Sustained-release hydrogels of topotecan for retinoblastoma

TAICH, PAULA; MORETTON, MARCELA; DEL SOLE, MARÍA JOSÉ; WINTER, ÚRSULA; BERNABEU, EZEQUIEL; CROXATTO, OSCAR; OPEZZO, JAVIER; WILLIAMS, GUSTAVO; CHANTADA, GUILLERMO; CHIAPPETTA, DIEGO; SCHAIQUEVICH, PAULA SUSANA

COLLOIDS AND SURFACES B-BIOINTERFACES

ELSEVIER SCIENCE BV

Lugar: Amsterdam; Año: 2016 vol. 146 p. 624 - 631

0927-7765

Treatment of retinoblastoma, the most common primary ocular malignancy inchildren, has greatly improved over the last decade. Still, new devices forchemotherapy are needed to achieve better tumor control. The aim of this projectwas to develop an ocular drug delivery system for topotecan (TPT) loaded inbiocompatible hydrogels of poly(ε-caprolactone)-poly(ethyleneglycol)-poly(ε-caprolactone) block copolymers (PCL-PEG-PCL) for sustained TPT release in thevitreous humor.Hydrogels were prepared from TPT and synthesized PCL-PEG-PCL copolymers.Rheological properties and in vitro and in vivo TPT release were studied. Hydrogel cytotoxicity was evaluated in retinoblastoma cells as a surrogate for efficacy and TPT vitreous pharmacokinetics and systemic as well as ocular toxicity were evaluated in rabbits. The pseudoplastic behavior of the hydrogels makes them suitable for intraocular administration. In vitro release profiles showed a sustained release of TPT from PCL-PEG-PCL up to 7 days and drug loading did not affect the release pattern. Blank hydrogels did not affect retinoblastoma cell viability but 0.4%(w/w) TPT-loaded hydrogel was highly cytotoxic for at least 7 days. After intravitreal injection, TPT vitreous concentrations were sustained above the pharmacologically active concentration. One month after injection, animals with blank or TPT-loaded hydrogels showed no systemic toxicity or retinal impairment on fundus examination, electroretinographic, and histopathological assessments. These novel TPT-hydrogels can deliver sustained concentrations of active drug into the vitreous with excellent biocompatibility in vivo and pronounced cytotoxic activity in retinoblastoma cells and may become an additional strategy for intraocular retinoblastoma treatment.