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1. 重庆医科大学附属第一医院金山医院体检部
2. 解放军第153中心医院科训办
3. 重庆医科大学附属第一医院体检部
4. 解放军第153中心医院肿瘤科
纸质出版日期:2017,
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杨雅娜, 岳玮, 王小林, 等. 聚乙烯醇-硫辛酸载多柔比星纳米颗粒的制备及其体外抗乳腺癌细胞活性的实验研究[J]. 重庆医科大学学报, 2017,42(11):1406-1410.
Yang Yana, Yue Wei, Wang Xiaolin, et al. Fabrication of Doxorubicin loaded poly(vinyl alcohol)-lipoic acid nanoparticles and characterization of the anti-breast cancer cell activity in vitro[J]. Journal of Chongqing Medical University, 2017,42(11):1406-1410.
杨雅娜, 岳玮, 王小林, 等. 聚乙烯醇-硫辛酸载多柔比星纳米颗粒的制备及其体外抗乳腺癌细胞活性的实验研究[J]. 重庆医科大学学报, 2017,42(11):1406-1410. DOI: 10.13406/j.cnki.cyxb.001070.
Yang Yana, Yue Wei, Wang Xiaolin, et al. Fabrication of Doxorubicin loaded poly(vinyl alcohol)-lipoic acid nanoparticles and characterization of the anti-breast cancer cell activity in vitro[J]. Journal of Chongqing Medical University, 2017,42(11):1406-1410. DOI: 10.13406/j.cnki.cyxb.001070.
目的:合成聚乙烯醇-硫辛酸聚合物
研究其载多柔比星纳米颗粒的制备及初步的体内、外实验研究。方法:采用"一步法"合成PVA27K-4%LA聚合物
激光粒径测定仪测定其粒径、多分散系数和ζ电位
电镜下观察其形态
分光光度法测定其载多柔比星的包封率
透析法研究其药物释放特性
以及MTS法研究其体外抗乳腺癌细胞的活性;建立荷乳腺癌裸鼠模型
行初步体内实验评价。结果:合成的PVA
27K
-4%LA聚合物在水相中形成纳米级颗粒
电镜下形态不规则
平均粒径、多分散系数和ζ电位分别为(8.30±3.02)nm、(0.129±0.063)和(-26.68±0.98)m V;对DOX的包封率为86.12%
平均粒径、多分散系数和ζ电位分别为(9.35±3.30)nm、(0.114±0.056)和(-28.57±1.63)mV
与PVA
27K
-4%LA相比较均无统计学差异(P值分别为0.023、0.0512和0.332);DOX在PBS溶液中随时间缓慢释放;乳腺癌细胞能快速摄取PVA27K-4%LA-DOX
IC50为537.3 ng/m L(与游离DOX组相比
P=0.005);纳米颗粒能靶向聚集在荷瘤裸鼠的肿瘤部位。结论:PVA27K-4%LA在水相中能自组装形成不规则的纳米颗粒
能有效装载DOX
通过缓释DOX实现对乳腺癌细胞的杀伤作用;PVA27K-4%LA在荷瘤裸鼠体内能靶向聚集在肿瘤部位。
Objective:To explore the fabrication of poly(vinyl alcohol)(PVA)-lipoic acid(LA) polymers and to study the basic physicochemical properties
as well as the anti-breast cancer cell activity;to preliminarily evaluate the biodistribution of PVA27 K-4%LA in breast cancer-bearing mice. Methods:"One-step"method was used to fabricate the PVA27 K-4%LA polymer. The mean particle size
poly dispersity and ζ potential were detected using dynamic light scattering;the morphology was observed under transmission electron microscope(TEM);the cytotoxicity of the polymer was studied. Dialysis method was employed to incorporate Doxorubicin(DOX)into PVA27 K-4% LA. The drug content
drug release rate
cell uptake and cytotoxicity were further investigated. The breast cancer-bearing mouse model was established
and study the biodistribution of the nanoparticles in vivo. Results:PVA27 K-4%LA can be self-assembled into nanoparticles in water solution
which was irregular in shape when observed under TEM. The mean particle size
poly dispersity and ζ potential were(8.30 ±3.02) nm
(0.129 ±0.063) and(-26.68 ±0.98) m V respectively. The encapsulation efficiency was 86.12%;dialysis method was used to incorporate DOX into PVA27 K-4%LA. The morphology of PVA27 K-4%LA-DOX was similar with that of PVA27 K-4%LA. The mean particle size
poly dispersity and ζ potential were(9.35 ±3.30) nm
(0.114±0.056) and(-28.57 ±1.63) m V respectively(P value were0.023
0.0512 and 0.332 respectively). The DOX released from PVA27 K-4%LA-DOX was much faster in the first 4 hours. On the24 th hours
about 60% of the DOX was released. The breast cancer cells MDA-MB-231 could uptake PVA27 K-4%LA-DOX quickly. The cancer cells could be killed efficiently
with the IC50 of537.3 ng/m L(P =0.005). PVA27 K-4% LA accumulated in tumor site
and reached highest dose at the 24 th hour. Liver
lung and spleen also had PVA27 K-4%LA distribution. Conclusion:PVA27 K-4%LA could be self-assembled into irregular nanoparticles in water solution. DOX could be incorporated into PVA27 K-4%LA efficiently. PVA27 K-4%LA-DOX could be uptaken by breast cancer cells MDA-MB-231
and could kill the cancer cells via releasing DOX gradually. PVA27 K-4%LA nanoparticles could targeted accumulate in the tumor site of breast cancer-bearing mice.
聚乙烯醇辛酸纳米颗粒多柔比星乳腺癌细胞
poly(vinyl alcohol)lipoic acidnanoparticledoxorubicinbreast cancer cell
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