A study concerning the feasibility of microsphere use as sustained delivery systems for N(6)-cyclopentyladenosine (CPA) administration has been performed. The release of this drug and the related stability effects in human whole blood have been tested. Moreover, the impact of the delivery system on CPA interaction toward human adenosine A1 receptor and the related cellular responses has been analyzed. The microspheres were prepared by an emulsion-solvent evaporation method using poly(lactic acid). Free and encapsulated CPA was incubated in fresh blood and the drug stability was analyzed with HPLC. The affinity of CPA to human A1 receptor expressed by CHO cells was obtained by binding experiments. Activity was evaluated by measurements of the inhibition of forskolin-stimulated 3',5'-cyclic adenosine monophosphate (c-AMP) performing competitive binding assays. Encapsulated CPA was released within 72 h and its degradation in blood was negligible. Affinity and activity values of CPA obtained in the absence and in the presence of unloaded microspheres were the same. CPA encapsulation in microspheres allows its sustained release and its stabilization in human whole blood to be obtained. The presence of this release system does not interfere with the CPA activity at its action site.
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|Anno di pubblicazione:||2001|
|Titolo:||Poly(lactic acid) microspheres for the sustained release of a selective A1 receptor agonist|
|Autori:||A. DAL PIAZ; A. SCATTURIN; B. PAVAN; C. BIONDI; M.A. VANDELLI; F. FORNI|
|Autori interni:||VANDELLI, Maria Angela |
|Rivista:||JOURNAL OF CONTROLLED RELEASE|
|Appare nelle tipologie:||Articolo su rivista|
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