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Intranasal Administration of Milnacipran in Rats: Evaluation of the Transport of Drugs to the Systemic Circulation and Central Nervous System and the Pharmacological Effect

机译:大鼠米那普仑的鼻内给药:药物向全身循环和中枢神经系统的运输及其药理作用的评估

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摘要

Recently, transnasal drug delivery has attracted a great deal of attention as an administration route to deliver drugs directly to the central nervous systems (CNS) and drug targeting of the CNS is expected to increase. In the present study, we investigated the possibility of using a transnasal delivery system for milnacipran, a serotonin?noradrenaline reuptake inhibitor (SNRI), by evaluating the transport to the systemic circulation and cerebrospinal fluid (CSF) and the pharmacological effect after intranasal (i.n.) administration. Moreover, the effect of chitosan as a bioadhesive material on the transport to the systemic circulation and CSF and the pharmacological effect after i.n. administration were evaluated. As a result, i.n. administration of milnacipran was found to produce a higher direct delivery to the CNS as well as to the systemic circulation, suggesting that this is a promising route of administration and an alternative to peroral (p.o.) administration. Furthermore, the i.n. co-administration with chitosan led to increased plasma and CSF concentrations and an enhanced pharmacological effect, evaluated by means of the forced swimming test. The results suggested that chitosan produced a long residence time of milnacipran in the nasal cavity due to its bioadhesive effect, leading to the enhanced transport of milnacipran from the systemic circulation to the CNS via the blood?brain barrier by an increase in systemic absorption as well as direct transport to the CNS, resulting in a higher antidepressant effect compared to that with p.o. administration.
机译:近来,作为将药物直接递送到中枢神经系统(CNS)的给药途径,经鼻给药已经引起了极大的关注,并且预期CNS的靶向药物将会增加。在本研究中,我们通过评估转运至全身循环和脑脊髓液(CSF)的剂量以及鼻内给药(in)后的药理作用,研究了使用米那普仑,5-羟色胺去甲肾上腺素再摄取抑制剂(SNRI)的鼻腔给药系统的可能性。 )管理。此外,壳聚糖作为生物粘附材料对输运至全身循环和脑脊液的作用以及i.n.之后的药理作用。管理进行了评估。结果,发现米那普仑的给药可产生更高的直接递送至中枢神经系统以及全身循环,这表明这是一种有希望的给药途径,也是经口(p.o.)给药的替代方法。此外,与壳聚糖合用可导致血浆和脑脊液浓度增加,并通过强制游泳试验评估其药理作用增强。结果表明,壳聚糖由于其生物粘附作用而在鼻腔中产生了较长的滞留时间,并通过增加全身吸收而导致了缓释剂从血液循环通过血脑屏障从全身循环到中枢神经系统转运。作为直接转运至中枢神经系统的药物,与抗抑郁药相比具有更高的抗抑郁作用管理。

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