Human repeated insult patch testing with an experimental pump spray antiperspirant formulation elicited sensitization reactions in two separate groups of panelists. After several rechallenges with variations of the formula components, isostearyl alcohol at 5% concentration in the product emerged as the causative agent in both groups. Due to the high content of alcohol in the pump spray antiperspirant, control patch testing was done with 100% ethanol, which served as the vehicle for testing isostearyl alcohol alone. All reactions were negative. Six out of 148 participants in the first group and one of 60 in the second group exhibited sensitization responses to isostearyl alcohol.
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http://dx.doi.org/10.1111/j.1600-0536.1980.tb04928.x | DOI Listing |
Biol Pharm Bull
June 2015
Department of Pharmacy Practice and Science, School of Pharmaceutical Science, University of Shizuoka.
A transdermal oil-in-water type emulsified formulation containing propiverine hydrochloride, used for treatment of an overactive bladder (OAB), was evaluated for in vitro skin permeation under finite conditions and in vivo transdermal absorption. Propiverine hydrochloride solubility was determined using 1,3-butyleneglycol, polyoxyethylene (2) oleylether, isostearyl alcohol, and lauryl alcohol. The solubility increased as the solubility parameter value increased.
View Article and Find Full Text PDFPhys Chem Chem Phys
March 2013
School of Physics, Key Laboratory of Cluster Science of Ministry of Education, Beijing Institute of Technology, Beijing, China 100081.
Understanding the role of kinetics in fiber network microstructure formation is of considerable importance in engineering gel materials to achieve their optimized performances/functionalities. In this work, we present a new approach for kinetic-structure analysis for fibrous gel materials. In this method, kinetic data is acquired using a rheology technique and is analyzed in terms of an extended Dickinson model in which the scaling behaviors of dynamic rheological properties in the gelation process are taken into account.
View Article and Find Full Text PDFInt J Pharm
August 2010
Stiefel - a GSK Company, 8 Macro Court, Rowville, Victoria 3178, Australia.
We demonstrate drug release properties from hydroethanolic formulations as a function of the drug's lipophilicity (logP), solvent lipophilicity and drug-polymer interactions, for the first time. A hydrophilic polymer, hydroxypropyl cellulose (HPC), provides the non-Fickian slower release of the lipophilic drug, lidocaine (logP=2.6) and the burst (Fickian) release of hydrophilic drug, lidocaine hydrochloride (logP
J Phys Chem B
December 2005
Department of Physics, National University of Singapore, 2 Science Drive 3, Singapore 117542.
The architecture of a biocompatible organogel formed by gelation of a small molecule organic gelator, N-lauroyl-L-glutamic acid di-n-butylamide, in isostearyl alcohol was investigated based on a supersaturation-driven crystallographic mismatch branching mechanism. By controlling the supersaturation of the system, the correlation length that determines the mesh size of the fiber network was finely tuned and the rheological properties of the gel were engineered. This approach is of considerable significance for many gel-based applications, such as controlled release of drugs that requires precise control of the mesh size.
View Article and Find Full Text PDFJ Control Release
August 2005
Department of Pharmacy, National University of Singapore, Republic of Singapore.
Small molecule gelling agent (SMGA) gels were developed using the gelator GP-1 in the solvents, namely, isostearyl alcohol (ISA) and propylene glycol (PG), to deliver haloperidol through the skin. The concentrations of the drug, haloperidol, the enhancer, farnesol and the gelator, GP-1 are 3 mg/ml, 5% (w/v) and 5% (w/v), respectively. The study employed a three-factor full factorial statistical design to investigate the influence of factor level changes on the permeability coefficient and permeation lag-time of haloperidol.
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