Faculty of Pharmacy and Pharmaceutical Sciences, Josai University, 1-1 Keyakidai, Sakado, Saitama, 350-0295, Japan.
Faculty of Pharmaceutical Sciences, Josai International University, 1 Gumyo, Togane, Chiba-Ken, 283-8555, Japan.
Pharm Res. 2023 Aug;40(8):1953-1963. doi: 10.1007/s11095-023-03529-6. Epub 2023 May 10.
Hollow microneedles (hMNs) have been gaining attention as a tool to enable the intradermal (i.d.) administration of pharmaceutical products. However, few reports have examined the effect of administration volume on distribution in the skin and pharmacokinetics parameters after i.d. injection. In the present study, a model middle molecular weight compound, fluorescein isothiocyanate dextran (M.W. 4,000, FD-4), was selected, and blood concentration-time profiles after i.d. and subcutaneous (s.c.) injections with different administration volumes were compared.
FD-4 solution was injected i.d. using a hMN or injected s.c. with a 27 G needle. Pharmacokinetics and dermatokinetics of FD-4 were analyzed using a compartment model. The skin distribution of iodine, as an X ray tracer, was used to evaluate drug disposition.
With the administered drug assumed to be absorbed from the broad injection site into blood vessels in the upper and lower dermis by rapid (k) and slow (k) first-order absorption rate constants, respectively, better agreement of observed and theoretical values was obtained. Furthermore, the fraction, F, of the administered dose absorbed with k decreased with the increase in injection volume after i.d. injection, although the pharmacokinetics parameters were almost the same regardless of administration volume after s.c. injection.
The drug distribution in the skin may be related to the obtained pharmacokinetics parameters suggested that the number of needles in the MN system and the total administration volume should be considered in designing hMN systems. The present results provide useful information that may support effective drug delivery with hMNs.
空心微针(hMN)作为一种能够实现药物经皮(i.d.)给药的工具,已引起人们的关注。然而,很少有报道研究给药体积对 i.d.注射后皮肤分布和药代动力学参数的影响。在本研究中,选择了一种模型中分子质量化合物,异硫氰酸荧光素葡聚糖(M.W. 4000,FD-4),并比较了不同给药体积 i.d.和皮下(s.c.)注射后 FD-4 的血药浓度-时间曲线。
使用 hMN 进行 FD-4 溶液 i.d.注射或使用 27 G 针头进行 s.c.注射。使用房室模型分析 FD-4 的药代动力学和皮肤动力学。用碘作为 X 射线示踪剂评估药物分布。
假设药物通过快速(k)和缓慢(k)一级吸收速率常数从广泛的注射部位被吸收到真皮的上下血管中,观察到的和理论值的一致性更好。此外,i.d.注射后,随着给药体积的增加,通过 k 吸收的给药剂量分数 F 减少,尽管 s.c.注射后药代动力学参数几乎相同。
皮肤内的药物分布可能与获得的药代动力学参数有关,这表明在设计 hMN 系统时应考虑 MN 系统中的针数和总给药体积。本研究结果提供了有用的信息,可能为 hMN 的有效药物输送提供支持。