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喷雾干燥制备的胃内滞留微粒作为脂溶性维生素的控释系统

Gastro-Resistant Microparticles Produced by Spray-Drying as Controlled Release Systems for Liposoluble Vitamins.

作者信息

Terracina Francesca, Caruana Roberto, Bonomo Francesco Paolo, Montalbano Francesco, Licciardi Mariano

机构信息

Dipartimento di Scienze e Tecnologie Biologiche Chimiche e Farmaceutiche (STEBICEF), Università degli Studi di Palermo, 90123 Palermo, Italy.

Technology Scientific S.r.l., Viale delle Scienze, Edificio 18, 90128 Palermo, Italy.

出版信息

Pharmaceutics. 2022 Jul 15;14(7):1480. doi: 10.3390/pharmaceutics14071480.

Abstract

In the present study, gastro-resistant microparticles (MPs) were produced using the spray-drying technique as controlled-release systems for some model liposoluble vitamins, including retinyl-palmitate, retinyl-acetate, β-carotene, cholecalciferol and α-tocopherol. The gastroprotective action of three different gastro-resistant excipients, the anionic methacrylic copolymer (Eudraguard Biotic, E1207), the cellulose acetate phthalate (CAP) and whey proteins (WPs), was compared. The latter was used to produce a novel delivery system manufactured with only food-derived components, such as milk, and showed several improvements over the two synthetic gastro-resistant agents. Scanning electron microscopy (SEM) images showed a quite homogeneous spherical shape of all microparticle batches, with an average diameter between 7 and 15 μm. FTIR analysis was used to evaluate the effective incorporation of vitamins within the microparticles and the absence of any degradation to the components of the formulation. The comparison graphs of differential scanning calorimetry (DSC) confirmed that the spray drying technique generates a solid in which the physical interactions between the excipients and the vitamins are very strong. Release studies showed a prominent pH-controlled release and partially a delayed-release profile. Ex vivo permeation studies of retinyl palmitate, retinyl acetate and α-tocopherol revealed greater transmucosal permeation capacity for microparticles produced with the WPs and milk.

摘要

在本研究中,采用喷雾干燥技术制备了胃滞留微粒(MPs),作为一些模型脂溶性维生素(包括棕榈酸视黄酯、醋酸视黄酯、β-胡萝卜素、胆钙化醇和α-生育酚)的控释系统。比较了三种不同胃滞留辅料(阴离子型甲基丙烯酸共聚物(优特奇生物,E1207)、邻苯二甲酸醋酸纤维素(CAP)和乳清蛋白(WPs))的胃保护作用。后者用于制备仅由食品衍生成分(如牛奶)制成的新型递送系统,与两种合成胃滞留剂相比有若干改进。扫描电子显微镜(SEM)图像显示所有微粒批次均为相当均匀的球形,平均直径在7至15μm之间。傅里叶变换红外光谱(FTIR)分析用于评估维生素在微粒中的有效掺入以及制剂成分未发生任何降解。差示扫描量热法(DSC)的比较图证实,喷雾干燥技术产生的固体中辅料与维生素之间的物理相互作用非常强。释放研究显示出显著的pH控制释放,部分呈现延迟释放曲线。棕榈酸视黄酯、醋酸视黄酯和α-生育酚的体外渗透研究表明,用WPs和牛奶制备的微粒具有更大的跨粘膜渗透能力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/49af/9319434/d2bf95863a94/pharmaceutics-14-01480-g001.jpg

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