Epperly Michael W, Wipf Peter, Fisher Renee, Franicola Darcy, Beumer Jan, Li Song, Brand Rhonda M, Falo Louis D, Erdos Geza, Greenberger Joel S
Department of Radiation Oncology, UPMC Hillman Cancer Center, Pittsburgh, PA, U.S.A.
Department of Chemistry, University of Pittsburgh, Pittsburgh, PA, U.S.A.
In Vivo. 2018 Sep-Oct;32(5):1009-1023. doi: 10.21873/invivo.11341.
BACKGROUND/AIM: The mitochondrial targeted GS-nitroxide, JP4-039, is an effective total body irradiation (TBI) mitigator when delivered intravenously (IV) up to 72 h after exposure. Effective systemic and localized administration to oral cavity/oropharynx and esophagus has been demonstrated. The objective of the study was to establish alternatives to IV administration suitable for JP4-039 delivery to mass casualties.
JP4-039 was administered to C57BL/6 mice by topically applied carboxy-methyl-cellulose microneedle arrays (MNAs) or by intramuscular (IM) injection. Three different formulations that have passed Food and Drug Administration review, namely Captisol, 2-hydroxypropyl-β-cyclodextrin (cyclodextrin), and Miglyol-812-N, were used for drug delivery. Intraoral (IO) administration with each formulation was also evaluated.
All tested formulations and MNAs successfully delivered JP4-039. However, IM delivery of the Miglyol-812-N displayed very efficient and highly reproducible radiation mitigation.
Effective IM delivery of JP4-039 in animal models after TBI or partial-body irradiation suggested the use of the Miglyol-812-N formulation in both medical indications and radiation countermeasures.
背景/目的:线粒体靶向性谷胱甘肽-氮氧化物JP4-039,在暴露后长达72小时静脉注射时,是一种有效的全身照射(TBI)减轻剂。已证明其可有效全身给药以及局部给药至口腔/口咽和食管。本研究的目的是确定适合向大量伤亡人员递送JP4-039的静脉注射替代方法。
通过局部应用羧甲基纤维素微针阵列(MNA)或肌肉注射(IM)将JP4-039给予C57BL/6小鼠。使用三种已通过美国食品药品监督管理局审查的不同制剂,即Captisol、2-羟丙基-β-环糊精(环糊精)和Miglyol-812-N进行药物递送。还评估了每种制剂的口腔内(IO)给药。
所有测试的制剂和MNA均成功递送了JP4-039。然而,Miglyol-812-N的肌肉注射显示出非常高效且高度可重复的辐射减轻效果。
在TBI或局部身体照射后的动物模型中,JP4-039通过肌肉注射有效递送,这表明Miglyol-812-N制剂可用于医疗适应症和辐射防护措施。