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Int J Pharm ; 224(1-2): 185-99, 2001 Aug 14.
Artigo em Inglês | MEDLINE | ID: mdl-11472828

RESUMO

A new polysoap, quaternary ammonium palmitoyl glycol chitosan (GCPQ, M(w)=178,000 g mole(-1)) with drug solubilising potential has been synthesised and characterised. In solution hydrophobic domains of GCPQ polymeric micelles were identified by the hypsochromic shift in the lambda(max) of methyl orange and by the increase in the ratio of the fluorescence emission intensity of the third and first pyrene vibronic peaks (I(3)/I(1)). At high aqueous concentrations (>10 mg ml(-1)) GCPQ presents as a gel which solubilises pyrene (2.5 mM, normal solubility in water approximately 2 microM) on probe sonication. Dilution of the gel to a liquid solution of polymeric micelles (< or =3.75 mg ml(-1) of GCPQ), results in the observation of fluorescent pyrene excimers (excited dimers) and a high excimer to monomer fluorescence ratio (I(E)/I(M)). However, attempts to solubilise pyrene at a concentration of 2.5 mM in a liquid solution of GCPQ (3.75 mg ml(-1)) results in a reduced I(E)/I(M) value and pyrene precipitation. Viscometry measurements show a more compact conformation for the polymer solubilising pyrene than the polymer alone. The polymer is non-haemolytic when present as the liquid solution and relatively non cytotoxic. In conclusion, a new biocompatible polysoap (potential drug solubiliser) is described which forms hydrophobic domains in solution and shows hysteresis in its solubilisation of pyrene.


Assuntos
Quitina/análogos & derivados , Quitina/química , Quitosana , Sistemas de Liberação de Medicamentos , Compostos de Amônio Quaternário/química , Compostos Azo/metabolismo , Linhagem Celular , Quitina/síntese química , Quitina/toxicidade , Corantes Fluorescentes/metabolismo , Indicadores e Reagentes/metabolismo , Espectroscopia de Ressonância Magnética , Modelos Químicos , Estrutura Molecular , Peso Molecular , Pirenos/metabolismo , Espectrometria de Fluorescência
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