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Tedavide H?zl? Sal?n?ml? ve Uzat?lm?? Sal?n?ml? Formülasyonlar?n Farklar?

机译:治疗快吗?萨尔吗?和扩展?萨尔吗?配方差异?

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?ZET?lac?n farmakokinetik ?zellikleri doz aral??? ba?ta olmak üzere, uygulama bi?imi, yükleme dozu, kararl? durum konsantrasyonuna ula?ma süresi gibi bir dizi ?l?ütü belirler. Bu ?l?ütlerin ideal uygulamaya uygun hale getirilmesi i?in ilac?n farmas?tik bi?imi de?i?tirilerek uzat?lm??, yava?lat?lm?? gibi de?i?tirilmi? sal?n?ml? formülasyonlar olu?turularak ilac?n emildi?i yerde serbestlenme paterninin farkl?la?t?r?lmas? s?k ba?vurulan bir y?ntemdir. B?ylece ilac?n daha seyrek aral?klarla uygulanmas?, tepe konsantrasyon artt?r?lmadan h?zl? yükleme yap?lmas?, kararl? durum konsantrasyonuna daha h?zl? ula??lmas? mümkün olur. Bunun klinik sonu?lar?; etkilili?in artt?r?lmas?, istenmeyen etkilerin azalmas?, farmako-kinetik ?l?ütlerde dolay?s?yla klinik etkide dalgalanmalar?n azalt?lmas?, hasta uyuncunun artmas? ve tedavi maliyetinin azalt?lmas? olabilir. Bu yaz?da an?lan a??lardan Ketiapin XR (uzat?lm?? sal?n?ml?) formülasyonu incelenmi?tir.The pharmacokinetics of drugs determine some of the parameters such as the dosing frequency, the route of administration, starting dose, time to reach the steady-state concentration etc. In order to adjust these parameters to provide the ideal administration; modifying the releasing pattern at the absorption site by creating formulations with different drug releasing patterns, such as extended or sustained release is a common practice. As a resu the drug can be applied less frequently, the initiation can be faster without increasing the peak plasma concentration and the steady-state concentration can be reached faster. The possible clinical outcomes are; increasing the efficacy, better tolerability, less variability of pharmacokinetic measures as well as the clinical effects, improving the treatment compliance and lower treatment costs. This article aims to evaluate quetiapine XR (extended release) from this point of view.
机译:ZET?Lac?N的剂量范围为?主要是给药形式,负荷剂量,稳定吗?达到情况集中所需的时间决定了铁的数量。为了使这些措施适合于理想的应用,对药物的药物形式进行了更改,扩展和减慢。喜欢吗?萨尔吗?通过创建制剂吸收药物的释放方式的差异?这是一种经常使用的方法。因此,在不增加峰值浓度的情况下,以较小的频率间隔快速给药是不是很快?安装?,稳定?更快地集中情况?达到?成为可能。这种临床后果?提高药效,减少不良作用,减少由于药代动力学措施引起的临床效果波动,提高患者依从性。并减少治疗费用?也许。药物的药代动力学决定了一些参数,例如给药频率,给药途径。 ,起始剂量,达到稳态浓度的时间等。为了调整这些参数以提供理想的管理;通过创建具有不同药物释放模式的制剂(例如延长释放或持续释放)来改变吸收部位的释放模式是一种常见的做法。结果是;可以减少药物的使用频率,在不增加血浆峰值浓度的情况下可以更快地启动药物,并且可以更快地达到稳态浓度。可能的临床结果是;提高疗效,更好的耐受性,药代动力学措施的可变性以及临床效果,改善治疗依从性并降低治疗成本。本文旨在从这种角度评估喹硫平XR(扩展版)。

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