首页> 外文会议>International Conference on Nanotechnology >CELLULOSE NANOPARTICLES BASED ESTER PRODRUGS FOR POTENTIAL COLON-SPECIFIC DRUG DELIVERY. SYNTHESIS PHYSICOCHEMICAL CHARACTERIZATION AND DRUG RELEASE STUDIES (PPT)
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CELLULOSE NANOPARTICLES BASED ESTER PRODRUGS FOR POTENTIAL COLON-SPECIFIC DRUG DELIVERY. SYNTHESIS PHYSICOCHEMICAL CHARACTERIZATION AND DRUG RELEASE STUDIES (PPT)

机译:纤维素纳米颗粒基酯前药,用于潜在的结肠特异性药物递送。合成物理化学表征和药物释放研究(PPT)

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Ester prodrug either of xylan based or of cellulose based has been successfully synthesized as confirmed by FT-IR and 1H/13C-NMR Spectroscopy. X-ray diffraction analysis showed that ester prodrugs have broader peak with less crystalline content. The decrease in crystallinity of prodrug might be facilitating the degradation of cellulose/xylan by produced enzymes in the colon. The crystallinity of cellulose based ester prodrugs of molar ratio 1:1 and 1:2 have almost constant, on the other hand ester prodrug of molar ratio of 1:3 has some what less crystallinity might be due to conjugation at C-6 carbon atom of cellulose. Smaller particle size of both cellulose/xylan based ester prodrugs provide large surface area for facilitating the enzyme action easily.
机译:基于Xylan或基于纤维素的酯前药已经成功地合成,如通过FT-IR和1H / 13C-NMR光谱证实。 X射线衍射分析表明,酯前药具有较宽的峰,具有较少的结晶含量。前药的结晶度降低可能通过在结肠中产生的酶来促进纤维素/木聚糖的降解。摩尔比的纤维素比1:1和1:2的结晶度几乎恒定,另一方面摩尔比的摩尔比为1:3的摩尔比具有一些较小的结晶度,由于C-6碳原子的缀合纤维素。纤维素/木聚糖基酯前药的较小粒径提供了大的表面积,以容易促进酶作用。

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