Valiante Salvatore, Falanga Annarita, Cigliano Luisa, Iachetta Giuseppina, Busiello Rosa Anna, La Marca Valeria, Galdiero Massimiliano, Lombardi Assunta, Galdiero Stefania
Department of Biology, University of Naples Federico II, Naples, Italy.
Department of Pharmacy, University of Naples Federico II, Naples, Italy ; DFM Scarl, University of Naples Federico II, Naples, Italy.
Int J Nanomedicine. 2015 Mar 10;10:1885-98. doi: 10.2147/IJN.S77734. eCollection 2015.
Peptide gH625, derived from glycoprotein H of herpes simplex virus type 1, can enter cells efficiently and deliver a cargo. Nanoparticles armed with gH625 are able to cross an in vitro model of the blood-brain barrier (BBB). In the present study, in vitro experiments were performed to investigate whether gH625 can enter and accumulate in neuron and astrocyte cell lines. The ability of gH625 to cross the BBB in vivo was also evaluated. gH625 was administered in vivo to rats and its presence in the liver and in the brain was detected. Within 3.5 hours of intravenous administration, gH625 can be found beyond the BBB in proximity to cell neurites. gH625 has no toxic effects in vivo, since it does not affect the maximal oxidative capacity of the brain or the mitochondrial respiration rate. Our data suggest that gH625, with its ability to cross the BBB, represents a novel nanocarrier system for drug delivery to the central nervous system. These results open up new possibilities for direct delivery of drugs into patients in the field of theranostics and might address the treatment of several human diseases.
源自单纯疱疹病毒1型糖蛋白H的肽gH625能够高效进入细胞并运载货物。携带gH625的纳米颗粒能够穿过血脑屏障(BBB)的体外模型。在本研究中,进行了体外实验以研究gH625是否能够进入神经元和星形胶质细胞系并在其中积累。还评估了gH625在体内穿过血脑屏障的能力。将gH625体内给药至大鼠,并检测其在肝脏和脑中的存在情况。静脉给药后3.5小时内,可在靠近细胞神经突的血脑屏障外发现gH625。gH625在体内无毒性作用,因为它不影响大脑的最大氧化能力或线粒体呼吸速率。我们的数据表明,具有穿过血脑屏障能力的gH625代表了一种用于向中枢神经系统递送药物的新型纳米载体系统。这些结果为在治疗诊断学领域直接向患者递送药物开辟了新的可能性,并可能解决几种人类疾病的治疗问题。