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Polyethylene glycol (PEG) and polyethylene oxide (PEO) are polymers having an identical structure except for chain length and end groups, and are the most commercially important polyethers. Polyethylene glycol refers to an oligomer or polymer with low molecular weight while polyethylene oxide is used for higher molecular weights. PEG generally is a liquid while PEO is a low-melting solid. Both are prepared by polymerization of ethylene oxide. While they find use in different applications and have different physical properties (i.e. more...

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viscosity) due to chain length effects, their chemical properties are nearly identical.

Polyethylene glycol has the following structure:

HO-(CH2-CH2-O)n-H

Pegylation is the act of adding a PEG structure to another larger molecule, for example, a protein (which is then referred to as pegylated).

PEG is soluble in water, methanol, benzene, dichloromethane and is insoluble in diethyl ether and hexane. It is coupled to hydrophobic molecules to produce non-ionic surfactants.

Clinical uses

Polyethylene glycol is non-toxic and is used in a variety of products. It is the basis of a number of laxatives (e.g. macrogol-containing products such as Movicol® and polyethylene glycol 3350, or MiraLax®). It is the basis of many skin creams, as cetomacrogol, and sexual lubricants, frequently combined with glycerin.

Polyethylene glycol with added electrolytes is used for bowel preparation and drug overdoses. It is sold under the brandnames GoLYTELY and Colyte.

When attached to various protein medications, PEG allows a slow release of the carried protein. This makes for a longer acting medicinal effect and/or reduces toxicity, and allows longer dosing intervals. Examples include PEG-interferon alpha (used to treat hepatitis C) and PEG-filgrastim (Neulasta®).

It has been shown that PEG can improve healing of spinal injuries in dogs .

Other uses

PEG is also used in liquid body armor and tattoos to monitor diabetes. Functional groups of PEG give polyurethane elastomers their "rubberiness", for applications such as foams (foam rubber) and fibers (spandex). Its backbone structure is analogous to that of silicone, another elastomer.

Since PEG is a flexible polymer, it can be used to create very high osmotic pressures (tens of atmospheres). It also is unlikely to have specific interactions with biological chemicals. These properties make PEG one of the most useful molecules for applying osmotic pressure in biochemistry experiments, particularly when using the osmotic stress technique.

PEO can serve as the separator and electrolyte solvent in lithium polymer cells. Its low diffusivity often requires high temperatures of operation, but its high viscosity even near its melting point allows very thin electrolyte layers. While crystallization of the polymer can degrade performance, many of the salts used to carry charge can also serve as a kinetic barrier to the formation of crystals. Such batteries carry greater energy for their weight than other lithium ion battery technologies.

Polyethylene glycol is also commonly used as a polar stationary phase for gas chromatography.

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Distal intestinal obstruction syndrome after surgery in cystic fibrosis - communications to the editor - Letter to the Editor
From CHEST, 12/1/03 by Michael P. Boyle

To the Editor:

We greatly appreciated the review by Gilljam et al (1) (January, 2003) on GI complications after lung transplantation in patients with cystic fibrosis (CF). Their experience mirrors our own: distal intestinal obstruction syndrome (DIOS) can be as important an issue after transplant in individuals with CF as management of pulmonary complications. In the initial days after lung transplant, the continuation of high-dose narcotics, postoperative ileus, poor oral intake, and bed rest creates a risk for DIOS that makes the estimate of 20% incidence seem optimistically low. Gill jam et al (1) wisely, suggest "prevention and early medical treatment" to prevent DIOS after transplant, and report success with a routine of early enteral feeding and, if needed, administration of electrolyte GI lavage solution 24 h after transplantation.

We too have noted a dramatic effect of a preventive protocol on the incidence of DIOS after lung transplant in individuals with CF. We now start this preventive protocol prior to surgery. After having three consecutive CF lung transplants complicated after surgery by DIOS, we adopted a protocol that included all individuals with CF awaiting lung transplant having access at home to polyethylene glycol lavage solution (GoLytely; Braintree Laboratories; Braintree. MA). As soon as they are contacted to come to the hospital for their transplant because donor lungs are available, they immediately drink 2 L of polyethylene glycol lavage solution. Combining this approach with the steps recommended in the article by Gilljam et al (1) has virtually eliminated the incidence of DIOS in our CF population immediately after transplant. This protocol has been adopted by other transplant centers, including the University of North Carolina at Chapel Hill, with similar success, Initial concern about patients drinking a large volume of liquid prior to surgery has been tempered by the much less complicated postoperative courses mid the observation that several hours invariably lapse between patient notification and actual surgery.

The principles of prevention and early treatment espoused by Gilljam et al (1) can be extended to apply to all surgeries in individuals with CF hi which Surgery will likely be followed by narcotic use and postoperative a dynamic ileus. After having postoperative DIOS occur in individuals with CF undergoing cholecystectomy and other ,abdominal surgeries, we have now made pretreatment with polyethylene glycol lavage solution a standard part of preoperative preparation.

Kudos to Dr. Gilljam and coworkers for their thorough review of an underrecognized complication of CF. By applying their principles of prevention and early treatment for DIOS, we should be able to dramatically decrease the incidence of GI complications not only after lung transplantation in CF, but after all surgeries.

REFERENCE

(1) Gilljam M, Chaparro C, Tullis E, et al. GI complications after lung transplantation in patients with cystic fibrosis. Chest 2003:1:23:37-41

Michael P. Boyle, MD, FCCP

Johns Hopkins Adult CF Program

Jonathan B. Orens, MD, FCCP

Johns Hopkins Lung Transplant Program

Baltimore, MD

Reproduction of tiffs article is prohibited without written permission from the American College of Chest Physicians (e-mail: permissions@chestnet.org).

Correspondence to: Michael P. Boyle, MD, FCCP, Assistant Professor of Medicine, Director, Johns Hopkins Adult CF Program The Johns Hopkins, Hospital, 1830 E. Monument St, Fifth Floor, Baltimore, MD 21205; e-mail: mboyle@jhmi.edu

COPYRIGHT 2003 American College of Chest Physicians
COPYRIGHT 2004 Gale Group

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