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首页> 外文期刊>Journal of Inclusion Phenomena and Macrocyclic Chemistry >Assessment of in-vitro bio accessibility and characterization of spray dried complex of astaxanthin with methylated betacyclodextrin
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Assessment of in-vitro bio accessibility and characterization of spray dried complex of astaxanthin with methylated betacyclodextrin

机译:虾青素与甲基化的β-环糊精喷雾干燥复合物的体外生物可及性评估和表征

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摘要

Astaxanthin (AXT) is a carotenoid which gained a lot of importance as a nutritional ingredient in Nutraceuticals and as a food additive. However this bioactive failed to gather absolute significance due to poor aqueous solubility. This study explores the improved dissolution rate of AXT by its complexation with methyl betacyclodextrin (M-βCD) using spray drying technique which is very much scalable and accepted in industry. The experimental methodology undertaken proved that at 1.0 molar concentration of M-βCD, the solubility of AXT was 0.012 mM, representing a 54-fold enhancement over baseline solubility (<0.025 µg/mL). A ten fold increase in the dissolution rate was observed within 45 min in case of spray dried complex of AXT with M-βCD as compared to plain AXT. HepG2 cell line study proved that the bio accessibility of AXT increased when complexed with M-βCD using spray drying technique. Also, these complexes were further characterized by FTIR, UV, DSC, 1H NMR, XRD and molecular modeling analysis. The results confirmed that the hexatomic side rings of the AXT molecule were partly incorporated into the M-βCD cavity. This study provides the basis for the development of soluble and bioavailable oral formulations of AXT using spray drying technology for cyclodextrin complexation.
机译:虾青素(AXT)是一种类胡萝卜素,在Nutraceuticals中作为营养成分和作为食品添加剂非常重要。然而,由于水溶性差,这种生物活性物质未能获得绝对的意义。这项研究探索了通过使用喷雾干燥技术将AXT与甲基β-环糊精(M-βCD)络合而提高的溶出速率,该技术在工业上具有很大的可扩展性和接受性。进行的实验方法论证明,在M-βCD的摩尔浓度为1.0时,AXT的溶解度为0.012 mM,比基线溶解度(<0.025 µg / mL)提高了54倍。与普通AXT相比,在AXT与M-βCD喷雾干燥的复合物中,在45分钟内观察到溶解速率增加了十倍。 HepG2细胞系研究证明,使用喷雾干燥技术将AXT与M-βCD复合时,其生物可及性增加。同样,这些复合物通过FTIR,UV,DSC,1H NMR,XRD和分子模型分析进一步表征。结果证实AXT分子的六毒侧环被部分地掺入M-βCD腔中。该研究为使用环糊精络合喷雾干燥技术开发可溶和生物利用的AXT口服制剂提供了基础。

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