کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
2505206 1557483 2008 6 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Physicochemical and pharmacokinetic characterization of water-soluble Coenzyme Q10 formulations
موضوعات مرتبط
علوم پزشکی و سلامت داروسازی، سم شناسی و علوم دارویی علوم دارویی
پیش نمایش صفحه اول مقاله
Physicochemical and pharmacokinetic characterization of water-soluble Coenzyme Q10 formulations
چکیده انگلیسی

Coenzyme Q10 (CoQ10) has been used as a drug for chronic heart failure. Furthermore, various biological effects of CoQ10 have also been applied for food supplements and cosmetics. However, CoQ10 was found to be poorly soluble in water, so that its bioavailability was low and variable depending on food intake. In the present investigation, a novel liquid (nano-emulsion, NE) and water-soluble powder formulations, including cyclodextrin–Q10 complex (CoQ10–CD) and dry-emulsion (DE), were prepared. The physicochemical properties of each formulation were characterized by dynamic light scattering (DLS), scanning electron microscopy (SEM), powder X-ray diffractometry (PXRD), and differential scanning calorimetry (DSC). In all powder formulations prepared, CoQ10 existed mainly as an amorphous form as determined by PXRD and DSC, and each powder formulation exhibited high solubility and dispersibility in water resulting in the formation of a nano-sized emulsion (NE; 60 nm) and micron sized particles (DEs and CoQ10–CD; 0.77–2.4 μm). The pharmacokinetic study of each dosage form, in comparison to a CoQ10 crystal suspension, was also carried out in rats after a single oral dose. Although similar kinetic values were seen with Tmax of 1.5 and 1.7 h, respectively, for NE and crystalline CoQ10, NE exhibited ca 1.7-fold higher AUC and Cmax than the crystalline CoQ10.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: International Journal of Pharmaceutics - Volume 363, Issues 1–2, 3 November 2008, Pages 112–117
نویسندگان
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