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Modeling and design of transdermal drug delivery patches containing an external heating device

机译:包含外部加热装置的透皮药物输送贴片的建模和设计

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摘要

Process modeling and design concepts were implemented to aid in the manufacturing of heat-enhanced transdermal drug-delivery systems. The simulated prototype consists of a corticosterone-loaded polymer patch applied to the skin and connected to a heating device in which an exothermic reaction occurs. To achieve a desired transdermal flux of 1.2 x 10~5 mg/cm2 h, this contribution focuses on the influences of the (1) initial reaction rate (-r_(AO)A0), (2) mass of filler material in the device (m), (3) initial concentration (Co) of medicament in the patch and (4) overall heat transfer coefficient (U). A regression technique yielded the following results:-r_(AO) = 3.000x 10~(-2) kg/m~3s,m = 1.251 × 10~(-8)kg, l/=6.124x 10J/m~2Ksand C_0 -1.966 × 10~(-1) kg/m~3. When m was fixed at 12.5g, the optimum design required the following specifications: r_(AO)=2.765× 10~(-2)kg/m~3 s,U= 1.402 × 10~3J/m~2 Ks and Co = 1.941 × 10~(-1) kg/m~3. The priority (Si) of the input factors (i) in reaching the target delivery rate is: S_(Co) > S_(rAO) > S_m > S_U.
机译:实施了过程建模和设计概念,以帮助制造热增强的透皮药物递送系统。模拟的原型包括一个皮质酮加载的聚合物贴剂,该聚合物贴剂涂在皮肤上,并连接到发生放热反应的加热装置上。为了获得1.2 x 10〜5 mg / cm2 h的理想透皮通量,该贡献集中在(1)初始反应速率(-r_(AO)A0),(2)设备中填充材料质量的影响上。 (m),(3)贴剂中药物的初始浓度(Co)和(4)总传热系数(U)。回归技术得出以下结果:-r_(AO)= 3.000x 10〜(-2)kg / m〜3s,m = 1.251×10〜(-8)kg,l / = 6.124x 10J / m〜2Ksand C_0 -1.966×10〜(-1)千克/米〜3。当m固定为12.5g时,最佳设计需要以下规格:r_(AO)= 2.765×10〜(-2)kg / m〜3 s,U = 1.402×10〜3J / m〜2 Ks和Co = 1.941×10〜(-1)千克/米〜3。输入因子(i)在达到目标传递速率时的优先级(Si)为:S_(Co)> S_(rAO)> S_m> S_U。

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