TY - JOUR
T1 - Polyanionic Biopolymers for the Delivery of Pt(II) Cationic Antiproliferative Complexes
AU - Ravera, Mauro
AU - Gabano, Elisabetta
AU - Zanellato, Ilaria
AU - Perin, Elena
AU - Arrais, Aldo
AU - Osella, Domenico
N1 - Publisher Copyright:
© 2016 Mauro Ravera et al.
PY - 2016
Y1 - 2016
N2 - Phenanthriplatin, that is, (SP-4-3)-diamminechlorido(phenanthridine)platinum(II) nitrate, an effective antitumor cationic Pt(II) complex, was loaded on negatively charged dextran sulfate (DS) as a model vector for drug delivery via electrostatic interactions. The free complex and the corresponding conjugate with DS were tested on two standard human tumor cell lines, namely, ovarian A2780 and colon HCT 116, and on several malignant pleural mesothelioma cell lines (namely, epithelioid BR95, mixed/biphasic MG06, sarcomatoid MM98, and sarcomatoid cisplatin-resistant MM98R). The in vitro results suggest that the conjugate releases the active metabolite phenanthriplatin with a biphasic fashion. In these experimental conditions, the conjugate is slightly less active than free phenanthriplatin; but both exhibited antiproliferative potency higher than the reference metallodrug cisplatin and were able to overcome the acquired cisplatin chemoresistance in MM98R cells.
AB - Phenanthriplatin, that is, (SP-4-3)-diamminechlorido(phenanthridine)platinum(II) nitrate, an effective antitumor cationic Pt(II) complex, was loaded on negatively charged dextran sulfate (DS) as a model vector for drug delivery via electrostatic interactions. The free complex and the corresponding conjugate with DS were tested on two standard human tumor cell lines, namely, ovarian A2780 and colon HCT 116, and on several malignant pleural mesothelioma cell lines (namely, epithelioid BR95, mixed/biphasic MG06, sarcomatoid MM98, and sarcomatoid cisplatin-resistant MM98R). The in vitro results suggest that the conjugate releases the active metabolite phenanthriplatin with a biphasic fashion. In these experimental conditions, the conjugate is slightly less active than free phenanthriplatin; but both exhibited antiproliferative potency higher than the reference metallodrug cisplatin and were able to overcome the acquired cisplatin chemoresistance in MM98R cells.
UR - http://www.scopus.com/inward/record.url?scp=84991369094&partnerID=8YFLogxK
U2 - 10.1155/2016/2380540
DO - 10.1155/2016/2380540
M3 - Article
SN - 1565-3633
VL - 2016
JO - Bioinorganic Chemistry and Applications
JF - Bioinorganic Chemistry and Applications
M1 - 2380540
ER -