Development of thermosensitive chitosan/glicerophospate injectablein situgelling solutions for potential application in intraoperative fluorescence imaging and local therapy of hepatocellular carcinoma: a preliminary study

吲哚青绿 自愈水凝胶 体内 离体 荧光寿命成像显微镜 壳聚糖 生物医学工程 荧光 材料科学 肝细胞癌 原位 生物物理学 体外 化学 外科 高分子化学 癌症研究 生物化学 医学 物理 生物技术 有机化学 量子力学 生物
作者
Andrea Salis,Giovanna Rassu,Mária Budai-Szűcs,Ilaria Benzoni,Erzsébet Csányi,Szilvia Berkó,Marcello Maestri,Paolo Dionigi,Elena Piera Porcu,Elisabetta Gavini,Paolo Giunchedi
出处
期刊:Expert Opinion on Drug Delivery [Taylor & Francis]
卷期号:12 (10): 1583-1596 被引量:37
标识
DOI:10.1517/17425247.2015.1042452
摘要

Objectives: Thermosensitive chitosan/glycerophosphate (C/GP) solutions exhibiting sol–gel transition around body temperature were prepared to develop a class of injectable hydrogel platforms for the imaging and loco-regional treatment of hepatocellular carcinoma (HCC). Indocyanine green (ICG) was loaded in the thermosensitive solutions in order to assess their potential for the detection of tumor nodules by fluorescence.Methods: The gel formation of these formulations as well as their gelling time, injectability, compactness and resistance of gel structure, gelling temperature, storage conditions, biodegradability, and in vitro dye release behavior were investigated. Ex vivo studies were carried out for preliminary evaluation using an isolated bovine liver.Results: Gel strengths and gelation rates increased with the cross-link density between C and GP. These behaviors are more evident for C/GP solutions, which displayed a gel-like precipitation at 4°C. Furthermore, formulations with the lowest cross-link density between C and GP exhibited the best injectability due to a lower resistance to flow. The loading of the dye did not influence the gelation rate. ICG was not released from the hydrogels because of a strong electrostatic interaction between C and ICG. Ex vivo preliminary studies revealed that these injectable formulations remain in correspondence of the injected site.Conclusions: The developed ICG-loaded hydrogels have the potential for intraoperative fluorescence imaging and local therapy of HCC as embolic agents. They form in situ compact gels and have a good potential for filling vessels and/or body cavities.
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