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PAMAM Dendrimers: Surface Modification and Potential in Oral Delivery of SN-38

机译:Pamam Dendrimers:SN-38口服递送的表面改性和潜力

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Poly amido amine (PAMAM) dendrimers are promising candidates for oral drug delivery due to their well-defined compact structure, versatility of surface functionalities, low polydispersity and the ability to enhance transepithelial transport. Here we report that surface acetylation of PAMAM dendrimers maintains their permeability across caco-2 cell monolayers while reducing cytotoxicity. We also report the potential of PAMAM dendrimers for oral delivery of SN-38, an active metabolite of camptothecin analogs.
机译:聚酰胺胺(PAMAM)树枝状大分子是由于其定义良好的紧凑结构,表面官能团,低多分散性和增强Transepearial运输能力的含量,用于口服药物递送的候选者。在这里,我们认为PAMAM树枝状大分子的表面乙酰化在降低细胞毒性的同时将它们的渗透性保持在Caco-2细胞单层的渗透性。我们还报告了PAMAM树枝状大分子的潜力,用于口服递送SN-38,一种活跃的Camptothecin类似物。

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