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Synthesis, physico-chemical properties and biomedical applications of poly(amidoamine)s

Identifieur interne : 001428 ( Main/Exploration ); précédent : 001427; suivant : 001429

Synthesis, physico-chemical properties and biomedical applications of poly(amidoamine)s

Auteurs : Paolo Ferruti [Italie] ; Maria Antonietta Marchisio [Italie] ; Rolando Barbucci [Italie]

Source :

RBID : ISTEX:E310A840734F8AF05E6F6147580A354D1FB0413F

English descriptors

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


Affiliations:


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Le document en format XML

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<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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