用于pH敏感药物释放的新型油改性丙烯酸聚合物:实验结果与统计分析

N. Panja, A. Chattopadhyay
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摘要

我们报告了一项实验研究的结果,并辅以对实验数据的详细统计分析,研究了一种使用pH敏感丙烯酸聚合物的更有效的药物递送控制方法。以十二烷基蓖麻油为原料,制备了以丙烯酸和脂肪酸为共聚物,并以甲基丙烯酸甲酯、丙烯酸和丙烯酰胺为共聚物。采用步变法研究了脂肪酸、丙烯酸共聚物和三共聚物在酸、碱溶液中的溶胀特性。抗生素药物头孢菌素和扑热息痛也通过溶解加入到聚合物混合物中,抗生素药物的释放在细菌染色介质和缓冲溶液中进行评估。结果表明,对乙酰氨基酚的释放速度受pH和聚合物共混物性质的影响。我们的实验数据后来进行了统计分析,以量化聚合物衰减率对相关聚合物溶剂pH密度的精确性质。聚合物衰变速率的时间演化表明,根据所选样品是一般共聚物(线性)还是三共聚物(非线性),从线性到严格非线性的显著转变。非线性数据外推技术已被用于对未来所有时间内保留聚合物重量百分比的变化进行概率预测,从而量化新药物递送方法的有效性程度。
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New oil modified acrylic polymer for pH sensitive drug release: Experimental results and statistical analysis
We report results of an experimental study, complemented by detailed statistical analysis of the experimental data, on the development of a more effective control method of drug delivery using a pH sensitive acrylic polymer. New copolymers based on acrylic acid and fatty acid are constructed from dodecyl castor oil and a tercopolymer based on methyl methacrylate, acrylic acid and acryl amide were prepared using this new approach. Water swelling characteristics of fatty acid, acrylic acid copolymer and tercopolymer respectively in acid and alkali solutions have been studied by a step-change method. The antibiotic drug cephalosporin and paracetamol have also been incorporated into the polymer blend through dissolution with the release of the antibiotic drug being evaluated in bacterial stain media and buffer solution. Our results show that the rate of release of paracetamol getss affected by the pH factor and also by the nature of polymer blend. Our experimental data have later been statistically analyzed to quantify the precise nature of polymer decay rates on the pH density of the relevant polymer solvents. The time evolution of the polymer decay rates indicate a marked transition from a linear to a strictly non-linear regime depending on the whether the chosen sample is a general copolymer (linear) or a tercopolymer (non-linear). Non-linear data extrapolation techniques have been used to make probabilistic predictions about the variation in weight percentages of retained polymers at all future times, thereby quantifying the degree of efficacy of the new method of drug delivery.
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