Chemical stability and physical compatibility of meropenem in admixtures for continuous and extended intravenous

Sara Giménez-Giner1, Antoni Llopis-Alemany1, Begoña Porta-Oltra1

  • 1Department of Pharmacy, Doctor Peset University Hospital, Valencia, Spain.

Abstract

Insights

Meropenem stability is maintained for prolonged infusions in critical care when refrigerated. Anticipated preparation in infusion bags is feasible for up to 24 hours, ensuring drug efficacy.

Area of Science:

  • Pharmacology
  • Critical Care Medicine
  • Pharmaceutical Chemistry

Background:

  • Prolonged intravenous beta-lactam infusions improve clinical cure rates in critical or septic patients.
  • Evaluating meropenem stability is crucial for optimizing its administration in clinical practice.
  • Assessing stability under various conditions informs the possibility of pre-prepared admixtures.

Purpose of the Study:

  • To determine the chemical stability and physical compatibility of meropenem admixtures.
  • To evaluate meropenem stability under conditions simulating clinical administration.
  • To assess the feasibility of anticipated preparation of meropenem infusions.

Main Methods:

  • Meropenem admixtures (6g or 1-2g) in 0.9% sodium chloride (NS) were prepared in infusors and infusion bags.
  • Tested at various temperatures (4.5°C, 32°C, 24.5°C) and infusion rates (2mL/h, 10mL/h).
  • Chemical stability assessed via HPLC; physical compatibility by pH and visual inspection.

Main Results:

  • Meropenem stability in infusors decreased with higher concentrations and temperatures.
  • Admixtures in infusion bags demonstrated stability and compatibility for at least 24 hours.
  • Refrigeration at 4.5°C is essential for maintaining stability in high-concentration infusor admixtures.

Conclusions:

  • Meropenem 6g in 24h infusion at 10mL/h is feasible at 4.5°C in infusors.
  • Extended infusions (3-4h) of 1-2g meropenem in infusion bags are viable.
  • Anticipated preparation of meropenem admixtures in infusion bags is possible with 24-hour stability.

Related Concept Videos

Factors Affecting Dissolution: Drug Permeability, Stability and Stereochemistry01:20

Factors Affecting Dissolution: Drug Permeability, Stability and Stereochemistry

Orally administered drugs primarily enter the systemic circulation via passive diffusion through the intestinal membranes. The drug's absorption is influenced by drug stability in the gastrointestinal GI tract, membrane permeability, the surface area available for absorption, luminal drug concentration, and residence time in the lumen. Drug permeability can be enhanced by adjusting the lipophilicity, polarity, or molecular size of the drug, promoting its passive transport across intestinal...
244
Waterproofing and Anti-Bacterial Admixtures in Concrete01:22

Waterproofing and Anti-Bacterial Admixtures in Concrete

Concrete's susceptibility to water absorption is due to the capillary action within the pores of its hydrated cement paste. This action draws water in, creating the need for waterproofing admixtures to prevent such penetration. The efficacy of these admixtures is contingent upon the water pressure, with variations arising from different conditions such as rain, capillary rise, or hydrostatic pressure in structures intended to hold water.
Waterproofing admixtures render concrete hydrophobic,...
109
Factors Affecting Dissolution: Polymorphism, Amorphism and Pseudopolymorphism01:21

Factors Affecting Dissolution: Polymorphism, Amorphism and Pseudopolymorphism

Polymorphism refers to the existence of a drug substance in multiple crystalline forms, known as polymorphs. Recently, this term has been expanded to include solvates (forms containing a solvent), amorphous forms (non-crystalline forms), and desolvated solvates (forms from which the solvent has been removed).
Some polymorphic crystals possess lower aqueous solubility than their amorphous counterparts, leading to incomplete absorption. For instance, the oral suspension of Chloramphenicol, which...
363
Factors Influencing Drug Absorption: Pharmaceutical Parameters01:28

Factors Influencing Drug Absorption: Pharmaceutical Parameters

Solid dosage forms such as tablets and capsules undergo rigorous manufacturing processes to ensure stability and effectiveness. Their dissolution and absorption properties are influenced significantly by the choice of excipients (inactive ingredients that serve various roles in the formulation), and the methodology applied during production. The manufacturing parameters, such as compression force and granulation techniques, significantly affect dissolution rates. Elevated compression forces...
177
Olefin Metathesis Polymerization: Acyclic Diene Metathesis (ADMET)00:53

Olefin Metathesis Polymerization: Acyclic Diene Metathesis (ADMET)

Acyclic diene metathesis polymerization or ADMET polymerization involves cross-metathesis of terminal dienes, such as 1,8-nonadiene, to give linear unsaturated polymer and ethylene. As ADMET is a reversible process, the formed ethylene gas must be removed from the reaction mixture to complete the polymerization process.
Similar to cross-metathesis, ADMET also involves the formation of metallacyclobutane intermediate by [2+2] cycloaddition of one of the double bonds of a terminal diene with...
2.0K
Routes of Drug Administration: Parenteral01:25

Routes of Drug Administration: Parenteral

The administration of drugs via parenteral routes allows for direct drug introduction into the systemic circulation, resulting in high bioavailability because the medication bypasses the harsh conditions of the gastrointestinal tract and hepatic metabolism.
The intravenous route (IV) of drug administration can be further categorized into two types. The bolus injection administers the entire dose rapidly, while an intravenous infusion slowly delivers smaller doses steadily.
The IV route is often...
2.0K