发明申请
US20150141414A1 Formulation of Stable Recombinant Alpha-Fetoprotein Conjugated with Anti-Tumor Substance in Target-Delivery System for Treatment of Cancer and Autoimmune Disease
审中-公开
![Formulation of Stable Recombinant Alpha-Fetoprotein Conjugated with Anti-Tumor Substance in Target-Delivery System for Treatment of Cancer and Autoimmune Disease](/abs-image/US/2015/05/21/US20150141414A1/abs.jpg.150x150.jpg)
基本信息:
- 专利标题: Formulation of Stable Recombinant Alpha-Fetoprotein Conjugated with Anti-Tumor Substance in Target-Delivery System for Treatment of Cancer and Autoimmune Disease
- 专利标题(中):在用于治疗癌症和自身免疫疾病的靶向递送系统中制备与抗肿瘤物质结合的稳定的重组甲胎蛋白
- 申请号:US14455249 申请日:2014-08-08
- 公开(公告)号:US20150141414A1 公开(公告)日:2015-05-21
- 发明人: Nana Legrand
- 申请人: Nana Legrand
- 申请人地址: US NJ Freehold
- 专利权人: LeGrand International LLC
- 当前专利权人: LeGrand International LLC
- 当前专利权人地址: US NJ Freehold
- 主分类号: A61K47/48
- IPC分类号: A61K47/48 ; A61K47/34 ; C07K14/47 ; A61K31/538
摘要:
Disclosed is a stable formulation based on rAFP conjugated with drug delivery system of various classes of pharmacological agents such as dactinomycin, cardionolide, and bufadinolide, among others. In another embodiment, the invention discloses a method of producing rAFP in a strain of methylotrophic Pichia pastoris yeast, allowing the yeast to replicate, and extracting the newly created rAFP. The method provides a nonpyrogenic, highly stable, recombinant, fully refolded rAFP and its fragments that are free from stable folding intermediates caused by non-native disulfide bridges and irreversible aggregates. The newly created rAFP is purified using a two-step chromatographic purification process in the presence of 0.5% polysorbate-20 and 10 mM inosine that prevents aggregation of the monomers of the target protein, increasing the yield of biologically active rAFP. The invented formulation of rAFP is conjugated with active pharmacological substances or target drug delivery system for prevention or treatment of oncological and autoimmune-diseases.
摘要(中):
公开了一种基于与药物递送系统结合的rAFP的稳定制剂,所述药物递送系统包括各种类型的药理学试剂,例如放线菌素,cardionolide和bufadinolide等。 在另一个实施方案中,本发明公开了一种在甲基营养型巴斯德毕赤酵母菌株中生产rAFP的方法,允许酵母复制并提取新产生的rAFP。 该方法提供非致死性,高度稳定,重组,完全重折叠的rAFP及其片段,其不含由非天然二硫键和不可逆聚集体引起的稳定折叠中间体。 在0.5%聚山梨醇酯-20和10mM肌苷存在下,使用两步色谱纯化方法纯化新产生的rAFP,以防止靶蛋白单体的聚集,提高生物活性rAFP的产量。 本发明的rAFP制剂与活性药理物质或靶药物递送系统结合,用于预防或治疗肿瘤和自身免疫疾病。
IPC结构图谱:
A | 人类生活必需 |
--A61 | 医学或兽医学;卫生学 |
----A61K | 医用、牙科用或梳妆用的配制品 |
------A61K47/00 | 以所用的非有效成分为特征的医用配制品,如载体、惰性添加剂 |
--------A61K47/48 | .非有效成分被化学键键合到有效成分上,例如聚合物药物轭合物 |