Paclitaxel stability and compatibility in polyolefin containers.

OBJECTIVE: To determine the compatibility and stability of paclitaxel in polyolefin containers. DESIGN: The following paclitaxel concentrations were determined by a stability-indicating HPLC method: 0.3 and 1.2 mg/mL diluted in dextrose 5% for injection, USP (D5W) or sodium chloride 0.9% for injection, USP (NS). The solutions were prepared in polyolefin containers and the stability and compatibility were monitored for 48 hours when stored at ambient temperature (20-23 degrees C) and normal fluorescent lighting. A mixture of the drug carrier consisting of approximately 10% polyoxyethylated castor oil (Cremophor EL) and 10% ethanol in D5W and NS, without paclitaxel, was studied to differentiate the effect of paclitaxel from the effect of the drug carrier on the container. Paclitaxel concentrations, pH changes, and visual clarity were used as stability and compatibility indicators. RESULTS: Paclitaxel concentrations remained at 96-99 percent of the initial concentration for up to 48 hours when placed in the polyolefin containers. No changes in color or visual clarity were noted. Only minor changes in the pH of the admixtures were observed. CONCLUSIONS: Paclitaxel diluted in D5W or NS at concentrations of 0.3 and 1.2 mg/mL is stable and compatible in flexible, polyolefin containers for up to 48 hours.

Myocardial injury following the intentional inhalation of typewriter correction fluid.

The first known case of myocardial injury, as documented by evolutionary electrocardiographic changes and echocardiographic septal wall motion abnormality associated with the voluntary inhalation of typewriter correction fluid, is reported. Typewriter correction fluid, which contains a combination of chlorinated hydrocarbons, is rapidly becoming a substance of abuse. Therefore, primary care practitioners should be alerted to specific organ system damages that may arise from the voluntary inhalation of this substance.