Lupi A, Perugini P, Genta I, Modena T, Conti B, Casado B, Cetta G, Pavanetto F, Iadarola P
Department of Biochemistry "A. Castellani", University of Pavia, V.le Taramelli 3/B, 27100 Pavia, Italy.
J Pharm Pharmacol. 2004 May;56(5):597-603. doi: 10.1211/0022357023349.
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.
脯氨酰寡肽酶缺乏症(PD)是一种罕见的常染色体隐性疾病,由胞质外肽酶脯氨酰寡肽酶(E.C. 3.4.13.9)水平不足引起,目前尚无根治方法。我们研究了负载脯氨酰寡肽酶的可生物降解微球是否能在细胞内释放活性酶,以考虑将该系统作为脯氨酰寡肽酶缺乏症的一种可能治疗方法。制备了聚(丙交酯-共-乙交酯)微球,改进了经典的双乳液溶剂蒸发法以减轻酶从微球中的突释效应。通过将微囊化的脯氨酰寡肽酶与来自PD患者和对照的培养成纤维细胞孵育进行体外实验,以确定递送至细胞的活性酶量。所述的微粒药物递送系统在成纤维细胞内携带少量活性脯氨酰寡肽酶,确保对X-脯氨酸二肽的细胞内积累作出反应,该机制被认为是导致人类这种疾病临床表现发展的原因。细胞内存在活性酶的一个积极结果是成纤维细胞形态得到改善。