[HTML][HTML] Migraine treatment: current acute medications and their potential mechanisms of action

JJY Ong, M De Felice - Neurotherapeutics, 2018 - Elsevier
Migraine is a common and disabling primary headache disorder with a significant
socioeconomic burden. The management of migraine is multifaceted and is generally …

Substrates, inducers, inhibitors and structure-activity relationships of human Cytochrome P450 2C9 and implications in drug development

SF Zhou, ZW Zhou, LP Yang… - Current medicinal …, 2009 - ingentaconnect.com
Cytochrome P450 2C9 (CYP2C9) is one of the most abundant CYP enzymes in the human
liver. CYP2C9 metabolizes more than 100 therapeutic drugs, including tolbutamide …

Synthetic and natural compounds that interact with human cytochrome P450 1A2 and implications in drug development

B Wang, SF Zhou - Current medicinal chemistry, 2009 - ingentaconnect.com
Human cytochrome P450 1A2 (CYP1A2) is one of the major CYPs in the liver (&sim13%)
and metabolizes about 20% of clinically used drugs. CYP1A2 is a 515-residue protein with a …

OCT1 mediates hepatic uptake of sumatriptan and loss‐of‐function OCT1 polymorphisms affect sumatriptan pharmacokinetics

J Matthaei, D Kuron, F Faltraco, T Knoch… - Clinical …, 2016 - Wiley Online Library
The low bioavailability of the anti‐migraine drug sumatriptan is partially caused by first‐pass
hepatic metabolism. In this study, we analyzed the impact of the hepatic organic cation …

Sex hormones and calcitonin gene–related peptide in women with migraine: a cross-sectional, matched cohort study

B Raffaelli, E Storch, LH Overeem, M Terhart… - Neurology, 2023 - AAN Enterprises
Background and Objectives Sex hormones may modulate calcitonin gene-related peptide
(CGRP) release in the trigeminovascular system. We studied CGRP concentrations in …

Cytochrome P450 and non–cytochrome P450 oxidative metabolism: Contributions to the pharmacokinetics, safety, and efficacy of xenobiotics

RS Foti, DK Dalvie - Drug Metabolism and Disposition, 2016 - ASPET
The drug-metabolizing enzymes that contribute to the metabolism or bioactivation of a drug
play a crucial role in defining the absorption, distribution, metabolism, and excretion …

Effect of chemical enhancers on the in vitro percutaneous absorption of sumatriptan succinate

A Femenia-Font, C Balaguer-Fernandez… - European Journal of …, 2005 - Elsevier
The effects of percutaneous enhancers on the transdermal absorption of sumatriptan
succinate were investigated by in vitro permeation studies. Pretreatment of porcine skin with …

Dissolving polyvinylpyrrolidone-based microneedle systems for in-vitro delivery of sumatriptan succinate

P Ronnander, L Simon, H Spilgies, A Koch… - European Journal of …, 2018 - Elsevier
In-vitro permeation studies were conducted to assess the feasibility of fabricating dissolving-
microneedle-array systems to release sumatriptan succinate. The formulations consisted …

Estimation of volume of distribution in humans from high throughput HPLC-based measurements of human serum albumin binding and immobilized artificial …

F Hollósy, K Valkó, A Hersey, S Nunhuck… - Journal of medicinal …, 2006 - ACS Publications
The volume of distribution (VD) in humans of 179 known drug molecules (acids, bases, and
neutrals) has been modeled using two biomimetic-binding measurements. The phospholipid …

Fungal hallucinogens psilocin, ibotenic acid, and muscimol: analytical methods and biologic activities

K Stebelska - Therapeutic Drug Monitoring, 2013 - journals.lww.com
Psychoactive drugs of fungal origin, psilocin, ibotenic acid, and muscimol among them have
been proposed for recreational use and popularized since the 1960s, XX century. Despite …