Biodistribution and Pharmacokinetic Evaluations of a Novel Taxoid DHA-SBT-1214 in an Oil-in-Water Nanoemulsion Formulation in Naive and Tumor-Bearing Mice

被引:15
作者
Ahmad, Gulzar [1 ]
Gattacecca, Florence [2 ]
El Sadda, Rana [3 ]
Botchkina, Galina [3 ,4 ]
Ojima, Iwao [3 ,5 ]
Egan, James [6 ]
Amiji, Mansoor [1 ]
机构
[1] Northeastern Univ, Dept Pharmaceut Sci, Sch Pharm, Boston, MA 02115 USA
[2] Univ Montpellier, IRCM, ICM, INSERM,U1194, Montpellier, France
[3] SUNY Stony Brook, Inst Chem Biol & Drug Discovery, Stony Brook, NY 11794 USA
[4] SUNY Stony Brook, Sch Med, Dept Pathol, Stony Brook, NY 11794 USA
[5] SUNY Stony Brook, Dept Chem, Stony Brook, NY 11794 USA
[6] Targagenix Inc, 25 Hlth Sci Dr, Stony Brook, NY 11790 USA
基金
美国国家卫生研究院;
关键词
biodistribution and pharmacokinetic; nanoemulsion formulation; prostate tumor; taxoid; OVERCOME MULTIDRUG-RESISTANCE; DRUG-DELIVERY SYSTEM; CANCER STEM-CELLS; VASCULAR-PERMEABILITY; MONOCLONAL-ANTIBODY; DHA-PACLITAXEL; NANOPARTICLES; THERAPEUTICS; MODULATION; MECHANISMS;
D O I
10.1007/s11095-018-2349-x
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Purpose The main purpose of this study was to formulate an oil-in-water nanoemulsion of a next generation taxoid DHA-SBT-1214 and evaluate its biodistribution and pharmacokinctics. Methods DHA-SBT-1214 was encapsulated in a fish oil containing nanoemulsion using a high pressure homogenization method. Following morphological characterization of the nanoemulsions, qualitative and quantitative biodistribution was evaluated in naive and cancer stem cell-enriched PPT-2 human prostate tumor bearing mice. Results DHA-SBT-1214 was successfully encapsulated up to 20 mg/ml in the nanoemulsion formulation and had an average oil droplet size of 200 nm. Using a DiR near infra-red dye encapsulated nanoemulsion, we have shown the delivery of nanoemulsion to mouse tumor region. By quantitative analysis, DHA-SBT-1214 encapsulated nanoemulsion demonstrated improved pharmacokinetic properties in plasma and different tissues as compared to its solution form. Furthermore, the nanoemulsions were stable and had slower in vitro drug release compared to its solution form. Conclusions The results from this study demonstrated effective encapsulation of the drug in a nanoemulsion and this nanoemulsion showed sustained plasma levels and enhanced tumor delivery relative to the solution form.
引用
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页数:13
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