Hara Kaori, Tsujimoto Hiroyuki, Huang C C, Kawashima Yoshiaki, Mimura Haruko, Miwa Nobuhiko
Hosokawa Powder Technology Research Institute, Tajika, Hirakata, Osaka 573-1132, Japan.
Oncol Rep. 2006 Dec;16(6):1215-20.
Poly (aspartic acid-co-lactic acid) (PAL) has been investigated as a new biodegradable material for Drug Delivery Systems (DDS). Similar to the poly (lactic acid-co-glycolic acid) (PLGA) nanospheres, the PAL nanospheres can control-release encapsulated drugs by hydrolysis and adhere to the mucous membranes to improve the drug absorption. In this study, the vitamin encapsulated PAL nanospheres were applied on mice to examine their effect on tumor metastasis and safety as an injectable DDS material for anti-cancer and other drugs. In the experiment, 6 C57BL/6 mice per group were intravenously administered with B16BL6 melanoma cells (1 x 10(5) per mouse) and non-encapsulated PAL nanospheres or pro-vitamin encapsulated nanospheres respectively, while the control group was administered with B16BL6 cells alone. Two weeks later, the lungs of the mice were excised and metastatic foci on the lung surface were counted. The melanoma cell metastasis to lungs was prevented by intravenous co-injection of B16BL6 melanoma cells with 1.7 microg of pro-vitamin E encapsulated PAL nanospheres. Its metastatic foci count (mean +/- SD) was 127+/-80, which was better than the control (246+/-95, p<0.02). Also, applying the pro-vitamin C and pro-vitamin A encapsulated PAL nanospheres as well as the non-encapsulated PAL nanospheres slightly decreased the number of metastasis colonies in the lungs as compared to that of the control. These results suggested that PAL nanospheres did not promote the lung metastasis of B16BL6 melanoma cells. Thus, the PAL nanospheres are safe material for injection applications.
聚(天冬氨酸 - 共 - 乳酸)(PAL)已被研究作为药物递送系统(DDS)的一种新型可生物降解材料。与聚(乳酸 - 共 - 乙醇酸)(PLGA)纳米球类似,PAL纳米球可通过水解控制释放包封的药物,并粘附于粘膜以改善药物吸收。在本研究中,将包封维生素的PAL纳米球应用于小鼠,以检查其作为抗癌和其他药物的可注射DDS材料对肿瘤转移的影响及安全性。实验中,每组6只C57BL / 6小鼠分别静脉注射B16BL6黑色素瘤细胞(每只小鼠1×10⁵个)和未包封的PAL纳米球或包封维生素原的纳米球,而对照组仅注射B16BL6细胞。两周后,切除小鼠的肺并计数肺表面的转移灶。通过将B16BL6黑色素瘤细胞与1.7微克包封维生素E的PAL纳米球静脉共同注射,可预防黑色素瘤细胞转移至肺。其转移灶计数(平均值±标准差)为127±80,优于对照组(246±95,p <0.02)。此外,与对照组相比,应用包封维生素C和维生素原A的PAL纳米球以及未包封的PAL纳米球也略微减少了肺中转移菌落的数量。这些结果表明,PAL纳米球不会促进B16BL6黑色素瘤细胞的肺转移。因此,PAL纳米球是用于注射应用的安全材料。