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含有二十碳五烯酸和二十二碳六烯酸的脂质体的配方、表征及优化;一种方法学途径。

Formulation, characterization and optimization of liposomes containing eicosapentaenoic and docosahexaenoic acids; a methodology approach.

作者信息

Hadian Zahra, Sahari Mohammad Ali, Moghimi Hamid Reza, Barzegar Mohsen

机构信息

Faculty of Agriculture, Tarbiat Modares University and Academic Staff of National Nutrition and Food Technology Research Institute, Shahid Beheshti University of Medical Sciences.

Department of Food Science and Technology, Faculty of Agriculture, Tarbiat Modares University, Tehran, Iran.

出版信息

Iran J Pharm Res. 2014 Spring;13(2):393-404.

Abstract

Omega-3 fatty acids (FAs) have been shown to prevent cardiovascular disease. The most commonly used omega-3 fatty acids like eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA) are highly vulnerable to oxidation and therefore, have short shelf life. Recent advances in nanoliposomes provided a biocompatible system for stabilizing omega-3 FAs. Several methods could be implemented to prepare nanoliposomes. To the best of our knowledge, the performances of these methods in preparation omega-3 FAs have not been examined. Nanoliposomes were prepared by thin film hydration followed by one of the following methods: 1- extrusion, ultrasonic irradiation; 2- bath sonication; 3- probe sonication; or 4- combined probe and bath sonication. The size of liposomes obtained from methods 1 to 4 were 99.7 ± 3.5, 381.2 ± 7.8, 90.1 ± 2.3, and 87.1 ± 4.10 nm with zeta potential being -42.4 ± 1.7, -36.3 ± 1.6, -43.8 ± 2.4, and 31.6 ± 1.9 mV, respectively. The encapsulation efficiency (EE) for DHA was 13.2 ± 1.1%, 26.7 ± 1.9%, 56.9 ± 5.2% and 51.8 ± 3.8% for methods 1 to 4, respectively. The corresponding levels for EPA were 6.5 ± 1.3%, 18.1 ± 2.3%, 38.6 ± 1.8%, and 38 ± 3.7%, respectively. The EE for DHA and EPA of liposomes for both methods 3 and 4 increased significantly (p<0.05). Propanal, as the major volatile product formed during liposomal preparations, amounts from 81.2 ± 4.1 to 118.8 ± 2.3 μg/Kg. The differential scanning calorimetry (DSC) study showed that DHA and EPA influence the phase transition temperature of small unilamellar vesicles (SUVs) of dipalmitoyl phosphatidyl choline (DPPC). Transmission electron microscopy (TEM) images of liposomes stained with uranyl acetate showed that the liposomes were spherical in shape and maintain high structural integrity. In conclusion, probe ultrasound of pre-formed liposomes facilitates significant loading of DHA and EPA into the nanoliposomal membrane.

摘要

ω-3脂肪酸(FAs)已被证明可预防心血管疾病。最常用的ω-3脂肪酸,如二十碳五烯酸(EPA)和二十二碳六烯酸(DHA),极易氧化,因此保质期较短。纳米脂质体的最新进展为稳定ω-3脂肪酸提供了一种生物相容性系统。可以采用几种方法来制备纳米脂质体。据我们所知,这些方法在制备ω-3脂肪酸方面的性能尚未得到检验。通过薄膜水化法制备纳米脂质体,然后采用以下方法之一:1-挤压、超声辐照;2-浴式超声处理;3-探头超声处理;或4-探头超声与浴式超声联合处理。通过方法1至4获得的脂质体大小分别为99.7±3.5、381.2±7.8、90.1±2.3和87.1±4.10纳米,ζ电位分别为-42.4±1.7、-36.3±1.6、-43.8±2.4和31.6±1.9毫伏。方法1至4中DHA的包封率(EE)分别为13.2±1.1%、26.7±1.9%、56.9±5.2%和51.8±3.8%。EPA的相应水平分别为6.5±1.3%、18.1±2.3%、38.6±1.8%和38±3.7%。方法3和4制备的脂质体中DHA和EPA的EE均显著增加(p<0.05)。丙醛作为脂质体制备过程中形成的主要挥发性产物,含量为81.2±4.1至118.8±2.3微克/千克。差示扫描量热法(DSC)研究表明,DHA和EPA会影响二棕榈酰磷脂酰胆碱(DPPC)小单层囊泡(SUVs)的相变温度。用醋酸铀酰染色的脂质体的透射电子显微镜(TEM)图像显示,脂质体呈球形且保持高度的结构完整性。总之,对预先形成的脂质体进行探头超声处理有助于将DHA和EPA大量负载到纳米脂质体膜中。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f352/4157015/05f8deb05b61/ijpr-13-393-g001.jpg

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