Data di Pubblicazione:
2004
Abstract:
Prolidase deficiency (PD) is a rare autosomal recessive disorder caused by inadequate levels of the
cytosolic exopeptidase prolidase (E.C. 3.4.13.9), for which there is not, as yet, a resolutive cure. We have
investigated whether biodegradable microspheres loaded with prolidase could release active enzyme
inside cells, to consider this system as a possible therapeutic approach for prolidase deficiency.
Poly(lactide-co-glycolide) microspheres were prepared,modifying the classical double emulsion solvent
evaporation method to mitigate the burst effect of the enzyme from the microspheres. Ex-vivo
experiments were performed, by incubating microencapsulated prolidase with cultured fibroblasts
from PD patients and from controls, to determine the amount of active enzyme delivered to the cells.
The microparticulate drug delivery system described carried small amounts of active prolidase inside
fibroblasts, ensuring a response to the intracellular accumulation of X-Pro dipeptides, the mechanism
that is supposed to be responsible for the development of clinical manifestations of this disorder in
man. A positive result of the presence of active enzyme inside cells was an improvement in fibroblast
shape.
cytosolic exopeptidase prolidase (E.C. 3.4.13.9), for which there is not, as yet, a resolutive cure. We have
investigated whether biodegradable microspheres loaded with prolidase could release active enzyme
inside cells, to consider this system as a possible therapeutic approach for prolidase deficiency.
Poly(lactide-co-glycolide) microspheres were prepared,modifying the classical double emulsion solvent
evaporation method to mitigate the burst effect of the enzyme from the microspheres. Ex-vivo
experiments were performed, by incubating microencapsulated prolidase with cultured fibroblasts
from PD patients and from controls, to determine the amount of active enzyme delivered to the cells.
The microparticulate drug delivery system described carried small amounts of active prolidase inside
fibroblasts, ensuring a response to the intracellular accumulation of X-Pro dipeptides, the mechanism
that is supposed to be responsible for the development of clinical manifestations of this disorder in
man. A positive result of the presence of active enzyme inside cells was an improvement in fibroblast
shape.
Tipologia CRIS:
1.1 Articolo in rivista
Keywords:
PROLIDASE; ENZYME; BIODEGRADABLE POLYMERS
Elenco autori:
Lupi, ANNA LISA; Perugini, Paola; Genta, Ida; Modena, Tiziana; Conti, Bice; B., Casado; Cetta, Giuseppe; Pavanetto, Franca; Iadarola, Paolo
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