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The History of Pluronic Lecithin Organogel: An Interview With Marty Jones, BSPharm, FACA, FIACP

Author(s):  Allen Loyd V Jr

Issue:  May/Jun 2003 - Diabetes and Wound Care
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Abstract:  A decade ago, Pluronic lecithin organogel was developed by Marty Jones. His colleague Lawson Kloesel suggested adding Pluronic F127 to stabilize the original formula. In this interview, Jones describes the process of creating this base for transdermal preparations and explains how and why it is effective. Topics discussed include the way Pluronic lecithin organogel was developed, its mechanism of action, ways the first formulation was improved, its clinical evaluation, steps in defining its uses, drugs not appropriate for use in this vehicle, storage or preparations and its future as a transdermal vehicle. Sample formulations for transdermal compounds using Pluronic lecithin organogel are provided, including Ketoprofen 10% in PLO, ABHR in PLO, Ketamine Hydrochloride 10%, Gabapentin 6%, Clonidine Hydrochloride 0.2% in PLO, and Methimazole 5 mg/0.l mL in PLO (Veterinary Formulation).

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Related Categories: DIABETES, HISTORY, PAIN MANAGEMENT

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