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抗肝癌免疫纳米颗粒的制备及其对肝癌细胞增殖的影响 被引量:3

Preparation of hepatocellular carcinoma-targeted immunonanoparticles and investigation of their effects on the proliferation of hepatocellular carcinoma cells
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摘要 目的:制备抗肝癌单链抗体二聚体高分子免疫纳米颗粒,观察其对肝癌细胞增殖的影响.方法:采用离子交联的方法,以壳聚糖水溶性衍生物多糖为基材,将已获得的抗肝癌单链抗体二聚体BDM制备成免疫纳米颗粒,检测纳米颗粒的表征、包封率及载药量,并通过MTT法观察免疫纳米颗粒对肝癌细胞株增殖的影响.结果:制备粒径为100-200nm的抗肝癌单链抗体二聚体高分子纳米颗粒,最佳包封率为53%,载药量为75μg/mg抗体二聚体,抗肝癌单链抗体二聚体高分子纳米颗粒显示较好的抗肿瘤作用,其对肝癌细胞的抑制率为34%左右,且有浓度依赖性.结论:成功制备了抗肝癌单链抗体二聚体高分子纳米颗粒,初步应用具有抑瘤性,为下一步开展体内肝癌的放射免疫诊断和靶向治疗奠定了基础. AIM:To prepare polyelectrolyte nanoparticles loaded with humanized single-chain Fv dimers for hepatocellular carcinoma (BDM diabody),and to investigate their effects on the proliferation of hepatocellular carcinoma (HCC) cells.METHODS:By means of infrared spectroscopy and transmission electron microscopy,the physicochemical characteristics of polyelectro-lyte nanoparticles were characterized,including particle size and morphology,the concentration of protein loaded,and the protein entrapment efficiency of the nanoparticles. The effects of BDM-loading nanoparticles on the proliferation of HCC cells were determined by methyl thiazol tetrazolium (MTT) assay. RESULTS:The particle size ranged from 100 to 200 nm. The concentration of protein loaded was 75 μg/mg. The protein entrapment efficiency was 53%. BDM-loading nanoparticles could sig-nif icantly inhibit the proliferation of HCC cells.CONCLUSION:HCC-targeted nanopaticles are successfully prepared,which provides a basis for future targeted diagnosis and therapy of HCC.
出处 《世界华人消化杂志》 CAS 北大核心 2010年第13期1326-1330,共5页 World Chinese Journal of Digestology
基金 广东省科技计划基金资助项目 No.2006B19901014~~
关键词 肝癌抗体二聚体 高分子纳米颗粒 肝癌 Diabody against hepatocellular carci-noma Polyelectrolyte nanopaticle Hepatocellular carcinoma
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  • 1盛洁,山登布卡,谢蜀生,魏树礼.单克隆抗体BDI-I导向的阿霉素白蛋白毫微球对人膀胱癌细胞的特异杀伤活性[J].药学学报,1995,30(9):706-710. 被引量:12
  • 2布卡,盛洁,谢蜀生,魏树礼.抗人膀胱癌免疫毫微球的制备及活性检测[J].中华微生物学和免疫学杂志,1996,16(1):54-57. 被引量:21
  • 3卢筱华,杨冬华,周旻,汤绍辉.抗肝癌单链抗体体外亲和力成熟的改造及意义[J].中华肝脏病杂志,2006,14(3):192-195. 被引量:11
  • 4李文俊.-[J].高分子学报,1997,2:106-110.
  • 5Adams GE Shaller CC,Dadachova E,et al.A single treatment of yttrium-90-1abeled CHX-A-C6.5 diabody inhibits the growth of established human tumor xenografts in immunodeficient mice.Cancer Res,2004,64:6200-6206.
  • 6Turner D J,Ritter MA,George AJ.Importance of the linker in expression of single-chain Fv antibody fragments:optimisation of peptide sequence using phage display technology.J lmmunol Methods,1997,205:43-54.
  • 7Bruix J,Sala M,Llovet JM.Chemoembolization for hepatocellular carcinoma.Gastroenterology,2004,127(5 Suppl 1):S179-188.
  • 8Omata M,Tateishi R,Yoshida H,et al.Treatment of hepatocellular carcinoma by percutaneous tumor ablation methods:Ethanol injection therapy and radiofrequency ablation.Gastroenterology,2004,127(5Suppl 1):S159-166.
  • 9Head HW,Dodd GD 3rd.Thermal ablation for hepatocellular carcinoma.Gastroenterology,2004,127(5 Suppl 1):S167-178.
  • 10Butterfield LH.Immunotherapeutic strategies for hepatocellular carcinoma.Gastroenterology,2004,127(5 Suppl 1):S232-241.

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