Stegman James R, Badin Jill K, Biles Kaitlyn A, Etienne Thamar, Fartash-Naini Sogand, Gordon Ariel D, Greeley Zachary W, Harding Benjamin W, Mack Ricardo J, Masica Danielle, Nelson Ashley N, Samra Amandeep K, Smith Sarah E, Thomas Gabrielle P, Zack Haley J, Brunker Timothy J, Margulies Barry J
Towson University Herpes Virus Lab, Department of Biological Sciences, Towson University, Towson, MD 21252, USA.
Department of Chemistry, Towson University, Towson, MD 21252, USA.
J Drug Deliv. 2018 Sep 26;2018:6161230. doi: 10.1155/2018/6161230. eCollection 2018.
Treatment for herpes simplex virus-1 and -2 (HSV-1 and -2) patients who suffer from recurrent outbreaks consists of multiple daily doses of the antiviral drugs acyclovir (ACV), penciclovir, or their more orally bioavailable derivatives valacyclovir or famciclovir. Drug troughs caused by missed doses may result in viral replication, which can generate drug-resistant mutants along with clinical sequelae. We developed a molecularly homogeneous mixture of ACV with the bioerodable polymer polycaprolactone. Through scanning electron microscopy, infrared spectroscopy, gel permeation chromatography, 1H NMR, and differential scanning calorimetry, our method of combining drug and polymer, termed Volatile Acid-Solvent Evaporation (VASE), does not compromise the integrity of polymer or drug. Furthermore, VASE creates materials that deliver therapeutic amounts of drug consistently for approximately two months. Devices with high enough drug loads diminish primary infection of HSV-1 in Vero cells to the same level as seen with a single dose of ACV. Our data will lead to further experiments in animal models, demonstrating efficacy in preventing reactivation of these viruses with a single intervention, and with other antiviral drugs amenable to such manipulation. Additionally, this type of treatment would leave no trace after its useful lifetime, as drug is released and polymer matrix is degraded .
对于患有复发性疱疹的单纯疱疹病毒1型和2型(HSV-1和HSV-2)患者,治疗方法包括每日多次服用抗病毒药物阿昔洛韦(ACV)、喷昔洛韦,或其口服生物利用度更高的衍生物伐昔洛韦或泛昔洛韦。漏服药物导致的药物谷浓度可能会引发病毒复制,进而产生耐药突变体并引发临床后遗症。我们研发了一种阿昔洛韦与可生物降解聚合物聚己内酯的分子均匀混合物。通过扫描电子显微镜、红外光谱、凝胶渗透色谱、1H核磁共振和差示扫描量热法,我们将药物与聚合物结合的方法,即挥发性酸-溶剂蒸发法(VASE),不会损害聚合物或药物的完整性。此外,VASE法制备的材料能够持续约两个月释放治疗剂量的药物。药物负载量足够高的装置可将HSV-1对Vero细胞的原发性感染降低到与单剂量阿昔洛韦相同的水平。我们的数据将推动在动物模型上开展进一步实验,以证明单次干预使用这种材料以及其他适合这种操作的抗病毒药物在预防这些病毒重新激活方面的疗效。此外,这种类型的治疗在其有效寿命结束后不会留下任何痕迹,因为药物会释放,聚合物基质会降解。