首页> 外文期刊>Investigative ophthalmology & visual science >Pharmacokinetics of bevacizumab and its effect on vascular endothelial growth factor after intravitreal injection of bevacizumab in macaque eyes.
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Pharmacokinetics of bevacizumab and its effect on vascular endothelial growth factor after intravitreal injection of bevacizumab in macaque eyes.

机译:玻璃猕猴眼玻璃体内注射贝伐单抗后,贝伐单抗的药代动力学及其对血管内皮生长因子的影响。

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PURPOSE: To evaluate the pharmacokinetics of intravitreally injected bevacizumab in the systemic circulation and the aqueous humor and its effect on vascular endothelial growth factor (VEGF) in the aqueous humor. METHODS: Bevacizumab (1.25 mg/50 microL) was injected into the vitreous cavity of the right eyes of three cynomolgus macaques. Aqueous humor and serum were obtained from the macaques just before injection and on days 1, 3, and 7 and weeks 2, 4, 6, and 8 after injection. The bevacizumab and VEGF concentrations were measured using enzyme-linked immunosorbent assay. RESULTS: Aqueous VEGF concentrations ranged from 63.2 to 106 pg/mL (mean, 80.0 +/- 22.6 pg/mL) before injection; decreased to <31.2 pg/mL, the lower limit of detection, in all eyes between 1 and 28 days after injection; and returned to the preinjection concentration at 42 days. Aqueous VEGF concentrations in the fellow eyes did not change throughout the experiment. Aqueous bevacizumab concentrations in the treated eyes reached a mean peak concentration of 49,500 +/- 10,900 ng/mL the day after injection and gradually declined, whereas those in the untreated eyes peaked at 3 days, with a mean concentration of 18.5 +/- 25.5 ng/mL, and declined to below 0.156 ng/mL, the limit of detection at 2 weeks. A maximum mean bevacizumab concentration of 1430 +/- 186 ng/mL was achieved in the serum 1 week after injection. CONCLUSIONS: Intravitreal injection of bevacizumab decreased the VEGF concentration in the treated eyes for at least 4 weeks and had no or a minimal effect on the untreated fellow eyes.
机译:目的:评价玻璃体内注射贝伐单抗在体循环和房水中的药代动力学及其对房水中血管内皮生长因子(VEGF)的影响。方法:将贝伐单抗(1.25 mg / 50 microL)注射到三只食蟹猕猴的右眼玻璃体腔中。在注射前以及注射后第1、3和7天以及第2、4、6和8周时从猕猴获得房水和血清。使用酶联免疫吸附测定法测量贝伐单抗和VEGF的浓度。结果:注射前VEGF水溶液的浓度范围为63.2至106 pg / mL(平均80.0 +/- 22.6 pg / mL)。在注射后1至28天之间的所有眼睛中,降至检测下限<31.2 pg / mL;并在第42天恢复到注射前浓度。在整个实验过程中,另一只眼睛中的VEGF水溶液浓度没有变化。注射后第二天,治疗眼中贝伐单抗的平均浓度达到49,500 +/- 10,900 ng / mL的峰值浓度并逐渐下降,而未治疗眼中的贝伐单抗的浓度在3天时达到峰值,平均浓度为18.5 +/- 25.5 ng / mL,并降至2周时的检出限以下0.156 ng / mL。注射后1周,血清中贝伐单抗的最大平均浓度为1430 +/- 186 ng / mL。结论:玻璃体内注射贝伐单抗可降低治疗眼中的VEGF浓度至少4周,对未治疗的另一只眼睛无影响或影响很小。

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