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[癌肉瘤发生发展过程中血卟啉、其衍生物及荧光素的药代动力学]

[The pharmacokinetics of hematoporphyrin, its derivative and fluorescein during the development of carcinosarcoma].

作者信息

Barabash R D, Skobelkin O K, Petukhov M I, Normanskiĭ V E, Riazhskiĭ G G, Mironova M I, Andreeva K P, Kolobanov A S

出版信息

Farmakol Toksikol. 1990 May-Jun;53(3):24-6.

PMID:2143733
Abstract

The pharmacokinetics of fluorescein, hematoporphyrin and a derivative of hematoporphyrin was studied microspectrofluorometrically on rats with transplanted carcinosarcoma. It was shown that in the rats in contrast to intact animals the tissue concentration of fluorescein exhibits a general tendency towards an increase, that of hematoporphyrin towards a decrease and that of hematoporphyrin derivative towards an increase in all parenchymatous organs and a decrease in the skin and mucosae of the hollow organs. At the equally short period of the maximal accumulation of luminophores, the tumour tissue differs from the normal one by a pronounced delay of excretion only of hematoporphyrin derivative.

摘要

采用显微分光荧光测定法,对移植癌肉瘤的大鼠进行了荧光素、血卟啉及其衍生物的药代动力学研究。结果表明,与正常动物相比,大鼠体内荧光素的组织浓度总体呈上升趋势,血卟啉呈下降趋势,血卟啉衍生物在所有实质器官中呈上升趋势,在中空器官的皮肤和黏膜中呈下降趋势。在发光体最大积累的相同短时间内,肿瘤组织与正常组织的不同之处在于,只有血卟啉衍生物的排泄明显延迟。

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