Tag: pharmacokinetics

Opioids and Methadone Equivalents for Clinicians

This 2005 article provides clinicians with guidance on opioid conversion, emphasizing methadone’s unique pharmacokinetic properties. Methadone’s potency varies with prior opioid exposure, necessitating careful dose adjustments. The article underscores the importance of individualized dosing and monitoring to ensure patient safety during opioid rotation, particularly when transitioning to methadone.

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A simple practice guide for dose conversion between animals and human

This 2016 review provides a practical framework for translating drug doses between animal models and humans using allometric scaling based on body surface area (BSA). It outlines a five-step method: determining the no observed adverse effect level (NOAEL) in animals, converting NOAEL to human equivalent dose (HED) using species-specific Km

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Vitamin C Pharmacokinetics: Implications for Oral and Intravenous Use

This 2004 study by Padayatty et al. investigated the pharmacokinetics of vitamin C administered orally and intravenously in 17 healthy volunteers. The study found that oral administration of vitamin C produces tightly controlled plasma concentrations due to limited absorption and renal excretion. In contrast, intravenous administration bypasses these controls, resulting

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Concentration-Dependent Activity of Hydromethylthionine on Cognitive Decline and Brain Atrophy in Mild to Moderate Alzheimer’s Disease

This 2019 study analyzed data from two Phase III trials involving 1,162 patients with mild to moderate Alzheimer’s disease (AD) to assess the relationship between hydromethylthionine (LMTM) plasma concentration and clinical outcomes. Findings revealed that even at a low dose of 8 mg/day, patients with higher plasma levels experienced significant

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Pharmacokinetics and safety of intravenously administered citrulline in children undergoing congenital heart surgery: potential therapy for postoperative pulmonary hypertension

This study evaluated the safety and pharmacokinetics of intravenous citrulline in infants and children undergoing congenital heart surgery. In Phase 1, a dose-escalation protocol (50, 100, 150 mg/kg) was used, with a target plasma citrulline trough of 80–100 µmol/L. The 150 mg/kg dose achieved this target. Due to citrulline’s short

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Topical Pharmacotherapy for Skin Cancer: Part I. Pharmacology

This review article provides a detailed examination of the pharmacologic properties of topical agents used in the treatment of superficial skin cancers such as actinic keratoses and basal cell carcinoma. It reviews the mechanisms of action, pharmacokinetics, formulations, clinical indications, adverse effect profiles, and contraindications of approved agents like 5-fluorouracil,

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Piracetam: a review of pharmacological properties and clinical uses

Piracetam, a cyclic derivative of GABA, exhibits neuroprotective, anticonvulsant, and nootropic properties. It modulates neurotransmission across cholinergic and glutamatergic systems, enhances neuroplasticity, and improves microcirculation by reducing erythrocyte adhesion and vasospasm. Clinically, piracetam has demonstrated efficacy in cognitive disorders, dementia, vertigo, cortical myoclonus, dyslexia, and sickle cell anemia. Despite requiring

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The Controversial Place of Vitamin C in Cancer Treatment

This 2008 review critically examines the role of vitamin C in cancer therapy. While early studies, notably by Linus Pauling, suggested benefits of high-dose vitamin C, subsequent randomized trials using oral administration did not confirm these findings. Recent pharmacokinetic data indicate that intravenous vitamin C can achieve plasma concentrations with

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Intravenously Administered Vitamin C as Cancer Therapy: Three Cases

This 2006 case series evaluated three patients with advanced cancers who received high-dose intravenous vitamin C (IVC) therapy. Each patient experienced unexpectedly prolonged survival and clinical improvement. Pharmacokinetic data indicated that IVC achieves plasma concentrations (~14,000 μmol/L) significantly higher than oral administration, levels at which vitamin C exhibits selective cytotoxicity

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