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首页> 外文期刊>Drug development and industrial pharmacy >Preparation of novel cationic copolymer microspheres and evaluation of their function by in vitro and in vivo tests as pH-sensitive drug carrier systems.
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Preparation of novel cationic copolymer microspheres and evaluation of their function by in vitro and in vivo tests as pH-sensitive drug carrier systems.

机译:制备新型阳离子共聚物微球并通过体外和体内试验(对pH敏感的药物载体系统)评估其功能。

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摘要

Novel pH-sensitive copolymer microspheres containing methylacrylic acid and styrene cross-linking with divinylbenzene were synthesized by free radical polymerization. The microspheres that were formed were then characterized by Fourier-Transform infrared (FT-IR) spectroscopy, differential scanning calorimetry (DSC), size analysis, and X-ray analysis. The copolymer microspheres showed pulsatile swelling behavior when the pH of the media changed. The pH-sensitive microspheres were loaded with diltiazem hydrochloride (DH). The release characteristics of the free drug and the drug-loaded microspheres were studied under both simulated gastric conditions and intestinal pH conditions. The in vivo evaluation of the pulsatile preparation was subsequently carried out using beagle dogs as experimental subjects. The results demonstrated that the drug release exhibited a pulsatile character both in vitro and in vivo.
机译:通过自由基聚合反应,合成了新型的含甲基丙烯酸和苯乙烯与二乙烯基苯交联的pH敏感共聚物微球。然后通过傅立叶变换红外(FT-IR)光谱,差示扫描量热法(DSC),尺寸分析和X射线分析对形成的微球进行表征。当介质的pH改变时,共聚物微球显示出脉动溶胀行为。 pH敏感的微球中装有盐酸地尔硫卓(DH)。在模拟的胃条件和肠道pH条件下研究了游离药物和载药微球的释放特性。随后使用比格犬作为实验对象进行搏动制剂的体内评估。结果表明药物释放在体外和体内均表现出搏动性。

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