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Tumour-localising and -photosensitizing properties of liposome-delivered Ge(IV)-octabutoxy-phthalocyanine.

作者信息

Cuomo V, Jori G, Rihter B, Kenney M E, Rodgers M A

机构信息

Department of Biology, University of Padova, Italy.

出版信息

Br J Cancer. 1991 Jul;64(1):93-5. doi: 10.1038/bjc.1991.247.

DOI:10.1038/bjc.1991.247
PMID:1854632
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1977328/
Abstract
摘要

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本文引用的文献

1
Plasma lipoprotein conversions.血浆脂蛋白转化
Methods Enzymol. 1986;129:347-66. doi: 10.1016/0076-6879(86)29079-5.
2
Pharmacokinetic studies with zinc(II)-phthalocyanine in tumour-bearing mice.锌（II）-酞菁在荷瘤小鼠体内的药代动力学研究。
Br J Cancer. 1987 Nov;56(5):597-600. doi: 10.1038/bjc.1987.247.
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Sites of photosensitization by derivatives of hematoporphyrin.血卟啉衍生物的光敏化位点。
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Tetra-n-propylporphycene as a tumour localizer: pharmacokinetic and phototherapeutic studies in mice.四正丙基卟吩作为肿瘤定位剂：小鼠体内的药代动力学和光治疗研究
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Distribution and elimination of Photofrin II in mice.二血卟啉醚在小鼠体内的分布与消除
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The time course of cutaneous porphyrin photosensitization in the murine ear.小鼠耳部皮肤卟啉光敏化的时间进程。
Photochem Photobiol. 1989 Mar;49(3):369-72. doi: 10.1111/j.1751-1097.1989.tb04121.x.
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Mechanisms of tumor necrosis induced by photodynamic therapy.光动力疗法诱导肿瘤坏死的机制。
J Photochem Photobiol B. 1989 Jun;3(3):299-318. doi: 10.1016/1011-1344(89)80035-1.
8
Liposome- or LDL-administered Zn (II)-phthalocyanine as a photodynamic agent for tumours. I. Pharmacokinetic properties and phototherapeutic efficiency.脂质体或低密度脂蛋白给药的锌（II）-酞菁作为肿瘤光动力剂。I. 药代动力学性质和光疗效率。
Br J Cancer. 1990 Mar;61(3):407-11. doi: 10.1038/bjc.1990.89.
9
Liposome-delivered Si(IV)-naphthalocyanine as a photodynamic sensitiser for experimental tumours: pharmacokinetic and phototherapeutic studies.脂质体递送的硅（IV）-萘酞菁作为实验性肿瘤的光动力敏化剂：药代动力学和光治疗研究
Br J Cancer. 1990 Dec;62(6):966-70. doi: 10.1038/bjc.1990.418.
10
Photosensitized processes in vivo: proposed phototherapeutic applications.
Photochem Photobiol. 1990 Aug;52(2):439-43. doi: 10.1111/j.1751-1097.1990.tb04201.x.