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Computational and experimental studies of controlled release drug delivery: Effect of microsphere diameter and drug size on in-vitro release kinetics.

机译:控释药物递送的计算和实验研究:微球直径和药物大小对体外释放动力学的影响。

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摘要

The use of devices for controlled release therapeutics is a thriving area of research today. Among the many controlled release devices available, poly(lactide-co-glycolide) (PLG) microspheres are perhaps the most popular. While a number of studies have investigated the effects of various parameters on the in-vitro release kinetics from microspheres, detailed studies of the effect of microsphere size have not been presented. This work is an examination of the effect of microsphere size on the in-vitro release kinetics of small-molecule drugs, proteins and oligonucleotides from uniform PLG microspheres.; For small-molecule release, increasing the microsphere diameter slows the release and the profile shifts from smooth, diffusive profile to sigmoidal profile. A model incorporating the effects of polymer degradation and the non-uniform initial drug distribution within the microspheres is developed to describe this transition. The variation of the drug's diffusivity with polymer molecular weight is also included. The model results agree well with experimental data despite using only one fit parameter.; In the case of in-vitro protein (human hemoglobin) and oligonucleotide release, an unusual phenomenon of faster release from larger microspheres is observed. Using polymer characterization techniques, larger microspheres are shown to degrade and erode faster, which explains the faster macromolecule release from them. The faster degradation of larger microspheres is believed to be due to the accumulation of acidic degradation products within the microspheres, which are known to further catalyze PLG degradation.; In order to verify the accumulation of acidic degradation products within larger microspheres, the pH within microspheres was monitored by encapsulating bovine serum albumin labeled with pH-sensitive and pH-insensitive fluorophores. Ratiometric confocal microscopy gives us a direct measure of the pH of the local environment. From these experiments, the increased acidity within larger microspheres is demonstrated.; Overall, the several ways microsphere size affects small-molecule, protein and oligonucleotide release have been clarified in this work.
机译:装置用于控释治疗是当今研究的一个蓬勃发展领域。在许多可用的控释装置中,聚丙交酯-共-乙交酯(PLG)微球可能是最受欢迎的。虽然许多研究已经研究了各种参数对微球体外释放动力学的影响,但尚未提出对微球尺寸影响的详细研究。这项工作是对微球尺寸对均匀PLG微球中小分子药物,蛋白质和寡核苷酸体外释放动力学的影响的研究。对于小分子释放,增加微球直径会减慢释放速度,并且轮廓会从平滑的扩散轮廓变为S形轮廓。建立了一个模型,该模型包含了聚合物降解和微球内初始药物分布不均匀的影响,以描述这种转变。还包括药物扩散率随聚合物分子量的变化。尽管仅使用一个拟合参数,但模型结果与实验数据非常吻合。在体外蛋白质(人血红蛋白)和寡核苷酸释放的情况下,观察到从较大的微球体快速释放的异常现象。使用聚合物表征技术,较大的微球显示出降解和侵蚀更快,这解释了大分子从其中释放得更快。较大的微球的更快降解被认为是由于酸性降解产物在微球内的积累,已知该酸性降解产物会进一步催化PLG降解。为了验证酸性降解产物在较大微球中的积累,通过封装用pH敏感和pH敏感的荧光团标记的牛血清白蛋白来监测微球内的pH。比例共聚焦显微镜可以直接测量当地环境的pH值。从这些实验中,证明了较大的微球内酸度增加。总体而言,这项工作已经阐明了微球大小影响小分子,蛋白质和寡核苷酸释放的几种方式。

著录项

  • 作者

    Raman, Chandrashekar.;

  • 作者单位

    University of Illinois at Urbana-Champaign.;

  • 授予单位 University of Illinois at Urbana-Champaign.;
  • 学科 Health Sciences Pharmacology.; Engineering Chemical.
  • 学位 Ph.D.
  • 年度 2005
  • 页码 107 p.
  • 总页数 107
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 药理学;化工过程(物理过程及物理化学过程);
  • 关键词

  • 入库时间 2022-08-17 11:41:15

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