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Preparation and Characterization of Cubosomal KIOM-C Suspension and Investigation on In Vitro Small Intestinal Absorption of Baicalin

机译:黄体苷KIOM-C悬浮液的制备,表征及黄ical苷的体外小肠吸收研究

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摘要

KIOM-C suspension and cubosome/KIOM-C suspension were prepared in various buffer solution of different pHs by a sonication method. KIOM-C particles were unstable in terms of time-dependent change in the size and the zeta potential. The fluctuation in the size and the zeta potential of KIOM-C particles was effectively damped by cubosome. The shape of KIOM-C particles was irregular and the size was hundreds to thousands of nm. Cubosome/KIOM-C particles exhibited stripes on their surfaces and the size was hundreds of nm. Regardless of the pH values (pH 2.0-10.0) of media, baicalin, a major component of KIOM-C, was chemically stable for 48 hours at a room temperature. Cubosome markedly enhanced the stability of baicalin particles against sedimentation. EDTA significantly enhanced the in vitro small intestinal absorption of baicalin, but MO cubosome hardly promoted.
机译:通过超声处理,在不同pH的各种缓冲溶液中制备KIOM-C悬浮液和立方核/ KIOM-C悬浮液。就尺寸和ζ电势的时间依赖性变化而言,KIOM-C颗粒不稳定。立方微粒可有效地抑制KIOM-C颗粒的尺寸和Zeta电位波动。 KIOM-C颗粒的形状不规则,尺寸为数百至数千纳米。立方体/ KIOM-C颗粒在其表面上显示出条纹,尺寸为数百纳米。无论培养基的pH值(pH 2.0-10.0)如何,黄ical苷(KIOM-C的主要成分)在室温下化学稳定48小时。立方体显着增强了黄ical苷颗粒抗沉淀的稳定性。 EDTA显着增强了黄ical苷的体外小肠吸收,但几乎没有促进MO立方体。

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