首页> 外文会议>5th International Photodynamic Association Biennial Meeting >Distribution and photodynamic effect of meta-tetrahydroxyphenylchlorin (mTHPC) in the pancreas and adjacent tissues in Syrian golden hamsters
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Distribution and photodynamic effect of meta-tetrahydroxyphenylchlorin (mTHPC) in the pancreas and adjacent tissues in Syrian golden hamsters

机译:叙利亚金仓鼠胰腺及邻近组织中间四羟基苯氯菊酯(mTHPC)的分布和光动力效应

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Abstract: Experimental study has been carried out using metatetrahydroxyphenylchlorin (m-THPC) in female Syrian golden hamsters. For quantitative fluorescence study, using a CCD camera, the dose of 1.0 mg/kg bodyweight of mTHPC was given intracaval and animals were sacrificed 1 and 4 hours and 1, 2, 3, 4, 5, 6 days afterwards and specimens from the pancreas, stomach, duodenum, gallbladder, aorta and vena cava were examined. A sensitizing dose of 0.3 mg/kg and 0.1 mg/kg respectively was given for PDT, which followed after 2 and 4 days and animals were sacrificed after 1, 2, 3, 4 and 7 days. The treated areas included the pancreas, antral part of the stomach, duodenum and wedge of lesser omentum. In the treated pancreas necrosis up to 3 - 4 mm, marked ulceration in treated duodenum up to 3 - 4.5 mm and in the stomach up to 2 - 2.5 mm in diameter were observed. No macroscopic and histological signs of necrosis were seen in bile duct and major blood vessels. Sealed duodenal perforation occurred in all treated animals with 0.3 mg/kg sensitizing dose and was not observed in 0.1 mg/kg dose with protected duodenum during PDT. Using breaks during PDT (3 $MUL 1; 3 $MUL 3 minutes, respectively) approximately 30% increase of pancreatic necrosis has been observed. In this model, only the duodenum is at risk of irreversible damage. The risk to normal organs in this region is similar to that of photofrin and sulphonated aluminum phtalocyanine. mTHPC is a promising photosensitizer for tumors in the region of the pancreas, although care is required in the region of the duodenum. !28
机译:摘要:已经使用间四羟基苯氯菊酯(m-THPC)在雌性叙利亚金仓鼠中进行了实验研究。为了进行定量荧光研究,使用CCD摄像机在车厢内给予1.0 mg / kg体重的mTHPC,并在第1和4小时以及第1、2、3、4、5、6天后处死动物并从胰腺中处死动物检查胃,十二指肠,胆囊,主动脉和腔静脉。对PDT分别给予0.3 mg / kg和0.1 mg / kg的致敏剂量,然后在2天和4天后进行,并在1、2、3、4和7天后处死动物。治疗区域包括胰腺,胃的胃窦部分,十二指肠和小网膜楔形。在治疗的胰腺坏死至3-4 mm中,观察到在治疗的十二指肠中至3-4.5 mm处明显溃疡,在胃中观察到最大2-2.5 mm直径。在胆管和主要血管中未见坏死的宏观和组织学迹象。在所有接受治疗的动物中,均以0.3 mg / kg的致敏剂量发生十二指肠穿孔,而在PDT期间未观察到以保护性十二指肠以0.1 mg / kg的剂量观察到十二指肠穿孔。在PDT期间使用中断(分别为3 $ MUL 1; 3 $ MUL 3分钟),已观察到胰腺坏死增加约30%。在此模型中,只有十二指肠有不可逆损害的风险。该区域对正常器官的风险类似于光敏蛋白和磺化酞菁铝。尽管需要在十二指肠区域进行护理,但mTHPC是一种有前景的针对胰腺区域肿瘤的光敏剂。 !28

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