| Literature DB >> 24914829 |
Na Qi1, Cuifang Cai2, Wei Zhang2, Yantao Niu2, Jingyu Yang2, Lihui Wang2, Bin Tian2, Xiaona Liu2, Xia Lin2, Yu Zhang2, Yan Zhang2, Haibing He2, Kang Chen2, Xing Tang3.
Abstract
This study described the development of vesicular phospholipid gels (VPGs) for sustained delivery of cytarabine (Ara-C) for the treatment of xenografted glioma. Ara-C-loaded VPGs in the state of a semisolid phospholipid dispersion looked like numerous vesicles tightly packing together under the freeze-fracture electron microscopy (FF-TEM), their release profiles displayed sustained drug release up to 384 h in vitro. The biodistribution of Ara-C in the rat brain showed that Ara-C-loaded VPGs could maintain therapeutic concentrations up to 5mm distance from the implantation site in brain tissue within 28 days. At the same time, fluorescence micrograph confirmed drug distribution in brain tissue visually. Furthermore, after single administration, Ara-C-loaded VPGs group significantly inhibited the U87-MG glioma growth in right flank in comparison with Ara-C solution (p<0.01). It was explained that the entrapped drug in VPGs could avoid degradation from cytidine deaminase and sustained release of drug from Ara-C-loaded VPGs could maintain the effective therapeutic levels for a long time around the tumor. In conclusion, Ara-C-loaded VPGs, with the properties of sustained release, high penetration capacity, nontoxicity and no shape restriction of the surgical cavity, are promising local delivery systems for post-surgical sustained chemotherapy against glioma.Entities:
Keywords: Cytarabine; Glioma; Local delivery; Sustained release; Vesicular phospholipids gels
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Year: 2014 PMID: 24914829 DOI: 10.1016/j.ijpharm.2014.06.005
Source DB: PubMed Journal: Int J Pharm ISSN: 0378-5173 Impact factor: 5.875