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Absorption, Uptake and Tissue Affinity of High-Molecular-Weight Hyaluronan after Oral Administration in Rats and Dogs

机译:大鼠和狗口服后高分子量透明质酸的吸收,吸收和组织亲和力

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The purpose of this study was to determine the absorption, distribution and excretion of ~(99m)technetium-labeled, high-molecular-weight hyaluronan ((~(99m)Tc-HA) and ~(99m)technetium pertechnetate (~(99m)Tc-P) after single dose, oral administration to Wistar rats and Beagle dogs. A pilot study utilized ~(99m)Tc-HA alone, and a second confirmatory study compared uptake of labeled ~(99m)Tc-HA with ~(99m)Tc-P. Urinary and fecal excretion after ~(99m)Tc-HA ingestion by rats showed 86.7-95.6% of radioactivity was recovered, almost all in feces. All tissues examined showed incorporation of radioactivity from ~(99m)Tc-HA starting at 15 min and persisting for 48 h, in a pattern significantly different from ~(99m)Tc-P. Whole-body scintigraphs and close-ups of the ventral chest region showed nenalimentary radioactivity from ~(99m)Tc-HA concentrated in joints, vertebrae and salivary glands four hours after administration. Autoradiography of skin, bone and joint tissue pieces after 24 h showed incorporation of radioactivity from ~(99m)Tc-HA, but not from ~(99m)Tc-P. Conversely, absorption, distribution and excretion of ~(99m)Tc was completely different from ~(99m)Tc-HA, showing an expected pattern of rapid absorption and excretion in urine, with accumulation in thyroid glands, stomach, kidney and bladder. This report presents the first evidence for uptake and distribution to connective tissues of orally administered, high-molecular-weight HA.
机译:这项研究的目的是确定〜(99m)-标记的高分子量透明质酸((〜(99m)Tc-HA)和〜(99m)高tech酸tech(〜(99m)的吸收,分布和排泄)Tc-P),单剂,口服给Wistar大鼠和Beagle狗口服。一项先导研究仅使用〜(99m)Tc-HA,另一项验证性研究比较了标记的〜(99m)Tc-HA与〜()的摄取。摄入〜(99m)Tc-HA后,大鼠尿和粪便排泄显示放射性回收率为86.7-95.6%,几乎所有粪便都被回收,所有检查的组织均显示〜(99m)Tc-HA吸收了放射性HA从15分钟开始并持续48 h,其模式与〜(99m)Tc-P明显不同。全身闪烁显像和腹侧胸腔特写显示浓缩的〜(99m)Tc-HA具有无放射性给药后四个小时,在关节,椎骨和唾液腺中发现皮肤,骨骼和关节组织碎片的放射自显影在24小时后显示〜(99m)Tc-HA的放射性公司,但不是〜(99m)Tc-P的公司。相反,〜(99m)Tc的吸收,分布和排泄与〜(99m)Tc-HA完全不同,显示出尿中快速吸收和排泄的预期模式,并在甲状腺,胃,肾和膀胱中积累。该报告为口服高分子量HA的结缔组织摄取和分布提供了第一个证据。

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