Liu K R, Peyman G A, She S C, Niesman M R, Khoobehi B
LSU Eye Center, New Orleans.
Ophthalmic Surg. 1989 May;20(5):358-61.
Cytarabine has been demonstrated to be a more potent inhibitor of fibroblast proliferation than fluorouracil. It is, however, more toxic to the retina. We evaluated the ocular toxicity of liposome-encapsulated cytarabine in vitrectomized and nonvitrectomized rabbit eyes by ophthalmic and histopathologic examination. In the vitrectomized group, doses of up to 26 micrograms were nontoxic to the retina. In nonvitrectomized eyes, doses of up to 55 micrograms were nontoxic. Doses of 85 micrograms resulted in loss of ganglion cells and disorganization of photoreceptor cells. The results obtained in this study demonstrated a substantial reduction in ocular toxicity of liposome-encapsulated cytarabine, as compared with a previous study which employed free drug. By virtue of its reduced toxicity, cytarabine in a liposomal vehicle may be of value in the treatment of ocular proliferative disorders.
已证明阿糖胞苷是比氟尿嘧啶更有效的成纤维细胞增殖抑制剂。然而,它对视网膜的毒性更大。我们通过眼科和组织病理学检查评估了脂质体包裹的阿糖胞苷在玻璃体切除和未切除玻璃体的兔眼中的眼毒性。在玻璃体切除组中,高达26微克的剂量对视网膜无毒。在未切除玻璃体的眼中,高达55微克的剂量无毒。85微克的剂量导致神经节细胞丧失和光感受器细胞紊乱。与先前使用游离药物的研究相比,本研究获得的结果表明脂质体包裹的阿糖胞苷的眼毒性大幅降低。由于其毒性降低,脂质体载体中的阿糖胞苷在治疗眼部增殖性疾病中可能具有价值。