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Improving drug loading of mucosal solvent cast films usinguda combination of hydrophilic polymers with amoxicillin andudparacetamol as model drugs

机译:使用 ud提高粘膜溶剂流延膜的载药量亲水性聚合物与阿莫西林和 ud的组合扑热息痛为模型药物

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摘要

Solvent castmucosal films with improved drug loading have been developed by combining carboxymethyl cellulose (CMC), sodium alginate (SA), and carrageenan (CAR) using paracetamol and amoxicillin as model drugs and glycerol (GLY) as plasticizer. Films were characterized using X-ray powder diffraction (XRPD), scanning electron microscopy (SEM), folding resilience, swelling capacity, mucoadhesivity, and drug dissolution studies. SA, CMC, and GLY (5 : 3 : 6) films showed maximum amoxicillin loading of 26.3% whilst CAR, CMC, and GLY (1 : 2 : 3) films had a maximum paracetamol loading of 40%. XRPD analysis showed different physical forms of the drugs depending on the amount loaded. Films containing 29.4% paracetamol and 26.3% amoxicillin showed molecular dispersion of the drugs while excess paracetamol was observed on the filmsurface when themaximum 40% was loaded. udWork of adhesion was similar for blank films with slightly higher cohesiveness for CAR and CMC based films, but the differences were significant between paracetamol and amoxicillin containing films. The stickiness and cohesiveness for drug loaded films were generally similar with no significant differences. The maximum percentage cumulative drug release was 84.65% and 70.59% for paracetamol and amoxicillin, respectively, with anomalous case two transport mechanism involving both drug diffusion and polymer erosion.
机译:通过将羧甲基纤维素(CMC),藻酸钠(SA)和角叉菜胶(CAR)以对乙酰氨基酚和阿莫西林为模型药物,并以甘油(GLY)为增塑剂进行组合,已开发出具有改善的药物载量的溶剂型粘膜膜。使用X射线粉末衍射(XRPD),扫描电子显微镜(SEM),折叠回弹性,溶胀能力,粘膜粘附性和药物溶解研究对膜进行表征。 SA,CMC和GLY(5:3:6)薄膜的最大阿莫西林负载量为26.3%,而CAR,CMC和GLY(1:2:3)薄膜的对乙酰氨基酚最大负载量为40%。 XRPD分析显示药物的不同物理形式取决于所加的量。含有29.4%对乙酰氨基酚和26.3%阿莫西林的薄膜显示出药物的分子分散性,而当最大装载量为40%时,在薄膜表面观察到过量的扑热息痛。粘合力对于空白膜相似,对于基于CAR和CMC的膜的粘合性稍高,但是对乙酰氨基酚和含阿莫西林的膜之间的差异是显着的。载药薄膜的粘性和内聚性通常相似,无显着差异。对乙酰氨基酚和阿莫西林的最大累积药物释放百分比分别为84.65%和70.59%,在异常情况下,两种转运机制均涉及药物扩散和聚合物侵蚀。

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