Ding Amy G, Shenderova Anna, Schwendeman Steven P
Department of Pharmaceutical Sciences, The University of Michigan, Ann Arbor, Michigan 48109-1065, USA.
J Am Chem Soc. 2006 Apr 26;128(16):5384-90. doi: 10.1021/ja055287k.
An equilibrium mathematical model that accurately predicts microclimate pH (mupH) in thin biodegradable polymer films of poly(lactic-co-glycolic acid) (PLGA) is described. mupH kinetics was shown to be primarily a function of: (i) kinetics of water-soluble acid content and composition in the polymer matrix and (ii) polymer/water partition coefficient of water-soluble degradation products (P(i)). Polymers were coated on standard pH glass electrodes, and mupH was measured potentiometrically. Water-soluble acid distribution and content in PLGA films were determined by pre-derivatization HPLC. Polymer degradation products partitioned favorably in the polymer phase relative to water (P(i) range: approximately 6-100), and P(i) increased with increasing hydrophobicity of the acidic species according to a linear free energy law related to reversed phase HPLC retention time for the corresponding derivatized bromophenacyl esters. The mupH predicted by the model was in excellent agreement with experimental mupH for several PLGAs as a function of time and PLGA lactic/glycolic acid ratio. These data may be useful to slowly release pH-sensitive PLGA-encapsulated bioactive substances and provide a general framework for predicting partitioning behavior of degradation products in biodegradable polymers.
本文描述了一种能准确预测聚乳酸-乙醇酸共聚物(PLGA)薄型可生物降解聚合物薄膜微气候pH值(mupH)的平衡数学模型。结果表明,mupH动力学主要取决于:(i)聚合物基质中水溶性酸含量和组成的动力学,以及(ii)水溶性降解产物的聚合物/水分配系数(P(i))。将聚合物涂覆在标准pH玻璃电极上,通过电位法测量mupH。采用衍生化高效液相色谱法(HPLC)测定PLGA薄膜中水溶性酸的分布和含量。相对于水,聚合物降解产物在聚合物相中具有良好的分配性(P(i)范围:约6 - 100),并且根据与相应衍生化溴苯甲酰酯的反相HPLC保留时间相关的线性自由能定律,P(i)随着酸性物质疏水性的增加而增大。该模型预测的mupH与几种PLGA随时间和PLGA乳酸/乙醇酸比例变化的实验mupH值高度吻合。这些数据对于缓慢释放pH敏感的PLGA包裹生物活性物质可能有用,并为预测降解产物在可生物降解聚合物中的分配行为提供了一个通用框架。