Linke Wu , Hui Li , Yunyun Wang, Chengyu Liu, Zhixin Zhao, Guisheng Zhuang, Quanmin Chen, Weichang Zhou, Jeremy Guo
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引用次数: 0
Abstract
The development of PFS requires a detailed understanding of the forces occurring during the drug administration process and patient’s capability. This research describes an advanced mathematic injection force model that consisting hydrodynamic force and friction force. The hydrodynamic force follows the basic law of Hagen-Poiseuille but refines the modeling approach by delving into specific properties of drug viscosity (Newtonian and Shear-thinning) and syringe shape constant, while the friction force was accounted from empty barrel injection force. Additionally, we take actual temperature of injection into consideration, providing more accurate predication. The results show that the derivation of the needle dimension constant and the rheological behavior of the protein solutions are critical parameters. Also, the counter pressure generated by the tissue has been considered in actual administration to address the issue of the inaccuracies of current injection force evaluation preformed in air, especially when the viscosity of the injected drug solution is below 9.0 cP (injecting with 1 mL L PFS staked with 29G ½ inch needle). Human factor studies on patients’ capability against medication viscosity filled the gap in design space of PFS drug product and available viscosity data in very early phase.
开发 PFS 需要详细了解给药过程中发生的力和患者的能力。本研究介绍了一种先进的注射力数学模型,该模型由流体动力和摩擦力组成。流体动力遵循哈根-普瓦耶基本定律,但通过深入研究药物粘度(牛顿和剪切稀化)和注射器形状常数的特定属性,对建模方法进行了改进,而摩擦力则是根据空桶注射力计算得出的。此外,我们还考虑了注射时的实际温度,从而提供了更精确的预测。结果表明,针头尺寸常数的推导和蛋白质溶液的流变行为是关键参数。此外,我们还考虑了实际给药过程中组织产生的反压力,以解决目前在空气中进行的注射力评估不准确的问题,尤其是当注射药物溶液的粘度低于 9.0 cP 时(使用 29G ½ 英寸针头注射 1 mL L PFS)。对患者针对药物粘度的能力进行的人为因素研究填补了 PFS 药物产品设计空间和早期可用粘度数据的空白。
期刊介绍:
The European Journal of Pharmaceutics and Biopharmaceutics provides a medium for the publication of novel, innovative and hypothesis-driven research from the areas of Pharmaceutics and Biopharmaceutics.
Topics covered include for example:
Design and development of drug delivery systems for pharmaceuticals and biopharmaceuticals (small molecules, proteins, nucleic acids)
Aspects of manufacturing process design
Biomedical aspects of drug product design
Strategies and formulations for controlled drug transport across biological barriers
Physicochemical aspects of drug product development
Novel excipients for drug product design
Drug delivery and controlled release systems for systemic and local applications
Nanomaterials for therapeutic and diagnostic purposes
Advanced therapy medicinal products
Medical devices supporting a distinct pharmacological effect.