Sustained Release of Antiinfectives
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[0075]The following is a detailed description of the manufacture of 150 mL of Liposomal / complexed amikacin.[0076]Total Initial Volume=1.5 L[0077]Ethanol Content=23.5% (v / v)[0078]Lipid Composition: DPPC / Chol (1:1 mole ratio)[0079]Initial [Lipid]=7.6 mg / ml[0080]Initial [amikacin sulfate]=57.3 mg / ml[0081]Final product Volume=150 mL
[0082]I) Compounding and Infusion:
[0083]7.47 g DPPC and 3.93 g Cholesterol were dissolved directly in 352.5 mL ethanol in a 50 C water bath. 85.95 g amikacin sulfate was dissolved directly in 1147.5 mL PBS buffer. The solution is then titrated with 10N NaOH or KOH to bring the pH to approximately 6.8.
[0084]352.5 mL ethanol / lipid was added or infused to the 1147.5 mL amikacin / buffer to give a total initial volume of 1.5 L. The ethanol / lipid was pumped @ 30 mL / min (also called infusion rate) with a peristaltic pump into the amikacin / buffer solution which was being rapidly stirred at 150 RPM in a reaction vessel on a stir plate at room temperature
[0085]The produ...
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