CD101, a novel echinocandin with exceptional stability properties and enhanced aqueous solubility

被引:74
作者
Krishnan, B. Radha [1 ,2 ]
James, Kenneth D. [1 ,2 ]
Polowy, Karen [2 ]
Bryant, B. J. [2 ]
Vaidya, Anu [2 ]
Smith, Steve [2 ]
Laudeman, Christopher P. [2 ]
机构
[1] Cidara Therapeut, San Diego, CA USA
[2] Seachaid Pharmaceut, Durham, NC USA
关键词
TISSUE DISTRIBUTION; ANTIFUNGAL AGENT; PHARMACOKINETICS; MICAFUNGIN; ANIDULAFUNGIN; CASPOFUNGIN;
D O I
10.1038/ja.2016.89
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The echinocandins are an important class of antifungal agents. However, instability and, in some cases, lack of solubility have restricted their use to situations in which daily infusions are acceptable. CD101 is a novel echinocandin in development for topical and weekly i.v. administration that exhibits prolonged stability in plasma and aqueous solutions up to 40 degrees C. After incubation for 44 h in rat, dog, monkey and human plasma at 37 degrees C, the percent of CD101 remaining (91%, 79%, 94% and 93%, respectively) was consistently greater than that of anidulafungin (7%, 15%, 14% and 7%, respectively). Similarly, after incubation in phosphate-buffered saline at 37 degrees C, the CD101 remaining (96%) was greater than that of anidulafungin (42%). CD101 exhibited <2% degradation after long-term storage at 40 degrees C as a lyophilized powder (9 months) and at room temperature in 5% dextrose (15 months), 0.9% saline (12 months) and sterile water (18 months). Degradation was <7% at 40 degrees C in acetate and lactate buffers (6 to 9 months at pH 4.5-5.5). The chemical stability and solubility of CD101 contribute to dosing, pharmacokinetic, formulation and safety advantages over other echinocandins and should expand utility beyond daily i.v. therapy.
引用
收藏
页码:130 / 135
页数:6
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