Comparative Evaluation of Cyclooxygenase Inhibition Profiles Across Various NSAID Forms and Doses: Implications for Efficacy and Adverse Effects.

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Tác giả: Hidekazu Kuma, Kenshu Shirakawa, Masafumi Takeno, Takaaki Terahara, Shigeki Yamaguchi

Ngôn ngữ: eng

Ký hiệu phân loại:

Thông tin xuất bản: New Zealand : Pain and therapy , 2025

Mô tả vật lý:

Bộ sưu tập: NCBI

ID: 175934

INTRODUCTION: Nonsteroidal anti-inflammatory drugs (NSAIDs) are commonly used for pain disorders and exert pharmacological effects by inhibiting cyclooxygenase (COX). Although previous studies have evaluated the COX inhibitory activity and selectivity of NSAIDs, none has compared COX inhibitory concentrations with the plasma concentrations of clinical doses or investigated the efficacy and adverse effects of different dosage forms. Therefore, in this study we evaluated the COX inhibitory activities and inhibition rates of clinical doses of the various NSAID formulations, especially diclofenac sodium. METHODS: Human blood and the drug (diclofenac sodium, celecoxib, ibuprofen, flurbiprofen, or etodolac) were mixed and incubated, and the supernatant was collected and quantified the COX inhibitory activity of each drug by ELISA. Logistic regression analyses were used to calculate the inhibition rates at maximum plasma drug concentration (C RESULTS: COX-2 inhibition rate at C DISCUSSION: This result explains why gastrointestinal disorders frequently occur with oral and suppository formulations of diclofenac sodium despite its relatively high COX-2 selectivity. Although the plasma drug concentration of the transdermal formulation is lower than oral and suppository formulations, it has an inhibition rate above IC CONCLUSION: The findings explain why the transdermal formulation exerts an analgesic effect despite having a lower C
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