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食管5-氨基酮戊酸光动力疗法的分次照射:对血流和卟啉原IX形成的影响

Fractionated illumination for oesophageal ALA-PDT: effect on blood flow and PpIX formation.

作者信息

van den Boogert J, van Staveren H J, de Bruin R W, Siersema P D, van Hillegersberg R

机构信息

Laboratory for Experimental Surgery, Erasmus University, PO Box 1738, 3000 DR Rotterdam, The Netherlands.

出版信息

Lasers Med Sci. 2001;16(1):16-25. doi: 10.1007/pl00011331.

Abstract

The effect of fractionating the 633 nm illumination of 5-aminolaevulinic (ALA)-based photodynamic therapy (PDT) of the normal rat oesophagus was studied. Fractionation of the illumination could enhance the PDT effect in two ways: (a) delay of the vascular shutdown or relaxation of the vasoconstriction induced by ALA-PDT and (b) use of newly formed protoporphyrin IX (PpIX), produced during the dark interval. Forty rats were randomly allocated to two groups of 20 animals each. To study vascular effects, in group 1 illumination with 633 nm (100 mW/cm) was performed at 3 h after oral ALA administration (200 mg/kg) either continuously with 20 J/cm diffuser length (n = 5) or fractionated 2 x 10 J/cm with a 150 s interval (n = 5), five animals served as controls. Blood flow was measured with a laser Doppler flowmeter. To study the effect of renewed PpIX forming, animals in group 2 were illuminated continuously at 3 h after ALA with 20 J/cm (n = 5) or 40 J/cm (n = 5) or fractionated 2 x 20 J/cm with a 3 h interval (n = 5), five animals served as controls. In all animals the in vivo fluence rate and PpIX fluorescence were measured during illuminations and animals were killed at 48 h after PDT. ALA-PDT did not cause any significant vasoconstriction. Fluorescence measurements and dosimetric results in group 1 did not differ between animals illuminated continuously or fractionated with a 150 s interval. In group 2, during a 3 h dark interval, PpIX fluorescence increased and was bleached during the second illumination. The tissue optical properties changed during the 3 h dark interval, resulting in a lower in vivo fluence rate (p < or = 0.001). Fractionation did not result in more oesophageal damage. It was concluded that a 150 s interval during illumination in ALA-PDT does not increase oesophageal blood flow. During an interval of 3 h new PpIX is formed. In the present study, fractionated illumination using short or long time intervals did not result in more damage. Thus, this study shows no evidence for improved PDT effect with fractionated light delivery.

摘要

研究了对正常大鼠食管进行基于5-氨基酮戊酸(ALA)的光动力疗法(PDT)时,633 nm光照分次照射的效果。光照分次照射可通过两种方式增强PDT效果:(a)延迟血管关闭或缓解ALA-PDT诱导的血管收缩,以及(b)利用在黑暗间隔期产生的新形成的原卟啉IX(PpIX)。40只大鼠随机分为两组,每组20只。为研究血管效应,在第1组中,口服ALA(200 mg/kg)后3小时,用633 nm(100 mW/cm)进行光照,连续照射20 J/cm扩散器长度(n = 5)或分次照射,每次10 J/cm,间隔150秒(n = 5),5只动物作为对照。用激光多普勒血流仪测量血流量。为研究新形成的PpIX的作用,第2组动物在ALA给药后3小时,连续照射20 J/cm(n = 5)或40 J/cm(n = 5),或分次照射,每次20 J/cm,间隔3小时(n = 5),5只动物作为对照。在所有动物中,在光照期间测量体内光通量率和PpIX荧光,并在PDT后48小时处死动物。ALA-PDT未引起任何明显的血管收缩。第1组中,连续照射或间隔150秒分次照射的动物之间,荧光测量和剂量学结果没有差异。在第2组中,在3小时的黑暗间隔期内,PpIX荧光增加,并在第二次光照期间被漂白。在3小时的黑暗间隔期内,组织光学性质发生变化,导致体内光通量率降低(p≤0.001)。分次照射并未导致更多的食管损伤。得出的结论是,ALA-PDT光照期间150秒的间隔不会增加食管血流量。在3小时的间隔期内会形成新的PpIX。在本研究中,使用短或长时间间隔的分次光照并未导致更多损伤。因此,本研究没有证据表明分次光传递能改善PDT效果。

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