Sharma Rishi, Kim Soo-Young, Sharma Anjali, Zhang Zhi, Kambhampati Siva Pramodh, Kannan Sujatha, Kannan Rangaramanujam M
Center for Nanomedicine, Department of Ophthalmology, Wilmer Eye Institute Johns Hopkins University School of Medicine , Baltimore, Maryland 21231, United States.
Department of Anesthesiology and Critical Care Medicine, Johns Hopkins University School of Medicine , Baltimore, Maryland 21287, United States.
Bioconjug Chem. 2017 Nov 15;28(11):2874-2886. doi: 10.1021/acs.bioconjchem.7b00569. Epub 2017 Oct 27.
Brain-related disorders have outmatched cancer and cardiovascular diseases worldwide as the leading cause of morbidity and mortality. The lack of effective therapies and the relatively dry central nervous system (CNS) drug pipeline pose formidable challenge. Superior, targeted delivery of current clinically approved drugs may offer significant potential. Minocycline has shown promise for the treatment of neurological diseases owing to its ability to penetrate the blood-brain barrier (BBB) and potency. Despite its potential in the clinic and in preclinical models, the high doses needed to affect a positive therapeutic response have led to side effects. Targeted delivery of minocycline to the injured site and injured cells in the brain can be highly beneficial. Systemically administered hydroxyl poly(amidoamine) (PAMAM) generation-6 (G6) dendrimers have a longer blood circulation time and have been shown to cross the impaired BBB. We have successfully prepared and characterized the in vitro efficacy and in vivo targeting ability of hydroxyl-G6 PAMAM dendrimer-9-amino-minocycline conjugate (D-mino). Minocycline is a challenging drug to carry out chemical transformations due to its inherent instability. We used a combination of a highly efficient and mild copper catalyzed azide-alkyne click reaction (CuAAC) along with microwave energy to conjugate 9-amino-minocycline (mino) to the dendrimer surface via enzyme responsive linkages. D-mino was further evaluated for anti-inflammatory and antioxidant activity in lipopolysaccharides-activated murine microglial cells. D-mino conjugates enhanced the intracellular availability of the drug due to their rapid uptake, suppressed inflammatory cytokine tumor necrosis factor α (TNF-α) production, and reduced oxidative stress by suppressing nitric oxide production, all significantly better than the free drug. Fluorescently labeled dendrimer conjugate (Cy5-D-mino) was systematically administered (intravenous, 55 mg/kg) on postnatal day 1 to rabbit kits with a clinically relevant phenotype of cerebral palsy. The in vivo imaging study indicates that Cy5-D-mino crossed the impaired blood-brain barrier and co-localized with activated microglia at the periventricular white matter areas, including the corpus callosum and the angle of the lateral ventricle, with significant implications for positive therapeutic outcomes. The enhanced efficacy of D-mino, when combined with the inherent neuroinflammation-targeting capability of the PAMAM dendrimers, may provide new opportunities for targeted drug delivery to treat neurological disorders.
在全球范围内,与脑相关的疾病已超过癌症和心血管疾病,成为发病和死亡的主要原因。缺乏有效的治疗方法以及相对枯竭的中枢神经系统(CNS)药物研发渠道构成了巨大挑战。对当前临床批准药物进行卓越的靶向递送可能具有重大潜力。米诺环素因其能够穿透血脑屏障(BBB)以及具有药效,已显示出治疗神经疾病的前景。尽管其在临床和临床前模型中具有潜力,但产生积极治疗反应所需的高剂量已导致副作用。将米诺环素靶向递送至脑内的损伤部位和损伤细胞可能非常有益。全身给药的第6代(G6)羟基聚(酰胺胺)(PAMAM)树枝状大分子具有更长的血液循环时间,并且已显示可穿过受损的血脑屏障。我们已成功制备并表征了羟基-G6 PAMAM树枝状大分子-9-氨基-米诺环素缀合物(D-米诺)的体外功效和体内靶向能力。由于米诺环素固有的不稳定性,它是一种难以进行化学转化的药物。我们使用了高效温和的铜催化叠氮化物-炔烃环加成反应(CuAAC)与微波能量相结合的方法,通过酶响应连接将9-氨基-米诺环素(米诺)缀合到树枝状大分子表面。进一步评估了D-米诺在脂多糖激活的小鼠小胶质细胞中的抗炎和抗氧化活性。D-米诺缀合物由于其快速摄取而提高了药物的细胞内可用性,抑制了炎性细胞因子肿瘤坏死因子α(TNF-α)的产生,并通过抑制一氧化氮的产生降低了氧化应激,所有这些均明显优于游离药物。在出生后第1天,将荧光标记的树枝状大分子缀合物(Cy5-D-米诺)以55 mg/kg的剂量静脉注射给具有脑性瘫痪临床相关表型的兔仔。体内成像研究表明,Cy5-D-米诺穿过受损的血脑屏障,并与脑室周围白质区域(包括胼胝体和侧脑室角)的活化小胶质细胞共定位,这对积极的治疗结果具有重要意义。D-米诺增强的功效与PAMAM树枝状大分子固有的神经炎症靶向能力相结合,可能为靶向药物递送治疗神经疾病提供新的机会。