Capsules Prepared(准备好的胶囊)研究综述
Capsules Prepared 准备好的胶囊 - The capsules prepared by the sol-emulsion-gel method demonstrated the highest release efficiency at pH 7. [1] In the Fe@SiO2 nanocapsules prepared with 900 μl TEOS, as the reaction temperature increases, the mean particle size of Fe@SiO2 nanocapsules increases from 328 to 546 nm. [2] In addition, the process makes it possible to increase the intake of soluble dietary fiber fraction thanks to the possibility of using beta-glucan as a wall material for the microcapsules prepared. [3] The results show that the nanocapsules prepared have the latent heat as high as 160. [4] Interestingly, SPVA/PVDF-Mcs-3 hollow composite microcapsules prepared using 70:30 ratio of water and isopropanol generated the highest amount of 570 mL hydrogen in 180 min at room temperature which can be attributed to the high porosity and less wall thickness. [5] Microcapsules prepared using the STM (ST-CC) were synthesized using sodium dodecyl sulphate (SDS) surfactant micelles as the soft-template, while the microcapsules prepared using the EM (EM-CC) were synthesized in an oil-in-water (O/W) in situ emulsion. [6] Capsules prepared with 1. [7] Herein we describe the synthesis of polysaccharide based nanocapsules prepared from furcellaran and chitosan via layer-by-layer deposition using electrostatic interaction. [8] Bovine serum albumin (BSA)-coated haemoglobin (Hb)-microcapsules prepared by co-precipitation of Hb and MnCO3 may present an alternative type of artificial blood substitute. [9] The nanocapsules prepared with AO and MCT presented mean particle size around 165 and 131 nm, respectively; polydispersity index values <0. [10] 4 phosphate buffer up to eight hours with microcapsules prepared with gelatin giving Felodipine release up to 86% after 8 hrs. [11] This paper aimed to obtain novel polymeric nanocapsules prepared from poly(ε-caprolactone)-poly(ethylene glycol) (PCL-PEG) blend containing CLZ. [12] The microcapsules prepared with WPI/IN (1:1) had the lowest lightness and the highest yellowness values. [13] In this work, we optimized the wall material composition (gelatin supplemented with gum Arabic, Tween 20, and β-cyclodextrin) of Turkish oregano microcapsules prepared by spray-drying technology to increase the product yield, the encapsulation efficiency, and to achieve narrower particle size distribution. [14] The core fraction of microcapsules prepared with optimum parameters was 66. [15] The microcapsules prepared by combining the two emulsification processes (HU) and at core and wall ratio of was 1:4 presented the smallest particles size and the greatest encapsulation efficiency (68. [16] Release systems for ATZ have been developed to minimize this contamination, such as nanocapsules prepared with poly (ε-caprolactone) (PCL). [17] The objectives of this study were to characterize zein fibers and capsules