Am J Health-Syst Pharm
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


This Article
Right arrow Order Full text via Infotrieve
Right arrow Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Driscoll, D.
Right arrow Articles by Bistrian, B.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Driscoll, D.
Right arrow Articles by Bistrian, B.
American Journal of Health-System Pharmacy, Vol 52, Issue 6, 623-634
Copyright © 1995 by American Society of Health-System Pharmacists


Articles

Physicochemical stability of total nutrient admixtures

DF Driscoll, HN Bhargava, L Li, RH Zaim, VK Babayan, and BR Bistrian


The effect of six independent factors on the stability of i.v. nutritional emulsions was studied. Forty-five i.v. nutritional admixtures were prepared, each containing the following: (1) amino acids (range, 2.5-7%), (2) hydrated glucose (range, 5-20%), (3) lipid emulsion (range, 2-5%), (4) monovalent cations (range, 0-150 meq/L), (5) divalent cations (range, 4-20 meq/L), and (6) trivalent cations (range, 0-10 mg of elemental iron/L). Stability assessments included particle-size analysis, pH determination, and visual inspection. Sizing and counting of fat particles was achieved by using light obscuration and dynamic light scatter methods. Light obscuration and visual assessments were performed at 0, 6, 12, 24, and 30 hours. Dynamic light scatter and pH determinations were performed at 0 and 30 hours. Multiple stepwise regression analysis revealed that trivalent cation concentration was the only variable that affected the stability of nutritional emulsions (p < 0.00001), accounting for approximately 60% of the potentially dangerous increases in fat particle sizes observed. In addition, a percentage of large fat particles (> 5 microns in diameter) greater than 0.4% was associated with unstable emulsions. However, this instability was visibly evident only 65% of the time. Changes in mean globule diameter, cream-layer thickness, and pH did not reveal instability in these emulsions. Emulsions in which > 0.4% of the initial fat concentration consists of particles of > 5 microns in diameter are likely to become unstable. Of the six factors studied, the trivalent cation in iron dextran was most disruptive to lipid-based parenteral nutrient admixtures.
 



This article has been cited by other articles:


Home page
Am J Health Syst PharmHome page
K. Nemec, H. Kopelent-Frank, and R. Greif
Standardization of infusion solutions to reduce the risk of incompatibility
Am. J. Health Syst. Pharm., September 1, 2008; 65(17): 1648 - 1654.
[Abstract] [Full Text] [PDF]


Home page
JPEN J Parenter Enteral NutrHome page
M. Skouroliakou, C. Matthaiou, A. Chiou, D. Panagiotakos, A. Gounaris, T. Nunn, and N. Andrikopoulos
Physicochemical Stability of Parenteral Nutrition Supplied as All-in-One for Neonates
JPEN J Parenter Enteral Nutr, March 1, 2008; 32(2): 201 - 209.
[Abstract] [Full Text] [PDF]


Home page
Am J Health Syst PharmHome page
D. F. Driscoll
Globule-size distribution in injectable 20% lipid emulsions: Compliance with USP requirements
Am. J. Health Syst. Pharm., October 1, 2007; 64(19): 2032 - 2036.
[Abstract] [Full Text] [PDF]


Home page
Nutr Clin PractHome page
G. P. Zaloga, A. J. Dunham, T. M. Gonyon, L. M. Best, and M. Groves
Safety and Stability of Lipid Emulsions
Nutr Clin Pract, June 1, 2007; 22(3): 367 - 369.
[Full Text] [PDF]


Home page
Nutr Clin PractHome page
D. F. Driscoll
Safety and Stability of Lipid Emulsions--Response
Nutr Clin Pract, June 1, 2007; 22(3): 370 - 372.
[Full Text]


Home page
JPEN J Parenter Enteral NutrHome page
D. F. Driscoll, P.-R. Ling, and B. R. Bistrian
Physical Stability of 20% Lipid Injectable Emulsions via Simulated Syringe Infusion: Effects of Glass vs Plastic Product Packaging
JPEN J Parenter Enteral Nutr, March 1, 2007; 31(2): 148 - 153.
[Abstract] [Full Text] [PDF]


Home page
Am J Health Syst PharmHome page
D. F. Driscoll, A. P. Silvestri, B. R. Bistrian, and B. A. Mikrut
Stability of total nutrient admixtures with lipid injectable emulsions in glass versus plastic packaging
Am. J. Health Syst. Pharm., February 15, 2007; 64(4): 396 - 403.
[Abstract] [Full Text] [PDF]


Home page
Nutr Clin PractHome page
T. Canada
Pathological Consequences From the Infusion of Unstable Lipid Emulsion Admixtures in Guinea Pigs
Nutr Clin Pract, December 1, 2006; 21(6): 636 - 637.
[Abstract] [Full Text]


Home page
Am J Health Syst PharmHome page
D. F. Driscoll, M. Parikh, A. P. Silvestri, K. Klutsch, B. R. Bistrian, and J. Nehne
Establishing a stability window for medium- and long-chain-triglyceride lipid-based total nutrient admixtures using USP standards.
Am. J. Health Syst. Pharm., November 1, 2006; 63(21): 2135 - 2143.
[Abstract] [Full Text] [PDF]


Home page
Nutr Clin PractHome page
D. F. Driscoll
Lipid Injectable Emulsions: 2006
Nutr Clin Pract, August 1, 2006; 21(4): 381 - 386.
[Abstract] [Full Text] [PDF]


Home page
Am J Health Syst PharmHome page
D. F. Driscoll, A. P. Silvestri, J. Nehne, K. Klutsch, B. R. Bistrian, and W. Niemann
Physicochemical stability of highly concentrated total nutrient admixtures for fluid-restricted patients
Am. J. Health Syst. Pharm., January 1, 2006; 63(1): 79 - 85.
[Abstract] [Full Text] [PDF]


Home page
Nutr Clin PractHome page
D. F. Driscoll
Total Nutrient Admixtures: Theory and Practice
Nutr Clin Pract, June 1, 1995; 10(3): 114 - 119.
[Abstract] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 1995 by the American Society of Health-System Pharmacists.