Laboratory of Vision and Optics, Ophthalmology, Medical School, University of Crete, Voutes, Heraklion, Greece.
Laboratory of Toxicology, Medical School, University of Crete, Heraklion, Greece.
Pharmacol Res Perspect. 2021 Apr;9(2):e00724. doi: 10.1002/prp2.724.
BNN27 is a novel 17-spiroepoxy derivative of the neurosteroid Dehydroepiandrosterone with neuroprotective properties. The purpose of this study was the detection and quantification of BNN27 after single intraperitoneal administration, in the serum and retina of normal rodents. Forty-two C57BL/6 mice and 48 Sprague-Dawley rats were used for the quantification of BNN27 in the blood serum and retina, respectively. BNN27 was injected intraperitoneally (i.p.) at concentrations of 100 and 30 mg/kg of body weight (b.w.), respectively. The blood was collected with retro-orbital bleeding and the retina was isolated after enucleation at various time points. The molecule concentrations were measured with Liquid chromatography-mass spectrometry (LC-MS). Non-compartmental analysis was used to determine pharmacokinetic parameters. BNN27 was found to have an elimination constant k = 0.465 h and mean residence time (MRT) 2.154 h in the mouse serum. The maximum concentration (C ) in the retina was detected at 2 h ( ) after intraperitoneal administration and was equal to 1100 ng/g. BNN27 is rapidly eliminated from both blood and retina. In the retina specifically, it is undetectable 6 h after injection. BNN27 shows a rapid systemic elimination as anticipated by its small size and lipophilicity. It is measurable in small peripheral tissues such as the rat retina, after one single i.p. injection, using a simple method such as LC-MS. Its detection in the retina corroborates the existing biological data that the molecule crosses the blood-retinal barrier, highlighting it as a potential neuroprotective agent for retinal disease.
BNN27 是一种新型的 17-螺环氧神经甾体脱氢表雄酮衍生物,具有神经保护作用。本研究的目的是检测和定量单次腹腔注射后正常啮齿动物血清和视网膜中的 BNN27。分别使用 42 只 C57BL/6 小鼠和 48 只 Sprague-Dawley 大鼠来定量血清和视网膜中的 BNN27。BNN27 分别以 100 和 30mg/kg 体重的浓度腹腔注射。用眼眶后采血法采集血液,眼球摘出后分离视网膜。用液相色谱-质谱法(LC-MS)测量分子浓度。采用非房室分析方法确定药代动力学参数。在小鼠血清中,BNN27 的消除常数 k 为 0.465h,平均驻留时间(MRT)为 2.154h。腹腔给药后 2 小时( )在视网膜中检测到最大浓度(C ),等于 1100ng/g。BNN27 从血液和视网膜中迅速消除。特别是在视网膜中,注射后 6 小时后无法检测到。BNN27 表现出预期的快速全身消除,这与其小尺寸和脂溶性有关。使用 LC-MS 等简单方法,单次腹腔注射后,在大鼠视网膜等小周边组织中仍可检测到该物质,表明其具有成为治疗视网膜疾病的潜在神经保护剂的潜力。