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pH --- Nanogel using pH sensitive block copolymer polyaspartic acid-graft-imidazole-polyethylene glycol and preparing method thereof
pH --- Nanogel using pH sensitive block copolymer polyaspartic acid-graft-imidazole-polyethylene glycol and preparing method thereof
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机译:pH敏感型嵌段共聚物聚天冬氨酸接枝咪唑聚乙二醇的pH ---纳米凝胶及其制备方法
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摘要
The present invention relates to a nano-gel using a pH-sensitive block copolymer, poly (aspartic acid-graft-imidazole) -polyethylene glycol, and a process for preparing the same. The present invention relates to a poly (aspartic acid-graft-imidazole) PH-sensitive nanogels were prepared through chemical cross-linking between polyethylene glycol and chemically modified bis-N-hydroxysuccinimide (bis-NHS) conjugated polyethylene glycols, (PH between 7.2 and pH 6.5) due to their chemical nature (appropriate pK a value, wide buffer pH range, nano size, positive zeta potential and morphology) and pH dependent properties Interaction can regulate drug release and increase drug efficacy on target cells through reversible swelling and endosomal destruction. Therefore, a nanogel using poly (aspartic acid-graft-imidazole) -polyethylene glycol having the above effect can be utilized as a drug delivery composition for tumor treatment.
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机译:本发明涉及使用pH敏感的嵌段共聚物,聚(天冬氨酸-接枝-咪唑)-聚乙二醇的纳米凝胶及其制备方法。本发明涉及一种聚天冬氨酸-接枝-咪唑PH敏感纳米凝胶,它是通过聚乙二醇与化学改性的双-N-羟基琥珀酰亚胺(bis-NHS)共轭聚乙二醇之间的化学交联制备的(PH在7.2之间和pH 6.5)的化学性质(适当的pK a Sub>值,较宽的缓冲液pH范围,纳米尺寸,正zeta电位和形态)和pH依赖特性相互作用可以调节药物的释放并提高通过可逆的肿胀和内体破坏破坏靶细胞。因此,具有上述效果的使用聚(天冬氨酸-接枝-咪唑)-聚乙二醇的纳米凝胶可以用作用于肿瘤治疗的药物递送组合物。
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