Allison B A, Waterfield E, Richter A M, Levy J G
Department of Microbiology, University of British Columbia, Vancouver, Canada.
Photochem Photobiol. 1991 Nov;54(5):709-15. doi: 10.1111/j.1751-1097.1991.tb02079.x.
The influence of lipoprotein association on in vitro tumor cell killing and in vivo tumor photosensitization with benzoporphyrin derivative (BPD) has been investigated in M-1 tumor bearing mice. The association of benzoporphyrin mono acid ring A with either low or high density lipoprotein increased tumor cell killing in an in vivo/in vitro cytotoxicity assay performed 3 h post intravenous drug administration. Eight hours following photosensitizer injection only low density lipoprotein (LDL) mixtures produced significant (P less than or equal to 0.005) increases in tumor cell killing compared to BPD in unfractionated plasma. The efficacy of in vivo photosensitization in the presence of lipoproteins correlated with the in vivo/in vitro cytotoxicity. Association of BPD with low or high density lipoproteins resulted in delayed tumor regrowth and higher cure rates when light exposure (125J/cm2) was performed 3 h post drug administration. When light exposure was performed 8 h post-injection only LDL-BPD mixtures led to enhanced tumor eradication compared to BPD administered in aqueous solution or unfractionated plasma.
在携带M-1肿瘤的小鼠中,研究了脂蛋白结合对苯卟啉衍生物(BPD)体外肿瘤细胞杀伤及体内肿瘤光致敏作用的影响。静脉给药3小时后进行的体内/体外细胞毒性试验表明,苯卟啉单酸环A与低密度或高密度脂蛋白的结合均增强了肿瘤细胞杀伤作用。注射光敏剂8小时后,与未分级血浆中的BPD相比,仅低密度脂蛋白(LDL)混合物显著(P≤0.005)增强了肿瘤细胞杀伤作用。脂蛋白存在时的体内光致敏效果与体内/体外细胞毒性相关。当给药后3小时进行光照(125J/cm2)时,BPD与低密度或高密度脂蛋白的结合导致肿瘤生长延迟且治愈率更高。当注射后8小时进行光照时,与水溶液或未分级血浆中给药的BPD相比,仅LDL-BPD混合物导致肿瘤根除增强。