Zoledronic acid, a new highly potent 3rd generation aminobisphosphonate, is the drug currently used to prevent bone resorption in patients with bone metastases. Moreover, ZOL is a potent inducer of apoptosis in several cancer cell types, suggesting a direct anti-cancer activity that may affect a broad range of tumours. However, the rapid elimination from plasma with the rapid uptake and accumulation within bone hampers the direct anti-cancer activity of ZOL in vivo. On the other hand, long circulating nanocarriers offer the opportunity to change pharmacokinetics of encapsulated drugs, targeting tissues with an increased permeability of the vessels (e.g. tumors). In this study, we proposed two different strategies in order to avoid ZOL accumulation into the bone and address the drug toward tumors. In particular, we designed and developed long circulating liposomes and self-assembly PEGylated nanoparticles for the delivery of ZOL into solid tumors.
NANOTECHNOLOGIES TO USE ZOLEDRONIC ACID AS A POTENT ANTITUMORAL AGENT / Salzano, Giuseppina; M., Marra; C., Leonetti; M., Porru; S., Zappavigna; A., Abbruzzese; LA ROTONDA, MARIA IMMACOLATA; M., Caraglia; DE ROSA, Giuseppe. - In: JOURNAL OF DRUG DELIVERY SCIENCE AND TECHNOLOGY. - ISSN 1773-2247. - STAMPA. - 21:3(2011), pp. 283-284.
NANOTECHNOLOGIES TO USE ZOLEDRONIC ACID AS A POTENT ANTITUMORAL AGENT
SALZANO, GIUSEPPINA;LA ROTONDA, MARIA IMMACOLATA;DE ROSA, GIUSEPPE
2011
Abstract
Zoledronic acid, a new highly potent 3rd generation aminobisphosphonate, is the drug currently used to prevent bone resorption in patients with bone metastases. Moreover, ZOL is a potent inducer of apoptosis in several cancer cell types, suggesting a direct anti-cancer activity that may affect a broad range of tumours. However, the rapid elimination from plasma with the rapid uptake and accumulation within bone hampers the direct anti-cancer activity of ZOL in vivo. On the other hand, long circulating nanocarriers offer the opportunity to change pharmacokinetics of encapsulated drugs, targeting tissues with an increased permeability of the vessels (e.g. tumors). In this study, we proposed two different strategies in order to avoid ZOL accumulation into the bone and address the drug toward tumors. In particular, we designed and developed long circulating liposomes and self-assembly PEGylated nanoparticles for the delivery of ZOL into solid tumors.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.