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. Author manuscript; available in PMC: 2016 Jun 30.
Published in final edited form as: Curr Opin Investig Drugs. 2005 Aug;6(8):845–853.
Study Type Result Reference
Synthesis. Partricin A was modified to generate analogs. Most of the amide derivates were more potent
antifungals, less toxic and produced less hemolysis than amphotericin B. Two analogs were selected for
further development, SPA-S-710 and SPA-S 752. SPA-S-753 is the diaspartate salt of SPA-S-752 and
SPK-843 is the diascorbate salt.
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Photostability. Light induced the formation of the E isomer. Violet and ultraviolet radiation yielded damaging effects.
The light emitted by red varnished wire lamps was much less damaging than the light of usual wire,
neon and sodium lamps. Lowering the light emission in the violet and ultraviolet regions reduced
photodegradation.
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Stability. Intralipid 10% emulsion containing SPK-843 (0.1 to 0.5 mg/ml) at mildly acid or basic pH was physically
stable. SPK-843 in Intralipid 10% emulsion, at natural and mildly basic pH, was chemically stable for 2 h
at 25°C even in a well-lit room.
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