首页> 美国卫生研究院文献>British Journal of Cancer >Protoporphyrin IX distribution following local application of 5-aminolevulinic acid and its esterified derivatives in the tissue layers of the normal rat colon
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Protoporphyrin IX distribution following local application of 5-aminolevulinic acid and its esterified derivatives in the tissue layers of the normal rat colon

机译:在正常大鼠结肠的组织层中局部应用5-氨基乙酰丙酸及其酯化衍生物后的原卟啉IX分布

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摘要

Photodynamic diagnosis and especially therapy after sensitization with 5-aminolevulinic acid (ALA) is hampered by limitations of uptake and distribution of ALA due to its hydrophilic nature. Chemical modification of ALA into its more lipophilic esters seems to be promising to overcome these problems. The aim of the present study was to investigate the comparative kinetics of protoporphyrin IX (PPIX) fluorescence in rat colonic tissue after topical application of ALA and its esterified derivatives, ALA-hexylester (h-ALA), ALA-methylester (m-ALA) and ALA-benzylester (b-ALA). Fluorescence intensity induced by PPIX in normal colonic tissue was quantified using fluorescence microscopy at 1, 2, 4, 6 and 8 h after sensitization. Mucosa exhibited higher fluorescence levels compared to the underlying submucosa or smooth muscle. Peak fluorescence intensities were seen 4 h after local sensitization with 86.0 mol ml−1 ALA (513 ± 0.57 counts per pixel), 6.6 mol ml−1 m-ALA (508 ± 35.50) and 4.8 mol ml−1 h-ALA (532 ± 128.80), and 6 h after sensitization with 4.6 mol ml−1 b-ALA (468 ± 190.27). A 13–18 times lower concentration of ALA esters was required for fluorescence intensities reached with ALA alone. A similar degree of the fluorescence ratio between mucosa and muscularis (5–6:1) was detected for ALA and its derivatives. The time point of the maximum value of this ratio was consistent with peak fluorescence levels for ALA and each ALA-ester. The clinical feasibility and the advantages of topical ALA ester-based fluorescence for detection of malignant and premalignant lesions need further investigations. © 2001 Cancer Research Campaign   
机译:由于其亲水性,限制了ALA的吸收和分布,阻碍了5-氨基乙酰丙酸(ALA)致敏后的光动力学诊断,尤其是治疗。将ALA化学修饰成更具亲脂性的酯似乎有望克服这些问题。本研究的目的是研究局部应用ALA及其酯化衍生物,ALA-己酸酯(h-ALA),ALA-甲酯(m-ALA)后大鼠结肠组织中原卟啉IX(PPIX)荧光的比较动力学。和ALA-苄基酯(b-ALA)。在致敏后1、2、4、6和8 h,用荧光显微镜对PPIX诱导的正常结肠组织中的荧光强度进行定量。与下层粘膜下层或平滑肌相比,粘膜显示出更高的荧光水平。局部敏化后4 h出现峰值荧光强度,分别为86.0μmolml -1 ALA(每个像素513±0.57个计数),6.6μmolml -1 m-ALA(508 ±35.50)和4.8μmolml -1 h-ALA(532±128.80),以及在4.6μmolml -1 b-ALA敏化后的6 h(468±190.27) )。单独使用ALA达到的荧光强度需要低13-18倍的ALA酯浓度。对于ALA及其衍生物,在粘膜和肌层之间的荧光比率(5-6:1)具有相似的程度。该比率的最大值的时间点与ALA和每个ALA-酯的峰值荧光水平一致。局部ALA酯基荧光检测恶性和恶变前病变的临床可行性和优势尚待进一步研究。 ©2001癌症研究运动

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