Lee Hung-Yen, Mohammed Kamal A, Goldberg Eugene P, Kaye Frederic, Nasreen Najmunnisa
Division of Pulmonary, Critical Care & Sleep Medicine, Department of Medicine, University of Florida P. O. Box 100225, Gainesville, FL 32611-6400, USA ; Biomaterials Center, Department of Materials Sciences and Engineering, University of Florida P. O. Box 116400, Gainesville, FL 32611-6400, USA.
Division of Pulmonary, Critical Care & Sleep Medicine, Department of Medicine, University of Florida P. O. Box 100225, Gainesville, FL 32611-6400, USA ; NF/SGVHS, Malcom Randall VA Medical Center, University of Florida P. O. Box 100225, Gainesville, FL 32611-6400, USA.
Am J Cancer Res. 2015 Jan 15;5(2):603-15. eCollection 2015.
The low solubility of cisplatin in aqueous solution limits the treatment effectiveness and the application of cisplatin in various kinds of drug-eluting devices. Although cisplatin has a high solubility in Dimethyl sulfoxide (DMSO), the toxicity of cisplatin can be greatly reduced while dissolved in DMSO. In this study, the solid powder of cisplatin-loaded albumin mesospheres (CDDP/DMSO-AMS), in a size range of 1 to 10 µm, were post-loaded with cisplatin and showed high cisplatin content (16% w/w) and effective cytotoxicity to lung cancer cells. Cisplatin were efficiently absorbed into the albumin mesospheres (AMS) in DMSO and, most importantly, the toxicity of cisplatin was remained at 100% after the loading process. This CDDP/DMSO-AMS was designed for the intratumoral injection through the bronchoscopic catheter or dry powder inhalation (DPI) due to its high stability in air or in solution. This CDDP/DMSO-AMS showed a fast cisplatin release within 24 hours. In the in vitro study, CDDP/DMSO-AMS showed high effectiveness on killing the lung cancer cells including the non-small cell lung cancer (NCL-H23 and A549), malignant mesothelioma (CRL-2081) and the mouse lung carcinoma (Lewis lung carcinoma) cell lines. The albumin based mesospheres provide an ideal loading matrix for cisplatin and other metal-based drugs due to the high swelling degree and fast uptake rate in the organic solvents with high polarity. In addition, to investigate the effects of polysaccharides, such as chitosan and chondroitin, on enhancing loading efficiency and lasting cytotoxicity of cisplatin, the polysaccharide-modified albumin mesospheres were synthesized and loaded with cisplatin in this study.
顺铂在水溶液中的低溶解度限制了其治疗效果以及在各种药物洗脱装置中的应用。尽管顺铂在二甲基亚砜(DMSO)中具有高溶解度,但溶解于DMSO时顺铂的毒性会大大降低。在本研究中,尺寸范围为1至10 µm的载顺铂白蛋白微球(CDDP/DMSO-AMS)固体粉末在载药后显示出高顺铂含量(16% w/w)且对肺癌细胞具有有效的细胞毒性。顺铂在DMSO中能有效被吸收到白蛋白微球(AMS)中,最重要的是,载药过程后顺铂的毒性仍保持在100%。这种CDDP/DMSO-AMS因其在空气或溶液中的高稳定性而被设计用于通过支气管镜导管进行瘤内注射或干粉吸入(DPI)。这种CDDP/DMSO-AMS在24小时内显示出快速的顺铂释放。在体外研究中,CDDP/DMSO-AMS对杀死肺癌细胞具有高效性,包括非小细胞肺癌(NCL-H23和A549)、恶性间皮瘤(CRL-2081)和小鼠肺癌(Lewis肺癌)细胞系。基于白蛋白的微球由于在高极性有机溶剂中的高溶胀度和快速摄取率,为顺铂和其他金属基药物提供了理想的载药基质。此外,为了研究多糖(如壳聚糖和软骨素)对提高顺铂载药效率和持久细胞毒性的影响,本研究合成了多糖修饰的白蛋白微球并进行了顺铂载药。