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首页> 外文期刊>Molecular pharmaceutics >Eudragit e PO as a complementary material for designing oral drug delivery systems with controlled release properties: Comparative evaluation of new interpolyelectrolyte complexes with countercharged eudragit L100 copolymers
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Eudragit e PO as a complementary material for designing oral drug delivery systems with controlled release properties: Comparative evaluation of new interpolyelectrolyte complexes with countercharged eudragit L100 copolymers

机译:Eudragit e PO作为用于设计具有控释特性的口服药物输送系统的补充材料:具有带负电荷的eudragit L100共聚物的新型聚电解质复合物的比较评估

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摘要

The design of new interpolyelectrolyte complexes (IPEC) between countercharged polymers (Eudragit EPO (EPO) and Eudragit L100 (L100)) was investigated. The formation and chemical composition of three new IPECs between EPO and L100 was established by elemental analysis. The structure and solid state properties of the synthesized IPEC were investigated using Fourier transform infrared (FTIR) spectroscopy and modulated temperatre differential scanning calorimetry (MTDSC). The binding ratio of a unit molecule of EPO with L100 was found to range between 1:0.98 (Z = 1.02) and 1:0.50 (Z = 2.00) while increasing the pH from 6.0 to 7.0. As a result of electrostatic interaction between the copolymer chains, the glass transition temperature of the IPEC increased significantly. Considerable pH-sensitive swelling in acidic and neutral media was observed for different type of IPECs. Through evaluation of diffusion-transportation properties of the IPECs, basic mechanisms controlling the delivery of chemically different drugs (diclofenac sodium and theophylline) were obtained. The results of swelling and release of the model drugs from the polycomplex matrices confirm that they have potential to be used in oral controlled drug delivery.
机译:研究了带电荷的聚合物(Eudragit EPO(EPO)和Eudragit L100(L100))之间的新型聚电解质复合物(IPEC)的设计。通过元素分析确定了EPO和L100之间的三个新IPEC的形成和化学组成。合成的IPEC的结构和固态性质使用傅立叶变换红外(FTIR)光谱和调制温度差示扫描量热法(MTDSC)进行了研究。发现EPO与L100的单位分子的结合比在1:0.98(Z = 1.02)和1:0.50(Z = 2.00)之间,同时将pH从6.0增加到7.0。由于共聚物链之间的静电相互作用,IPEC的玻璃化转变温度显着提高。对于不同类型的IPEC,在酸性和中性介质中观察到相当大的pH敏感溶胀。通过评估IPEC的扩散-运输特性,获得了控制化学上不同药物(双氯芬酸钠和茶碱)递送的基本机制。模型药物从多复合基质中溶胀和释放的结果证实,它们有潜力用于口服控制药物的递送。

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