prepared by electrospinning and electrospraying techniques, respectively, and then use them to encapsulate folic acid. [18] The spherical microcapsules prepared in this study were 1–20 μm in diameter. [19] The capsules prepared under the optimal conditions are about 2 mm in diameter and show a latent heat of up to 122. [20] The first demonstration of microcapsules prepared from minimally grafted silk ionomers (silk fibroin modified with cationic/anionic charge groups) are presented here. [21] The intestine-targeted delivery performance of the gum Arabic (GA) - O-carboxymethyl chitosan (OCMC) microcapsules prepared by layer-by-layer (LbL) assembly and genipin crosslinking was evaluated by using an acid-susceptible compound omeprazole as the model. [22] The structure-property relationship in alginate microparticles (microspheres and microcapsules prepared with or without Trichoderma viride spores (Tv) was investigated. [23] rubrum) from microcapsules prepared by cross-linking emulsion method with chitosan as wall material. [24] The results showed that the microcapsules prepared in the experiment were of uniform size, with the sustained release of essential oil exceeding 168 h. [25]通过溶胶-乳液-凝胶法制备的胶囊在 pH 7 时表现出最高的释放效率。 [1] 在用 900 μl TEOS 制备的 Fe@SiO2 纳米胶囊中，随着反应温度的升高，Fe@SiO2 纳米胶囊的平均粒径从 328 nm 增加到 546 nm。 [2] 此外，由于可以使用 β-葡聚糖作为制备的微胶囊的壁材，该方法可以增加可溶性膳食纤维部分的摄入量。 [3] 结果表明，制备的纳米胶囊的潜热高达160。 [4] 有趣的是，使用 70:30 比例的水和异丙醇制备的 SPVA/PVDF-Mcs-3 中空复合微胶囊在室温下 180 分钟内产生最多 570mL 氢气，这可归因于高孔隙率和较小的壁厚。 [5] 使用十二烷基硫酸钠（SDS）表面活性剂胶束作为软模板合成使用STM（ST-CC）制备的微胶囊，而使用EM（EM-CC）制备的微胶囊在水包油（O /W) 原位乳液。 [6] 用 1 制备的胶囊。 [7] 在本文中，我们描述了使用静电相互作用通过逐层沉积从furcellaran 和壳聚糖制备的基于多糖的纳米胶囊的合成。 [8] 通过 Hb 和 MnCO3 的共沉淀制备的牛血清白蛋白 (BSA) 包被的血红蛋白 (Hb)-微胶囊可能是一种替代类型的人工血液替代品。 [9] AO和MCT制备的纳米胶囊的平均粒径分别在165和131nm左右；多分散指数值<0。 [10] 4 磷酸盐缓冲液长达 8 小时，使用明胶制备的微胶囊在 8 小时后释放高达 86% 的非洛地平。 [11] 本文旨在获得由含有CLZ的聚（ε-己内酯）-聚（乙二醇）（PCL-PEG）混合物制备的新型聚合物纳米胶囊。 [12] 用 WPI/IN (1:1) 制备的微胶囊具有最低的亮度和最高的黄度值。 [13] 在这项工作中，我们优化了喷雾干燥技术制备的土耳其牛至微胶囊的壁材组成（明胶辅以阿拉伯树胶、吐温 20 和 β-环糊精），以提高产品收率、包封效率并实现更窄的颗粒。尺寸分布。 [14] 以最佳参数制备的微胶囊的核心分数为66。 [15] 结合两种乳化工艺（HU）制备的微胶囊，在核壁比为1：4的情况下，粒径最小，包封率最高（68. [16] 已经开发了用于 ATZ 的释放系统以最大限度地减少这种污染，例如用聚 (ε-己内酯) (PCL) 制备的纳米胶囊。 [17] 本研究的目的是分别表征通过静电纺丝和电喷雾技术制备的玉米醇溶蛋白纤维和胶囊，然后用它们封装叶酸。 [18] 本研究中制备的球形微胶囊直径为1-20 μm。 [19] 在最佳条件下制备的胶囊直径约为 2mm，潜热高达 122。 [20] 此处介绍了由最小接枝的丝离聚物（用阳离子/阴离子电荷基团改性的丝素蛋白）制备的微胶囊的首次演示。 [21] 以酸敏感化合物奥美拉唑为模型，评价了逐层（LbL）组装和京尼平交联制备的阿拉伯胶（GA）-O-羧甲基壳聚糖（OCMC）微胶囊的肠靶向给药性能。 [22] 研究了用或不用绿色木霉孢子 (Tv) 制备的藻酸盐微粒（微球和微胶囊）的结构-性能关系。 [23] 以壳聚糖为壁材，采用交联乳液法制备的微胶囊。 [24] 结果表明，实验制备的微胶囊尺寸均匀，精油缓释时间超过168 h。 [25]
% w v % wv
The CINA-NCs capsules prepared with 30% (w/v) MCC, 8% (w/v) CCNa and 2% (w/v) talcum powder by orthogonal experimental design presented an enhanced in vitro dissolution rate in four media compared with commercial tablets Sensipar® and raw material. [1]通过正交实验设计，用 30% (w/v) MCC、8% (w/v) CCNa 和 2% (w/v) 滑石粉制备的 CINA-NCs 胶囊在四种介质中的体外溶出率均高于商业片剂 Sensipar® 和原材料。 [1]