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Synthesis of Substituted Gelatine Grafted Maleic Anhydride as Drug Copolymer

机译:取代明胶接枝马来酸酐药物共聚物的合成

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In this research the structural modification of gelatin(A 1 ) was carried out with maleic anhydride as a grafted copolymer(A 2 ) to enhance and add new function groups such as acid anhydride which can used to be easy substituted with amino drug such as Amoxilline (A 3 ) ,this design of carries for controlled delivery of therapeutic agent which could release the entrapped drug over an extended period of time ,due to its non toxic ,biodegradable and slow digesting nature ,the new drug carries copolymer was characterized by FTIR and UV Spectroscopes. Thermal analysis was studied the prepared drug copolymer was analyzed in different pH values.at 37C 0 ,as in vitro study and controlled drug release was compared at zero time and after four days .Swelling percentage were calculated in water ,acidic and basic medium .
机译:在这项研究中,以马来酸酐为接枝共聚物(A 2)进行明胶(A 1)的结构改性,以增强和添加新的官能团,例如酸酐,该官能团过去很容易被氨基药物如阿莫西林取代(A 3),这种载体设计可控制治疗剂的输送,由于其无毒,可生物降解和缓慢消化的特性,可以长时间释放被包裹的药物,该新型药物的共聚物具有FTIR和紫外光谱仪。对热分析进行了研究,在37°C 0下对所制备的药物共聚物进行了不同的pH值分析,进行了体外研究,比较了零时和四天后药物的控制释放情况。计算了在水,酸性和碱性介质中的溶胀百分比。

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