Mizuno Satoshi, Gake Shintaro, Takabayashi Makiko, Ito Yuriko, Sanada Hiroko, Sugimoto Natsumi, Maeda Akari, Tamamura Takuto, Sawamoto Kazuki, Hara Yusuke, Ohi Yoshiko, Tsuji Chiaki, Shiomoto Yukiko, Kato Yukio, Fujita Arimi, Shimada Tsutomu, Miyamoto Ken-Ichi, Sai Yoshimichi
Department of Clinical Pharmacokinetics, Graduate School of Medical Sciences, Kanazawa University, Kanazawa, Japan.
Department of Hospital Pharmacy, University Hospital, Kanazawa University, Kanazawa, Japan.
Drug Metab Pharmacokinet. 2025 Feb;60:101035. doi: 10.1016/j.dmpk.2024.101035. Epub 2024 Nov 5.
A retrospective study and an animal study were conducted to investigate factors affecting the transdermal fentanyl dose to achieve adequate pain relief in patients switched from other opioids. In the retrospective study, patient factors were included as gender, age, body mass index (BMI), and serum albumin concentration. In obese (BMI ≥25) patients, the post-titration dose of transdermal fentanyl was significantly lower than in normal (BMI 18.5-25) patients despite the initial dose was the same. To support this unexpected finding, fentanyl was administered intravenously and transdermally to Zucker (fa/fa) rats as an obese model and Zucker (+/+) rats as a control. No difference in systemic clearance (CL) after intravenous administration was observed between the two groups. However, transdermal bioavailability (F) and fentanyl release ratio from the formulation (F) were significantly increased in Zucker (fa/fa) rats compared to Zucker (+/+) rats. Skin availability (F), calculated as F divided by F, was also significantly increased. These results indicated that obesity should be considered as a factor in the titration of transdermal fentanyl dose.
开展了一项回顾性研究和一项动物研究,以调查在从其他阿片类药物转换过来的患者中,影响透皮芬太尼剂量以实现充分疼痛缓解的因素。在回顾性研究中,纳入的患者因素包括性别、年龄、体重指数(BMI)和血清白蛋白浓度。在肥胖(BMI≥25)患者中,尽管初始剂量相同,但透皮芬太尼滴定后的剂量显著低于正常(BMI 18.5 - 25)患者。为支持这一意外发现,将芬太尼静脉注射和经皮给药于作为肥胖模型的 Zucker(fa/fa)大鼠以及作为对照的 Zucker(+/+)大鼠。两组之间静脉给药后的全身清除率(CL)未观察到差异。然而,与 Zucker(+/+)大鼠相比,Zucker(fa/fa)大鼠的经皮生物利用度(F)和制剂中芬太尼释放率(F)显著增加。以 F 除以 F 计算的皮肤可利用性(F)也显著增加。这些结果表明,肥胖应被视为透皮芬太尼剂量滴定中的一个因素。