Nature of precipitation resulted from intravenous drugs incompatibility

In critical care, the co-administration of intravenous drugs often leads to physical incompatibilities, resulting in harmful precipitates. This study evaluated the nature of drug-induced precipitation in terms of size, shape, and quantity. Twelve drugs previously reported to be incompatible were tested with infusion fluids. Particle detection was conducted using an Olympus CX41 microscope with a 1 µm detection limit, enhanced by darkfield microscopy for better sensitivity. Particle size was analyzed using Feret’s diameter via the Optilab imaging system. Precipitates ranged from 5– 150 µm, with smaller particles (<10 µm) seen in furosemide and subvisible particles (10–50 µm) in cefotaxime, chloramphenicol, and paracetamol. Visible particles were noted in acyclovir, ampicillin, meropenem, phenobarbital, and phenytoin. Most macro-precipitates were acicular, while micro-precipitates tended to be irregular. Particle counts ranged from 80 to 2,000 particles/mL. The findings highlight the clinical risk of particulate contamination due to drug incompatibilities, emphasizing the need for careful medication management.

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Charles Sturt University Research Output (CRO)
Published
2025-09-01
Primary Topic
Inhalation and Respiratory Drug Delivery
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article
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article

Nature of precipitation resulted from intravenous drugs incompatibility

Suci HANIFAH, Ross A. Kennedy, Patrick A.; id_orcid 0000-0001-8918-2119 Ball
Charles Sturt University Research Output (CRO)
Inhalation and Respiratory Drug Delivery
article

Nature of precipitation resulted from intravenous drugs incompatibility

Suci HANIFAH, Ross A. Kennedy, Patrick A.; id_orcid 0000-0001-8918-2119 Ball
article en

Abstract

In critical care, the co-administration of intravenous drugs often leads to physical incompatibilities, resulting in harmful precipitates. This study evaluated the nature of drug-induced precipitation in terms of size, shape, and quantity. Twelve drugs previously reported to be incompatible were tested with infusion fluids. Particle detection was conducted using an Olympus CX41 microscope with a 1 µm detection limit, enhanced by darkfield microscopy for better sensitivity. Particle size was analyzed using Feret’s diameter via the Optilab imaging system. Precipitates ranged from 5– 150 µm, with smaller particles (<10 µm) seen in furosemide and subvisible particles (10–50 µm) in cefotaxime, chloramphenicol, and paracetamol. Visible particles were noted in acyclovir, ampicillin, meropenem, phenobarbital, and phenytoin. Most macro-precipitates were acicular, while micro-precipitates tended to be irregular. Particle counts ranged from 80 to 2,000 particles/mL. The findings highlight the clinical risk of particulate contamination due to drug incompatibilities, emphasizing the need for careful medication management.

Charles Sturt University Research Output (CRO)
University of Wolverhampton (GB), Islamic University of Indonesia (ID)
Good health and well-being
Openalex Percentile: Top 24%
Inhalation and Respiratory Drug Delivery
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Nature of precipitation resulted from intravenous drugs incompatibility — Suci HANIFAH, Ross A. Kennedy, et al. · Charles Sturt University Research Output (CRO) (2025) | TGRS Research Map | TGRS