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首页> 外文期刊>Applied Surface Science >Simultaneous determination of drug surface concentration and polymer degradation kinetics in biodegradable polymer/drug membranes: a model drug delivery system
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Simultaneous determination of drug surface concentration and polymer degradation kinetics in biodegradable polymer/drug membranes: a model drug delivery system

机译:可生物降解的聚合物/药物膜中药物表面浓度和聚合物降解动力学的同时测定:模型药物递送系统

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摘要

This paper reports new simultaneous ToF-SIMS analysis to determine both the earliest stage of polymer degradation and the surface concentration of a drug additive. The static SIMS spectra of a model Ph_3N/poly(L-lactic acid) (PLLA) (20:80 wt.%) blend matrix (t ~ 0.4 μm on 1.0 cm~2) hydrolyzed in buffered conditions are simultaneously and independently analyzed in the low mass range for the surface accumulation profile of Ph_3N and in the high mass for the hydrolytic degradation kinetics of PLLA, respectively. The rate of PLLA degradation at pH 10.0 is ~ 2 times faster than that at pH 7.4, but the corresponding rate of Ph_3N accumulation at the surface is accelerated by a factor of ~ 10.5 times faster. The results provide new insight in evaluating the surface concentration of Ph_3N (pK_b = 0) from the blends, indicating that the initial rapid increase in surface concentration of Ph_3N is related to but not singularly dependent on the rate of PLLA degradation.
机译:本文报告了同时进行的ToF-SIMS分析,以确定聚合物降解的最早阶段和药物添加剂的表面浓度。同时并独立分析了在缓冲条件下水解的Ph_3N /聚(L-乳酸)(PLLA)(20:80 wt。%)混合基质(t〜0.4μm,1.0 cm〜2)的静态SIMS光谱。 Ph_3N的表面累积曲线的质量范围较小,而PLLA的水解降解动力学的质量范围较高。 pH 10.0时的PLLA降解速率比pH 7.4时的降解速率快约2倍,但相应的Ph_3N在表面的积累速率却加快了约10.5倍。结果为评估掺混物中的Ph_3N表面浓度(pK_b = 0)提供了新的见识,表明Ph_3N表面浓度的初始快速增加与PLLA降解速率有关,但并非唯一。

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