"><term>Amido groups</term>
<term>Amine</term>
<term>Aminic</term>
<term>Aminic groups</term>
<term>Aminic nitrogens</term>
<term>Amino</term>
<term>Amino acids</term>
<term>Amino nitrogens</term>
<term>Ammonium salts</term>
<term>Aqueous media</term>
<term>Aqueous solution</term>
<term>August</term>
<term>Average charge</term>
<term>Barbucci</term>
<term>Barone</term>
<term>Basic nitrogens</term>
<term>Basic strength</term>
<term>Basicity</term>
<term>Basicity constants</term>
<term>Bertoglio riolo</term>
<term>Biomedical</term>
<term>Biomedical applications</term>
<term>Carbonyl groups</term>
<term>Casolaro</term>
<term>Catalytic activity</term>
<term>Catalytic power</term>
<term>Chem</term>
<term>Chemical applications</term>
<term>Complex formation</term>
<term>Conference issue</term>
<term>Conformational freedom</term>
<term>Conformational transition</term>
<term>Contact time</term>
<term>Corresponding models</term>
<term>Crosslinked</term>
<term>Crosslinking</term>
<term>Crosslinking agent</term>
<term>Crosslinking agents</term>
<term>Crosslinking units</term>
<term>Dacron</term>
<term>Ferruti</term>
<term>First group</term>
<term>First protonation</term>
<term>Form complexes</term>
<term>Further reactions</term>
<term>Heavy metal ions</term>
<term>Heparin</term>
<term>Heparinization studies</term>
<term>Large extent</term>
<term>Last step</term>
<term>Linear polymer</term>
<term>Linear polymers</term>
<term>Linear portion</term>
<term>Linear portions</term>
<term>Macromolecular chain</term>
<term>Macromolecule</term>
<term>Main chain</term>
<term>Metal ions</term>
<term>Monomeric units</term>
<term>N2ll</term>
<term>Naoh</term>
<term>Other hand</term>
<term>Other words</term>
<term>Pergamon press</term>
<term>Phosphate buffer</term>
<term>Polym</term>
<term>Polymer</term>
<term>Polymer acts</term>
<term>Polymeric</term>
<term>Polymeric amines</term>
<term>Polymerization process</term>
<term>Practical applications</term>
<term>Previous study</term>
<term>Protamine sulphate</term>
<term>Protonation</term>
<term>Protonation constants</term>
<term>Protonation enthalpies</term>
<term>Reaction steps</term>
<term>Resin</term>
<term>Results show</term>
<term>Retentive power</term>
<term>Same monomeric unit</term>
<term>Second group</term>
<term>Second protonation</term>
<term>Side substituents</term>
<term>Similar results</term>
<term>Spectrophotometric measurements</term>
<term>Stability constants</term>
<term>Substantial independence</term>
<term>Tertiary</term>
<term>Various materials</term>
<term>Viscosimetric titrations</term>
<term>Whole macromolecule</term>
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<front><div type="abstract" xml:lang="en">The aim of this article is to provide a comprehensive survey on synthesis, chemical and physico-chemical properties, and applications in several fields, including the biomedical field, of a family of tertiary amino polymers, the poly(amido-amine)s.</div>
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