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Lyophilized wafers comprising carrageenan and pluronic acid for buccal drug delivery using model soluble and insoluble drugs

机译:包含角叉菜胶和普罗糖酸的冻干薄饼,用于使用模型可溶性和不溶性药物进行颊部药物递送

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摘要

Lyophilized muco-adhesive wafers with optimum drug loading for potential buccal delivery have been developed. A freeze-annealing cycle was used to obtain optimized wafers from aqueous gels containing 2% κ-carrageenan (CAR 911), 4% pluronic acid (F127), 4.4% (w/w) polyethylene glycol with 1.8% (w/w) paracetamol or 0.8% (w/w) ibuprofen. Thermogravimetric analysis showed acceptable water contentudbetween 0.9 and 1.5%. Differential scanning calorimetry and X-ray diffraction showed amorphous conversion for both drugs. Texture analysis showed ideal mechanical and mucoadhesion characteristics whilst both drugs remained stable over 6 months and drug dissolution at a salivary pH showed gradual release within 2 h. The results show the potential of CAR 911 and F127 based wafers for buccal mucosauddrug delivery.
机译:已经开发了具有最佳药物载量的冻干粘膜胶粘片,用于潜在的颊部递送。冷冻退火循环用于从含水凝胶中获得优化的晶圆,该含水凝胶包含2%κ-角叉菜胶(CAR 911),4%普鲁尼克酸(F127),4.4%(w / w)聚乙二醇和1.8%(w / w)扑热息痛或0.8%(w / w)布洛芬。热重分析表明可接受的水含量在0.9至1.5%之间。差示扫描量热法和X射线衍射显示两种药物的无定形转化。质地分析显示出理想的机械和粘膜粘附特性​​,而两种药物均在6个月内保持稳定,并且在唾液pH值下药物溶解显示在2小时内逐渐释放。结果显示了基于CAR 911和F127的威化饼在颊粘膜药物输送中的潜力。

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