TL;DR: A sustained-release pharmaceutical preparation comprising an admixture of uncoated and/or single walled water soluble drugs, such as aspirin, and dual walled coated drugs is described in this paper.
Abstract: A sustained-release pharmaceutical preparation comprising an admixture of uncoated and/or single walled water soluble drug, such as aspirin, and dual walled coated drug. The dual wall structure has an inner wall microencapsular control coating, such as ethyl cellulose, and an outer wall enteric coating such as cellulose acetate phthalate. The dual walled coated drug has a delayed, gradual, long-term release which takes place in the intestines while the uncoated and/or single walled drug has immediate therapeutic properties upon dissolution in the stomach. The outer wall enteric coating may be applied to microencapsulated core drug by a coacervation, spray coating or other process.
TL;DR: In this article, a phase change material (PCM) and a encapsulation material are studied, where the PCM is a mixture of sodium and potassium eutectic salts and the encapsulation is diatomite, and it is observed that the PCMs are distributed homogeneously in the composite materials.
TL;DR: The results showed that spherical micro Capsules were obtained for all conditions except for 30 min of hardening time, which did not result in microcapsules.
Abstract: Microcapsules of vitamin A palmitate were prepared by gelatin-acacia complex coacervation The effects of colloid mixing ratio, core-to-wall ratio, hardening agent, concentration of core solution, and drying method on the coacervation process and the properties of the microcapsules were investigated The microcapsules of vitamin A palmitate were prepared using different weight ratios of gelatin and acacia, that is, 2:3, 1:1, and 3:2 under controlled conditions The other factors studied were 1:1, 1:2, and 1:3 core-to-wall ratios; 30, 60, and 120 min of hardening time; 2, 5, and 10 ml of formaldehyde per 280 g of coacervation system as a hardening agent; and 30%, 40%, and 50% w/w vitamin A palmitate in corn oil as a core material The drying methods used were air drying, hot air at 40 degrees C, and freeze-drying The results showed that spherical microcapsules were obtainedfor all conditions except for 30 min of hardening time, which did not result in microcapsules The optimum conditions for free-flowing microcapsules with a high percentage of entrapped drug were 1:1 gelatin-to-acacia ratio and 1:2 core-to-wall ratio when hardening with 2 ml formaldehyde for 60 min and using 40% w/w vitamin A palmitate in corn oil as the core concentration In addition, drying the microcapsules by freeze-drying provided microcapsules with excellent appearance
TL;DR: In this article, a micro-encapsulation method for procyanidins was proposed to extend the shelf life of grape seeds by using gum arabic and maltodextrin as wall materials.
TL;DR: In this article, the folic acid was encapsulated in horse chestnut starch and β-cyclodextrin by spray drying technique and the release behavior of capsules were investigated during simulated gastric conditions.